Mitarbeiter/in in der Tierpflege (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

Seit fast 75 Jahren arbeiten die Mitarbeiter von Charles River zusammen, um bei der Entdeckung, Entwicklung und sicheren Herstellung neuer Arzneimitteltherapien zu helfen. Wenn Sie sich unserer Familie anschließen, haben Sie einen bedeutenden Einfluss auf die Gesundheit und das Wohlbefinden der Menschen auf der ganzen Welt. Ob Ihr Hintergrund in Life Sciences, Finanzen, IT, Vertrieb oder einem anderen Bereich ist, Ihre Fähigkeiten werden eine wichtige Rolle bei der Arbeit spielen, die wir durchführen. Im Gegenzug helfen wir Ihnen, eine Karriere zu bauen, die Sie begeistern wird.

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierpfleger / Mitarbeiter in der Tierbetreuung (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

Betreuung, Zucht und Haltung unserer Labornager
Einhaltung der internen Qualitätsvorgaben und Arbeit unter sterilen Bedingungen
Dokumentationserstellung
Mitarbeit an der Verbesserung von Arbeitsabläufen

Die Anforderungen:

Freude am professionellen Umgang mit Tieren
Teamgeist
Einsatzbereitschaft und Sorgfalt
Körperliche Belastbarkeit
EDV-Kenntnisse erwünscht

Unser Angebot:

· eine ausführliche und betreute Einarbeitung im Rahmen unseres Trainingskonzepts

· ein leistungsgerechtes Einkommen

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

· Teilnahme an diversen Unternehmensveranstaltungen

· zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, Tankgutschein, VWL-Förderung u.v.m.)

Auch Bewerber ohne spezifische Vorkenntnisse/ Quereinsteiger sind uns willkommen!

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com, www.criver.com

Für Vorabinformationen stehen wir Ihnen gerne unter der Telefonnummer 09761 406-11 zur Verfügung.

Über Research Models & Services

Für die Grundlagenforschung ist die Verwendung von In-vivo-Modellen zur Identifikation von Zielkrankheiten und potentieller biologischer Pfade, welche Krankheiten bestimmen, notwendig. Als eines der weltweit führenden Unternehmen für die Produktion und den Vertrieb von Versuchstieren der höchsten Qualität, welches die Hälfte aller Versuchstiermodelle weltweit für die präklinische Forschung liefert, verstehen wir, wie wichtig dieser Schritt ist. Mit sieben Jahrzehnten Erfahrung ist unser Know-how unerreicht, sodass wir das perfekte Modell liefern können, einschließlich krankheitsspezifischer und konditionierter Optionen, für die Grundlagenforschung und darüber hinaus.

Über Charles River

Charles River ist ein auf die Frühphase der Wirkstoffentwicklung spezialisiertes Auftragsforschungsunternehmen (CRO). Wir haben auf der Grundlage unserer Erfahrungen mit Versuchstiermedizin und -wissenschaft ein vielseitiges Portfolio von Discovery- und Sicherheitsprüfungsdienstleistungen aufgebaut, sowohl mit Good Laboratory Practice (GLP) und ohne GLP, um Kunden von der Wirkstoffidentifikation bis zur präklinischen Entwicklung zu unterstützen. Charles River bietet auch eine Reihe von Produkten und Dienstleistungen für klinische Labortestbedürfnisse und Herstellungsaktivitäten. Die Nutzung dieses breiten Portfolios von Produkten und Dienstleistungen ermöglicht unseren Kunden, ein flexibleres Medikamentenentwicklungsmodell zu entwickeln, wodurch die Kosten gesenkt, die Produktivität erhöht und die Markteinführung beschleunigt wird.

Mit über 20.000 Mitarbeitern in 110 Standorten in 20 Ländern rund um den Globus sind wir strategisch positioniert, weltweite Ressourcen zu koordinieren und multidisziplinäre Projekte für die Entwicklung und Herausforderungen unserer Kunden zu entwickeln. Unsere Kundenbasis umfasst globale Pharmaunternehmen, Biotechnologieunternehmen, Behörden und Krankenhäuser sowie akademische Institutionen in der ganzen Welt.

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von etwa 86% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Bei Charles River Laboratories erkennen wir alle Talente an und stellen sie ein. Wir sind ein Unternehmen, das sich dem Grundsatz der Vielfalt und Inklusion verpflichtet hat und täglich in diese Richtung arbeitet.

Weitere Informationen finden Sie unter www.criver.com.

Veterinary Technician I - $5,000 Sign On Bonus! (Reno, NV, US, 89511)

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

***Position is eligible for a $5,000 sign on bonus!***

The Veterinary Technician 1 is responsible for assisting the veterinarians in documentation, triage, and management of laboratory animal health cases. Also responsible for daily health observations, preventive health care, environmental enrichment and handling and restraining of laboratory animals.

Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Attending Veterinarian.
Perform routine veterinary technical skills including the following:
Assess and follow-up on animal health concerns
Generate animal treatment records and perform, track and schedule follow-ups
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/teeth clipping/trimming.
Venipuncture techniques.
Perform radiographs as required.
Daily walk through of animal rooms
Proficient animal restraint techniques.
Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
Monitor animal health, visually, and by following detailed schedules.
Generate animal treatment records and perform, track and schedule follow-ups.
Maintain appropriate medical records for each animal in accordance with study and regulatory requirements. Assist in maintaining accurate record keeping procedures for the veterinary department.
Maintain and follow complex procedures to ensure appropriate animal health and treatment.
Assist in providing leadership, animal health training, and guidance to other laboratory personnel.
Assist in keeping inventory and stocking the vet rooms (i.e., drugs and supplies). Assist in organizing and maintaining the vet exam rooms.
Responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.

Job Qualifications

Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above if the individual is credentialed as a Certified Veterinary Technician.
LVT license or CVT/RVT certification preferred. Uncertified candidates must have Vet Tech in Training (VTIT) and will be required to receive certification within 12-18 months or show that certification has been substantially completed. AALAS certification desired.

The pay range for this position is $28.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Pendant 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Sommaire de l'emploi

En tant que Commis aux soins des animaux pour notre site d’élevage situé à St-Constant, vous serez responsable du bien-être de nos animaux de recherche. Votre réussite assurera la santé de nos animaux.

Dans ce poste, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie (nettoyer les salles d’animaux ainsi que les cages);
Manipuler les animaux avec soins;
Participer aux activités physiques/sociales des animaux.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

AEP en soins animaliers (atout);
Apte à travailler physiquement (soulever jusqu’à 20-25kg, marcher, rester debout, s’accroupir, etc.);
Avoir un bon esprit d’équipe;
Passion pour les animaux.

Informations spécifiques au poste:

Localisation : 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Du lundi au vendredi, entre 6h00 et 14h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaire ainsi que des fin de semaine;
Poste temps plein, 40 heures par semaine;
Poste temporaire à l’embauche & après la période de probation de 6 mois, poste permanent.

Pourquoi Charles River?

Aucune expérience préalable requise;
Des heures garanties, car le milieu de la recherche est très en demande;
Excellent programme de formation continue;
Opportunités de développement professionnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos des modèles et services de recherche
Indispensable dans la recherche fondamentale et la découverte, l'utilisation de modèles in vivo nous aide à cibler certaines maladies et à déterminer les voies d'intervention biologiques potentielles qui permettent de contrôler l'évolution de la maladie. En notre qualité de leader mondial dans la production et la distribution d'animaux de recherche de qualité supérieure, avec un modèle sur deux produit pour la recherche préclinique à l'échelle mondiale, nous sommes bien placés pour comprendre l'importance de cette étape. Grâce à nos sept décennies d'expérience, notre expertise est inégalée, ce qui nous permet de mettre à votre disposition le modèle parfait, y compris des options spécifiques à une maladie et pré-conditionnées, pour la recherche fondamentale et au-delà.

À propos de Charles River
Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Avec plus de 20 000 collaborateurs sur 110 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

As an Animal Care Clerk for our Husbandry facility located in St-Constant, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals.

In this role, primary responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry (clean the animal rooms and the cages);
Handle animals with care;
Participate in the physical/social activities of the animals.

Job Qualifications

If you possess the following qualifications, we will train you in the rest:

AEP in Animal Care (asset);
Able to work physically (lift up to 20-25 kg, walk, stand, stoop, etc.);
Have a good team spirit;
Passion for animals.

Role Specific Information:

Location: 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport: Free parking;
Salary: $18/hrs;
Schedule: Monday to Friday, between 6:00 am to 2:15 pm. Depending on the needs, you may have to do weekends and/or overtime;
Full-time position, 40 hours per week;
Temporary position at the hiring & after the probation period of 6 months, permanent position.

Why Charles River ?

No experience needed;
Guaranteed hours - The research field is in high demand;
Paid development training;
Professional development opportunities.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Research Models & Services
Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Data Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Data Scientist, you will play a critical role in the process to help unlocking the value of data.

In this role, primary responsibilities include:

Lead and execute end to end data science projects, including problem formulation, data exploration, model development, validation, deployment and ongoing optimization for mission critical applications;
Collaborate closely with the Data Analysts team, Data Engineering team and DataOps team to automate and integrate data science solutions seamlessly into production pipelines;
Work collaboratively, in a consultative way, across the business units, advising on best approaches to leveraging data science in the most effective and efficient manner, including utilizing Generative AI technologies where applicable to develop cutting-edge solutions.

Key Elements

We are looking for the following minimum qualifications for this role:

Master’s with a minimum of 5 years’ experience or Bachelor’s with a minimum of 7 years’ experience in Data science, Computer science, Statistics, Operations research, applied mathematics, applied physics or any related field;
Excellent analytical and problem-solving skills with the ability to approach challenges creatively;
Strong communication skills to translate the findings into actionable business recommendations through rich data visualization;
Familiar with Agile methodologies and tools;
Self-driven and capable of working both independently and collaboratively within a team setting.

Technical Expertise required:

Minimum of 5 years’ hands-on experience processing and analyzing large data sets;
Minimum of 3 years’ experience with the full Machine Learning product lifecycle process and able to take the initiative in making sure deadlines and requirements are met proactively;
Minimum of 5 years’ experience working with development toolsets such as SQL, PySpark, Python, Pandas, Scala;
Minimum of 2 years’ experience in data science projects focused on marketing, sales, or customer experience, delivering insights that drive business impact.

Role Specific Information:

Location: Remote
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientifique de données sénior (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique de données sénior, vous allez jouer un rôle essentiel dans le processus visant à libérer la valeur des données.

Dans ce poste, les principales responsabilités incluront:

Diriger et exécuter des projets de science des données de bout en bout, y compris la formulation de problèmes, l'exploration de données, le développement de modèles, la validation, le déploiement et l'optimisation continue pour les applications critiques;
Collaborer étroitement avec l'équipe d'analystes de données, l'équipe d'ingénierie de données et l'équipe DataOps afin d'automatiser et d'intégrer les solutions de science des données de manière transparente dans les pipelines de production;
Travailler en collaboration, de manière consultative, avec les unités opérationnelles, en donnant des conseils sur les meilleures approches pour tirer parti de la science des données de la manière la plus efficace et la plus efficiente, y compris en utilisant les technologies d'IA générative, le cas échéant, pour développer des solutions de pointe.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Maitrise avec un minimum de 5 ans d'expérience ou Baccalauréat avec un minimum de 7 ans d'expérience en science des données, informatique, statistiques, recherche opérationnelle, mathématiques appliquées, physique appliquée ou tout autre domaine connexe;
Excellentes compétences en matière d'analyse et de résolution de problèmes, avec la capacité d'aborder les défis de manière créative;
Solides compétences en communication pour traduire les résultats en recommandations commerciales exploitables par le biais d'une riche visualisation des données;
Familiarité avec les méthodologies et les outils Agile;
Autonome et capable de travailler à la fois de manière indépendante et en collaboration au sein d'une équipe.

Expertise technique requise :

Au moins 5 ans d'expérience pratique dans le traitement et l'analyse de grands ensembles de données;
Au moins 3 ans d'expérience avec le processus complet du cycle de vie d'un produit d'apprentissage automatique et capacité à prendre l'initiative pour s'assurer que les délais et les exigences sont respectés de manière proactive;
Au moins 5 ans d'expérience dans l'utilisation d'outils de développement tels que SQL, PySpark, Python, Pandas, Scala;
Minimum 2 ans d’expérience dans des projets de science des données axés sur le marketing, les ventes, ou l’expérience client, fournissant des informations qui ont un impact sur les affaires.

Informations spécifiques au poste:

Localisation: Télétravail
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos de l'évaluation de la sécurité
Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

Pour plus d'information, consultez www.criver.com.

Technicien de Laboratoire en Immunologie - H/F - CDI (Evreux, FR, 27930)

Depuis plus de 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Qui sommes-nous ?

Le site Charles River d’Evreux est un site unique de 2 hectares, situé aux portes de la Normandie. Il offre un environnement scientifique innovant, dynamique et convivial où près de 500 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Le département Biomarkers recrute un Technicien en Immunologie pour intégrer son équipe composée de 15 techniciens.

Les missions

Au sein du Département Biomarkers, vous aurez pour principales missions sous la responsabilité du responsable du service :
•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique et possédez au minimum 3 ans d’expérience sur un poste similaire.
Connaissances en culture cellulaire (Elispot).
Vous maitrisez l’anglais et possédez une aisance relationnelle et un sens du contact et du service.
Vous êtes organisé(e), vous appréciez de travailler en équipe.
Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.

Les modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 3
•   Contrat : CDI Non-cadre (accord de modulation 35h)
•   Salaire : A compter de 24 500 € bruts / an sur 13 mois
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Primes de transport, d’intéressement/participation, accord d’ancienneté
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

À propos de Charles River

Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Avec plus de 20 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.

Pour plus d'information, consultez www.criver.com

Production Technician (m/f/d) 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit, die Teil unseres Produktionsteams für Reagenzien werden möchte.

Ihre Tätigkeit:

• Sie arbeiten direkt an den Produktionsmaschinen zur Abfüllung und Etikettierung von Reagenzien und dokumentieren die Tätigkeiten nach Vorgabe.

• Sie unterstützen beim Reinigen und Einrichten der Maschinen nach externen (GMP, ISO 9001) und internen Standards

• Sie helfen beim Reinigen von Hilfsmitteln und Vorbereiten von Rohmaterialen für die Produktion

• Sie stellen die Ausführung der übertragenen Aufgaben und Aufträge gemäß den vorliegenden Arbeitsstandards sicher.

Gerne mit einer abgeschlossenen Berufsausbildung, gleich welcher Branche, gerne Quereinsteiger (m/w/d) mit oder ohne produktionstechnische Kenntnisse.

Sie verfügen über:

• Interesse und Verständnis für technische Zusammenhänge und unsere hohen Hygieneanforderungen.

• Sichereren Umgang mit automatisierten Maschinen, handwerkliches Geschick.

• Hohes Sicherheitsempfinden und Verantwortungsbewusstsein

• Strukturiertes, zielorientiertes Arbeiten, hohe Verlässlichkeit und Flexibilität,

• Team- und Kommunikationsfähigkeit, Serviceorientierung

• Gute Deutschkenntnisse sind unerlässlich. Englischkenntnisse sind wünschenswert.

Wir bieten:

• Eine befristete Vollzeitstelle mit abwechslungsreichen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen

• Aktive Mitgestaltung Ihres Aufgabengebietes in einem hoch motivierten Team mit flachen Hierarchien

• Weiterentwicklung und die Möglichkeit, mehr Verantwortung zu übernehmen und innerhalb des Unternehmens zu wachsen

• Eine intensive Einarbeitung

• Flexible Arbeitszeiten

• Wettbewerbsfähige Vergütung

We are looking for a full-time person to become part of our reagent production team.

Your Tasks:

• You work directly on the production machines for filling and labelling reagents and document the activities according to specifications.

• You assist in cleaning and setting up the machines according to external (GMP, ISO 9001) and internal standards.

• You assist in cleaning auxiliary materials and preparing raw materials and for production.

• You ensure the execution of the assigned tasks and orders in accordance with the present work standards.

A completed vocational training is desirable, regardless of the industry, we welcome career changers (m/f/d) with or without technical production knowledge.

You have:

• Interest in and understanding of technical interrelationships and our high hygiene requirements.

• Confident handling of automated machines, manual dexterity.

• High sense of safety and responsibility

• Structured, goal-oriented work, high reliability and flexibility,

• Team and communication skills, service orientation

• Good German language skills are essential. Knowledge of English is desirable.

We offer:

• A full-time position (2 year fixed term contract) with varied, challenging activities in a future-oriented company

• Active participation in shaping your area of responsibility in a highly motivated team with flat hierarchies.

• Further development and the opportunity to take on more responsibility and grow within the company.

• An intensive induction

• Flexible working hours

• Competitive remuneration

About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

For more information, please visit www.criver.com.

Production Technician (m/w/d) 1 1 1 1 1 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit mit chemisch/biologischem Hintergrund (BTA,CTA,PTA, auch B.Sc. oder M.Sc.) die Teil unseres Produktions-Teams unserer Reagenzien werden möchte.

Unterstützen Sie uns bei:
•   der Bulk-Herstellung der Reagenzien (im 1-200 L Maßstab),
•   In-Prozess-Kontrollen und Freigabe-Prüfungen
•   der Aufreinigung einiger unserer Rohstoffe mittels HPLC
•   weiteren Prozessschritten (Abfüllung, Gefriertrocknung, Autoklavieren etc.)
•   der Aufrechterhaltung unseres ISO Systems und der Einhaltung der Vorgaben der Guten Herstellungspraxis (GMP)

Überzeugen Sie uns durch:
•   gute Team- und Kommunikationsfähigkeit
•   strukturiertes und auf das Ziel fokussiertes Arbeiten, Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
•   Gute Deutsch- und Englisch Sprachkenntnisse

Wir bieten:
•   eine unbefristete Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
•   eine aktive Mitgestaltung Ihres Tätigkeitsfeldes in einem sehr motivierten Team mit flachen Hierarchien
•   Weiterentwicklung uns Spezialisierung
•   eine intensive Einarbeitung
•   flexible Arbeitszeiten
•   eine angemessene Vergütung

Haben wir Ihr Interesse geweckt?
Wenn ja, bewerben Sie sich bitte unter Angabe der Referenz „Production Technician“ mit Ihren aussagekräftigen Bewerbungsunterlagen, Ihrem frühestmöglichen Eintrittstermin sowie Ihren Gehaltsvorstellungen. Wir freuen uns auf Ihre Bewerbung.

Über Microbial Solutions

Unsere Gruppe „Microbial Solutions“ verfügt über ein umfassendes Portfolio für Endotoxin-Tests, mikrobielle Detektion sowie mikrobielle Identifikationsprodukte und -dienstleistungen, das seinesgleichen sucht und das gezielt entwickelt wurde, um die komplexen und sich ständig ändernden Anforderungen der Branche zu erfüllen. Wir helfen unseren Kunden, die Produktsicherheit und -qualität durch einfach zu verwendende und robuste Testlösungen sicherzustellen, die behördliche Anforderungen erfüllen, kritische Entscheidungsfindung ermöglichen und die operative Effizienz verbessern.

Über Charles River

Mit über 20.000 Mitarbeitern in 90 Standorten in 20 Ländern rund um den Globus sind wir strategisch positioniert, weltweite Ressourcen zu koordinieren und multidisziplinäre Projekte für die Entwicklung und Herausforderungen unserer Kunden zu entwickeln. Unsere Kundenbasis umfasst globale Pharmaunternehmen, Biotechnologieunternehmen, Behörden und Krankenhäuser sowie akademische Institutionen in der ganzen Welt.

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von etwa 85% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Information en finden Sie unter www.criver.com.

Scientific Research In Vitro - Associate (Szeged, HU)

A Charles River munkatársai 75 éve dolgoznak azon, hogy új gyógyszeres terápiák felfedezésében, fejlesztésében és biztonságos előállításában segédkezzenek. Ha csatlakozol ehhez a nagy családhoz, lehetőséged nyílik arra hogy jobbá tedd az emberek egészségét és jóllétét világszerte. Minannyiunk tudása és képessége fontos szerepet játszik a munkánkban függetlenül attól, hogy eddigi tapasztalataidat élettudományi, pénzügyi, informatikai, értékesítési vagy más területen szerezted. Cserébe segítünk egy sikeres karrier felépítésében.

Job Summary

Főbb feladatok:

- Validálásokhoz, kutatásokhoz kapcsolódó in-vitro mérések elvégzése (elsődleges feladat)
- Emlős sejtek fenntartása és kezelése, steril munkavégzés
- Laboratóriumi munka technikai előkészítése
- Oldatok, pufferek, törzsoldatok készítése
- Laboreszközök, műszerek használata, karbantartása
- Adminisztratív jellegű laboratóriumi feladatok ellátása

Job Qualifications

Az álláshoz tartozó elvárások:

- Legalább középfokú szakirányú végzettség
- Hasonló területen szerzett laboratóriumi tapasztalat - min. 2 év
- Jártasság általános laboreszközök használatában
- Önálló, precíz, felelősségteljes munkavégzés
- Dinamikus, nyitott, rugalmas, csapatjátékos személyiség
- Angol nyelvismeret
- Felhasználói szintű MS Office alkalmazások ismerete (Word, Excel)
- ISO 9001 minőségbiztosítási rendszerben való jártasság előny

A Discovery részlegről

A Charles River Discovery részlege az ipar által is bizonyítottan sikeres új terápiák fejlesztése terén. Az elmúlt 17 évben 320 új szabadalmat és 74 preklinikai gyógyszerkészítményt állítottunk elő megbízóink részére. Több mint 650 tudós által kidolgozott átfogó, integrált portfóliónk a legújabb technológiákat és platformokat alkalmazza, hogy kémiai, biológiai és farmakológiai szolgáltatásokat nyújtson, ezzel támogatva ügyfeleinket a preklinikai gyóyszerfejlesztési folyamaton át. Ügyfélközpontúak vagyunk, és együttműködéssel érjük el a valódi partnerkapcsolatok kialakulását, melyek során felmérjük az esetleges kihívásokat, legyőzzük az akadályokat és együtt haladunk azon az úton mely során új gyógyszereket juttatunk a piacra.

A Charles Riverről

A Charles River egy szolgáltató cég, mely a gyógyszerfejlesztés korai fázisára nyújt megoldásokat. Építkezve a laboratóriumi állatgyógyászati és tudományos alapjainkra egy széleskörű portfóliót hoztunk létre a gyógyszerfejlesztés preklinikai fázisaira koncentrálva (discovery és safety). Mind GLP és non-GLP rendszerben kínálunk vizsgálatokat a kezdeti lépésektől (target identification) a preklinikai fejlesztésekig. A Charles Rivernél termék- és szolgáltatáscsomagot is kínálunk, hogy segítsük ügyfeleink klinikai vizsgálatait és gyártási tevékenységüket. Ennek a széles termék- és szolgáltatás portfóliónak köszönhetően ügyfeleink egy rugalmasabb gyógyszerfejlesztési modellt hozhatnak létre, mely csökkenti a költségeiket, növeli a termelékenységüket és hatékonyságukat, hogy ezáltal gyorsabban léphessenek piacra.

A világ 20 országában, 110 telephelyen több, mint 20.000 munkavállalónkkal stratégiai helyzetben vagyunk, hogy összehangoljuk az erőforrásainkat és multidiszciplináris szempontokat alkalmazzunk ügyfeleink egyedi kihívásainak megoldásában. Ügyfélkörünk globális gyógyszergyárakból, biotechnológiai cégekből, kormányszervekből, klinikákból és akadémiai intézményekből áll szerte a világon.

A Charles Rivernél elkötelezettek vagyunk hogy javítsuk az emberek életminőségét. Küldetésünk, kitűnő tudományos hátterünk és erős céltudatosságunk vezérel minket mindenben amit teszünk, és minden napot azzal a nézettel közelítünk meg, hogy a munkánk segít az emberek egészségén és jóllétének javításán világszerte. Büszkék vagyunk arra, hogy az elmúlt öt évben az FDA által jóváhagyott gyógyszerek mintegy 80%-át mi fejlesztettük ki.

További információért látogass el a honlapra www.criver.com

Manufacturing Specialist (Rockville, MD, US, 20850)

Job Summary

The Manufacturing Specialist is a key technical contributor responsible for process optimizations, manufacturing troubleshooting, continuous improvement initiatives to ensure Manufacturing consistently produces quality product. This role sits at the intersection of operational excellence, quality, training & development, and MSAT supporting efficient, compliant, and ever improving operations.

The ideal candidate will have a strong understanding of cGMP compliance, quality event investigation, lean production methodologies, and process technology to drive reliability in operations.

Key Responsibilities and Duties:

Process Improvement & Optimization

Identify and implement continuous improvement projects using Lean methodologies to improve and stabilize yield, efficiency, and process success.
Partner with MS&T and Process Development to monitor process performance to identify data-driven solutions and enhancements.
Support technology transfer, process scale-up, and process validation to ensure smooth transitions into manufacturing.
Partner with MS&T and Engineering to optimize equipment utilization, automation strategies, and data analytics for real time adjustments and support.

Compliance & Manufacturing Support

Conduct timely batch record reviews and deviation investigations, ensuring long term resolution of documentation/instructional issues.
Lead root cause analysis and corrective/preventive action (CAPA) for process deviations, non-conformances, and quality issues.
Work close with Quality and Manufacturing teams to ensure documentation supports data integrity & good documentation practices (GDP) incompliance with FDA, EMA, guidelines.

Training and Documentation Management

Develop and maintain SOPs, training materials, and documentation systems for manufacturing compliance and process improvements.
Partner with MS&T and Training to conduct training programs for manufacturing staff to ensure adherence to cGMP, process guidelines, and quality requirements.
Work cross-functionally to ensure employees remain qualified and up to date on process and compliance expectations.

Job Qualifications

Bachelor’s degree in relevant Science or Engineering discipline preferred.
Minimum 3 years working within industry. Strong technical writing capabilities a plus.
Experience within cell/gene therapies, biologics, and/or cGMP regulated environment preferred
Knowledge of process improvement and lean methodologies preferred.
Ability to interpret and present complex scientific data in a clear and concise manner.
Proficient in Microsoft office suite and document management systems.
Strong organizational and project management skills.

Compensation Data

The pay range for this position is $68,712 - $87,200 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

In-Vivo Scientist I - Oncology (Worcester, MA, US, 01608)

Job Summary

We are seeking an experienced Scientist I, Oncology for our Discovery site located in Worcester, MA.

We are seeking a motivated, skilled scientist to work within the Oncology team in our Worcester site. While retaining an element of hands-on responsibility, this position is also largely focused upon leveraging the individual’s scientific strengths through the mentoring of more junior staff. This position requires competency of all aspects of oncology studies including the skills and techniques necessary to satisfy the overall study objectives.

Successful candidates in this position will:

Possess strong interpersonal skills with strong scientific curiosity, initiative and resourcefulness
Possess exceptional organizational and planning skills enabling management of multiple, concurrent tasks & priorities
Careful attention to detail and the accurate, organized and timely documentation of study data and report generation
Team orientation, highly collaborative and results-oriented focus
Self-driven and enthusiastic with the ability to thrive in a dynamic environment
Design and plan projects/protocols with occasional direction from senior staff.
Follow company BOPs and guidelines.
Mentor and train technicians.

The pay range for this position is $70,000 to $74,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

The following are minimum requirements related to the Scientist I position.

Education: Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Master's degree (M.S./M.A.) or Ph.D. preferred.
Experience: Minimum of 5 years previous directly related laboratory experience in a pharmaceutical or contract laboratory environment. Animal handling in lab setting is required. Experience with cancer tumor models and imaging is preferred.
Other: Exceptional analytical and problem solving capabilities. Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and Good Laboratory Practices (GLPs), as appropriate. Excellent written and verbal communication skills in a team environment. Able to prioritize work and meet deadlines under minimal direction. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Proficiency in the use of analytical instrumentation software with the ability to troubleshoot for routine and non-routine work.

Compensation Data

Competencies

Care - We show we care when we respect each other, our animals and the communities where we work and live, when we create a positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the right thing.

Collaborate -We collaborate when we partner with each other and promote teamwork, when we communicate clearly and effectively across the hall or around the globe, and when we welcome all forms of diversity and encourage inclusiveness.

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Own - We act like owners when we hold ourselves accountable for our actions, when we respond to internal and external client needs with speed and accuracy, when we set and achieve meaningful goals, and when we strive towards continuous improvement.

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

For more information, please visit www.criver.com.

Director, Pharmacology (Shrewsbury, MA, US, 01545)

Job Summary

Provide senior level business, scientific, and strategic leadership for Pharmacology (Oncology and Metabolism) locally with input globally:

o Manage and scale the Pharmacology (Oncology and Metabolism) business responsibly, with a balanced approach of prioritizing employees, client satisfaction, and operational efficiency while growing topline revenues and maintaining consistently high margins.

o Identify and foster science-related initiatives and capabilities.

o Provide a focal point for assessing program related needs and proposals for improvement and effect their implementation.

o Identify key science-based issues needing discussion at the appropriate meeting venue and contribute exemplary leadership in determining resolution of issues and advancement of scientific programs.

o Contribute to problem resolution of study related science-based issues.

o Provide scientists with guidance in the interpretation and reporting of data.

o Support key business financial, operational, client service, employee, quality goals and achieve targets.

o Encourage and support global collaboration across all sites involved in Pharmacology.

· Scope of work, report and protocol scientific review: Contribute to the interactions of the study directors, clients, and sponsors and provide scientific oversight for study design, preparation of protocols, interpretation of data, and preparation of reports. Interact with study directors and their supervisors to ensure reports are of high quality.

· Functional area(s) of expertise: Provide scientific oversight through both direct and indirect management of the Pharmacology (Oncology and Metabolism) functional areas including PDX, CDX, syngeneic tumor models, DIO, Type I and Type II diabetes, NASH, and new therapies. Identify and recommend innovative technologies, techniques, and/or cross-functional management of staff responsible for the specialty area. Work directly with operations staff in the functional area to resolve scientific and technical issues.

· Responsible for personnel management activities such as: macro scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.

· Work effectively with technical operations groups and direct activities of assigned group(s) to ensure optimal performance of the group/function. Identify and implement collaborative projects and synergies with other departments and sites.

· Support strategic planning in the functional area of Pharmacology (Oncology and Metabolism).

· Business development: Engage clients directly and as part of co-travel with Charles River commercial teams. Identify and evaluate new capabilities to expand the scientific base of the company. Represent Charles River at scientific meetings and support sales and marketing at local Charles River sponsored meetings on request.

· Preclinical function: Participate in cross-site initiatives related to scientific initiatives, harmonization of procedures, and standardization of Pharmacology processes, templates for protocols, and reports. Provide scientific and regulatory advice to the Pharmacology group and interact with colleagues in Laboratory Sciences and Toxicology.

The pay for this position is between $185,000 - $230,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: Veterinary or Medical degree (DVM/VMD, MD) and/or Ph.D. in Pharmacology- (Oncology and Metabolism) related discipline is preferred. Post-doctoral experience in a related discipline is a plus.
An equivalent combination of education and experience with documentation as a subject matter expert in the discipline of Pharmacology (Oncology and Metabolism) may be accepted as a satisfactory substitute for the requirements listed above.
Experience: Minimum of 10 years related experience in research or pharmaceutical environment. Management experience is essential.
Certification/Licensure: None required.
Other: Experience in use of desktop applications (word processing, spreadsheets, databases) and network navigation required.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Cagewash Technician I (Chicago, IL, US, 60637)

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.

Job Summary

We are seeking a Cagewash Attendant for our Insourcing Solutions site located in Chicago, IL.

As the Cagewash Technician, you will use existing SOPs and quality assurance standards to perform general housekeeping, as well as maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

Additional responsibilities include:

Sanitize, maintain, and repair animal caging materials
Ensure cagewash and animal holding facilities are kept in a clean and organized manner
Assist with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position:

High school diploma, General Education Degree (G.E.D.) or equivalent

Experience and/or training working with mechanical equipment preferred

The pay for this position is $17.94 per hour.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Insourcing Solutions
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

For more information, please visit www.criver.com.

研究模型饲养- 支持类-DIRECT LABOR 1 1 (Changping District, BJ, CN, 100107)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融，IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

关于研究模型与服务
基础研究和发现的基本方法是使用体内模型来帮助寻找疾病靶标并确定调节相应病症的潜在生物学通路。作为世界上生产和销售最优质研究动物的领军企业，其中全球临床前研究中使用的动物模型中有一半是我们生产的，我们了解这一步的重要性。凭借七十年的经验和无与伦比的的技术专长，我们能够为您提供完美的动物模型，包括特定疾病模型和预处理模型，可用于基础研究等等。

关于Charles River
Charles River是一家早期药物研发授权研究机构（CRO）。我们的业务是建立在实验室动物医学和科学基础之上，我们开发多样化的发现和安全评估服务组合，包括与实验室管理规范（GLP）和非实验室管理规范有关的服务，以在从靶标鉴定到临床前开发的整个流程中为客户提供支持。Charles River还提供一套支持客户的临床实验室测试需求和制造活动的产品和服务。利用广泛的产品和服务组合，我们的客户可以创建更灵活的药物开发模式，从而降低成本、提高效率和功效，并加快上市速度。

我们在全球各地20个国家和地区拥有110家设施及20000多名员工，我们在战略上能够协调全球资源并采取多学科视角来解决客户面对的独特挑战。我们的客户群包括世界各地的全球性制药公司、生物技术公司、政府机构、医院和学术机构。

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。我们支持了2021年FDA批准的所有药物中约86％的药物的开发工作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com。

Animal Care Technician I (San Diego, CA, US, 92121)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team, located in San Diego, CA.

As the Animal Care Technician I, you will provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

Required:
- Education: High school diploma, General Education Degree (G.E.D.)
Preferred:
- Education: Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred
- Experience: Directly related laboratory animal experience in a laboratory animal facility preferred.
- Certification/Licensure: Assistant Laboratory Animal Technician (ALAT) certification from AALAS preferred.

The pay range for this position is $20-22 USD per hour. Please note that salaries vary within the range based on factors including , skills, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Senior Associate Scientist- Manual Ion Channel Testing (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Senior Associate Scientist for our Manual Ion Channel Testing team at our Safety Assessment site located in Cleveland, Ohio.

The Manual Ion Channel Testing group is responsible for evaluating test article effects on ion channels in vitro. Personnel are responsible for operating and maintaining manual patch clamp electrophysiology workstations. Validated hardware and software systems are used to collect and analyze data under regulated (GLP) or non-regulated conditions. The group prepares, collects and transfers test article formulation samples to the CLE analytical chemistry unit (or other appropriate laboratory) for concentration verification and homogeneity analyses, and is responsible for interpretation and reporting of data outcomes

Essential Duties and Responsibilities: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight
Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area
Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight
Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations
Assist in problem solving for technical and/or regulatory issues with oversight
Responsible for writing and preparing study plans/protocols/amendments with minimal oversight
Participate in Sponsor visits/tours with minimal oversight
Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight
Perform data analysis using appropriate software with minimal oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with minimal oversight
Ensure scientific integrity of studies with minimal oversight
Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Write, review and approve deviations with oversight
Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Effectively manage a small portfolio of research projects including assay development and validation while ensuring timelines are met in a single operational area with oversight
Perform all other related duties as assigned

The pay range for this role is $75-78K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience. Master’s degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice
Ability to work under specific time constraints

Equal Employment Opportunity

For more information, please visit www.criver.com.

Directeur des Productions - F/H - CDI (L'Arbresle, FR, 69592)

Qui sommes-nous ?

Le site Charles River de Lyon est un site unique de 14 hectares, situé dans la vallée d'Azergues. Il offre un environnement scientifique innovant, dynamique et convivial où près de 1000 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Nous recherchons notre nouveau Directeur des productions F/H en CDI en charge de définir et piloter la stratégie pour l'ensemble des activités de production des modèles animaux, des services supports afférents (pré-zone, conditionnement et logistique) et des activités soumises au BPF et/ou cGMP sur les sites de l'Arbresle (69) et Châtillon sur Chalaronne (01) dans un contexte évolutif pour ces activités.

En tant que membre de Comité de direction, vous impulsez la définition d’actions garantissant l’intégration de votre département dans les objectifs et politiques générales de l’entreprise et du Groupe, en alignement avec la réglementation et nos standards exigeants.
Directement rattaché à notre Directeur Général, vous êtes responsable d’un département d'une centaine de personnes.

Vous jouez ainsi un rôle déterminant en assurant le bon déroulement, la conformité et la performance de l'ensemble des opérations de votre périmètre dans un environnement multisites, dans le respect des budgets, des procédures de l'entreprise et ce en vue d'obtenir le meilleur niveau de qualité possible.

Responsabilités principales

Garantir le développement de la culture, de la maturité et de la performance des activités de votre périmètre autour de 7 piliers majeurs : HSE, biosécurité, bien-être animal, sûreté, qualité, productivité et service client.

Sécuriser les activités en anticipant les risques, renforçant la culture sécurité et développant des actions de prévention en matière de sécurité, biosécurité et sûreté en lien avec les objectifs site
Assurer la productivité de votre département via le pilotage d’indicateurs clés de performance, en maîtrisant les coûts et garantissant l’efficacité de l’organisation
Être garant du respect des exigences réglementaires et de l’application des directives du groupe, proportionnellement aux réalités terrain et enjeux des activités.
Organiser et animer les équipes de votre département par un management structurant, engageant et orienté résultats. Assurer le développement des compétences et des talents en impulsant au quotidien une culture de transparence et de progrès.
Identifier et conduire des projets significatifs d'amélioration continue, de transformation ou d'investissement, dans un souci constant d'efficience.
Proposer aussi souvent que nécessaire les évolutions d'organisation permettant d'accomplir l'ensemble des missions ci-dessus de manière efficace
Tenir le rôle de représentant de l'entreprise auprès des clients, autorités, sociétés du groupe et autres partenaires extérieurs dans le périmètre de votre responsabilité.
Participer activement à la vie du Comité de direction, en apportant une vision opérationnelle, transverse et stratégique afin de faire progresser l’ensemble de l’organisation.

Profil recherché

Formation : Diplôme de niveau bac+5 minimum (Ingénieur, master ou équivalent)
Expérience d’au moins 7 ans dans des postes de management de production en environnement industriel structuré à forte exigence qualité et réglementaire
Appétence démontrée pour le pilotage en environnement multisites et la conduite de projets transverse
Leadership, capacité à fédérer vos équipes et à incarner au quotidien les valeurs fondamentales de l'entreprise.
Sens poussé de l'analyse et de la résolution de problèmes, avec une forte orientation résultat.
Capacités confirmées de communication, de présentation et de collaboration avec des publics très variés, en interne comme en externe.
Enfin, notre groupe international requiert un niveau d’anglais courant (lu, écrit et parlé).

Modalités

Convention collective de l’industrie pharmaceutique
Contrat : Poste cadre
Localisation : Basé à l'Arbresle (69) et déplacements réguliers à prévoir à Châtillon sur Chalaronne (01)
Salaire : A discuter selon profil, sur 14 mois + bonus + intéressement et participation
Indemnités de transport, accord de télétravail, prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Site non accessible en transport en commun : moyen de locomotion indispensable

Pour plus d'information, consultez www.criver.com.

Customer Service Team Lead (Charleston, SC, US, 29407)

Job Summary

The Customer Service Team Leader oversees and provides direction to the Microbial Solutions, North American, Customer Service team.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Supervisory Duties
⦁ Oversee daily operational activities and training for a group of non-exempt employees. Ensure optimum group performance.
⦁ Coordinate activities of customer service department to ensure efficient and timely availability of product.
⦁ Resolve all customer disputes, including counseling Customer Service staff in dispute resolution, complaint memos, and Trackwise cases.
⦁ Establishes and maintains close working relationships with the customer, Account Managers, Key Account Managers, Customer Service Representatives, and other support resources
⦁ Supports management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing feedback and coaching on performance, preparing reports and KPIs for annual performance reviews.
⦁ May assist in development of departmental budget.
⦁ Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
⦁ Coordinate vacation/time off schedules.
⦁ Ensure optimum performance of group function. Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.

Functional SME Duties
⦁ Maintain records in SAP and generate reports. Work with Global Supply Chain team to provide sales forecast. Interact with accounting to provide sales reporting information required for SOX compliance.
⦁ Act as backup for sign off requirements
⦁ Work with Accounts Receivable to resolve discrepancies in billing and customer accounts
⦁ Perform UAT, Integration, and Regression testing prior to implementation of new processes within platforms
⦁ Provide post go-live production support in Salesforce and SAP
⦁ Assist with inter and intra-company orders

These responsibilities are in addition to the basic requirements of a Customer Service Representative.
⦁ Perform customer service functions, including processing orders, providing documentation (e.g., health certificates), and communicating availability of product to customers, telephoning/emailing/faxing quotes/delivery/product information, and order confirmations.
⦁ Ensure coordination between Customer Service, freight forwarders and domestic carries to ensure efficient and timely delivery of product.
⦁ Work closely with global distributers for accurate and timely allocation of products.
⦁ Perform all other related duties as assigned.

Job Qualifications

⦁ Education: Bachelor’s degree (B.A./B.S.) or equivalent in Business or related discipline.
⦁ Experience: 2-3 years related experience with a Bachelor’s degree or 4-6 years related experience in customer service or business.
⦁ Experience using SAP ECC Order Management and Salesforce Service Cloud and/or ServiceMax
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None
⦁ Other: Supervisory and dispute resolution skills; excellent verbal and written communication skills; computer skills.

PHYSICAL DEMANDS:
⦁ Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
⦁ Must occasionally move about inside the office to access file cabinets, office machinery, etc.
⦁ Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to accurately exchange accurate information in these situations.

WORK ENVIRONMENT:
⦁ General office working conditions
⦁ The noise level in the work environment is usually quiet.

Comments:
⦁ This position requires occasional domestic travel.

Compensation Data

The pay range for this position is $55,000 to $58,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Alternance : Technicien de Toxicologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

Choisir Charles River Evreux, c’est intégrer un site unique de 500 personnes dans la province Normande, dans un environnement scientifique en constante évolution, ayant pour objectifs l'avancée de la recherche et le bien-être animal.

L’équipe

L’équipe de Toxicologie regroupe environ une vingtaine de personnes. Elle assure les techniques demandées dans le cadre des études scientifiques et est garante du bon report des tâches réalisées, dans le suivi des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
•   Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
•   Procéder à des prélèvements sanguins, d’urine ou de fèces,
•   Saisir l’intégralité des actes réalisés sur informatique,
•   Assurer la qualité des données recueillies et de résultats,
•   Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2 dans le domaine de la biologie médicale (BTS BMB, Anabiotech...) et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique, et êtes reconnu pour vos capacités d’organisation et votre proactivité.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milano, IT, 20122)

Da quasi 75 anni, i dipendenti di Charles River hanno lavorato insieme per assistere alla scoperta, allo sviluppo e alla produzione sicura di nuove terapie farmacologiche. Quando si unisce alla nostra famiglia, avrai un impatto significativo sulla salute e il benessere di persone in tutto il mondo. Se il tuo background è in scienze della vita, finanza, IT, vendite o in un'altra area, le tue abilità avranno un ruolo importante nel lavoro che svolgiamo. In cambio, ti aiuteremo a costruire una carriera che puoi sentirti appassionata.

Riepilogo del lavoro

Di cosa si occupa la Charles River

Charles River è un’organizzazione di ricerca a contratto (CRO) per le fasi precoci della ricerca farmacologica. Sulla base della nostra scienza e medicina degli animali da laboratorio abbiamo costituito e sviluppato un portafoglio diversificato di servizi di scoperta e di valutazione della sicurezza, sia GLP che non-GLP, per supportare i clienti a partire dall’identificazione del bersaglio fino allo sviluppo preclinico. Charles River offre inoltre una gamma di prodotti e servizi a supporto delle esigenze di analisi cliniche di laboratorio e delle attività di produzione dei nostri clienti laboratorio. L’utilizzo di questo portafoglio variegato di prodotti e servizi permette ai nostri clienti di creare modello di sviluppo dei farmaci più flessibile, che riduce i costi e migliora la produttività e l’efficienza al fine di ridurre i tempi di immissione sul mercato.

Con oltre 20.000 dipendenti in 110 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milan, IT, 20122)

Da 75 anni, i dipendenti di Charles River hanno lavorato insieme per assistere alla scoperta, allo sviluppo e alla produzione sicura di nuove terapie farmacologiche. Quando si unisce alla nostra famiglia, avrai un impatto significativo sulla salute e il benessere di persone in tutto il mondo. Se il tuo background è in scienze della vita, finanza, IT, vendite o in un'altra area, le tue abilità avranno un ruolo importante nel lavoro che svolgiamo. In cambio, ti aiuteremo a costruire una carriera che puoi sentirti appassionata.

Job Summary

Per cliente sito in Perugia ricerchiamo un operaio stabularista

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione dello stabulario

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro part-time nelle giornate di venerdì - sabato e domenica

Di cosa si occupa la Charles River

Con oltre 20.000 dipendenti in 90 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosamente ha collaborato allo sviluppo di ~85% dei farmaci approvati dalla FDA nel 2021.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Cuidador/a Animalario MAD (Madrid, M, ES, 28029)

Durante casi 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando se une a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentirte apasionada.

Charles River Laboratories España, S.A., empresa dedicada a la investigación y desarrollo experimental en biotecnología, necesita incorporar CUIDADORES/AS DE ANIMALARIO en Madrid.

• Jornada laboral de 40 h de lunes a viernes.

• Contrato laboral temporal por suplencia. Duración en función de la suplencia a cubrir.

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

• Tareas de mantenimiento de animales con fines experimentales (cambio de jaula, rejilla y cobertor)

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

• Desinfecciones de material de estabulación (racks ventilados, cabinas de cambio, jaulas, cobertores, etc.)

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

• Mantenimiento de registros ambientales (Tª, humedad, ciclos de luz, etc.)

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

• Desinfección de salas de estabulación, pasillos, almacenes, zona de lavado, etc.

Requisitos

Experiencia 3 meses. Experiencia mínima de 3 meses, aunque formamos a nuestro propio personal.
Título CFGM
Técnico/a superior anatomía patológica y citodiagnóstico
Idioma español
Competencias / conocimientos: se valorará acreditación para funciones A y B o formación como ATV (asistente técnico veterinario)

Acerca de Charles River

Charles River es una organización de investigación por contrato (CRO) en fase temprana. Hemos ampliado nuestra oferta sobre la base de la medicina y ciencia con animales de laboratorio para desarrollar una cartera diversificada de servicios de descubrimiento y evaluación de la seguridad, tanto por medio de buenas prácticas de laboratorio (GLP) como sin ellas, para apoyar a los clientes desde la identificación de los objetivos hasta el desarrollo preclínico. Charles River también proporciona una serie de productos y servicios para apoyar las necesidades de pruebas de laboratorio clínico y actividades de fabricación de nuestros clientes. El uso de esta extensa cartera de productos y servicios permite a nuestros clientes para crear un modelo más flexible de desarrollo de fármacos, lo cual reduce sus costes y mejora su productividad y eficacia, logrando así incrementar la velocidad con la que llega al mercado.

Con más de 20,000 empleados en 90 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo de ~85 % de los fármacos aprobados por la FDA en 2021.

En Charles River Laboratories, reconocemos y contratamos a todos los talentos. Somos una empresa comprometida con el principio de la diversidad y la inclusión y trabajamos diariamente en esta dirección.

Charles River España está comprometido con una política a favor de la integración y el empleo continuo de las personas con discapacidad. Todos nuestras vacantes están abiertas a trabajadores con discapacidad y se les dará especial consideración en los procesos de selección.

Para más información, visite www.criver.com.

Zootecnia de vivarios de investigación - Colaborador 1 1 (Madrid, M, ES, 28029)

Durante 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando se une a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentirte apasionada.

Resumen de trabajo

Acerca de Microbial Solutions

Nuestro grupo de negocios Microbial Solutions posee una exclusiva y completa cartera de productos y servicios de pruebas de endotoxinas, detección microbiana e identificación microbiana, que ha sido diseñada específicamente para cumplir con las necesidades complejas y siempre cambiantes de la industria. Ayudamos a los clientes a asegurar la seguridad y calidad del producto con soluciones de pruebas fáciles de usar pero robustas que satisfacen los requisitos regulatorios, apoyan el proceso de toma de decisiones críticas y mejoran las eficiencias operacionales.

Acerca de Charles River

Con más de 20,000 empleados en 110 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo del 80% de los fármacos aprobados por la FDA en los últimos cinco años.

Para más información, visite www.criver.com.

Manager Virology Scientific Support (Wayne, PA, US, 19087)

Job Summary

Responsible for the management of a team dedicated to scientific development and assay optimization as it pertains to the Virology laboratory. Will provide operational supervision, technical support and professional and scientific expertise, as needed, to ensure operational excellence.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Planning and ensuring on-time delivery of client projects.
Lead the development, qualification and validation of new assays that meet industry expectations and current regulatory guidelines. As Virology Subject Matter Expert, provide guidance for resolution of technical problems affecting Virology assays.
Oversees the optimization of existing Virology assays and their life cycle management, which will include monitoring to assess the need for subsequent requalification.
Support and manage the technical transfer of in vitro Virology assays.
Work with Sales to identify and fill gaps in Virology testing.
Partner with Business Development in providing and reviewing pricing and proposals, and provide excellent service to clients.
Act as a liaison with other departments to ensure that any method development appropriately aligns with Virology processes and subsequent routine testing.
Supports other operational areas in relation to virus based work, as needed, by providing guidance for R&D.
Participate in client technical calls to assist with Virology assay development or trouble shooting.
Supervise technical staff and perform personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions, time and vacation approval and preparing and delivering annual performance and salary reviews.
Develop and maintain departmental systems and SOPs. Maintain compliance of operating documents through review and revision as required by SOPs. Assist in the development and communication of departmental policies and procedures.
Participate in and support cross-functional communication and laboratory activities, as necessary.
Assist in the development of the departmental budget, including resource allocations and needs, and authorize expenditures.
Ensure adherence to pertinent regulatory requirements and to departmental policies.
Perform all other related duties as assigned.
With respect to all Virology assays and tests, the manager assures that:
Study or assay protocols are approved as provided by applicable regulatory requirements and that the protocols are followed.
All experimental data, including unanticipated observations, are accurately recorded and verified.
Unforeseen circumstances that may affect the quality and integrity of the study are noted when they occur, and corrective action is taken and documented.
Test systems, including reagents, live cells, equipment or other materials are as specified in the protocol.
All applicable good laboratory or manufacturing practice regulations are followed, as applicable.
All raw data, documentation, protocols, specimens, and final reports are transferred for archiving during or at the close of the study.

Job Qualifications

Education: Bachelor's degree or equivalent in biology or a related discipline. Master's degree preferred.
Experience: Minimum of 4-5 years related laboratory experience in Virology or related field.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Demonstrated leadership skills required. Working knowledge of cGMPs or regulatory requirements pertaining to the pharmaceutical and biotechnology industries required.

PHYSICAL DEMANDS:

May have exposure to potential chemical, electrical, biological and waste-handling hazards.
Must regularly operate a computer and other office machinery (i.e., calculator, copy machine, and computer printer).
Regularly moves about to access file cabinets, equipment, and personnel.
Ability to observe laboratory test results using a microscope to differentiate shapes, colors and other qualitative properties.

WORKING ENVIRONMENT:

General office and laboratory working conditions.
Laboratory working conditions may occasionally require wearing personal protective equipment, including but not limited to: goggles, face shield, surgical mask, cap, gloves, scrubs and/or shoe covers.
Work with or near toxic or caustic chemicals and biological agents including potential biohazards. Possible exposure to fumes or airborne particles.

Compensation Data

The pay range for this position is $105,000-$110,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Alternance : Technicien de Toxicologie Non-Rongeurs - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

Votre quotidien

Pourquoi nous rejoindre ?

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Alternance : Technicien de Laboratoire en Immunologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

L’équipe d'Immunologie regroupe environ 15 personnes. Elle assure la réalisation des techniques d’Immunologie, dans le respect des normes des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2/3 dans le domaine de la Biologie et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique et proactif et recherchez une expérience avec beaucoup de technique.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.
Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Scheduler I (Reno, NV, US, 89511)

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

The pay range for this position is $20.50 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

We are seeking an experienced Scheduler (Technical Operations) for our Safety Assessment site located in Reno, Nevada.

The Scheduler schedules all protocol-required tasks for in-life studies, ensuring proper placement of employees into specific study activities based on competency and responsibilities. Additionally, schedule employee department and global trainings, and manage the department level study schedule and resources.

The following are minimum requirements related to the Scheduler position.

Associate’s degree (A.A./A.S.) or equivalent in scientific support/administrative or related discipline.
2 years of related experience in a laboratory or research environment. Previous experience in a GLP environment preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to interact with all levels of staff and sponsors. Strong communication and interpersonal skills and attention to detail. Proficient in the use of word processing, spreadsheet and database desktop applications.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

Head of CSD (Sulzfeld, Bavaria (Bayern), DE, 97633)

Wir suchen ab sofort eine/n

Head of CSD (kaufmännische/r Angestelle/r) (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld

DAS SIND IHRE AUFGABEN:

Planung und Koordination von Kundenprojekten
- - Leitung des Customer-Service-Department-Teams am Standort Sulzfeld
  - Spezialwissen zur Logistik in Deutschland und EU-weit
  - Aufbereitung, Informationssammlung und Analyse über europäische Logistik
  - Effiziente Fehlerbehebung und Optimierungen in SAP und anderen angewandten unterstützenden IT-Tools

DAS BRINGEN SIE MIT:

Abgeschlossene kaufmännische Ausbildung
Sie verfügen über mindestens 5 Jahre Berufserfahrung im Bereich Customer Service

Sie haben Spaß an der Kundenbetreuung
Sie bringen Erfahrung in SFDC und E-Commerce-Plattformen mit sowie im Bereich Zoll und Logistik
Sie sind offen für Arbeiten in großen Netzwerken auf internationaler Ebene
Sie sind zuverlässig, belastbar, flexibel, verantwortungsbewusst und teamfähig
Sie beherrschen die englische Sprache in Wort und Schrift
Der versierte Umgang mit Microsoft Office (Excel, PowerPoint, Word) sowie mit SAP und Inventarmanagementsystemen wird vorausgesetzt
Hohe Resilienz
Wünschenswert wären Personalführungserfahrung und Versiertheit bei Behördenkontakten

DAS BIETEN WIR:

eine ausführliche und betreute Einarbeitung
eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team mit Raum für Kreativität
ein internationales Arbeitsumfeld
attraktive Fort-/Weiterbildungsangebote
ein wettbewerbsfähiges Vergütungspaket
zahlreiche soziale Leistungen und Zuschüsse

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com , www.criver.com

Vorabinfos unter: 09761-40611

Über Research Models & Services

Über Charles River

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von rund 80% der von der FDA in den letzten fünf Jahren zugelassenen Arzneimittel unterstützt haben.

Weitere Informationen finden Sie unter www.criver.com.

Technicien de laboratoire en Histologie - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Pathologie recrute un Technicien en Histologie pour intégrer son équipe composée de 33 techniciens.

Les missions 

Au sein du Département Pathologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Réaliser les techniques de laboratoire en Histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
Assurer la réalisation des autopsies pour toutes les espèces utilisées dans le cadre de nos études,
S’assurer de la conformité des résultats obtenus,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine scientifique.

Vous maitrisez l’anglais scientifique (compréhension écrite)

Vous savez faire preuve d’autonomie mais vous appréciez également le travail en équipe

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.
Contact avec les animaux.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
CDD de 09 mois
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 400 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de Laboratoire en Génomique - H/F - CDD 9 mois (Evreux, FR, 27930)

Pendant de 70 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Qui sommes-nous ?

Le poste

Le département de Biologie Moléculaire recrute un Technicien de Laboratoire en Génomique pour intégrer son équipe composée de 17 techniciens.

Les missions 

Au sein du Département Biologie Moléculaire, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Réaliser progressivement certaines techniques de laboratoire : extractions d’acides nucléiques, dosages quantitatifs et qualitatifs, réalisation de PCR,
Assurer la saisie informatique des résultats et leurs conformités,
Lire les protocoles, avenants et notices en anglais,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine de la Biologie Moléculaire.

Vous maitrisez l’anglais scientifique (compréhension écrite).

Vous savez faire preuve d’autonomie mais vous appréciez également le travail en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 24 000 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de l'évaluation de sécurité

Avec plus de 17 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2019.

Electronic Technician - Hybrid (Charleston, SC, US, 29407)

Job Summary

We are seeking an experienced Electronic Technician, for our Microbial Solutions site located in Charleston, SC.

The Electronic Technician’s primary role is testing, troubleshooting, repairing, performing preventative maintenance, and calibrating Microbial Solutions instruments. The Electronic Technician must be able to troubleshoot to the component level. Support of our Field Technicians and production staff is included in this position. They must be able to operate test equipment including DVM’s, oscilloscopes, and soldering irons. All associated paperwork as required by cGMP and FDA, along with updates to our database are also part of the responsibilities. We are seeking a motivated individual with good communication skills and attention to detail. Your ability to handle these tasks in a timely manner will be a major part of meeting the service needs of our customers.

The following are the job duties & responsibilities related to the Electronic Technician:

Administer test, trouble shoot and repair electronics to the component level.
Understand and read schematics.
Mechanically assembly and disassemble new and existing equipment
Perform and operate on test equipment and solder equipment when needed.
Create, develop and continuously improve SOP’s pertaining to the PTS and MCS machines.
Able to analyze situations and apply own judgment when accessing mechanical problems, independently.
Coordinate scheduling and support department personnel in the absence of the PTS Engineer.
Responsible for proficiency in all SOPs in areas of responsibility.
Responsible for documentation as required by company policy, cGMP and FDA.
Support and serve as second back-up to Technical Services by loading software, calibration of new equipment and ensuring proper packaging of new equipment.
Perform and assess data entry in software program in order to track machine repairs.
Interpret past repairs on PTS and MCS machines, historically, in order to resolve and diagnosis new machine issues.
Perform all other related duties as assigned.

Job Qualifications

The following are minimum requirements related to the Electronic Technician position.

Education: Associates Degree(A.S) in Electronic Engineering Technology, or related discipline
Experience: 0-1 years related experience in a regulated environment.
Computer literacy with Windows Office Suite programs including data entry and tracking.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

The pay range for this position is $25.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Research Scientist LC-MS/MS - F/H - CDI (Saint-Nazaire, FR, 44600)

Depuis plus de 75 ans, les salariés de Charles River travaillent ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Le poste

Notre Laboratoire de chromatographie recrute un Research Scientist LC-MS/MS - H/F en CDI, basé sur le site de Saint-Nazaire (44).

Le site est spécialisé dans la mise en place de tests de bioanalyse pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération (LC-MS/MS). Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Vous ferez partie d’une équipe dans laquelle votre rôle sera la réalisation technique et la responsabilité de conduite d'études de développements de méthode de bioanalyse sur de nouveaux médicaments.

Les missions

Réaliser techniquement des développements de méthode de bioanalyse pour tout type de matrices biologiques (plasma, sang,tissus,…) de façon autonome et efficace
Assumer la responsabilité générale de la conduite d'étude de développement et y apporter son expertise technique et scientifique
S’assurer de la disponibilité du matériel et des réactifs pour respecter le planning établi
Interpréter les données avec précision et faire preuve de minutie dans la vérification et la validité des informations
Produire des documents analytiques précis et de haute qualité pour transférer efficacement les méthodes développées aux collègues chargés de la partie réglementaire (validation)
Travailler en étroite collaboration avec l’ensemble des personnes du laboratoire (techniciens de laboratoire, responsables d’études, responsables d’équipe) et des services supports (planification, Archiviste, Publisher et coordinateur scientifique, Magasin et achats, etc…)
Communiquer régulièrement avec les clients, fournisseurs, auditeurs, etc…

Qualifications recherchées

De formation Bac + 2 minimum, vous disposez idéalement d'une expérience technique d'au moins 5 ans en bioanalyse (préparation d’échantillons biologiques, LC-MS/MS).

Vous avez de bonnes connaissances des normes BPL/BPC ou du travail en contexte qualité/réglementaire (suivi et respect de procédures et consignes).

Rigoureux et autonome, vous êtes reconnu(e) pour votre bon sens du relationnel et êtes à l’aise avec les outils informatiques.

Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI cadre (forfait jours, RTT)
Salaire : Environ 34 000 € bruts/an, sur 12 mois, selon expérience
Prise en charge de la mutuelle à 60% et tickets restaurants

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Cagewash Technician I (Bldg 35) 1 (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The duties of the Cagewash Technician I are to maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

You will also perform the following duties:

Sanitize, maintain, and repair animal caging materials as needed.
Ensure cagewash and animal holding facilities are kept in a clean and organized manner.
Assist with the receipt, stocking, and maintenance of supply inventories.
Prepare and submit required written records, charts, logs, and inventories.
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Other duties will include general housekeeping, in addition to reviewing, comprehending and complying with all SOPs and quality assurance standards pertaining to specific areas.

Qualifications

Experience and/or training working with mechanical equipment preferred.

Obtain ALAT certification within 1 year of employment with HS Diploma/GED or within 2 years of employment if no HS Diploma/GED.

The pay for this position is $17.50-18.47 USD per hour.

For more information, please visit www.criver.com.

Technicien animalier - F/H - CDI (Paris, FR)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

L’activité Insourcing désigne la prestation de gestion d’animalerie, dans laquelle le client confie à Charles River le soin de réaliser les prestations définies dans un contrat au sein de ses installations adaptées à l’hébergement des animaux de laboratoire.

Dans le cadre de cette activité, nous recherchons un Technicien animalier F/H en CDI pour travailler au sein d'animaleries de recherche au sein de nos sites client basés à Paris.

A ce titre, vous intégrerez une équipe de zootechniciens engagés au cœur du bien-être animal et travaillerez en interface directe avec les équipes de recherche.

Missions principales

Gestion d'élevage (rongeurs)

Gestion les animaux selon les instructions données par équipes de recherche via un logiciel de gestion d'animalerie
- Contrôle de l'état de gestation, suivi des animaux, sexage et sevrage
- Réalisation des accouplements contrôlés
Identification des animaux
Réalisation de prélèvements à des fins de génotypage/phénotypage
Mise à jour et suivi des données d'élevages sur le logiciel d'animalerie
Travail en lien avec les équipes de recherche

Entretien, soin et surveillance des animaux

Assurer le bien-être des animaux au quotidien : observation, abreuvement, alimentation, enrichissement et la vérification des paramètres d'ambiance
Assurer l'hébergement des animaux: change des cages sous hotte de change
Nettoyage et désinfection des locaux en respectant les règles de prophylaxie et de biosécurité
Gestion des stocks de consommables, déclenchement des commandes et suivi des réceptions

Profil recherché

Idéalement niveau 2/Fonction A en Expérimentation animale
Expérience requises: expérience dans la gestion d'élevage de rongeurs
Savoir travailler en milieu confiné ou en zone protégée avec des équipements de protection individuelles (EPI)
Respect des procédures et de la réglementation en expérimentation animale
Esprit d'équipe et capacité à collaborer avec différents interlocuteurs
A l'aise avec les outils informatiques

Modalités

Convention collective pharmaceutique
Permanences ponctuelles les week-ends et/ou jours fériés
Rémunération à partir 30 K€ brut annuel sur 14 mois, selon profil.
Indemnité de transport, prime d’Intéressement et participation, accord d’ancienneté
Prise en charge de la mutuelle à 60%, tickets restaurants, comité d'entreprise

Pour plus d'information, consultez www.criver.com.

Medical Technologist I (Reno, NV, US, 89511)

Job Summary

BASIC SUMMARY:
Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain and perform basic troubleshooting procedures on analyzers. Process additional study samples. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist in the preparation of appropriate paperwork and materials prior to clinical pathology blood collection days. Assist with the computer protocol work schedule for each study, as needed.
•   Perform basic medical technology procedures such as record blood slide differentials, reticulocyte counts, and urinalysis with minimal supervision; prepare blood and cytology slide smears.
•   Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
•   Maintain proficient knowledge of hematology, clinical chemistry, coagulation, and urinalysis.
•   Analyze proficiency survey samples.
•   Review documentation of functions performed as part of quality requirements.
•   Input raw data into the computer system and review data.
•   Operate, maintain, and troubleshoot clinical pathology analyzers.
•   Perform daily maintenance and quality control of instruments.
•   Perform all other related duties as assigned.

Job Qualifications

Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) desired.
Experience: 2-3 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is desirable. Effective organizational and leadership skills desired.

The pay range for this position is $30.00-32.00 an hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Environmental Health and Safety Specialist (Cambridge, MA, US, 02142)

Job Summary

Responsible for implementing/maintaining the Environmental, Health, Safety & Sustainability (EHS&S) Program(s) for adherence to local, state, and federal regulations. Identify and mitigate potential hazards to reduce/eliminate risk exposure.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Establish, administer, and update specific EHS&S programs for compliance with state and federal Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), Department of Transportation (DOT) and other regulations as necessary.
Manage OSHA and EPA records and maintain reporting and documentation standards.
Provide initial and periodic safety and environmental training to all employees as required and advise management on safety and environmental issues.
Review new regulatory standards and make compliance recommendations.
Inspect the facility for compliance with OSHA and EPA regulations as applicable. Recommend solutions to management that address deficiencies in EHS&S compliance. Submit work orders for facility corrective action on EHS&S concerns.
Assist in the development of EHS&S programs and metrics.
Manage the hazardous waste (RCRA) and medical waste disposal function including waste profiling, permitting, manifesting, and record keeping and reporting.
Assist management team in emergency response and function as EHS&S Emergency Coordinator for 24-hour incident response.
Serve or Co-chair as a member of the Safety Committee(s)
Assist in the investigation of injuries resulting in lost time claims and/or safety violations and property damage. Make recommendations for corrective action.
Provide regulatory guidance on EHS&S issues to all staff.
Available to clients and federal and state investigators to explain procedures and produce written documentation as proof of compliance.
Request and maintain necessary facility permits, licenses and compliance reports to federal, local and state regulatory authorities.
Obtain necessary licenses to function as wastewater and underground storage tank operator.
Coordinate communications to regulatory agencies and client inspections on EHS&S related matters.
Provide initial and periodic safety and environmental training to all employees as required by regulation and as needed for ‘best practice’.
Liaise with Document Control team to ensure SOPs and BOPs are properly formatted, updated, and entered.
Recommend and implement changes to facility SOPs, Global Operating Framework (GOFs) and Business Operating Procedures (BOPs) relating to EHS&S.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in Environmental Science, Occupational Health and Safety, Environmental Engineering or related discipline.
Experience: 3 – 5 years related experience in Environmental Health, Safety.& Sustainability.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Ability to interpret federal and state regulation and apply them to address compliance solutions as required. Effective writing, organizational and time management skills. Computer skills including MS Office and database management. Ability to speak Spanish is a plus.

Compensation Data

The pay range for this position is $95,000 - $105,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Technician II, Formulations (Ashland, OH, US, 44805)

Job Summary

We are seeking an experienced Formulations Tech II for our Formulations Team at our Safety Assessment site located in Ashland, OH.

Basic Summary:

A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight.

Prepare basic to complex dosing material and samples for solutions, suspensions, diets, and dispensations.
Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).
Independently sterilize laboratory equipment using autoclave or other methods.
Assist in washing and maintenance of glassware and lab cleanliness.
Assist with the disposal of residual dosing material.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Independently be able to identify equipment issues for troubleshooting and notify proper personnel.
Actively participate in process improvement initiatives.
Be able to provide feedback on laboratory investigations and quality observations.
Utilize various mixing methods and apparatuses to prepare formulations.
Prepare aseptic and glovebox formulations with oversight.
Prepare formulations under observation of Study Directors.
Performs all other related duties and functions as assigned.

The pay for this position is $20.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education & Experience: Associate’s degree (A.A./A.S.) or equivalent with a minimum of 1-2 years of relevant experience and CPhT with 1-2 years of compounding experience recommended. Bachelor’s degree (B.A./B.S.) in a relevant field with no experience strongly recommended. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Good written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, and extended shifts sometimes with short notice or unscheduled.
Ability to work under specific time constraints.

Physical Demands:

Must be able to lift, move, manipulate and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or supplies.
Must be able to perform procedures, standing or sitting, for long periods of time, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently hold and manipulate work materials while utilizing fine motor skills.
Must be able to regularly provide information to and receive information from/through various technologies, media, sources, and contacts. Must be able to accurately exchange information in these situations.
Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
Move about inside the work area to access file cabinets, office machinery, etc.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

General office and lab working conditions, the noise level in the work environment is usually moderate.
While performing the duties of this job the employee is regularly required to wear protective clothing (i.e., goggles, face shield, cap, gloves, scrubs, shoe covers), work near toxic or caustic chemicals, work with biohazards.
The employee may occasionally be exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and extreme temperature conditions.
The noise level in the work environment ranges from moderate to high depending upon the task being performed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Histology Technician II (Shrewsbury, MA, US, 01545)

Job Summary

BASIC SUMMARY:
Independently perform basic histology laboratory procedures. Assist with specialized histology procedures. Review data for quality control.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform basic histology procedures independently (trimming, processing, embedding, microtomy, staining, coverslipping).
•   Assist with and perform advanced histology procedures (slide QC, special stains, thin/thick sections, IHC, serial/step sectioning).
•   Review laboratory documents for accuracy, completeness and compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), and study specific requirements.
•   Assist in training of staff junior to this position.
•   Assist in the preparation of responses, deviations and other documentation resulting from internal and external reviews and/or audits.
•   May assist with basic necropsy procedures (basic dissection, tissue collection/preservation, fresh tissue trimming).
•   May cross-train in other areas of pathology and/or other laboratory departments (flow cytometry, clinical pathology, special pathology, bioanalytical, reproductive toxicology, etc.).
•   Perform all other related duties as assigned.

The pay rate for this position is between $29.00 and $30.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
•   Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (B.A./B.S.) or equivalent in a biological science preferred.
•   Experience: Minimum 2 years of pathology laboratory experience required.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: HT (ASCP) or HLT (ASCP) preferred.
Other: Placement at this level requires successful completion/competency of the required tasks of the position preceding this level and continued ability to perform those tasks are required. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, maintain a positive work atmosphere, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Experience with computer software programs is required.

PHYSICAL DEMANDS:
•   Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
•   Must be able to perform laboratory procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
•   Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
• Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

COMMENTS:
• May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Medical Technologist II - Clinical Pathology (Horsham, PA, US, 19044)

Job Summary

A Medical Technologist II is responsible for performing and maintaining proficient knowledge of basic medical technology techniques on primary benches. Performs basic operation, daily maintenance, quality control, and basic troubleshooting on all clinical pathology analyzers. Performs manual urine microscopy, cell counting, and manual differentials.

Essential Duties and Responsibilities:
Performs basic medical technology techniques on primary benches (urinalysis, coagulation, hematology, and chemistry).
Performs urine microscopy, cell counting, and manual differentials.
Maintains proficient knowledge of hematology, coagulation, chemistry, and urinalysis.
Performs basic operation, daily maintenance, quality control, and basic troubleshooting on all analyzers.
Records and reviews hand recorded or computer generated raw data.
Trains in MVP training (System Administrator role)
Trains and gains proficiency in Medical Technologist II core skills and values.
Perform all other related duties as assigned.

The pay range for this position is between $32-$34 . Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

Qualifications:
Education: Associate degree (A.A./A.S.) or Bachelor’s degree (B.A./B.S.) or equivalent in medical technology certification (MT) preferred.
Experience: 1-4 years of experience in a clinical pathology laboratory required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MLT, MT, or MLS with certification or certification eligible (ASCP or HEW) required.

Demonstrated ability to learn and perform clinical laboratory procedures, both manually and using instrumentation.
Excellent written and verbal communication skills inside and outside the organization.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Assembler - Associate (Charleston, SC, US, 29407)

Job Summary

An essential member of the larger production team, responsible for mechanical assembly, rework, documentation, instrument release, and installation of software for automation equipment, as well as support instrument production deliverables. Reports to the production supervisor.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Test and release instrumentation, and robotics systems
• Perform rework on instrumentation and robotics systems as necessary
• Perform onsite service and instrumentation of robotics systems as required in support of the Field Service Team
• Draft/Edit MPIs (Manufacturing Process Instructions)
• Draft/Edit SOPs (Standard Operating Procedures) related to primary job function
• Mechanically assemble and disassemble new and existing equipment
• Receive, sort, inspect and stock components in a warehouse area
• Identify and report defects, including potential defects to aid in product improvement
• Operate hand and power tools such as torque drivers, screw drivers, wire cutters and other tools for instrument assembly
• Perform rework including but not limited to soldering, crimping, separating, cutting etc.
• Read and understand CAD drawings, BOM etc.
• Assist in:
   Perform general housekeeping and adhere to safety procedures.
   Production process development
   Continuous improvement
Product improvements
Manufacturing processes
Testing processes
• Perform SAP operations to facilitate the processing of components and instruments
• Set up instruments in Service Max, track defects and RMAs.
• Work with PLM system and work instructions
• Perform general housekeeping and adhere to safety procedures.
• Proficient in all SOPs in areas of responsibility
• Perform all other related duties as assigned.
• Responsible for adhering to all documentation as required by company policy, cGMP and FDA.
• Cross train as required for all other roles within the department
   Periodically assist in those roles with direction as needed
LEADERSHIP:
• Onboard and train new team members, cross train other team members
ADDITIONAL RESPONSIBILITIES:
• Equipment safety / manuals etc.
• Trained by Hamilton in the service of the nexus instrument.
• Capable of traveling internationally. 10% travel as necessary.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.)
Experience: 2 years+ experience working in assembly with basic mechanical knowledge.

PHYSICAL DEMANDS:

Specific vision abilities required by this job include close vision and the ability to adjust focus..
Sitting and standing for periods of time.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General production working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

Employee is responsible to verify and validate his or her job output as specified through verbal and/or written instructions. Verbal and written instructions may include training, policy statements, work instructions, Standard Operating Procedures, or workmanship standards.

For more information, please visit www.criver.com.

Supervisor - Bioanalytical (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Supervisor for our Bioanalytical & Analytical Chemistry group in Laval, you will be responsible for the management of technical staff, services, and standards, qualify and cost-effectiveness of all relevant activities. Your contribution will ensure maximum efficiency of the team and help resolve more challenging issues.

In this role, primary responsibilities include:

Coach, train and support employees to ensure maximum efficiency of teams and resolve more challenging issues;
Schedule work of departmental staff to maximize efficiency and productivity;
Oversee the training process of all staff;
Provide performance appraisal and development opportunities for staff members.

Key Elements

We are looking for the following minimum qualifications for this role:

Bachelor’s degree in Chemistry, Biochemistry, Biology or any related scientific field;
Minimum of 2 years’ experience in a management role;
Good interpersonal and communication skills;
Strong problem-solving skills;
Good listener and strategic vision;
Bilingualism in French and English is mandatory. However, the level of English can be intermediate to advanced.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station
Annual bonus based on performance;
Schedule: Daytime Monday to Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Clinical Pathology Lab Assistant (Reno, NV, US, 89511)

Job Summary

We are seeking a Clinical Pathology Assistant for our Safety Assessment site located in Reno, NV.

The following are responsibilities related to the Clinical Pathology Assistant:

*Perform a wide variety of basic laboratory tasks.
*Maintain and perform recordkeeping.
*Review data recorded for others for quality control.
*Prepare all materials required for sample receipt and processing.
*Maintain data files for department.
*Perform all tasks in compliance with Good Laboratory Practice (GLP) regulations and with Standard Operating Procedures (SOPs).

Job Qualifications

Education: High school diploma or General Education Degree (GED)
Experience: None
Certification/Licensure: None
Other: Good keyboarding skills, proficient in utilizing personal computer, email, and standard office software packages.

The pay range for this position starts at $18.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Superviseur.e - Bioanalyse (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Superviseur.e pour notre équipe de Bioanalyse & Chimie Analytique à notre site de Laval, vous serez responsable de la gestion du personnel technique, des services et des normes, de la qualité et de la rentabilité de toutes les activités concernées. Votre contribution assurera une efficacité maximale de l’équipe et aidera à résoudre les problèmes les plus difficiles.

Dans ce poste, les principales responsabilités incluront:

Encadrer, former et soutenir les employés pour assurer une efficacité maximale des équipes et résoudre les problèmes les plus difficiles;
Planifier le travail du personnel du département afin de maximiser l’efficacité et la productivité;
Superviser le processus de formation de tout le personnel;
Offrir des opportunités d’évaluation des performances et de développement aux membres du personnel.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat en Chimie, Biochimie, Biologie ou toutes autres disciplines reliées à un domaine scientifique;
Au minimum de 2 ans d’expérience dans un poste en gestion de personnel;
Bonnes aptitudes interpersonnelles et de communication;
Bonnes compétences en résolution de problème;
Bon sens de l’écoute et vision stratégique.
Le bilinguisme français & anglais est obligatoire. Toutefois, le niveau d'anglais peut être de niveau intermédiaire à avancé.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Regional Environmental Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Regional Environmental Specialist for our Health & Safety team at the Senneville location, you will be responsible for managing environmental programs in compliance with local, provincial, and federal regulations for our regional sites: Senneville, Ville St-Laurent, Laval, and Sherbrooke.

In this role, primary responsibilities include:

Establish, manage, and update specific environmental programs to ensure compliance with municipal, provincial, and federal administrations and organizations;
Help sites conduct environmental audits as well as establish and implement an action plan to address the gaps identified during the audits (internal and external);
Inspect the facilities to ensure they comply with local regulations, where applicable. Advise management on environmental issues and recommend solutions to address gaps;
Manage the disposal function for hazardous and medical waste, including permits, reporting, releases, record keeping, and establishing disposal profiles related to this waste;
Explain the procedures and produce written documents as evidence of compliance for clients and municipal, provincial, and federal investigators. Coordinate communications with regulatory bodies and clients on environmental issues;
Promote sustainable development on the sites by keeping updated and communicating monthly the data and key performance indicators (KPIs) related to the environment and sustainable development.

Key Elements

We are looking for the following minimum qualifications for this role:

Bachelor's degree or equivalent in environmental sciences or sustainable environmental engineering;
Minimum 5 years of related experience in environmental and sustainable development work;
Experience in a laboratory or a scientific organization is an asset;
Bilingual (French & English).
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Ability to effectively manage multiple projects simultaneously;
Commitment to excellence and attention to detail, ability to work within a complex and fast-moving environment.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Day schedule from Monday to Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Spécialiste régional.e en environnement et développement durable (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Spécialiste Régional.e, Environnement et développement durable pour notre équipe de Santé et Sécurité située au site de Senneville, vous gérerez les programmes environnementaux dans le respect des réglementations locales, provinciales et fédérales de nos sites régionaux :Senneville, Ville St-Laurent, Laval et Sherbrooke.

Dans ce poste, les principales responsabilités incluront:

Établir, administrer et mettre à jour des programmes environnementaux particuliers afin d’assurer la conformité avec les administrations et les organismes municipaux, provinciaux et fédéraux;
Aider à réaliser les audits environnementaux ainsi qu’établir et mettre en œuvre un plan d’action pour combler les lacunes décelées lors des audits (internes et externes);
Inspecter les installations pour s’assurer qu’elles sont conformes aux réglementations locales, le cas échéant. Conseiller la direction sur les questions environnementales et recommander des solutions pour remédier aux lacunes;
Gérer la fonction d’élimination des déchets dangereux et des déchets médicaux, notamment les autorisations, la production de rapports, les communiqués, la tenue de registres et l’établissement des profils d’élimination relatifs à ces déchets;
Expliquer les procédures et produire des documents écrits comme preuve de conformité à la clientèle et aux enquêteur.trices de niveau municipal, provincial et fédéral. Coordonner les communications avec les organismes de réglementation et la clientèle sur les questions liées à l’environnement;
Promouvoir le développement durable sur les sites, en tenant à jour et en communiquant mensuellement les données et les indicateurs de rendement clés (IRC) en matière d’environnement et de développement durable.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Baccalauréat ou équivalent en sciences de l’environnement ou en ingénierie de l’environnement durable;
Minimum de 5 ans d’expérience en environnement et développement durable;
Expérience dans un laboratoire ou une organisation scientifique est un atout;
Bilingue (français et anglais).
Capacité à inspirer confiance grâce à de solides compétences interpersonnelles et à une collaboration efficace ;
Capacité à gérer efficacement plusieurs projets simultanément ;
Engagement envers l'excellence et le souci du détail, tout en ayant la capacité à travailler dans un environnement complexe et en évolution rapide.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Director, Human Resources (Mattawan, MI, US, 49071)

Job Summary

The Human Resources Director will serve as the strategic HR partner and site HR leader for the Safety Assessment business at the Mattawan, Michigan site. As the HR Director, you understand that in today’s market, innovative and forward-thinking people strategy is essential to short and long-term business success. To achieve this, you will collaborate with business leaders to turn strategy into action, resolving talent gaps and seizing opportunities that support our goals of hiring, engaging, developing, and retaining outstanding talent.

Essential Duties & Responsibilities:

Provides high-level consultation to senior leaders in areas such as organizational assessment, compensation, succession planning, organizational structure, work force planning and change management in order to strengthen overall organizational capability.
Lead, develop and coach a team of HR Professionals, ensuring they deliver exceptional HR services.
Acts as a senior trusted advisor and strategic partner to leadership by gathering and analyzing HR and client information to drive the development and implementation of solutions.
Understands the site business model and drivers. Partners closely with the site leader and other senior leaders to anticipate and address issues impacting the business as it relates to talent and organizational issues.
Undertakes diagnostics and analysis of complex data, to facilitate HR Leadership decision making.
Collaborates with internal process experts to execute and implement large scale HR initiatives (i.e., roll out of annual programs, new programs, policies, etc.).
Provides consultation and leadership on the handling and resolution of complex employee relations issues ensuring consistency with corporate policies and practices.
Directs annual HR processes such as performance reviews, succession planning, bonus and merit programs.
Bring solutions to continuously improve HR support to the business around efficiency, process and performance.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in Human Resources, or related discipline.
Experience: 8+ years related Human Resources experience serving in a business partnership oriented role for executive leaders.
Must have demonstrated skills in change management and organizational development. Must possess excellent interpersonal communication and influencing skills.
Key skills and abilities include coaching, influencing, facilitation, process development, project management, analysis, presentation, written & verbal communication and problem solving.
Working knowledge of EEO, Federal & State employment laws, Worker’s Comp, STD and LTD issues.
Proficient in collaborating effectively and utilizing networks.
High degree of autonomy and strong decision-making skills.
Ability to analyze and interpret relevant data to inform business decisions.
Keeps commitments; exhibits candor and courage – is not afraid to establish a visible presence and point of view, to engage in spirited and constructive debate, to hold others accountable.
Demonstrated experience in HR strategy development and fostering continuous improvement.

Compensation Data

The pay range for this position is $140,000-$190,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien animalier en élevages rongeurs (F/H) - Mission temporaire (Paris, FR, 75012)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

L'activité Insourcing désigne la prestation de gestion d'animalerie, dans laquelle le client confie à Charles River le soin de réaliser les prestations définies dans un contrat au sein de ses installations adaptées à l'hébergement des animaux de laboratoire.

Dans le cadre de cette activité, nous recherchons un Technicien animalier en élevages rongeurs (F/H) en pour une mission temporaire de plusieurs mois pour travailler au sein d'une animalerie sur l'un de nos site client à Paris. A ce titre, vous intégrerez une équipe de zootechniciens engagés au cœur du bien-être animal et travaillerez en interface directe avec les équipes du client.

Missions principales

En tant que Technicien animalier en élevages rongeurs (F/H), vous serez directement impliqué dans la gestion des élevages transgéniques destinés à des projets de recherche. Vos responsabilités incluront :

Gestion d'élevage transgénique (rongeurs)

Gestion des colonies murines transgéniques via un logiciel de gestion d'animalerie :
Accouplement, suivi des gestations et naissances
Identification des animaux
Sevrage
Saisies des données d'élevages sur le logiciel Anibio et sur des fichiers Excel

Participation aux suivis des projets expérimentaux

Pesées des animaux
Mise en place d'accouplements contrôlés
Injections intra-péritonéales ou sous-cutanées

Entretien, soin et surveillance des animaux

Assurer le bien-être des animaux au quotidien : observation, abreuvement, alimentation, enrichissement et vérification des paramètres d'ambiance
Assurer l'hébergement des animaux : change des cages sous hotte ou PSM
Contrôle des équipements et des installations
Entretien des zones de stabulation et des parties communes de l'animalerie
Participation aux activités de laverie

Profil recherché

Vous êtes idéalement expérimenté en gestion d'élevage de rongeurs transgéniques, rigoureux, passionné par le travail des animaux et vous avez à cœur de contribuer à la progression des projets scientifiques.
Niveau 2/Fonction A en Expérimentation animale
Savoir travailler en milieu confiné ou en zone protégée avec des équipements de protection individuelles (EPI)
A l'aise avec les outils informatiques
Esprit d'équipe et capacité à collaborer avec différents interlocuteurs
Organisation et rigueur au quotidien, sens de l'observation et capacité à identifier des anomalies
Autonomie et proactivité

Modalités

•   Convention collective pharmaceutique
•   Permanences ponctuelles les week-ends et/ou jours fériés : (1 à 2 fois par mois) pour contrôler le bien-être des animaux et vérifier les paramètres d'ambiance
•   Indemnité de transport, prime d'Intéressement et participation, accord d'ancienneté
•   Prise en charge de la mutuelle à 60%, tickets restaurants, comité d'entreprise

À propos des modèles et services de rechercheIndispensable dans la recherche fondamentale et la découverte, l’utilisation de modèles in vivo nous aide à cibler certaines maladies et à déterminer les voies d’intervention biologiques potentielles qui permettent de contrôler l’évolution de la maladie. En notre qualité de leader mondial dans la production et la distribution d’animaux de recherche de qualité supérieure, avec un modèle sur deux produit pour la recherche préclinique à l’échelle mondiale, nous sommes bien placés pour comprendre l’importance de cette étape. Grâce à nos sept décennies d’expérience, notre expertise est inégalée, ce qui nous permet de mettre à votre disposition le modèle parfait, y compris des options spécifiques à une maladie et pré-conditionnées, pour la recherche fondamentale et au-delà.

À propos de Charles RiverCharles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d’évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d’apporter à nos clients un soutien complet, de l’identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l’appui des besoins en matière d’essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Avec plus de 20 000 collaborateurs sur 110 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l’élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d’enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d’innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d’avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d’information, consultez www.criver.com.

Senior Infosec Analyst (Vulnerability Management) (Ahmedabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

Job Summary

As an Infosec vulnerability analyst, you will be a hands-on practitioner and representative of the vulnerability management practice in cyber security defence. This is a technical role, and candidates must possess a solid understanding of information security, applications, operating systems, networking, cloud infrastructure, and attacker tactics, techniques, and procedures (TTPs). Responsibilities of this position include vulnerability management, reporting, remediation and continuous assessment, penetration testing, and red teaming.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Manage vulnerabilities across applications, endpoints, databases, networking devices, and mobile, cloud, and third-party assets.
•   Conduct continuous discovery and vulnerability assessment of enterprise-wide assets.
•   Support auditors in their duties that focus on compliance and risk reduction.
•   Perform penetration tests against company-owned assets, including internal and cloud-based assets, as well as web applications and APIs.
•   Perform other duties as assigned.

QUALIFICATIONS:

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in computer science, information technology, or related discipline.
• Very strong experience in information security operations, vulnerability management, or related disciplines.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Understanding of OWASP, CVSS, the MITRE ATT&CK framework, and the software development lifecycle.
•   Capable of scripting in Python, Bash, Perl, or PowerShell.
•   Certification/Licensure: IT security-related certification desired (e.g., Security +, CISSP, CISA, GCED, GPEN, GCIH, or similar professional certification).
•   Other:
   Must have strong interpersonal, teamwork, and self-initiative skills.

WORK ENVIRONMENT:
• This position has been designated as permanently remote.

Comments:
• May require occasional domestic or international travel.

About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

For more information, please visit www.criver.com.

Head of Continuous Improvement (Charleston, SC, US, 29407)

For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

We are looking for a hands-on Continuous Improvement Lead to drive improvement projects by working directly with all stakeholders including Operators on the plant floor. The ideal candidate will have a background in lean manufacturing and Six Sigma, with experience coaching and mentoring teams to solve problems and implement process improvements. This role is a member of the Production team, collaborating cross functionally with manufacturing teams, manufacturing support teams, and site leadership.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Lead and manage continuous improvement projects in the manufacturing areas. Will also plan a key leadership role in CI projects in other areas across the site.
⦁ Strong communication, influencing and stakeholder management skills, with the ability to engage and present recommendations to senior leadership
⦁ Oversight for training, introduction and optimization of lean tools and processes across the site such as 6S, Standard Work, Visual Management, Meeting Effectiveness, Gemba and Kaizen.
⦁ Lead value stream mapping workshop in order to identify and drive improvement projects
⦁ Excellent strategic thinking and problem-solving skills
⦁ Develop 3-5 Year C.I. Strategic Plan in conjunction
⦁ Strong analytical skills and data-driven decision-making capabilities
⦁ Ability to work collaboratively and build strong relationships across the organization
⦁ Demonstrated ability to drive change and foster a culture of continuous improvement
⦁ A strong sense of prioritization and time management
⦁ Ability to prioritize work, influence team members to execute, and measure success
⦁ Overall success leads to annual P&L financial savings target and execution of plans for process improvement
⦁ Work with Operators and area leaders to implement Lean and Six Sigma tools
⦁ Coach and train plant floor teams to improve processes
⦁ Identify and eliminate inefficiencies to drive operational excellence

Job Qualifications

⦁ Education: B.S./B.A./M.S. or equivalent in engineering and/or related discipline. Formal Black Belt Qualification or experience of oversight of signification continuous improvement change programs is desired.
⦁ Experience:
⦁ 6+ years related experience.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure:
⦁ PMP or project management experience.
⦁ Six Sigma green belt or black belt certification a plus.
⦁ Other:
⦁ Effective communication and interpersonal skills required.
⦁ Demonstrated computer skills (data input, word processing) required.
⦁ Experience with project management software and tools such as Microsoft project, smart sheet or similar.
⦁ Extensive experience in biotech industry in process development, process scale up, tech transfer and manufacturing.
⦁ Experience in the design, installation, and operations of GMP processes and equipment.

PHYSICAL DEMANDS:
⦁ Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁ Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to accurately exchange accurate information in these situations.
⦁ Ability to move about the manufacturing environment, including operating within clean rooms and other controlled areas

WORK ENVIRONMENT:

⦁ The employee must be able to follow site safety procedures as they will occasionally work near moving mechanical parts; in high, precarious places; and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock.
⦁ The noise level in the work environment is moderate.

Compensation Data

The pay range for this position is $130,000 - $145,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Technicien en Chimie Analytique - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui-sommes-nous ?

Le poste

Intégré(e) au département Formulations & Contrôle du site, nous recrutons un Technicien en Chimie Analytique (F/H) en CDI pour rejoindre notre laboratoire dès que possible.
Rattaché(e) à la manager d'équipe, le technicien en chimie pratique les analyses de routine (prinpalement UPLC) et participe activement à la vie du laboratoire. Il sait identifier les anomalies, problèmes et difficultés rencontrés dans son quotidien.

Les missions

Participer au développement et à la validation de méthodes analytiques en apportant une expertise technique
Réaliser toutes les étapes d’une analyse de routine (méthode validée) jusqu’à la constitution des dossiers
Utiliser des logiciels assurant le pilotage des équipements analytiques (chromatographie et spectrophotométrie)
Réaliser l’acquisition et le traitement des données analytique
Transmettre les résultats d’analyse en interne
Effectuer le contrôle interne des dossiers des analyses de routine
Préparer les rapports et les transmettre aux Directeurs d’étude
Transférer des données aux Directeurs d’Etude (compilation des dossiers, fichiers Excel transférés sur réseau…)

Conditions spécifiques du poste

Amplitude horaire : 7h30/18h avec planning à la semaine

Qualifications souhaitées

Vous êtes titulaire d'un diplôme de niveau Bac +2/3 en chimie et disposez d'une première expérience professionnelle concluante en chimie analytique (UPLC).
Vous appréciez le travail en équipe, mais savez évoluer en autonomie.
Organisé(e), vous êtes capable de vous adapter à des changements de planning avec flexibilité et rigueur.
Vous avez de bonnes bases de compréhension en anglais, écrit et lu.

Modalités

Convention collective de l’industrie pharmaceutique : groupe 3
Contrat : CDI non-cadre (accord de modulation 35h)
Salaire : A partir de 25 500€ bruts/an, sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun : moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Research Scientist Biomarker - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui-sommes-nous ?

Le site Charles River de Lyon est un site unique de 14 hectares, situé dans la vallée d’Azergues. Il offre un environnement scientifique innovant, dynamique et convivial où près de 1000 personnes travaillent chaque jour dans l’objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Afin de renforcer notre équipe de 15 scientifiques impliquée dans la gestion d'études de type immunoessais pour la détection d’anticorps ou protéines, nous recherchons un Reseach Scientist en Immunologie (F/H) en CDI sur notre site de Saint-Germain-Nuelles (69), à 30 minutes de Lyon. Vous interviendrez plus spécifiquement pour nos études liées aux biomarqueurs (plate-based assays et cell-based assays).

Vous travaillerez ainsi en support analytique afin de démontrer l'efficacité et la potentielle toxicologie de produits lors d’études animales ou d’essais cliniques humains. Pour cela, vous démontrez une connaissance approfondie du développement d’immunoessais sur les plateformes suivantes : ELISA, MSD, Gyrolab, cytométrie en flux et ELISpot.

Vous aimez également les défis techniques et l’opportunité de travailler sur plusieurs projets variés en parallèle est stimulante pour vous afin de faire avancer concrètement les projets clients préclinique et clinique.

Les missions

1/ Assurer un rôle de Directeur d'Etudes dans la gestion scientifique de développement, validation et analyse d'échantillons sur des études de toxicologie animale ou bien cliniques (80%) :

Etablir la faisabilité technique et scientifique des projets
Assurer un rôle de chef de projet (supervision des résultats générés, rédaction de rapports en anglais)
Prendre en charge l'analyse des données générées et leur acceptation sur Watson (LIMS)
Interpréter les données générées et être garant de leur fiabilité
Construire les procédures analytiques et plans expérimentaux préalable aux études (plan de plaque, détail de l'annexe technique)
Conseiller et orienter le client dans le design de l'essai et les démarches analytiques associées entreprises
Communiquer les informations clés aux équipes techniques de manière à faciliter les changes et travailler de manière efficiente

2/ Assurer également un rôle d’expert technique lors des phases de développement et validation (20%) :

Assurer de manière autonome la réalisation des essais ou bien s'assurer de leur réalisation, leur analyse, la vérification des données générées et leur communication dans le respect des délais et des procédures en vigueur.
Participer activement à la gestion opérationnelle de l'activité et des études (planification des essais, suivi des stocks de réactifs critiques, rédaction et vérification des annexes techniques)
Dispenser des formations ciblées aux techniciens et les développer en cas de besoin identifié
Être force de propositions pour améliorer les process et les méthodes analytiques

Qualifications souhaitées

Titulaire d'un Doctorat dans les domaines de l'immunologie, l'hématologie ou des biotechnologies, vous bénéficiez d’une expérience minimale de 5 ans en CRO, en développement et validation d’immunoessais en biomarqueurs et/ou cytométrie en flux.
Vous appréciez le travail en équipe dans un environnement collaboratif et évolutif.
Vous êtes reconnu(e) pour votre côté pédagogue, votre capacité à transmettre votre savoir aux collègues avec qui vous travaillez.
Vous êtes à même de convaincre des clients que votre approche analytique est pertinente et permettra d’atteindre les objectifs souhaités.
Une connaissance des exigences BPL serait un atout supplémentaire ; de même que la connaissance des logiciels suivants : Watson, Softmax, Gyrolab, sector S600, DIVA, FCS Express,...
Enfin, un niveau d’anglais confirmé (C1 minimum) est indispensable en vue des interactions avec nos clients ou avec les autres entités du groupe réparties à travers le monde.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI Cadre (forfait jours + 12 RTT)
Salaire : A partir de 48 000€ bruts/an, sur 13 mois
Indemnités de transports (site non accessible en transport en commun : moyen de locomotion indispensable)
Accord de télétravail (jusqu'à 3 jours/semaine), prise en charge de la mutuelle à hauteur de 60%, restaurant d’entreprise, CSE, primes de participation et d’intéressement, ...

À propos de Safety Assessment

À propos de Charles River

Au sein des laboratoires Charles River, nous reconnaissons et recrutons tous les talents. Nous sommes une entreprise attachée au principe de mixité, de diversité et d’inclusion et œuvrons quotidiennement en ce sens. Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.

Pour plus d'information, consultez www.criver.com.

Research Analyst I - Immunology (Ashland, OH, US, 44805)

Job Summary

We are seeking a Research Analyst 1- for our Immunology team at our Safety Assessment site located in Ashland, OH.

Basic Summary:

Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting.

Essential Duties and Responsibilities: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus.
Perform density gradient cell separations.
May act a lead/primary technician on basic studies.
Utilize micropipettes for all assays.
Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling.
Receive and log in reagents, solutions, and samples.
Prepare simple to complex lab solutions.
Assist in method development studies, method validation studies, and equipment validations as needed.
Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations.
Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed.
Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans.
Input, print, and edit basic to complex data.
Prepare materials for shipment and archival.
Review documentation for quality control.
Perform all other related duties as assigned.

The pay for this position is $21 USD per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: Bachelor’s degree (B.A/B.S.) in scientific field required.
Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and 4 years related experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experience preferred.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Technician I - In Vivo PK (Worcester, MA, US, 01608)

Job Summary

This position is working Full Time - Tuesday - Saturday 6:00 a.m. to 2:30 p.m.

Collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform in-life technical procedures (e.g., clipping, handling, binding, removals, body weight, dosing).
• Administer test substances by various basic methods (e.g., oral gavage).
• Input, print and edit computer entries (e.g., in life numbers, body weights, food consumption and clinical observation).
• Under supervision may act as lead/primary technician on basic studies.
• Observe animals for general health and overall well being. • Collect and record research data and biological specimens in compliance with applicable guidelines and regulations (GLPs, SOPS). • Read basic study protocols and extract pertinent information.
• Review documentation of functions performed as part of quality control requirements.
• Retrieve and view SOPs using appropriate database.
• Use applicable GLPs, SOPs, processes and company policies when performing all job functions.
• Handle, restrain, and provide care for all species of laboratory animals at the site.
• Perform study preparation activities including collection tube labeling and room setup.
• Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
• Receive animals (e.g., general health observation, sexing and identification) of all species, if applicable for the site.
• Perform all other related duties as assigned.

Job Qualifications

Qualifications:

Education: High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline.
Experience: 6 months related experience in animal research and/or husbandry or must have fully satisfied technical and experience requirements for the previous level.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred.
Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay for this position is $22.50/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Technicien de Toxicologie Rongeurs - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service Toxicologie recrute un Technicien en Toxicologie pour intégrer son équipe composée de 30 techniciens (rongeurs).

Les missions 

Au sein des services de Toxicologie In Vivo, vous aurez pour principales missions sous la responsabilité de votre supérieur :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
Procéder à des prélèvements sanguins, d’urine ou de fécès,
Saisir l’intégralité des actes réalisés sur informatique,
Assurer la qualité des données recueillies et de résultats,
Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Conditions spécifiques du poste

Travail en milieu confiné avec port obligatoire d’équipements de protection individuelle.

Travail le WE.

Retours et horaires décalés possibles (Discutés en amont avec le Responsable).

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique.

Vous êtes à l’aise au contact des animaux, notamment des rongeurs.

Vous maitrisez l’anglais

Vous possédez une aisance relationnelle et un sens du contact et du service, vous êtes organisé(e), vous appréciez de travailler en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h) - CDI
Salaire : A compter de 25 400 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Veterinary Pathologist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Veterinary Pathologist 2, for our team located in Senneville, Quebec, Canada, you will mainly be responsible for tissue evaluation and interpretation of assigned studies. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.
Record pathology findings in data capturing system(s).
Prepare complex reports delineating pathological findings and detailing all test article effects.
Interact with clients to assure satisfaction and to market services.
May assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation.
As needed, work with study directors to ensure data is accurately integrated into study reports.
Provide training, technical guidance and leadership to laboratory staff and to less experienced pathologists, as needed.
Provide advanced scientific expertise for experimental design and other aspects of research studies as needed.
Perform all other related duties as assigned.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Open to new graduates, eligible for ACVP/ECVP board exam.
Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.
Working knowledge of clinical pathology preferred; specialized training and/or experience in medical device pathology preferred.
Board certification with the American College of Veterinary Pathologists (A.C.V.P.) or European College of Veterinary Pathologists (E.C.V.P) required to enter the level grade.
Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought.
Ability to work on problems of diverse scope in which analysis of data requires evaluation of multiple factors.
Ability to exercise judgement within generally defined practices and policies in selecting methods or techniques for obtaining solutions.
Working knowledge of related computer applications.

Role Specific Information:

Place of work: Senneville.
Schedule: Onsite, Monday to Friday.

Why Charles River?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage)
Relocation amount and assistance.
Retention Bonus.
Paid development training.
Paid ACVP / ECVP yearly license.
Employee and family assistance program.
Access to a doctor and various health professionals (telemedicine).
4 weeks’ vacation & 10 Personal days per year.
Many social activities.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us, THIS IS YOUR MOMENT!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Pathologiste Vétérinaire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Pathologiste Vétérinaire 2, pour notre équipe située à Senneville, Québec, Canada, vous serez principalement responsable de l'évaluation des tissus et de l'interprétation des études assignées. Votre contribution assurera la santé de nos animaux ainsi que l'intégrité de nos études précliniques.

Dans ce rôle, les principales responsabilités sont les suivantes:

Effectuer l'évaluation et l'interprétation macroscopique et microscopique de tissus.
Entrer les observations microscopiques dans le(s) système(s) de capture de données.
Rédiger des rapports narratifs exhaustifs détaillant tous les effets de la substance évaluée.
Interagir avec les clients pour assurer leur satisfaction.
Supervision de nécropsie, possible de participer directement à des nécropsies, incluant la collecte et la fixation des échantillons et la description des observations macroscopiques.
Au besoin, collabore avec les directeurs d'étude pour s'assurer que les données de pathologie sont intégrées avec précision dans les rapports d'étude.
Effectuer toutes les autres tâches connexes assignées.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Diplôme de doctorat (D.V.M./V.M.D.) d'une école vétérinaire accréditée ou équivalent international acceptable en médecine vétérinaire.
Certification du Collège américain ou européen des pathologistes vétérinaires (A.C.V.P ou E.C.V.P).
Capable de travailler sur des problèmes complexes dans lesquels l'analyse de situations ou de données nécessite une évaluation approfondie de divers facteurs. Il a fait preuve de compétence technique, de créativité scientifique, de collaboration avec d'autres personnes et d'indépendance d’esprit; il a la réputation d'être un leader émergent avec des performances et des réalisations soutenues.
Maîtrise des logiciels de traitement de texte, de feuilles de calcul et de bases de données.

Informations spécifiques au poste:

Lieu de travail: Senneville.
Horaire: Du lundi au vendredi

Pourquoi Charles River?

Avantages compétitifs dès l'embauche. Nous payons jusqu'à 85% des primes (santé et dentaire).
Montant et aide à la relocalisation.
Prime de rétention.
Formation de développement payée.
Licence annuelle ACVP / ECVP payée.
Programme d'aide aux employés et aux familles.
Accès à un médecin et à divers professionnels de la santé (télémédecine).
4 semaines de vacances et 10 jours personnels par an.
Nombreuses activités sociales.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais partout dans le monde, joignez-vous à nous, C’EST VOTRE MOMENT.

Pour plus d'information, consultez www.criver.com.

Junior Technical Service (Hyderabad, IN)

Job Summary

Responsible for technical support for Endosafe® (including automated NEXUS system) and/or Celsis™ and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™)
Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales.
Supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management.
Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products.
Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line.
Performs instrument qualification and installation for new customers.
Establishes regular interface and communication with the Account Management and Field Services team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients.
Builds relationships with customers to influence the acceptance and use of Microbial portfolio.
Input, manage and monitor cases on Service Cloud or SFDC.Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate.

GENERAL REQUIRMENTS

Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements.
Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate.
Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements.
Must be willing to travel domestically and internationally to customers’ sites.
Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements.
Performs all other related duties as assigned.

Job Qualifications

Education: Minimally M.Sc. or equivalent in Biology, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline.
Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities.
Salary range : 4 to 7 LPA.
Understanding of Biology/Microbiology in the Pharma setting is an advantage.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Animal Care Technician I (Shrewsbury, MA, US, 01545)

Job Summary

Full Time - 40 Hours/Week - Tuesday-Saturday Day Shift

Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. May serve as lead/primary technician and perform technical duties with guidance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• May serve as lead/primary technician and perform technical duties with guidance.
• Handle, restrain, and provide care for all species of animals at the site.
• Observe animals for general health and overall well being.
• Clean primary enclosure and enclosure area for animals.
• Sanitize cages, enrichment devices and other related equipment.
• Measure and distribute feed to animals in accordance with established procedures.
• Provide environmental enrichment.
• Inspect feeding and watering devices for proper function.
• Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
• Review documentation of functions performed as part of quality control requirements.
• Perform quarantine & isolation procedures as they relate to husbandry tasks.
• Perform duties associated with the transportation, receipt, transfer and distribution of animals as assigned.
• Perform cagewash duties as assigned.
• Collect laboratory data and independently use equipment related to the collection of data.
• May perform basic veterinary technical and husbandry tasks with guidance, including the following:
o    Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
o    Bandage/wrapping techniques.
o    Nail/hoof/teeth clipping/trimming.
o    Venipuncture techniques.
o    Vaginal swabs.
o    Proficient animal restraint techniques.
o    Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
• Perform all other related duties as assigned.

The pay for this position is $20.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) required.
• Experience: Minimum of 6 months related experience in animal research and/or husbandry preferred or must have demonstrated full knowledge of competencies and positive performance at the previous level. Experience working in a regulated environment preferred.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: AALAS certification at the ALAT level preferred
• Other: Ability to handle common laboratory animal species. Basic knowledge of GLP regulations preferred. Ability to work on assignments that are semi-routine in nature in which ability to recognize deviation from accepted practice is required. Ability to receive and understand general instructions on routine work and detailed instructions on new assignments.

PHYSICAL DEMANDS:
• Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
• Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
• Must be able to frequently firmly hold species while utilizing fine motor skills.
• Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
• Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
• The employee regularly works with live animals with risk of exposure to dander, allergens, zoonotic disease, and biohazards.
• The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:
• This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Clinical Veterinarian (Ashland, OH, US, 44805)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

The Clinical Veterinarian is a full-time role meant to provide top notch and ethical veterinary health care for laboratory animals and ensure CRL’s mission of saving human and animal lives! A successful individual will also advise regarding the husbandry, care and maintenance of laboratory animals as well as facilitating training for technicians. This responsibility extends to promoting animal well-being during all phases of the animal's life as well as roles in compliance monitoring, quality management and safe work practices when working with animal models. Our goal is to save human and animal lives in the most ethical and humane way by not only adhering to regulations and guidance's such as the animal welfare act, the 3R's of ethical research, the AVMA guidance on human euthanasia, and “The Guide for the Care and Use of Lab Animals," but pursuing continuous improvement to approaches in research animal care.

Note: This posting is for networking purposes for future opportunities.

For successful hires we offer:

PAID TIME OFF TO STUDY FOR BOARDS AND TUITION ASSISTANCE FOR CONTINUING EDUCATION
STRONG BONUS INCENTIVES AS WELL AS RETENTION BONUSES FOR 3 YEARS
SUPPORT FOR ANNUAL CONFERENCE ATTENDANCE, CONTINUING EDUCATION AND JOURNAL PUBLICATIONS IF DESIRED
THE SATISFACTION OF BEING PART OF A TEAM THAT IS COMMITED TO ANIMAL WELFARE AND ON THE CUTTING EDGE OF DRUG DISCOVERY

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
expertise/advice to facilitate protocol development.
Develop and deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment. May also consult on the planning, conduct, and reporting of studies.
May assist in sentinel animal monitoring and other monitoring programs.
Write, review and update veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
May assist in management of the activities of assigned section, including supervising
employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring.
Perform special projects and assist with administrative efforts as needed.

Job Qualifications

QUALIFICATIONS:

Education: Veterinary degree (D.V.M./V.M.D.) or international equivalent.
Experience: 0 to 2 years related experience with animal care. Preferred but not required as we have a training program to assist with joining the CRL team.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable.
Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

Compensation Information:

Base salary + short-term and long-term incentive plans
Professional development and continuing education (e.g., CE (national/local meetings, virtual & in-person), leadership development, cross-site and international collaboration within CRL)
Other academic and credentialed pursuits (e.g., ACLAM Boards, Toxicology specialty boards). 
Enhanced flexibility/consistency of hours, valued support for work/life balance
Comprehensive onboarding, mentorship during transition, and training opportunities
Access to a global network of veterinarians across Safety Assessment and other business units.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Staff Veterinarian (Reno, NV, US, 89511)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

We are seeking an experienced Staff Veterinarian for our Safety Assessment site located in Reno, Nevada, or Houston, Texas

Note: This posting is for networking purposes for future opportunities.

Job Summary

This position is responsible for overseeing and performing veterinary procedures that support all studies. This position will also oversee all aspects of the animal care and use program.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
expertise/advice to facilitate protocol development.
Develop and deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment. May also consult on the planning, conduct, and reporting of studies.
May assist in sentinel animal monitoring and other monitoring programs.
Write, review and update veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
May assist in management of the activities of assigned section, including supervising
employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring.
Perform special projects and assist with administrative efforts as needed.

Qualifications

The following are minimum requirements related to the Staff Veterinarian position:

Veterinary degree (D.V.M./V.M.D.) or international equivalent required
Licensure to practice veterinary medicine in at least 1 U.S. state required
Computer literacy, good communication, interpersonal, and organizational skills

Preferred:

Ability to practice veterinary medicine in the work state highly desirable
ACLAM eligibility or accreditation preferred
Minimum 3 years experience in laboratory animal medicine preferred
2 years management experience preferred
Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles (GLP) and current methodology of laboratory animal medicine and management is important

Compensation information:

Base salary + short-term and long-term incentive plans
Professional development and continuing education (e.g., CE (national/local meetings, virtual & in-person), leadership development, cross-site and international collaboration within CRL)
Other academic and credentialed pursuits (e.g., ACLAM Boards, Toxicology specialty boards). 
Enhanced flexibility/consistency of hours, valued support for work/life balance
Comprehensive onboarding, mentorship during transition, and training opportunities
Access to a global network of veterinarians across Safety Assessment and other business units.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

For more information, please visit www.criver.com.

Senior Business Development Executive - Cell Solutions (West Coast Territory) (Northridge, CA, US, 91325)

For over 40 years, Charles River Cell Solutions has worked to making a positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and developing novel cell-based therapies.

We recognize that our success depends on the vision and passion of our employees; that is why we are devoted to making Cell Solutions a rewarding and valuable place to work. We believe in making a difference, and at Cell Solutions, you will make a difference every day.

Job Summary

The Senior Business Development Executive is primary responsibility is to develop new business relationships and expand existing relationships by analyzing account potential; initiating, developing, and closing sales that drive profitable revenue growth. The Senior Business Development Executive is directly responsible for achieving or exceeding quarterly and annual area sales targets and gross profit growth within an assigned geographic territory and various market segments such as Cell and Gene Therapy, Pharmaceutical, Biotechnology, Regenerative Medicine, Vaccine, and Academic R&D.

This position is remote and will work from a home office, located in the West Coast of the USA.

Travel is expected to be 50% of the time.

Essential Responsibilities

•   Demonstrate technical, negotiation, and selling skills.
•   Work with management to develop, prepare, and implement a comprehensive territory business plan to identify new target accounts and target opportunities within an assigned geographic area to achieve quarterly and annual revenue targets.
•   Develop and maintain short- and long-term sales pipeline to consistently generate revenue.
•   Build team relationships with other Sales and Operational staff to maximize sales revenue and territory pipeline.
•   Serve as the voice of the customers in their territory by collecting and communicating VOC to Marketing to improve customer experience and anticipate market changes to adapt and respond to new product and service needs.
•   Enhance job knowledge by participating in local educational opportunities, reading professional publications, maintaining personal networks, and participating in professional organizations.
•   Work with management to prepare and provide accurate territory forecasts throughout the year to track achievements versus goals.
•   Comfortable working with ambiguity in a dynamic and changing environment.
•   Assist with updating and maintaining applicable databases (e.g., SalesForce.com)
•   Assist with executing other daily tasks or special projects, as assigned.
•   Independently travel to meet with current and prospective customers, attend vendor shows and seminars, and sales meetings. In person travel should achieve the goal of increasing revenue and building territory pipeline via prospecting, increasing brand awareness and building relationships and strategic partnerships with end users of the product portfolio.

Job Qualifications

To perform this job successfully, an individual must be able to perform each essential responsibility satisfactorily using the skills and abilities outlined in this job description. The requirements listed below are representative of the knowledge, skills, and abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
•   Strong communication and interpersonal skills
•   Organizational skills and attention to detail required
•   Well-developed math and business skills
•   High level of understanding of the market
•   Discretion in handling confidential and sensitive matters
•   Building and maintaining relationships with internal stakeholders and external customers
•   Closing skills
•   Ability to learn and understand highly technical content
•   Positive attitude and resilience
•   Ability to adapt and succeed in an evolving, dynamic environment
•   Independent decision making & problem-solving skills
•   Flexibility to work both autonomously and part of a larger team
•   Presentation skills

Education, Experience, and Licensure

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, business or marketing related discipline; master’s degree preferred and/or Ph.D. preferred. Certified Sales Professional designation preferred.
•   Experience: Six to nine years previous experience in a similar sales role, preferably in selling to academic, biotechnology, or pharmaceutical researchers and organizations.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Familiar with primary human cells, stem cells, immunology, life science research, drug screen, toxicity test, cell-based assay, hematology, or flow cytometry

Compensation Data

The pay range for this position is $130K - 140K USD + 50% commission. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River Cell Solutions

Charles River Cell Solutions is a global leader and trusted brand in the customization of human-derived biological products and services for biomedical research, drug discovery, and cell and gene therapy development. Cell Solution’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.

In January 2020, HemaCare was acquired by Charles River Laboratories, an early-stage contract research organization (CRO). Combined with Charles River’s integrated, early-stage portfolio of discovery, safety assessment, and manufacturing support services, the acquisition creates a unique, comprehensive solution for researchers and cell therapy developers and manufacturers worldwide to help accelerate their critical programs from basic research and proof-of-concept to regulatory approval and commercialization. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs and enhances their productivity and effectiveness to increase speed to market. We work closely with our clients throughout the clinical process to maximize success and drive positive clinical outcomes.

Together, with over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Cell Solutions, we are passionate about our role in improving the quality of people’s lives. We have proudly supported the development of 100% of the current commercially available FDA-approved immunocellular therapies. Our mission is to provide a best-in-class portfolio of high quality, customizable human cellular material and services to support drug discovery, scientific research, and cell therapy. This resonates from our employees and impacts our customers because we know that every day is an opportunity to advance discoveries and make a difference in someone’s life.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Technician I, Animal Care (Cage Wash) (Ashland, OH, US, 44805)

We are seeking an experienced Animal Care Technician I for our Safety Assessment site located in Ashland, OH. Shift Monday-Friday 8am-430pm, every 4th weekend and every other holiday. *This role will primarly work within our Cage Wash discipline within the Animal Care department*

A Technician 1 – Animal Care Services is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study which may include animal husbandry needs, animal handling, cage changes, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. The technician is working under close supervision to gain proficiency

ESSENTIAL DUTIES AND RESPONSIBILITIES: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cage changes, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements. 
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The starting pay for this position is 18.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles.
The employee regularly works with live animals with risk of exposure to dander, allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Business Development Director - Biologics Testing (New England territory) (Wilmington, MA, US, 01887)

Job Summary

The Business Development Director will support the Biologics Testing Commercial team in the New England region.

Position will work from home office and ideally live within Boston or the New England area.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Lead sales program in assigned territory applying technical/scientific skills to compete for customers.
Develop and qualify leads through customer contact and prospecting. Communicate available Charles River products and services and inform customers of new products and services in a timely manner.
Fulfill subject matter expertise role, working with marketing to assure design, development and implementation of marketing tools and programs that support company goals.
Handle initial inquires and qualify all prospective opportunities. Identify the drug development business model at these accounts and effectively communicate the value proposition of the company's products and services.
Prepare and implement a comprehensive territory management plan to indicate target opportunities, potential new accounts, expansion of existing accounts and an analysis of competitor accounts.
Build relationships with customers to influence the acceptance and use of company products and services.
Work with other specialists within Biologics and across the organization to generate major account specific sales strategies to close opportunities.
Assist Global Account Management with presenting global capabilities, qualifying leads, demonstrating added value and closing new business opportunities by providing scientific support during sponsor teleconference calls, field visits and at scientific trade shows.
As required, give overview of assigned product line and services to internal and external contacts. Share portfolio opportunities with Account Manager from other divisions withing Charles River.
As required gather data on market trends and competitive products and pricing. Gather data on potential competitors in the designated geographic region.
Share customer problems/concerns with relevant departments for quality resolution.
Participate and assume support role in national and international tradeshows and aid in the coordination of tradeshow events and or presentations.
Participate in sales meetings as required.
Complete all required sales documentation and training in a timely manner.
Utilize CRM to capture customer information and maintain all communications within the CRM system with routine status reporting.
Perform as organizational lead for CRM system monitoring and reporting. Specifically, ensuring all proposals are followed up on in a timely manner.
Develop and maintain reports for tracking and reporting on Sales Initiatives within CRM and/or other tools.
Assist Sales Specialists and Management with specific assigned customer projects as needed.
Perform all other related duties as assigned.
Responsible for ensuring that a safe working environment is maintained for him/herself and his/her colleagues by observing all safety procedures and working methods, by making proper use of protective clothing and equipment and by reading, understanding and following all safety documents issued or notified to him/her.
To participate in overtime as is reasonably required for the successful completion of your role.

Job Qualifications

Education: Bachelor's degree (B.A. /B.S.) or equivalent in business or related discipline.
Experience: Three to Five years related experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid driver's license required.
Other: Fluent in verbal and written English and German. Must possess excellent communication and presentation skills. Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail).

Compensation Data

The pay range for this position is $110,000 - $125,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier en Toxicologie Non-Rongeurs - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Toxicologie recrute un Animalier pour intégrer son équipe composée de 10 animaliers.

Les missions 

Au sein du Département de Toxicologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Participer à l’entretien des locaux (change de cages, matériel) et soins des animaux selon les règles d’hygiène et de sécurité et les bonnes pratiques de laboratoire ,
Réaliser progressivement certaines techniques sur toutes espèces (contention,…) ,
Assurer la saisie informatique des résultats,
Appliquer les procédures standards et protocoles d’études avec toute la rigueur requise,
Assurer un suivi et transmettre toutes informations sur tout évènement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BEP/BAC type STL .

Vous êtes organisé(e) et vous appréciez le travail en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.

Contact avec les animaux.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : CDD de 09 mois - Non-cadre (accord de modulation 35h)
Salaire : A compter de 23 946€ bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animalier en Toxicologie Non-Rongeurs - F/H - CDD 09 mois 1 (Evreux, FR, 27930)

Résumé du travail

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Trade Show Manager (Life Sciences), DSA (Wilmington, MA, US, 01887)

Job Summary

The Events Manager is responsible for the planning, execution, and review of conference / tradeshow participation and customer-focused events within the Discovery & Safety Assessment (DSA) division globally.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage, plan, and execute a section of conferences, tradeshows and CRL hosted events assigned for the DSA division.
• Understand the strategic business objectives and collaborate with both commercial and operational stakeholders to build and execute on a comprehensive plan of events that results in visible impact on revenue.
• Oversee and build on the successful range of CRL hosted scientific summit events across the manufacturing portfolio.
• Perform extensive research on each potential event; strategize on key initiatives to drive success, enforce a culture of continuous evaluation, and implement change to drive improvement.
• Establish and communicate out KPI’s (leads, pre-set meetings, attendees, survey results) for each event. Provide KPI metrics to the wider team and stakeholders, provide suggestions on improvements.
• Perform pre-event planning strategies to provide historical, demographic, and statistical analysis and return on investment.
• Provide advice and guidance to senior management regarding event budget requirements, ROI, suggested level of participation and recommendations for future event involvement.
• Select, manage, and build relationships with a selection of third-party vendors associated with event execution. Where possible provide expertise and advice to enhance ROI and the overall CRL experience at events.
• Manage the global event schedule, including all aspects of negotiation, contracting, preparation and logistics for CRL’s event involvement.
• Provide clear and concise information for stakeholders and attendees on participation, roles & responsibilities and expectations.
• Assist in the development and recommendation of departmental budget. Authorize expenditures in accordance with budget. Manage event expenses, including negotiation whilst striving to provide maximum value on investment by means of bundling, value adding and discount discussions.
• Evaluate event involvement, including effectiveness of activities, content, and messaging, and make changes and improvements as needed.
• Identify and research potential new events that meet the objective for growing new CRL business or acquisition.
• Ensure adequate staffing at all events and provide appropriate selection of marketing literature and materials.
• Organize, chair and record pre and post event planning meetings for each event. Develop event strategy from group discussion, assign tasks to complete strategy, and manage completion of all tasks to ensure prominent presence for CRL at the event.
• Identify and take advantage of all promotional opportunities available for each event.
• Determine and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s degree (B.A./B.S.) or equivalent.
• Experience: 5-10 years related experience, ideally working within the life sciences tradeshow arena.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None
• Other: Negotiation, organization, statistical analysis, problem solving and strong communication skills required.

This position requires regular domestic travel.

Compensation Data

The pay range for this position is $75,000 - $100,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier en Toxicologie Rongeurs - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Toxicologie recrute un Animalier pour intégrer son équipe composée de 10 animaliers.

Les missions 

Au sein du Département de Toxicologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Participer à l’entretien des locaux (change de cages, matériel) et soins des animaux selon les règles d’hygiène et de sécurité et les bonnes pratiques de laboratoire,
Réaliser progressivement certaines techniques sur toutes espèces (contention,…),
Assurer la saisie informatique des résultats,
Appliquer les procédures standards et protocoles d’études avec toute la rigueur requise,
Assurer un suivi et transmettre toutes informations sur tout évènement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BEP/BAC type STL.

Vous êtes organisé(e) et vous appréciez le travail en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.
Travail de Week-End.
Contact avec les animaux (rongeurs).

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 2
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 23 940 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Chargé(e) HSE - H/F - CDI (Ecully, FR, 69130)

Qui sommes-nous ?

Aux portes de Lyon, le site Charles River d'Ecully offre à ses 90 collaborateurs un environnement dynamique et une cuture d'entreprise certifiés Great Place To Work® pour la 4ème année consécutive. Nos équipes, passionnées et impliquées, contribuent aux efforts que nous accomplissons chaque jour pour améliorer la santé et le bien-être du plus grand nombre possible de personnes.

Le poste

Dans le cadre d'une création de poste et afin de répondre à l'intégralité de nos enjeux dans le domaine, nous recherchons un(e) Chargé(e) HSE en CDI.
Votre rôle sera de participer à la définition de la politique HSE et à sa mise en œuvre afin d’assurer la prévention des risques pour le personnel, les prestataires et l’environnement, par le développement et le maintien d’une dynamique et d’une culture HSE.
Il s'agit d'un poste polyvalent et autonome, en interface avec de nombreuses parties prenantes internes et externes. Sur ce poste, vous rapporterez directement au Responsable des Services Généraux du site, et indirectement au pôle HSE du groupe.

Missions :

1/ Responsabilités générales :

Participer à la définition de la politique HSE, en lien avec la stratégie globale et locale, en étant force de proposition
Veiller et participer au bon avancement et mise en œuvre de la politique HSE
Conduire et coordonner des projets et des initiatives et surveiller leur avancement
Faire le lien avec les équipes HSE globales et des autres sites, notamment pour déployer la politique HSE globale et échanger sur les bonnes pratiques
Assurer la veille réglementaire en matière HSE et anticiper les évolutions afin de garantir la conformité HSE du site
Proposer et suivre des indicateurs HSE et en dégager une analyse
Contrôler la bonne application des réglementations et préconisations HSE
Planifier et suivre les audits HSE
Communiquer sur les bonnes pratiques et les réalisations du site en matière HSE

2/ Hygiène et Sécurité :

Identifier, analyser et hiérarchiser les risques professionnels en observant les conditions de travail des salariés, et proposer des actions d’amélioration
Assurer la mise en place et/ou la mise à jour de la documentation HSE et des moyens nécessaires pour garantir le travail en toute sécurité de l’ensemble du personnel
Informer et sensibiliser les différents acteurs et le personnel de l’entreprise aux enjeux HSE, et être moteur dans le développement de la culture sécurité
Superviser et animer le comité PRAP (Prévention des Risques liés à l’Activité Physique)
Analyser les accidents et mettre en place des plans d’actions correctives et préventives
Proposer, concevoir et animer des formations sur les modalités, les règles et les consignes de sécurité et environnement
Veiller à la bonne qualité de services des prestataires, et notamment la prestation de ménage

3/ Environnement :

Gérer les dossiers réglementaires sécurité et environnement de la société (DUERP, assurances, etc.)
Superviser les flux de déchets générés par les activités et proposer des actions d’amélioration
Piloter la maintenance des infrastructures, principalement liée aux contrôles règlementaires réguliers
Participer aux projets de travaux et au suivi de leur réalisation sur le site

Qualifications requises :

Vous êtes issu(e) d'une formation de niveau bac+5 spécialisée en management HSE, ou vous disposez d'une expérience équivalente de 5 ans minimum sur un poste similaire.

Au-delà de vos connaissances techniques et de votre savoir-faire, vos qualités relationnelles seront vos principaux atouts : empathie et écoute, excellent niveau de communication, aisance relationnelle, capacité à animer en transversale et à fédérer.

Notre entreprise ayant un rayonnement international, une bonne maîtrise de l’anglais est indispensable à l’oral comme à l’écrit.

Modalités contractuelles :

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat CDI cadre, forfait 217 jours par an
Salaire annuel à partir de 39 663 € bruts sur 14 mois + variable
Primes de transport et titres restaurant
Prime d’intéressement

Dans le cadre de sa politique en faveur de la diversité et de l’inclusion, Charles River s’engage à respecter les principes d’égalité des chances et de non-discrimination tout au long du process de recrutement.

À propos de Microbial Solutions

Notre groupe Microbial Solutions dispose d'un portefeuille très complet de services de test d'endotoxines, et de services et produits de détection et d'identification de microbes sans égal, qui a été spécialement conçu pour répondre aux besoins complexes et changeants de l'industrie. Nous aidons nos clients à garantir la qualité et l'innocuité de leurs produits grâce à des solutions de test faciles à utiliser et néanmoins extrêmement fiables qui sont conformes aux exigences réglementaires, qui sont axées sur le processus de prise de décisions critiques et qui visent à améliorer l'efficacité opérationnelle.

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Bioanalytical Chemistry - Director (Mattawan, MI, US, 49071)

Job Summary

Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

Job Functions:

Efficiently perform supervisory responsibilities in accordance with organizational policies and applicable laws to include interviewing, hiring, training and developing employees
Develop organizational strength by hiring, identifying and developing personnel who are scientifically and/or technically strong
Establish culture and atmosphere to maintain good retention and low turnover using available tools and metrics
Assist with providing costing estimates for components of applicable studies
Provide short- and long-term solutions that support continuous improvement
Maintain critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, team, cross-site, and externally with collaborators and sponsors
Ensure laboratory tasks and operations are executed in compliance with SOPs, protocols, regulatory requirements as needed
Review and approve Standard Operating Procedures (SOPs), protocols, policies, best practices and study procedures
Maintain contemporaneous knowledge of regulatory requirements
Effectively plan, assign and direct work within one or more operational areas
Establish and monitor performance metrics for one or more operational areas
Skillfully oversee the design, conduct, interpretation and reporting of studies as needed
Lead implementation of new procedures and refinement of existing procedures to meet current and future business needs
Align operational resources with the current needs in one or more operational area
Manage cross-service line interdependencies in collaboration with organizational leadership
Collaborate with multiple departments within and outside of site
Lead planning (resource management, budgets and study coordination) as well as track budgets and spend vs. revenue for one or more operational areas
Collaborate and consult with prospective Sponsors, providing scientific expertise and developing ongoing Sponsor relationships
Provide leadership, expert consultation and mentorship to cross-functional company teams
Provide vision and determines business priorities for one or more operational areas
Performs all other related duties as assigned

Job Qualifications

Bachelor’s degree or equivalent with 15+ years of relevant experience. Greater than 8 years of management experience required
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
LCMS/MS Experience Preferred
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints

The pay range for this position is $165-175k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientific Associate (Chemistry) 12 Month FTC (Tranent, GB, EH33 2NE)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

The Chemistry Department at Charles River Edinburgh is seeking a talented and flexible individual for a role as a Scientific Associate.

In order to support our Agrochemical, Animal Health and Pharmaceutical Sponsors, the Chemistry department provides accurate quantification and elucidation of chemical structures. This is conducted as a key component of the full range of ADME, Crop Metabolism, Field & Veterinary Residue and Environmental Fate studies that we provide.

The successful applicant will be primarily laboratory-based, supporting studies that involve analysis of drug, agrochemical and animal health compounds in complex matrices. These projects require the application of selective extraction methods followed by chromatographic-mass spectrometry techniques such as LC MSMS, LC-high resolution-MS, GC-MS(MS), SFC-MSMS and may include radio-chromatographic techniques. You may also support studies which involve the purification/isolation of compounds using (semi-) prep scale flash chromatography.

Accurate data recording is imperative to ensure compliance with company and regulatory policies. We are therefore seeking a highly organised individual with an eye for detail. The successful applicant will have excellent communication skills, working effectively with others to overcome scientific challenges and learn new skills. This role also requires the ability to work independently in the laboratory.

Profile and Requirements

The successful applicant will be educated to at least Degree level in a discipline containing a significant chemistry or analytical chemistry component. 

A working knowledge of sample preparation and chromatographic techniques such as UPLC/HPLC/GC and triple quadrupole/high resolution MS is highly advantageous but not essential as training will be provided.

Key responsibilities:

• Follow written instructions (standard operating procedures, protocols, analytical methods)

• Preparation of samples for chromatography

• Sample analysis (LC MSMS, LC-high resolution-MS, GC-MS(MS), SFC-MSMS)

• Data processing

• Reporting and Quality control checking of data

• Working to agreed deadlines

The salary for this role is £27,163.48

Due to high volume of applications we are receiving if you have not heard anything from Charles River Laboratories Edinburgh regarding the next steps of our recruitment process within 3 weeks of the closing date then please conclude you have been unsuccessful.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

For more information, please visit www.criver.com.

Biomanufacturing Supervisor 12:00pm - 8:00pm (Memphis, TN, US, 38118)

Job Summary

We are seeking a Biomanufacturing Supervisor for our Cell Therapy Manufacturing Business located Memphis, TN.

NOTE: The shift for this position is rotating schedule 12:00pm - 8:00pm

The following are responsibilities related to the Biomanufacturing Supervisor.

• Oversees manufacturing personnel in equipment setup, equipment operation, and processes in accordance with cGMPs, Quality System, and process documents.
• Conducts and/or schedules training for new employees including media fills.
• Schedule’s personnel to support all production related activities.
• Provides assistance to management in the revision and/or writing of process documents to assure accuracy and completeness. This includes but is not limited to reviewing BPRs and associated documentation for accuracy, compliance, and presence of all verification signatures.
• Assures employees understand duties, responsibilities, policies, and procedures.
• Advises management on personnel management functions.
• Leads and implements continuous improvement activities and assists with projects as assigned.
• Enforces adherence to regulatory guidelines and internal policies.
• Takes part in Technology Transfer. May collect, analyze and summarize information and trends.
• Lead, mentor, and develop direct reports.
• Perform other duties, as assigned.

Job Qualifications

The following are minimum qualifications related to the Biomanufacturing Supervisor position:

• Minimum of an Associate degree required.
• Minimum of 3 years of applicable experience.
• 1 year of leadership and/or supervisor experience preferred.
• Exhibits exceptional leadership qualities.
• Must be detail oriented and have excellent organizational skills.
• Must possess effective written and oral communication skills.
• Must display a high degree of professionalism and confidentiality.

Compensation Data

The pay range for this position is $74,700 - $83,500. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Animal Care Technician I (San Diego, CA, US, 92121)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team, located in San Diego, CA.

As the Animal Care Technician I, you will provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

Required:
- Education: High school diploma, General Education Degree (G.E.D.)
Preferred:
- Education: Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred
- Experience: Directly related laboratory animal experience in a laboratory animal facility preferred.
- Certification/Licensure: Assistant Laboratory Animal Technician (ALAT) certification from AALAS preferred.

The pay range for this position is $20-22 USD per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Validation Engineer (Wayne, PA, US, 19087)

Job Summary

Provide engineering oversight for validation of legacy and new equipment.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure optimum performance of the validation group's metrology function.
Oversee and support the testing phase of equipment monitoring systems validation efforts.
Oversee equipment validation efforts regarding the execution, development and training for the site.
Manage and maintain the site's DI water system and associated drops.
Maintain, coordinate and schedule vendor certifications of clean rooms and associated equipment.
Represents the validation group with all site and equipment change control
Review vendor standard operating procedures, reports and protocols and maintain revision status as current.
Work closely with contractors, suppliers and vendors to troubleshoot or install equipment.
Assist in identifying what equipment in the lab needs to be replaced or removed.
Assist with developing equipment requirements for laboratory purchases.
May train others on proper use of equipment.
Oversee daily operational activities of one non-exempt employee.
Recommend short-range operating objectives, organizational structure, staffing requirements and succession plans.
May assist in development of departmental budget.
As required, oversee maintenance of group training manual and training records.
Support the policy of equal employment opportunity through affirmative action in personnel actions.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
Author and revise qualification protocols and SOPs.
Perform technical review of vendor generated calibration and certification reports.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor's degree (B.A. /B.S.) in engineering or related discipline.
Experience: 2-4 years related experience in a cGMP regulated environment. Experience involving active participation in metrology, equipment qualification and system validation efforts, preferably at the project management level.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Computer files organizational skills. Computer application skills. Ability to read and follow all company SOPs and guidelines and demonstrated knowledge of cGMP regulations. Ability to work effectively as a member of a team, interact with internal and external clients during client site audits, conducting vendor audits, and interact with all levels of employees at the site for training and team events. Ability to manage multiple priorities, problem-solve and meet deadlines. Excellent verbal and written communication skills and ability to respond effectively to change. Champion new procedures which will improve or add value to new and existing assays. Knowledge of compendial monographs, 21 CFR Part 11 requirements, ICH guidelines and ISO standards as they apply to a regulatory environment.

Compensation Data

The pay rate for this role is $75,000 - $79,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Formulations Technician I (Spencerville, OH, US, 45887)

Job Summary

We are seeking a Formulations Technician I for our Formulations Technician I at our Safety Assessment site located in Spencerville, OH.
A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include disposal of Formulation material, assisting with the preparation of test materials and dietary admixtures for dose administration, as well as maintaining the general cleanliness of the lab. The technician is working under close supervision to gain proficiency.

Essential Functions (The fundamental Duties & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards (protocols, methods, SOPs, etc.).
Train in formulations skills which may include disposal and transport of residual dosing material, non-regulated pharmaceutical solids, accumulated single-use containers to designated waste receiving areas; sterilization of laboratory equipment using autoclave or other methods; perform and document preparation of vehicle/control article/substance dosage solutions/suspensions under supervision; and wash and maintain glassware and lab cleanliness and appearance. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Assist with use and maintenance of instrumentation and equipment.
Read protocols and extract pertinent study information including a general understanding of the protocol format and its content with minimal help.
Learn Good Laboratory Practices (GLP) regulations and understand compliance through in-house training.
Develop knowledge of company SOPs and policies, and begin to apply the knowledge to ensure compliance when performing functions throughout the lab with minimal help.
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned

The pay for this position is $19.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
A mathematical aptitude required.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP),
Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Maintenance Technician IV Automation - Mon - Friday 3:00pm - 11:30pm (Mattawan, MI, US, 49071)

Job Summary

Note: This position is 3:00pm - 11:30pm EST Monday thru Friday with w/e rotation every 2 months

A Building Automation System Operator is responsible for: maintaining the building environment, environmental monitoring systems and controls; performing maintenance functions; and recommending improvements. The individual in this role works with minimal supervisor on complex projects and handles work orders for facility equipment control issues in a highly regulated environment.

Essential Duties & Responsibilities:

Maintain the building environment, environmental monitoring systems and controls.
Perform equipment maintenance functions associated with monitoring of a laboratory research environment.
Make recommendations to improve efficiency or operations.
Assist with the design of new facility heating, ventilation, and air conditioning (HVAC) and other monitored systems.
Remediate routine/nonroutine work orders and facility equipment control issues.
Coordinator correspondence for corrective action preventative action (CAPA) issues for Good Laboratory Procedures (GLP) documentation of errors and deviations.
Remediate HVAC deviations and repairs encountered in the facility.
Other duties as assigned.

Job Qualifications

Education & Experience:

HS/GED/Associate's/Bachelor's degree with 2 or more years of relevant experience; contract research organization experience preferred.
Building control system experience required.
Commercial HVAC and systems experience preferred.
EPA Certified preferred.
Demonstrated ability to problem-solve, make decisions, work effectively independently and as part of a team.
Demonstrated knowledge of plant mechanical functions, Standard Operating Procedures (SOPs), policies, GLPs and associated requirements.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate wit Essential Duties and Responsiblities, including the ability to learn a validated systems.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under time constraints.
Ability to push, pull, lift 50lbs +.

The pay range for this position is $28-35/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Technician Assistant (Reno, NV, US, 89511)

Job Summary

We are seeking an experienced Research Technician Assistant for our Safety Assessment site located in Reno, Nevada.

As a Research Technician Assistant, you will have the opportunity to care for all species of animals at our state-of-the-art safety sites. You will learn new skills ranging from animal care and handling of laboratory animals, perform clinical observations, blood collection, drug dosing, and perform accurate data collection and reporting.

The following are minimum requirements related to the Research Technician Assistant position.

High School Diploma or General Education Degree (G.E.D.)
0-6 months related experience in animal research and/or husbandry preferred.
Ability to handle common laboratory animal species.
Basic knowledge of Good Laboratory Practice regulations preferred.

Job Qualifications

The training and development offered to our entry level technicians is state of the art and designed to help you succeed. The work you will be doing will impact the lives of patients and animals across the world and is the kind of work that is truly rewarding.

If you possess the following qualities, we will train you in the rest:

Enjoys working within a team
Has the ability to work in a fast-paced and challenging environment
Pays attention to detail
Dependable
Ability to work independently
Ability to multitask
Ability to think on your feet

With plenty of room for growth, you can enjoy a long and meaningful career in a positive work environment. Take your first step, patients are waiting.

The pay for this position is $22.00 USD per hour.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sample Management Technician 1 1 1 (Reno, NV, US, 89511)

Job Summary

***Please note this position is for 2nd shift Monday- Friday 2pm - 11pm***

Perform a wide variety of basic laboratory support tasks. Perform routine maintenance on basic laboratory equipment. Prepare all materials required for reagent receipt and storage. Compile required documentation and package reagents for shipping. Assist in the maintenance of general laboratory supply inventory and reagents within the Laboratory Sciences group.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs), Good Clinical Practice Regulations (GCP), and Standard Operating Procedures (SOPs).
• Perform all other related duties as assigned.
• May generate reports, data, and forms.
• Maintain and perform record keeping.
• Review data recorded by others for quality control.
• May record observations and measurements for basic lab/research tasks
• Perform clerical duties (e.g.: filing, making copies, etc.).
Lab maintenance
• Perform routine laboratory maintenance of lab equipment.
• Remove biohazard and recycle waste from lab to appropriate locations for disposal.
• Wash and dry laboratory supplies and distribute to appropriate locations within the laboratory.
• Label tubes, devices and containers and perform laboratory set-up/clean-up
• Monitor and stock lab supplies in assigned areas.
Outgoing shipment preparations
• Help to prepare materials and data for shipment and archiving.
• Package biological reagents and ensure accurate completion of all required documentation for the shipment (i.e.: verify shipping lists).
• Prepare shipping documentation and assist in preparation of CITES permits as needed. Fax shipping documentation to sponsors as needed.
• Prepare domestic and international packages according to applicable guidelines.

Job Qualifications

• Education: High school diploma or General Education Degree (G.E.D.) required.
• Experience: none
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None.
• Other: Must be detail oriented and have general familiarity with lab procedures. Good verbal and written communication skills required. Basic computer skills; familiarity with Microsoft Office and Excel software. Ability to organize and prioritize work and meet timelines.

The pay range for this position is $19.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Manager RMS Client Portfolio Management (Wilmington, MA, US, 01887)

Job Summary

We are seeking a Manager, RMS Client Portfolio Management to support our GEMS group within Research Models Services. This is a remote opportunity.

The Manager, RMS Client Portfolio Management, provides leadership to a team of client portfolio managers and project managers supporting the Genetically Engineered Models and Services (GEMS) client portfolio. The portfolio management team spans numerous key client accounts for GEMS across multiple US sites. The client portfolio includes large pharmaceutical, biotech, and academic institutions. Position requires complex planning and in-depth analysis to ensure that project managers meet client expectations and deadlines.

In addition to leading a team, the Manager, RMS Client Portfolio Management, will function as a primary client contact, with guidance from senior scientific staff, for activities related to the planning and execution of client programs. They will interact with clients to understand their requirements to disseminate and partner with Business Development, Client Services, Operational Staff, and Quality Assurance Staff. Essential for this position is the careful organization, preparation, and distribution of information necessary to ensure operational milestones are met from contract development to final reporting.

The Manager, RMS Client Portfolio Management, will work in collaboration with Key Strategic Account Managers to develop and execute on GEMS strategies. They will also collaborate across departments to ensure quality customer service is provided for client account programs. Furthermore, they will ensure communication and strong governance with all stakeholders both internal and external.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:
• Master’s degree or equivalent in life sciences or related discipline, two years’ experience managing projects and working in a leadership role.
• Bachelor's degree (B.A./B.S.) or equivalent in life sciences or related discipline, two years’ experience managing projects and working in a leadership role.
• Associate’s degree or equivalent in life sciences or related discipline, three years’ experience managing projects and working in a leadership role.
• High school diploma, five years’ experience managing projects and working in a leadership role.

In addition:
• Ability to multi-task, excellent written and verbal communication skills, organizational skills and attention to detail required.
• Must possess excellent analytical thinking and problem-solving skills and be able to prioritize and re-evaluate priorities as situations change.
• Working knowledge of computer software (MS Word, MS Excel, SAP, Colony Management Systems).

PREFERRED QUALIFICATIONS:

• Working knowledge of scientific/technical aspects of rodent genetics.
• Experience with Client Resource Management systems (e.g., Salesforce).

The pay range for this position is $90K - $110K annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Cagewash Attendant I (33) (Bethesda, MD, US, 20892)

Job Summary

We are seeking a Cagewash Attendant I to join our Insourcing Solutions team located in Bethesda, MD

    As the Cagewash Attendant I, you will sanitize, maintain and repair animal cagewash materials.

Additional responsibilities include:

Follow SOPs and quality assurance standards
Perform routine preventative maintenance on cagewash and autoclaves
Maintain animal holding facilities clean and organized
Other tasks may include assist with receipt, stocking and maintenance of inventory supplies
Become involved in animal care and husbandry of multiple animal species

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

  The pay for this position is $18.50 USD per hour. Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekend and holidays if necessary

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Laboratory Animal Technician I (14BS) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Laboratory Animal Technician to join our Insourcing Solutions team located in Bethesda, MD.

As the Laboratory Animal Technician, you will maintain and monitor the health, technical, and physical environments within the animal care facility. You'll work closely with the Clinical Veterinarians and Veterinary support staff to perform daily health assessments, clinical observations and providing treatments to the lab animals.  

Additional responsibilities include:

Technical support: animal handling and restraint, weaning, timed mating, tail snips, ear tagging, injections (Sub-Q, IP, tail vein), blood/tissue collections (mandibular, tail vein, term bleed: IC or RO), treatments, microinjections, surgical preparations, and post-operative observations. 
Familiarity with and ability to use various forms of anesthetic (Gas/Injectable). '
Provide environmental enrichment feed, other enrichment stimuli as well as behavioral assessments.
Provide quality assurance to include animal health surveillance, HVAC, animal shipments, facility sanitation and other procedures.
Maintain accurate records of animal importations, breeding, and health checks. 
Assist in assessing training needs; develop and present to staff and PIs. 
Prepare and submit written reports, charts, logs, and inventories.

Job Qualifications

The following are minimum requirements for the Lab Animal Technician:

High school diploma or GED.
A minimum of 3 years' lab animal facility experience performing animal husbandry and clinical support.
Must have LAT certification.  
Schedule: Monday through Friday: 7AM-3:30PM, weekends and holidays if necessary.

The pay range for this position is $27 to $30 USD per hour.  Please note that salaries vary within the range based on factors including skills, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien de laboratoire en Immuno-Histo-Chimie - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service d'Immunohistochimie recrute un Technicien pour intégrer son équipe composée de 10 techniciens.

Les missions 

Au sein du service d'Immunohistochimie, vous aurez pour principales missions sous la responsabilité de la responsable d’équipe :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsable, conformément aux bonnes pratiques de laboratoire, aux procédures standards et aux protocoles d’études,
Réaliser progressivement certaines techniques de laboratoire en histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
S’assurer de la conformité des résultats obtenus,
Lire les protocoles, avenants et notices en anglais,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,

En contact avec notre équipe de Vétérinaires Pathologistes :

Effectuer la digitalisation des lames : digitalisation, mise à disposition aux pathologistes et archivage,
Réaliser la digitalisation en fluorescence,
Préparer et envoyer des disques durs,
Réaliser de l’analyse d’images (développement & validation & application algorithmes, compilation des résultats, mise en forme et partage),
Construire des banques de lames pour de l'analyse d’images.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique (type BUT Génie Biologique).

Vous possédez idéalement une première expérience professionnelle dans le domaine.

Vous possédez une aisance relationnelle et un sens du contact et du service.

Vous êtes organisé(e) et vous appréciez le travail en équipe.

Votre anglais est opérationnel ; vous êtes à l’aise à l’écrit et à la compréhension scientifique.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail, ...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Chef de Projet Junior - F/H - Alternance (Saint Germain Nuelles, FR, 69210)

Le poste :

Au sein de l’équipe Excellence Opérationnelle, en tant que Junior Project Manager en Alternance , vous participez au développement de l’amélioration continue, le suivi des programmes de projets et la réalisation de ces derniers.

Véritable acteur du changement, vous accompagnez les opérationnels dans la réalisation des projets et changements nécessaires pour garantir l’efficacité et la rentabilité des activités en collaboration avec la direction du site, l’équipe Finance et vos homologues des autres sites du groupe Charles River.

Les missions proposées au cours de votre alternance :

Recueillir, comprendre et construire le cahier des charges les besoins fonctionnels exprimés,
Concevoir et développer des solutions à l'aide de la suite Office (Power Platform : Power BI, Automate, etc.),
Accompagner le développement et suivre la gestion du projet : suivi de planning, charte projet, analyse de risques, clôture et retour d'expérience.
Assurer la documentation de votre travail,
Maintenir et supporter les solutions développées dans un esprit d'amélioration continue.

Profil recherché :

De formation supérieure Master ou formation Ingénieur,
Vous avez une réelle appétence pour les technologies Low-Code/No-code,
Vous êtes reconnu(e) pour votre curiosité, votre adaptabilité et votre relationnel
Vous appréciez le travail en équipe et transverse,
Les + : vous avez de bonnes connaissances des outils de développement No Code de la suite Office 365 et le domaine de l'amélioration continue

Modalités:

Restaurant d’entreprise, CSE
Primes de transport
Site non-accessible en transport en commun – Moyen de locomotion indispensable (Saint-Germain-Nuelles)

Pour plus d'information, consultez www.criver.com.

Scientific Manager, Bioassay (Wayne, PA, US, 19087)

Job Summary

Serve as the Scientific Manager responsible for the management and scientific oversight of assigned studies within the Bioassay laboratory including development and execution of highly complex method development and characterization studies related to the testing characterization and analysis of biotherapeutics using analytical instrumentation and methodologies. Independently responsible for method feasibility, method development, method optimization, method transfers, method qualifications, method validations and routine testing under both R&D and cGMP environments. Responsible for guidance and oversight of junior Staff. Additionally, serve as subject matter expert for key Clients, Business Development and Management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Functioning independently as the technical expert on highly complex studies, develop, perform, and troubleshoot laboratory experiments, tests, and procedures within accepted regulatory compliance for the characterization and analysis of biotherapeutics through use of cell culture and analytical testing techniques and methodologies.
Maintain a safe working environment by adhering to Company policies or procedures. Actively participate in laboratory experiments and maintenance.
Provide oversight of laboratories and mentor and/or supervise research staff in areas such as protocol interpretation, method development and refinement, study related problem resolution, and technique validation, as well as providing scientific expertise in study conduct, design, and interpretation.
Oversee Sponsor interactions, including scientific program development, consulting on study and program design, scheduling, conduct, and reporting. Communicate and provide guidance for client issue resolution and interaction concerning regulatory issues.
Generate and finalize high quality method and study protocols for sponsor and internal characterization and sample testing programs.
Ensure that study protocols are amended to accurately reflect any changes in scope of work or deliverables in a timely fashion.
Provide mentoring and technical guidance to resolve Bioassay challenges in a timely fashion.
Implement techniques to improve productivity, increase efficiencies and maintain laboratory state-of-the-art practices.
Perform routine testing techniques, such as the following, with a high degree of reliability, efficiency, accuracy, and a well-versed skill set in regulatory compliance
Cell culture and various cell handling techniques including expertise with: Adherent Cell Lines, Non-Adherent Cell Lines and Lightly Adherent cell lines
Experience and comfort with plate reader platforms including but not limited to: Softmax Pro, Tecan Magellan, Biotek Gen-5, and/or Stegmann PLA
High level of capability with ADC, ADCC, CDC assays
High level of capability with Potency assays
ELISA/ Immunoassay Analyses – Experience in kit and custom ELISA
RT-PCR – Experience with general methods
Independently review, interpret, analyze, evaluate, integrate, present, and discuss experimental data with research staff and Sponsor.
Independently perform tabulation and statistical analyses of study data, as required.
Prepare high quality final reports appropriate for assigned study, including integration of supporting subcontractor(s)’s reports into final reports as required, independently.
Perform all other related duties as required.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in Cellular/Molecular Biology or related scientific discipline. M.S. or Ph.D. strongly preferred.
Experience: Minimum 7 year’s relevant experience within a contract research, academic or pharmaceutical industry, including experience in the core competencies of characterization and analysis of biotherapeutics.
An equivalent combination of education and experience with contract research or the pharmaceutical industry may be accepted as a satisfactory substitute for the specific education and experience listed above.

Compensation Data

Pay rate for this role is $128,500 - $140,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

IT Engineer - Backup & Recovery Level 3 (Bangalore, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

IT Engineer – Backup & Recovery Level 3

For nearly 70 years, Charles River employees have worked together to assist in the discovery, development, and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales, or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

ROLE SUMMARY: CRL is seeking an energetic professional to provide engineering and architecture expertise in the Global Technology group as a member of a cross-functional team. The Global Technology team is accountable for technology at a global scale, supporting 20,000 employees across 100 locations. The Backup and Recovery Engineer Level 3 is key to delivering effective and secure technologies for on-prem and cloud environments. The role requires a mix of expertise in cloud computing, on-prem virtual infrastructure, and backup and recovery technologies. You will create solutions to enable the appropriate backup and recovery methodologies for multi-region, hybrid cloud infrastructures.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•    Design, implement, and manage backup and recovery technologies in global data centers, sites, and public cloud environments (AWS, Azure)
•    Be an escalation point for operational support teams to troubleshoot complex issues
•    Ensure backup and recovery solutions achieve RTO\RPO targets
•    Design and maintain capacity and licensing reports
•    Plan and coordinate hardware and software upgrade cycles
•    Document technical designs and procedures for compliance and support teams
•    Advise Technical Product Owner and management on service enhancements.

Required Qualifications:
Education: Bachelor’s degree (B.A./B.S.) or equivalent experience in computer science, engineering, or related discipline.

Experience:
•    At least 5 years of experience in the IT field in large enterprise environments
•    At least 4 years of experience with VMware
•    At least 4 years hands-on experience managing Rubrik, AWS Backup, and\or Azure Backup
•    1-2 years of experience with hybrid and\or public cloud infrastructures (AWS, Azure, etc)
•    Experience designing, implementing, and managing backup and recovery technologies in multi-region, on-prem, or public cloud environments
•    Experience managing backup and recovery technologies for both physical and virtual server infrastructures hosting Windows, Linux, Oracle, and SQL.

Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Biomanufacturing Manager, Cell & Gene Therapy (Memphis, TN, US, 38118)

Job Summary

The Biomanufacturing Manager is responsible for leading all manufacturing activities related to the start-up and GMP production of novel cellular products for new and existing clients in compliance with regulatory agencies and associated guidelines. The Manager will also schedule appropriate resources to meet production schedules and maintain a state of safety, compliance, and control within manufacturing.

Oversee all activities related to the start-up and production of new and existing client processes in accordance with Charles River quality and production timelines and agreements.
Schedule and manage manufacturing staff ensuring adherence to production schedules; coordinate with relevant functions to ensure schedule adherence.
Ensure a safe and compliant working environment by enforcing safety and quality policies and practices.
Serve as manufacturing representative on cross-functional teams ensuring on-time completion of deliverables related to technology transfer, operations, production, and disposition.
Advise and inform site and company leadership of issues with the potential to impact production timelines or Critical Quality Attributes of client products.
Participate in Regulatory, Quality, and Customer inspections and audits as manufacturing systems and production process SME.
Work closely with clients and internal functions to troubleshoot and solve issues related to client processes and production.
Build, train, and develop highly skilled production teams capable of producing cell therapy products in accordance with regulatory guidelines and Cognate quality standards.
Oversee the drafting, review, and approval of process specific and Internal Quality System documents.
Foster a culture of continuous improvement; identify opportunities and lead implementation of improvement activities, as required.

Job Qualifications

BS or MS in a scientific field.
Minimum of 3 years or equivalent applicable experience
Minimum of 2 years demonstrated success in a supervisory role
Exhibits exceptional leadership skills and deep knowledge of GMP
Must be detail oriented and have excellent organizational skills
Must possess effective written and oral communication skills
Must display a high degree of professionalism and confidentiality
Must demonstrate initiative to remain apprised of relevant industry and regulatory trends

Compensation Data

The pay range for this position is $94,000 - $120,000. Please note that salaries vary within the range based on factors but not limited to experience, skills, education and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Cage Wash Operator (Day Shift) (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Cage Washer Operator – Day shift – No experience necessary.

As a Cage Washer Operator for our Toxicology team in Sherbrooke, you will be responsible for ensuring the equipment used to maintain the animal’s living conditions is cleaned according to the highest wellbeing standards in the industry.

In this role, key responsibilities include:

Operating and performing daily checks on cage washer machines.
Monitor the use of soaps and various needs of the cage washers.
Clean all types of animal housing and accessories (cage, toys, bowl, waterbottle, etc…)
Perform basic maintenance on all cages and accessories to ensure that everything is safe for the animals.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Organized and self-driven.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role specific information:

Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station;
Salary: 18,25$/hrs
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
Access to a doctor and various health professionals (telemedicine).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. This is Your Moment!

Equal Employment Opportunity

For more information, please visit www.criver.com.

Opérateur.trice de lave-cage (poste de jour) (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Opérateur.trice de Lave-Cage – Horaire de jour – Aucune Expérience nécessaire

En tant qu’Opérateur.trice de Lave-Cage pour notre équipe de Toxicologie à notre site de Sherbrooke, vous aurez la charge d’assurer la propreté des équipements utilisés pour maintenir les conditions de vie des animaux selon les plus hauts standards de bien-être de l'industrie.

Dans ce rôle, les principales responsabilités incluront:

Faire fonctionner et effectuer les vérifications quotidiennes des laves-cages.
Surveiller l’utilisation des savons et les besoins divers des lave-cages.
Nettoyer tous types d’habitation d’animaux ainsi que leurs accessoires (jouet, bouteille, bols, etc…).
Effectuer l’entretien de base sur toutes les cages et accessoires afin de s’assurer que tout est sécuritaire pour les animaux.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Organisé et Autonome.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Informations spécifiques au poste :

Localisation: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transport: Facilement accessible avec le transport en commun. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire : 18,25$/HR.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/hr).

Pourquoi Charles River?

3 semaines de vacances et des congés personnels.
Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire).
Accès à un programme d’épargne et de retraite qui comprend une contribution de l’employeur.
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne.
Gym gratuit sur place.
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine).

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe! C’est Votre Moment!

Pour plus d'information, consultez www.criver.com.

Mechanical Engineer (Margate, GB, CT9 4LT)

Salary D.O.E + On Call Allowance

Mechanical Engineer

Rota - 35 Hrs per week

Monday - Thursday 8.00 am - 4.30 pm

Friday 8.00 am - 1.00 pm

Out of hours callouts - rostered - 1 in 4 weeks (Paid at additional rate)

* Please not due to nature of role flexibilty surrounding core hours is essential.

Overall responsibility

To be responsible for site steam systems and the maintenance, modification of all site mechanical services and equipment as directed by the Facilities Manager. To carry out mechanical repairs, tests and reports as and when necessary.

Main duties/responsibilities

To carry out mechanical repairs and improvements to Company properties, both on a responsive basis and strategic basis.
To carry out Mechanical tests and reports on company property and carry out the necessary repairs.
To carry out preventative planned maintenance and complete relevant job documentation
To respond to reactive work orders and complete as necessary
To promote customer satisfaction through the repair and improvements process
To advise the facilities Manager re. future mechanical maintenance requirements, and any changes to Mechanical practice and legislation.
Installation of pipe work throughout site both copper and iron
Responsible for the operation and monitoring of site boilers both oil and steam ( steam training can be provided)
Responsible for the operation and upkeep of this site biomass boiler
Assist with training of new team members on department procedures.
Responsible for monitoring stock levels for all plumbing and pipe fitting and assist with stock takes.
Provide on call cover to ensure correct operation of systems and equipment out of normal working hours.
Complete specific tasks or projects as requested by the Facilities Manager or Maintenance Manager.
Promote good work practices and enhance working relationships.
Contribute to continuous improvement with an enthesis on sustainability.
Ensure that all Health and Safety regulations are always adhered to.
Where appropriate, be able to report leading and lagging indicators with regards to safety and health to the EHS team.
Ensure a safe and tidy work area.
Provide cover for other members of the team as and when necessary.
Carry out other reasonable duties that may or may not be related to the job as requested by the management.
Must at all times adhere to the Company’s Equal Opportunities Policy in the planning and execution of their duties.

Qualifications, Skills & Abilities

At a minimum City& Guilds Mechanical installation
5 years’ work experience
Steam qualification / or equivalent time served
Some IT literacy
Experience of working in a busy environment to tight deadlines.
Maintaining Steam Boilers
Planned preventive maintenance
HVAC
LTHW Boilers
Some controls experience
Installation experience
Fault finding

Benefits: Life assurance, bonus, career development, training opportunities, free onsite parking, subsidised staff room, pay for participation on volunteer days, on-site team building, charity fundraising days, employee engagement programs.

Pension plan: 1st year employee -Company contribution 5% - Employee 4%, After 3 years: Company contribution 9% and employee 1%

Holidays - 26 days + 8 for Public holidays

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Biotechnician - Rodents (Groningen, NL)

Al 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u zich gepassioneerd over kunt voelen.

Baan Samenvatting

Heb jij een achtergrond in dierverzorging, paraveterinair of biotechniek en werk je graag met dieren, dan zoeken wij jou! 
Voor ons team in Groningen zoeken wij een:

Biotechnicus (32-40 uur)

Afdeling:
Met bijna 30 medewerkers is onze Discovery site een toegewijde groep die zich richt op farmacokinetische en farmacologische studies om de pathofysiologie van neurologische aandoeningen beter te begrijpen. 

Team:
Als biotechnicus bij Charles River Discovery kom je te werken in een collegiaal team. Iedereen staat voor elkaar klaar en naast dat er hard wordt gewerkt, is ook ruimte voor gezelligheid. Je werkt binnen jouw team zelfstandig en met elkaar aan de verschillende studies. Daarnaast spreek je regelmatig met de analisten en de Study Directors van de site over het verloop van de studies.

Over je rol:
Je bent als biotechnicus bij onze Discovery site onderdeel van de afdeling biotechniek, waar diverse studies uitgevoerd worden voor onderzoek naar de ontwikkeling van medicijnen. Samen met jouw collega’s draag jij, kwaliteitsbewust, de zorg voor het goed verlopen van de studies. Daarbij verlies je nooit het welzijn van de dieren uit het oog. Het onderzoek dat je uitvoert wordt gedaan met zowel ratten als muizen.

Primaire verantwoordelijkheden:
•   Verrichten van uiteenlopende biotechnische handelingen zoals het doseren, observaties en gedragstesten. Maar ook de bloedafnames in uiteenlopende studies;
•   Verrrichten van onder andere stereotactische operaties en jugularis cannulaties;
•   Verzamelen en documenteren van de experimentele gegevens;
•   Nauw samenwerken met je collega`s en goed contact houden met de betrokken Study Directors. 

Wat is vereist?
•   Een afgeronde opleiding MBO-4 of HBO met artikel 9 of 13F;  
•   De bereidheid om regelmatig weekend- of avondwerk te verrichten;
•   Functioneren zowel zelfstandig als in teamverband;
•   Een flexibele en kwaliteitsbewuste instelling;
•   Interesse om jezelf verder te ontwikkelen met betrekking tot de diverse biotechnische handelingen en operaties.

Wat zou prettig zijn:
•   Kennis van de Engelse taal.

Ons aanbod: 
Werken bij onze organisatie betekent werken in een dynamische internationale organisatie.
Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder: 
•   25 vakantiedagen; 
•   Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar; 
•   Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris; 
•   Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat; 
•   Korting op je zorgverzekering;
•   Reiskostenvergoeding à € 0,23 cent per kilometer met een max van € 250 netto per maand;
•   Collectief pensioen
•   Elke dag gratis vers fruit. 
 

Voor verdere informatie over de functie kun je contact opnemen met Janneke Basten, +31638857962. Heb je belangstelling voor deze functie, dan nodigen wij je uit te reageren via onze carreer site: Charles River Laboratories, Inc. Jobs (criver.com)

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld

Over Discovery

De discovery bij Charles River heeft zich in de branche bewezen, met de succesvolle ontwikkeling van nieuwe therapieën, meer dan 320 octrooien en levering van 74 kandidaat-geneesmiddelen aan sponsors in de afgelopen 17 jaar. Met de steun van meer dan 650 wetenschappers gebruikt onze complete en geïntegreerde portefeuille de allernieuwste technologie en platformen voor het aanbieden van diensten op het gebied van chemie, biologie en farmacologie die cliënten terzijde staan, vanaf de eerste fasen van 'hit identification' tot en met experimentele nieuwe geneesmiddelen (IND). Onze cliëntgerichte, collaboratieve aanpak resulteert in werkelijke partnerships waarin problemen worden voorzien, obstakels worden weggenomen en wij samen met de cliënt op pad gaan om nieuwe geneesmiddelen op de markt te brengen.

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogd zodat producten eerder op de markt gebracht kunnen worden.

Met meer dan 20.000 medewerkers bij 110 vestigingen in 20 landen wereldwijd zijn wij strategisch gepositioneerd voor het coördineren van wereldwijde middelen en kunnen wij multidisciplinaire inzichten inzetten om de unieke uitdagingen van onze cliënten op te lossen. Onze cliënten omvatten farmaceutische multinationals, biotechnologiebedrijven, overheidsinstellingen en medische en universitaire instellingen over de gehele wereld.

Bij Charles River zijn wij gepassioneerd over onze rol bij de verbetering van de levenskwaliteit van andere mensen. Onze missie, onze uitstekende wetenschap en onze doelgerichte instelling werken door in alles wat we doen, en we gaan elke dag opnieuw aan de slag met de kennis dat ons werk de gezondheid en het welzijn van vele mensen helpt te verbeteren. Wij zijn trots te kunnen zeggen dat wij een rol hebben gespeeld bij de ontwikkeling van circa 86% van de geneesmiddelen die in 2021 door de Amerikaanse FDA werden goedgekeurd.

Bij Charles River Laboratories herkennen en werven wij talenten. Wij zijn een bedrijf dat zich inzet op het gebied van diversiteit en gelijkheid en we werken op inclusieve wijze.

Meer informatie vindt u op www.criver.com.

Analist Ecotoxicologie en biodegradatie (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Al bijna 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u over gepassioneerd kunt voelen.

Ben jij op zoek naar een functie waarin je bij kunt dragen aan een betere leefomgeving voor mens en dier? Dan zal deze vacature op de afdeling ecotoxicologie jou zeker aanspreken!

Ben jij naast oplossingsgericht een echte proactieve teamspeler met een grote dosis enthousiasme? Dan komen wij graag met jou in contact.

Wegens uitbreiding van onze werkzaamheden zijn wij op zoek naar een:

ANALIST Ecotoxicologie en biodegradatie

Afdeling:

De afdeling Discovery & Environmental Sciences bestaat uit circa 90 medewerkers. Binnen deze afdeling wordt onderzoek uitgevoerd naar de veiligheid van bestaande en nieuwe stoffen. Kenmerkend voor het werk is de grote diversiteit aan testen, teststoffen, klanten en samenwerkingen.

Sectie Ecotox (Environmental Sciences): 

De Ecotox afdeling is een unieke groep binnen CRL waar effecten van producten vanuit  diverse industrieën op het milieu worden getest zowel voor de korte als de lange termijn.

Team:
Het team waarin je komt te werken, bestaat uit 14 collega analisten met daarnaast twee teamleiders en een Technisch Sectiehoofd (leidinggevenden). Daarnaast werk je nauw samen met een team van circa 7 studieleiders en draag  je zorg voor een goed verloop van de projecten van onze wereldwijde klantenkring. 

Over je rol:
Als analist werk je zelfstandig en in teamverband, onder leiding van de studieleider. Je onderzoekt hoe acuut toxisch de producten zijn voor bacteriën, algen, watervlooien en  vissen. Daarnaast onderzoek je lange termijn effecten door in chronische testen te kijken naar bijvoorbeeld groei van vissen, opname (accumulatie) in visweefsels of reproductie van watervlooien.  

Naast de toxiciteit testen werk je ook aan biodegradatie testen. Bij dit soort experimenten wordt onderzocht of bacteriën in staat zijn om de testmaterialen af te breken.

 Primaire verantwoordelijkheden: 

Werken volgens Good Laboratory Practice (GLP) of een vergelijkbaar kwaliteitssysteem; 
Uitvoeren van dagelijkse handelingen zoals; het controleren/kalibreren apparatuur, voeren van de dieren en onderhoud van kweken;
Contacten onderhouden met verschillende afdelingen binnen de organisatie;
Assisteren je bij de verwerking van de resultaten in de rapportage van de studies.

Wat is vereist?

Een achtergrond in:microbiologie, medische biologie; MBO/HBO
in het bezit van artikel 13F;
Bereidheid tot incidenteel weekendwerk;
32-40 uur beschikbaar;
Ervaring met laboratoriumwerkzaamheden: hierbij is zelfstandig en accuraat werken heel belangrijk;
Een goede beheersing van de Nederlandse taal;
Goede communicatieve en sociale vaardigheden;

Nice to Have:

Kennis van werken onder steriele omstandigheden;
Beheersing van de Engelse taal.

Ons aanbod:

Werken bij onze organisatie betekent werken in een dynamische internationale organisatie met een modern laboratorium en een grote diversiteit aan apparatuur en technieken tot je beschikking.

Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

27,5 vakantiedagen en 2 collectieve dagen per jaar;
Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
Reiskostenvergoeding à € 0,23 cent per kilometer met een max. van € 250 netto per maand, of een NS-Businesscard;
Fiets(lease)plan;
Collectief pensioen met een eigen bijdrage van 2.9%;
Bedrijfsfitness
De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
De mogelijkheid tot een consult van onze in house ergonoom;
Elke dag gratis vers fruit.

Heb je vragen over deze vacature?
Voor verdere informatie over de functie kun je contact opnemen met her-recruitment@crl.com. Heb je belangstelling voor deze functie, dan nodigen wij je uit te reageren via onze carreer site: Charles River Laboratories, Inc. Jobs (criver.com)

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld

Over Safety Assessment

Charles River helpt zijn partners bij het versneld uitvoeren van preklinische geneesmiddelontwikkeling dankzij uitstekende programma's voor veiligheidsbeoordeling, de allernieuwste voorzieningen en deskundig advies op het gebied van wet- en regelgeving. Van individuele gespecialiseerde toxicologie- en “IND enabling”-onderzoeken tot pakketten op maat en complete laboratoriumondersteuning: ons ervaren team kan programma's ontwerpen en uitvoeren die anticiperen op problemen en obstakels uit de weg gaan, voor een probleemloze en efficiënte ontwikkelingsgang naar de markt. Bij onze Safety Assessment-vestigingen lopen jaarlijks zo'n 300 programma's voor experimentele nieuwe geneesmiddelen (investigational new drugs [IND's]).

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogt zodat producten eerder op de markt gebracht kunnen worden.

Meer informatie vindt u op www.criver.com.

Scientifique sénior de recherche - Bioanalyse (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique Sénior de Recherche au sein de notre équipe Bioanalyse située à Senneville, vous serez responsable de la conception, de la conduite et des rapports d'études de sciences de laboratoire de manière efficace, rentable et avec une qualité scientifique maximale. Vous dirigez également, sur le plan scientifique, les analystes et les autres membres du personnel technique associés à la réalisation, à l'interprétation et à l'établissement des rapports d'études.

Dans ce poste, les principales responsabilités incluront:

Conçoit, rédige, examine et révise, le cas échéant, les plans d'étude, les modifications et les calendriers d'étude qui définissent et planifient toutes les activités de l'étude;
Superviser et coordonner tous les aspects des procédures d'étude, qu'elles soient réalisées au sein du service ou par des services de maintenance;
Veiller à ce que les projets soient réalisés conformément aux procédures opératoires normalisées et aux bonnes pratiques de laboratoire, et connaître les réglementations, les lignes directrices et les orientations appropriées;
Rédiger, examiner et réviser, le cas échéant, des projets de rapports ou des rapports finaux qui documentent toutes les procédures et tous les résultats liés à l'étude;
Communiquer rapidement, oralement ou par écrit, avec les commanditaires sur les questions liées à l'étude.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

5 ans d'expérience en LCMS et extractions;
Baccalauréat / Maîtrise avec 5 ans d'expérience ou bien Doctorat avec 1 à 2 ans d'expérience;
Bonnes compétences en matière de relations interpersonnelles et en communication;
Expérience dans un environnement BPL et/ou en toxicologie préclinique (atout);
Bonnes compétences en matière de résolution de problèmes.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: De jour en semaine du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Senior Research Scientist - Bioanalysis (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Research Scientist for our Bioanalysis team located in Senneville, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. You will also, scientifically directs the Analysts and other technical staff associated with the conduct, interpretation and reporting of studies.

In this role, primary responsibilities include:

Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities;
Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments;
Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidance’s;
Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results;
Prompt verbal or written communication with Sponsors on study related business.

Key Elements

We are looking for the following minimum qualifications for this role:

5 years’ experience with LCMS and extractions;
Bachelor’s / master’s degree with 5 years' experience or PHD with 1-2 years' experience;
Good interpersonal and communication skills;
Experience in a GLP environment (asset);
Strong problem-solving skills.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Daytime Monday to Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Supervisor Quality Assurance (Wayne, PA, US, 19087)

Job Summary

Supervise and provide support in the management of daily work flow operations of Quality Assurance (QA) staff. Ensure staff assignments are in alignment with regulatory inspection and reporting requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Oversee daily operational activities/schedules and ensure QA resources are properly assigned to manage regulatory oversight.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures.
Review, revise and approve (GMP QA) SOPs, protocols/batch records, reports, and other quality and regulated records involving technically complex issues and processes for accuracy and compliance with all applicable regulations and internal policies.
Participate in the preparation and review of study and QA files in preparation for sponsor site visits and regulatory inspections; assure that QA audit files are retained.
Participate in client site visits and regulatory inspections.
Participate in the development of recommendations for corrective and preventative actions to respond to client visit and regulatory inspection findings.
Routinely provide recommendations to Regulatory Affairs and Compliance management for improvements in auditing of Quality Systems based on extensive knowledge and understanding of regulations and quality principles.
Perform data audits to assess that records are attributable, legible, contemporaneous, original, accurate, and in compliance with regulations, international standards, SOPs, protocols/batch records, and corporate policies and procedures as needed to support departmental workload.
May participate in inspections and audits of subcontractors, vendors, and suppliers of products and services.
Assure the suitability of materials and supplies for compliance with specifications (GMP QA).
Review and approve all procedures related to production and maintenance, approving or rejecting incoming materials, in-process materials and finished product (GMP QA).
As required, oversee maintenance of group training manual and training records.
May assist in development of departmental budget.
Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development.
Support the policy of equal employment opportunity through affirmative action in personnel actions.
Provide regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent, preferably in a life science or related discipline.
Experience: Minimum 5 years experience in a Quality Assurance role or a GLP environment including 1 year supervisory experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Knowledge of Microsoft Office applications (e.g. Word, Access, Excel). Must be able to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements. Excellent judgment, decision-making, training/mentoring skills and verbal/written communication skills. Strong leadership, organizational skills and detail oriented. Able to prioritize workload and manage multiple tasks.

Compensation Data

The pay rate for this role is $90,000 - $94,500 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Instrument Field Support Specialist - Nexus (US)

Job Summary

We are seeking an Instrument Field Support Specialist for our Nexus Robot and Endosafe range within our Microbial Solutions business covering North America.

The following are responsibilities related to the Instrument Field Support Specialist for our Nexus Robot and Endosafe range:

Provide customer-facing technical repair and maintenance services for endotoxin, and microbial detection laboratory instruments on site at customer locations.
•   Schedule and perform on-site service visits within an assigned region for product installations, annual qualification, routine preventive maintenance and analysis of product performance.
•   Provide technical assistance and problem resolution to customers via telephone, email, or on-site communication.
•   Complete all required field service activities and documentation as assigned based on specific product, customer and/or standard operating procedural requirements.
•   Assisting field sales personnel in product demonstrations, new customer training, and product validations.
•   Responsible for completing all service and compliance documentation as required by company policy, cGMP and FDA.
•   Responsible for resolving client testing laboratory instrument service issues.

Job Qualifications

The following are minimum qualifications related to the Instrument Field Support Specialist for our Nexus Robot and Endosafe range:

Qualification in Engineering, Chemistry, Microbiology, Biology or equivalent experience in the field
•   High level of Technical ability and able to work under pressure
•   3+ years of related experience
•   Ability to work from a home-based office
•   Frequent travel, sometimes with short notice

Compensation Data

The pay range for this position is $73.7k-80k. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Facilities Engineer 1 (Mattawan, MI, US, 49071)

Job Summary

The Facilities Engineer is responsible for supporting the facilities/engineering for the building utilities and equipment that supports office, laboratory, and vivarium operations; responsible for capital project efforts and supporting facilities operations. The individual in this position will also monitor facility conditions, support the site master plan associated with reliability and maintenance engineering functions. This individual is expected to be an expert in their discipline while serving as a CRL representative on advanced projects. This individual will act as an advisor to Facilities leadership and external customers on advanced technical projects.

Essential Duties and Responsibilities:

Provide Engineering / Project Management activities supporting the execution capital projects and support of facilities operations.
Provide oversite and voice of the customer for onsite third-party engineering support.
Act as Subject Matter Expert (SME) to review and approve drawing packages provided by internal or external engineering support.
Prepare and review bid packages from external suppliers and A&E firms.
Assist in development and implementation Engineering department capital budget for the facility.
Work closely with local facilities departments, corporate project managers and site operations management to coordinate design efforts; compile user requirements in alignment with design guidelines, commissioning, validation, and operational delivery of small to large-scale capital projects to meet project objectives.
Assist Facilities team with engineering oversight of distribution of chilled water, steam, power, gas and other utilities.
Ensuring compliance with national and local safety codes and regulations
Work with leadership in developing site master plans; prepare maintenance and engineering plans to support master plan objectives.
Monitor the condition of the facilities through assessments and condition evaluations.
Compile and maintain information on plant facilities; establish and maintain engineering and construction standards and drawings.
Support reliability / maintenance engineering functions.
Implement and oversee site energy savings strategies to align with corporate sustainability initiatives.
Support local and corporate safety program.
Leverage engineering expertise (i.e., automation/BMS, CQV, GxP, HVAC/Electrical, LEED and maintenance) throughout the CRL Engineering network.
Other duties as assigned.

Job Qualifications

Bachelor’s degree (BA/BS) or equivalent in mechanical or chemical engineering or related discipline required.
Eight to ten years related experience in managing multiple capital projects / supporting utilities equipment (central utilities) up to $25MM
Certifications: Plant Engineering and or Building trades license helpful.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated working knowledge of LEED, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs), AAALAC, FDA/EU and government regulatory requirements and guidelines.
Demonstrated ability to handle multiple projects, prioritize work and meet deadlines.
Demonstrated ability to assess and troubleshoot facility systems.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite, knowledgeable with Microsoft Project, AutoCAD, Bluebeam (REVU CAD).
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ensure project timelines and Budgets are maintained
Ability to work under specific time constraints.

The pay range for this position is $115K - 135k/year. Please note that salaries vary within the range based on experience and education.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Assembler - Associate (Charleston, SC, US, 29407)

Job Summary

An essential member of the larger production team, responsible for mechanical assembly, rework, documentation and installation of software. Reports to the production manager, receives direction from the production manager, production engineer, and general production coordination direction from the Instrument Release and Production Coordinator.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
The following statements are intended to describe the general nature and level of work being performed by individuals assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

Mechanically assemble and disassemble new and existing equipment
Receive, sort, inspect and stock components in a warehouse area
Identify and report defects, including potential defects to aid in product improvement
Operate hand and power tools such as torque drivers, screw drivers, wire cutters and other tools for instrument assembly
Perform rework including but not limited to soldering, crimping, separating, cutting etc.
Read and understand CAD drawings, BOM etc.
Assist in:
- Perform general housekeeping and adhere to safety procedures.
- Production process development
- Continuous improvement
  - Product improvements
  - Manufacturing processes
  - Testing processes
Perform SAP operations to facilitate the processing of components and instruments
Work with PLM system and work instructions
Perform general housekeeping and adhere to safety procedures.
Proficient in all SOPs in areas of responsibility
Perform all other related duties as assigned.
Responsible for adhering to all documentation as required by company policy, cGMP and FDA.
Cross train as required for all other roles within the department
Periodically assist in those roles with direction as needed

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.)
Experience: Experience working in ESD and production of electronic assemblies is preferred

PHYSICAL DEMANDS:

Specific vision abilities required by this job include close vision and the ability to adjust focus..
Sitting and standing for periods of time.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General production working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

Employee is responsible to verify and validate his or her job output as specified through verbal and/or written instructions. Verbal and written instructions may include training, policy statements, work instructions, Standard Operating Procedures, or workmanship standards.

Compensation Data

The pay range for this position is $19.00 to $20.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Plant Service Engineer (Tranent, GB, EH33 2NE)

Job Summary

A Plant Service Engineer vacancy now exists within the Building/Workshop department based in Tranent, East Lothian. This is a permanent full-time role.

Working as a Plant Service Engineer, you’ll join a team who carry out a range of maintenance, fault finding and repair duties in a large campus style estate and associated satellite sites.

Duties and responsibilities include:-

Carrying out maintenance and repairs
Ensuring the continuation of a fit for purpose working environment in accordance with company procedures

Applicants should have:-

A time-served mechanical engineer qualification
Experience of HVAC systems, air compressors and steam condensers
Competence in fabrication using a variety of materials
Experience in the use of basic machine tools would be an advantage
Welding experience and certification would be an advantage
A full driving licence

Working within a small maintenance team on a wide variety of plant there is an expectation that the successful applicant will be multi skilled and flexible. The post requires the ability to work at height as well as in enclosed spaces, and the post holder must also be able to negotiate crawl spaces. Practical experience of fault finding on a range of plant and equipment systems is desirable.

Due to the nature of this role, you must also be able to work outwith normal office hours, as required and as a member of a rotational on-call response team, for which an on-call allowance will be payable.

Closing date: 16 July 2025

The salary on offer for this role is up to £40,000 per annum, depending on skills and experience.

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Cleaner (Edinburgh, GB, EH14 4AP)

Job Summary

We are looking to recruit a Cleaner for our site in Riccarton, Edinburgh. We are flexible in start and finishing times.

As a Cleaner you will have responsibility of cleaning services for office, laboratory and general areas within the Company including cleaning of surfaces, floors, benches and corridors as required.

The following is required for this role:

Previous cleaning experience would be a distinct advantage
Ability to work within a team
Good attention to detail
Flexible and hard-working attitude

The salary for the role is £23,842.35 per annum, which equates to £12.60 per hour.

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Electrical and Controls Engineer (Mattawan, MI, US, 49071)

Job Summary

This role is responsible for the design, start-up, commissioning, and maintenance of the electrical systems (480V and below), Building Automation System (BAS), and stand-alone Process Logic Controllers (PLC’s). This position will oversee electrical and controls projects, troubleshoot systems, and be the lead point of contact for electrical and controls systems used throughout the facility.

Essential Functions

Responsible for the site’s electrical and Building Automation System (BAS), including changes, upgrades, programming, installations, and overall proper operation.
Generate and review reports from the Building Automation System (BAS) to maintain proper system health and ensure data capture to maintain GLP compliance.
Plan and perform preventative maintenance and repair of controls-related HVAC and plant equipment.
Analyze plant electrical and automation/control systems; design and implement improvements.
Provide remote support as needed to troubleshoot and maintain the Building Automation System and other control systems.
Work with Engineering and Facilities personnel to design and implement control sequences for the Building Automation System that improve plant efficiency.
Basic familiarity with Microsoft Office Suite, knowledgeablewith Microsoft Project, AutoCAD, Bluebeam (REVU CAD).
Oversee the programing of various standalone PLC platforms for systems that include mechanical equipment, waste management, cold storage, etc., that are not controlled by the Building Automation System.
Provide expertise and direction to technicians and contractors, execute activities as needed, and ensure successful completion of all electrical and control components.
Partner cross-functionally and work with various departments regarding the implementation and maintenance of electrical and automated equipment, systems and controllers.
Troubleshoot and repair electronic control system malfunctions, including both hardware and software.
Oversee the installation, setup, and commissioning of various third-party integration devices.
Integrate low-voltage sensors and building sub-systems using various industry protocols such as BACNet, N2, Modbus, etc.
Create and/or work with vendors to create graphics for Building Automation System interface.
Act as the project manager for assigned projects to ensure successful completion of all project activities.
Work cross-functionally with Charles River Information Technology teams and/or automation contractors to support the operations and maintenance of the Building Automation System and other network systems as required.
Oversee the installation, setup and commissioning building automation system controllers as required to support site growth, expansion, maintenance, and upgrades.
Ensure that project timelines and budgets are maintained.
Ensure clear communication among all groups involved in successful delivery of projects.
Interface with vendors relating to control systems, automation, and facilities/laboratory equipment.
Plan, coordinate, and supervise the work of Building Automation System service contractors to ensure satisfactory completion of work.
Ensuring compliance with national and local safety codes and regulations
Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:

Education: Bachelor’s degree in electrical engineering or controls system engineering
Experience: 3-5 years designing and implementing installations or improvements to HVAC building automated systems.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education listed above.
Certification/Licensure: Building Automation System certifications regarding programming and operation highly preferred.
Certified Energy Manager (CEM) or LEED certification preferred.
AutoCAD Certified Professional (ACP) or AutoCAD Certified User (ACU).
Other: Must have experience in writing computer programs and software applications related to the HVAC industry.
Experience with any of the following platforms preferred: Schneider EcoStruxure, Allen Bradley, Siemens, Johnson Controls, Tridium, Delta, Honeywell, Allerton, Automated Logic Controls, etc.
Experience in the integration of low voltage building sub-systems using various industry protocols, such as BACNet, N2, Modbus, etc. preferred.
Basic knowledge of Good Laboratory Practice (GLP) regulations preferred.

PHYSICAL DEMANDS:

Ability to work in a variety of circumstances, including climbing ladders, scaffolds, and high lift equipment, working in ducts, crawl spaces, roofs, basements, above ceilings, and in outside/inside/heat/cold/day/night conditions.
While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

The pay range for this position is $110k - 120k/year. Please note that salaries vary within the range based on experience and education.

WORK ENVIRONMENT:
General office working conditions; the noise level is usually quiet.

Comments:
This position may require occasional domestic travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Analist Bioanalyse (LC-MS/MS) (Groningen, NL)

Voor de uitbreiding van de afdeling Bioanalyse zijn wij op zoek naar een

Analist Bioanalyse (LC-MS/MS)

Afdeling: 
Met bijna 30 medewerkers is onze Discovery site een toegewijde groep die zich richt op farmacokinetische en farmacologische studies om de pathofysiologie van neurologische aandoeningen beter te begrijpen.  

Team: 
Als Analist Bioanalyse bij Charles River Discovery kom je te werken in een collegiaal team. Iedereen staat voor elkaar klaar en naast dat er hard wordt gewerkt, is ook ruimte voor gezelligheid. Je werkt binnen jouw team zelfstandig en met elkaar aan de verschillende studies aan analysemethoden voor pre-klinisch onderzoek. Daarnaast spreek je regelmatig met de Study Directors van de site over het verloop van de studies.  

Over je rol:
Je werkt op de afdeling Bioanalyse (non-GLP) in een collegiaal team van analisten dat verantwoordelijk is voor LS-MS/MS analyses van potentiële nieuwe geneesmiddelen in uiteenlopende monsters (microdialysaat, CSF, plasma, serum, volbloed, weefsels). Hierbij worden verschillende monster voorbewerkingstechnieken gebruikt. Je werkt samen continu aan het implementeren en optimaliseren van bestaande en nieuwe technieken.

Primaire werkzaamheden:
•   Het voorbereiden, uitvoeren en rapporteren van analytische data;
•   Het ontwikkelen van analyse methodes voor nieuwe teststoffen of biomarkers;
•   Het beheer van apparatuur en materialen die bij ons onderzoek gebruikt worden;
•   Het uitvoeren van kwaliteitscontroles op bioanalyse data.

Jouw profiel:
•   Je bent een teamspeler die graag met je collega’s meedenkt en het teamresultaat net zo belangrijk vindt als je eigen doelen;
•   Je hebt een relevante en afgeronde opleiding op minimaal HBO niveau;
•   Je hebt ervaring in kwantitatieve analyse met LC-MS/MS;
•   Ervaring met het ontwikkelen van methodes voor zowel kleine als grote moleculen is een pré;
•   Goede communicatieve en sociale vaardigheden;
•   Je hebt een kritische werkhouding, zet kwaliteit voorop en neemt graag het initiatief.

Nice to have:
• Ervaring met het ontwikkelen van methodes voor zowel kleine als grote moleculen is een pré.

Ons aanbod:
Werken bij onze organisatie betekent werken in een dynamische internationale organisatie. 
Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:  
•   25 vakantiedagen;  
•   Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;  
•   Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;  
•   Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;  
•   Korting op je zorgverzekering;
•   Reiskostenvergoeding à € 0,21 cent per kilometer met een max van € 225 netto per maand;
•   Collectief pensioen;
•   Elke dag gratis vers fruit.  
  
 
Voor verdere informatie over de functie kun je contact opnemen met Maaike Verrijt via
her-recruitment@crl.com. Heb je belangstelling voor deze functie, dan nodigen wij je uit te reageren via onze carreer site: Charles River Laboratories, Inc. Jobs (criver.com) 

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Senior Business Development Executive - Cell Solutions (New England Territory) (Wilmington, MA, US, 01887)

Job Summary

This position is remote and will work from a home office, ideally located in CT, MA, PA, NY.

Travel is expected to be 50% of the time.

Essential Responsibilities

Job Qualifications

Education, Experience, and Licensure

Compensation Data

The pay range for this position is $130K - 140K USD + commission. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Charles River Cell Solutions

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Job Etudiant : Technicien Animalier - F/H - CDI Week-end Intermittent (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste

Pour travailler au sein de nos animaleries (rongeurs ou non-rongeurs) pendant les week-ends et vacances scolaires, nous recherchons plusieurs étudiants.
En contrat CDI Intermittent, vous interviendrez en tant que Technicien Animalier (F/H) après une formation initiale de 6 semaines, à temps complet, dispensée sur l'été 2025.

Les missions

Assurer le bien-être et les soins aux animaux dans les conditions optimales d’hébergement en étude : alimentation, abreuvement, change des animaux
Participer à l’entretien des installations : nettoyage et rangement du matériel
Observer l’état physiologique et sanitaire des animaux
Assurer les soins et traitements prescrits par les vétérinaires, les techniques de contention
Effectuer le relevé des observations cliniques et l’acquisition des données selon le plan d’étude et les protocoles

Qualifications souhaitées

Vous êtes reconnu(e) pour votre rigueur et votre adaptabilité. Vous savez travailler seul(e) comme en équipe.
A l'aise avec les outils informatiques, vous maitrisez les logiciels bureautiques (Word, Excel).
Notre environnement est propice aux étudiants de formations en biologie ou sciences.

Modalités contractuelles

Convention collective de l'industrie pharmaceutique, groupe : 2
Salaire de base : 11,65€ bruts/h + majoration forfaitaire de 45%
Contrat : CDI Intermittent (environ 200h par an, hors formation initiale)
Formation rémunérée à temps plein de 6 semaines minimum sur les mois de juin à août 2025 selon disponibilités
Planning annuel donné en août
Lieu de travail : St Germain Nuelles (69) - Permis B et véhicule obligatoire.

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Principal Scientist I - Discovery Bioanalysis (Worcester, MA, US, 01608)

Job Summary

We are seeking a Principal Scientist 1 for our Discovery site located Worcester, MA

We are seeking a highly-motivated individual with extensive hands-on experience in developing large and small molecule bioanalytical assays by LC-MS/MS to join our discovery bioanalytical team. The scientist will be responsible for method development and execution of quantitative assays, critical review of data, mentoring junior staff, and maintaining analytical equipment. Individuals in this role will also serve as primary point of communication with the clients. The scientist is expected to work independently to deliver high-quality non-GLP data in a fast-paced environment.

The successful candidate in this position will have:

A solid understanding of analytical approaches and experience of LC-MS bioanalysis.
Experience in extraction and analysis of biological samples, data generation, review of results and scientific presentation
Excellent scientific communication and interpersonal skills
Demonstrated ability to work collaboratively in a team environment with colleagues at various levels
Attention to detail and the ability to critically analyze and verify data prior to data release
Exceptional method development and assay troubleshooting skills
Technical proficiency in operation of analytical instrumentation including chromatography and mass spectrometry systems.

Other: Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs, as appropriate. Knowledge of applicable international guidelines for all types of studies. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and analytical instrumentation software.

Job Qualifications

The following are minimum qualifications related to the Principal Scientist 1 position:

Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or Ph.D. preferred.
Experience: Minimum of 7 years related experience in the contract research, academic, or pharmaceutical industry.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Certification as appropriate for specialty preferred.
Other: Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs, as appropriate. Knowledge of applicable international guidelines for all types of studies. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and analytical instrumentation software.

Compensation Data

The pay range for this position is between $100,000/yr. -$110,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Batch Release Co-Ordinator (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Batch Release Co-Ordinator for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Analytical Functional Manager and the main duties & responsibilities shall be:

Project Management of routine batch release testing in the Analytical Services Department (client correspondence,/weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
Generation of GMP compliant SOPs, Protocols and reports.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
Receipt and processing of test samples in LIMS
Carry out data calculations ,basic statistics and trending. Provide additional information at the clients request as required.
Assist in internal, regulatory and client visits/audits and respond to findings.
Carry out test method procedures like generic ELISA, MAT assay, microplate assays or client specific immunoassays.
Safe and compliant disposal of all laboratory generated waste.

Profile and Requirements

The following are minimum requirements related to this Position;

A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
Experience in project management essential.
BSc/M.Sc. in a relevant science discipline (e.g. Analytical Chemistry)
Experience in analytical techniques/immunoassays desirable but not essential.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Administratieve Projectondersteuner (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Zou jij als Administratief Projectondersteuner graag willen bijdragen aan onderzoek naar de veiligheid van bestaande en nieuwe stoffen?
Ben jij oplossingsgericht, nauwkeurig, flexibel en ben je communicatief vaardig?
Heb je affiniteit met softwareprogramma’s?

Heb je alle bovenstaande vragen met ja beantwoord, dan zijn wij op zoek naar jou!

Administratief Projectondersteuner voor de afdeling Toxicologie

Afdeling:
Met meer dan 240 medewerkers voert de afdeling Toxicologie onderzoek uit naar de veiligheid van bestaande/nieuwe medicijnen en chemische stoffen. Kenmerkend voor het werk is de grote diversiteit aan projecten, teststoffen en opdrachtgevers.

Over jouw rol:

Als administratief projectondersteuner fungeer je als assistent, ben je een energiek steun- en schakelpunt voor de afdeling Toxicologie en werk je nauw samen met de huidige drie administratieve projectondersteuners en de Lead Electronic File Processing. Je ondersteunt op dagelijkse basis een team van ca. 30 studie directors en zorgt ervoor dat alle processen soepel en efficiënt verlopen.

Primaire werkzaamheden:
•   Projectadministratie (o.a. het omzetten van studieplannen, amendementen en rapporten in PDF format met behulp van Adobe; het versturen van deze documenten; het verzamelen en opslaan van digitale handtekeningen met behulp van Docusign);
•   Voorbereiden van studieplannen en draft rapporten voor projecten en het monitoren van deze projecten;
•   Genereren van wetenschappelijke electronische rapporten en rapportonderdelen (publishen) via M-Files/AdLib volgens de regels van de geldende autoriteiten en verzoeken van klanten;
•   Vergunning gerelateerde werkzaamheden (controleren en registreren van data voor indiening bij de NVWA);
•   Onboarding van nieuwe collega’s;
•   Algemene werkzaamheden zoals het verwerken van emailcorrespondentie; het onderhouden van in- en externe contacten en overige voorkomende (ad-hoc) werkzaamheden.

Wat is vereist:
•   MBO-4/HBO werk- en denkniveau;
•   32 - 36 uur per week; mogelijkheid om 1x per week vanuit huis te werken;
•   Je bent communicatief sterk en kunt onder druk van deadlines werken;
•   Je beschikt over goede computervaardigheden en hebt affiniteit met het jezelf eigen maken van verschillende software;
•   Ervaring met MS office (Ecxel, Word, Outlook) en Adobe is een pré;
•   Je staat organisatorisch sterk in je schoenen;
•   Je kunt zelfstandig en in teamverband werken;
•   Je fungeert als aanspreekpunt voor interne partijen en bent in staat om problemen met een oplossingsgerichte houding af te handelen;
•   Draagt actief bij aan procesverbeteringen;
•   Je hebt uitstekende communicatieve vaardigheden, zowel mondeling als schriftelijk in Nederlands en Engels;
•   Je kunt omgaan met vertrouwelijke informatie;
•   Je bent accuraat, kunt prioriteiten stellen, structuur aanbrengen en het overzicht behouden;
•   Je hebt een flexibele, proactieve en servicegerichte houding.

Wij bieden:
Werken bij onze organisatie betekent werken in een dynamische internationale organisatie met een modern laboratorium en een grote diversiteit aan apparatuur en technieken tot je beschikking.
Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

•   27,5 vakantiedagen en 2 collectieve dagen per jaar;
•   Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
•   Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
•   Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
•   Reiskostenvergoeding á 0,23 cent per kilometer met een max. van 250 netto per maand, of een NS-Businesscard;
•   Fiets(lease)plan;
•   Collectief pensioen met een eigen bijdrage van 2.9%;
•   Bedrijfsfitness;
•   De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
•   De mogelijkheid tot een consult van onze in house ergonoom;
•   Elke dag gratis vers fruit.

Over Safety Assessment

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogt zodat producten eerder op de markt gebracht kunnen worden.

Meer informatie vindt u op www.criver.com.

Lab Assistant, Bioanalytical Chemistry (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Lab Assistant I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH.

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Perform all laboratory maintenance functions with minimal oversight
Perform laboratory support functions such as labeling and solution preparations with oversight
Assist with maintaining discipline-level inventory of laboratory consumables with oversight
Write both study and non-study deviations with oversight
Performs all other related duties as assigned

The pay range for this position is $19-20/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

HS/GED/Associate’s degree with no experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Necropsy Technician (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Technician for our Necropsy team located in Senneville, you will mainly be responsible for performing the post-mortem examination of animals while following the ethical regulations and directives from study plans. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Dissecting and evaluating animal tissues for pathologists;
Weigh and document all abnormalities of the organs;
Euthanize animals prior to performing the necropsy.

Key Elements

We are looking for the following minimum qualifications for this role:

Collegial Diploma in Animal Health or any other Biology related field;
Bachelor’s degree in biology or any other Animal Science related field;
Dissection experience (asset);
Ability to work in a team environment, independently, and detail-oriented;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $22/hrs;
Annual bonus based on performance;
Schedule: Daytime schedule, Monday to Friday. Depending on the needs, you may have to do weekends rotations and overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Free gym on site
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien.ne en Nécropsie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Technicien.ne pour notre équipe de Nécropsie située à Senneville, vous serez responsable d'effectuer les examens post-mortem des animaux tout en suivant les règlements éthiques et les directives des plans d'étude. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Effectuer les dissections et évaluer les tissus des animaux pour les pathologistes;
Peser et documenter toutes les anomalies des organes;
Euthanasier les animaux avant de procéder à la nécropsie.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Santé animale ou toutes autres disciplines en lien avec la Biologie;
Baccalauréat en Biologie ou toutes autres disciplines en lien avec la Science animale;
Expérience en dissection (atout);
Capacité à travailler en équipe;
Être autonome et minutieux;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 22$/hrs;
Bonus annuel basé sur la performance;
Horaire: Horaire de jour en semaine du lundi au vendredi. Selon les besoins de l’entreprise vous pourriez avoir à effectuer des rotations de fin de semaine et du temps supplémentaires;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Gym gratuit sur place;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all nonhuman primates at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint, generating and recording data and related tasks. Assist with the movement of animals and stocking of supplies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

•    Education: High school diploma or General Education Degree (G.E.D.) required.
•    Experience: None.
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•    Certification/Licensure: None.

***The pay range for this position starts at $19.75. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Mitarbeiter für den internen Produktions- und Logistikbereich (Sulzfeld, Bavaria (Bayern), DE, 97633)

Wir suchen ab sofort

eine/n Mitarbeiter/in (m/w/d)

für Außenbereichstätigkeiten

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

· Warenannahme und -lagerung

· Bau, Wartung und Abbau von Isolatoren

· Bestückung des Autoklaven mit Materialien für Reinräume

· Abfallbeseitigung gemäß Vorschrift

· Reinigung und Desinfektion von Außenbereich, Lagerhallen

Die Anforderungen:

Körperliche Belastbarkeit
Ordentlichkeit
Personalhygiene
Einsatzbereitschaft
Sorgfalt
Technisches Verständnis

Unser Angebot:

· eine ausführliche und betreute Einarbeitung

· ein leistungsgerechtes Einkommen

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

· Teilnahme an diversen Unternehmensveranstaltungen

· zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, Tankgutschein, VWL-Förderung u.v.m.)

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com, www.criver.com

Vorabinfos unter: 09761/406-11 oder 09761/406-280

Über Research Models & Services

Über Charles River

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von rund 80% der von der FDA in den letzten fünf Jahren zugelassenen Arzneimittel unterstützt haben.

Weitere Informationen finden Sie unter www.criver.com.

生产副主管 (Changping District, BJ, CN, 100107)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融， IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。在过去五年中，美国食品和药物管理局 (FDA) 批准的药品中有 80% 都与我们合作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com。

Technician I-Histology-2nd shift (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our 2nd shift Histology Team located in Ashland, OH. Candidate will transition to Mon-Thu 2pm-1230am after training.

A Histology Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, including various tasks within Pre-Trim with an introduction to Trimming. Technician is working under close supervision to gain proficiency.

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which includes GLP Training, Animal Welfare Training and New Hire Orientation. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements. 
Use and maintain instrumentation and equipment.
Reading and understanding of protocols.
Excellent written and verbal communication skills. Knowledge of English.
Manage multiple tasks and priorities to achieve goals.
Ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Work under specific time constraints.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Perform all other related duties as assigned.

The pay rate for this position is $19/hour plus a 10% shift differential. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. 
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

Comments:

May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Elektriker / Elektroniker (m/w/d) - allgemeine Gebäudetechnik (Erkrath, NW, DE, 40699)

Am Standort Erkrath suchen wir ab sofort und unbefristet
eine/n

Elektriker / Elektroniker (m/w/d) für das Management der allgemeinen Gebäudetechnik

(Equipment, Safety &-Facility Management Specialisten (m/w/d)

Zu Deinen Aufgaben zählen:

Elektrotechnische Arbeiten
- Installationen, Reparaturen, Wartungen & Prüfungen von z.B. Lüftungs- & Klimaanlagen, Lampen etc.
das Management der allgemeinen Gebäudetechnik
die Verantwortlichkeit für (Labor)-Geräte nach der Einarbeitung
- Gerätewartungen & Gerätequalifizierungen
Dokumentation nach GMP-Richtlinien:
- Erstellung und Revision von SOPs
- Erstellung von einheitlichen Vorlagen für die Gerätedokumentation
Beratung von Mitarbeitenden in Hinblick auf
- Gerätequalifizierung und die Auswahl neuer Geräte

Überzeuge uns durch:

eine erfolgreiche abgeschlossene Ausbildung als Elektriker, Elektroniker, Betriebstechniker o.ä.
Erfahrung im Bereich der Instandhaltung und / oder Qualifizierung von technischen Anlagen und Geräten wünschenswert
Erfahrung im zertifizierten oder GMP-regulierten Umfeld wünschenswert
idealerweise Erfahrung im Bereich der Erstellung und Pflege von technischer Dokumentation
schnelles Erfassen und grundlegendes Verständnis von Arbeitsabläufen und Netzwerken sowie diplomatisches Geschick
hohes Maß an interdisziplinärem Denken und der Bereitschaft auch Arbeiten in angrenzenden Arbeitsgebieten durchzuführen
lösungsorientiertes Arbeiten und flexibler Umgang mit ungeplanten Situationen
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung
eine intensive Einarbeitung mit Onboarding Programm
kostenfreie Parkplätze / Fahrkostenzuschuss
Fortbildungsmöglichkeiten
Engagement Programm

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb Dich bitte unter der Job-ID 227053 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Clinical Veterinarian II (Stilwell, KS, US, 66085)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

A Clinical Veterinarian II is responsible for providing consultation, oversight, and direct support of veterinary care activities for all animals used by Charles River Laboratories; supporting the IACUC to ensure compliance with animal welfare standards and regulations by AAALAC, Int., USDA, and PHS-OLAW; and supporting the evaluation of test article effects by performing examinations and making assessments to interpret study effects on animals.

Essential Duties and Responsibilities:

Oversee daily animal health assessment program including both routine stock and study examinations which support research.
Respond to requests for veterinary care, planned or emergency, by examining the animal, communicating with staff, and following the case until resolution, and address veterinary concerns.
May perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice.
Functions as departmental representative for interdepartmental communications and initiatives as required.
Supports and contributes to occupational health and safety program.
Support the overall training program for veterinary techniques/treatments performed by veterinary technicians/technical staff and ensure that training is properly documented and regularly updated. Contributes to training others in research animal techniques and other aspects of vivarium operations.
May assist in the development of operating objectives and Standard Operating Procedures (SOP's).
May serve as a full or ad-hoc member of the Institutional Animal Care and Use Committee (IACUC), assisting in protocol review and other efforts as identified.
Develop understanding of animal welfare regulations and standards and their application.
Development of understanding of the 3Rs and considers where refinements may be applied within the animal care program. Works with cross-site team members to implement refinements.
In consultation with the Study Director is a contact for Sponsor discussion on veterinary care and animal responses to the test article as well as review study plans as needed.
Actively engages with internal and external customers and demonstrates understanding of customers’ needs, requirements, and expectations.
Other duties as assigned

Job Qualifications

Education: DVM or equivalent degree required
Experience: 2+ years of experience in veterinary medicine required; experience in laboratory animal medicine or relevant area/education preferred
Licensure to practice veterinary medicine in at least 1 U.S. state required
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Must be able to obtain a veterinary license, controlled substances license, and USDA accreditation in state of employment.
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions and including ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively, and lead/manage staff in a growing, changing environment

Compensation Data

The starting salary for this opportunity is $155,000 USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Note: Relocation assistance, sign-on bonus and a retention bonus will be part of the overall compensation package as well.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

BTA / Biologielaborant /BSc als Technical Officer (m/w/d) - Bioassays (Erkrath, NW, DE, 40699)

Für die Abteilung Bioassays am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Technical Officer (m/w/d)

Zu Deinen Aufgaben gehören:

die Entwicklung und Durchführung zellbasierter Bioassays unter einem GMP-System
Laborarbeiten mit Zellkulturen und Viren bis hin zur Risikogruppe S2
die Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GMP-Systems u.a. Pflege und Wartung von Labor-Geräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen.
die permanenten Verbesserung unserer Prozesse und Techniken

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-Technischer Assistent / Biologielaborant (m/w/d), ein B.Sc. im Bereich Biologie / Biotechnologie oder eine vergleichbare Qualifikation
vorzugsweise Berufserfahrung in einem Arbeitsumfeld, das dem unseres Unternehmens ähnelt (Biotechnologie, Pharmazie, etc.)
nach Möglichkeit praktische Fähigkeiten in den gängigen zellkulturtechnischen Verfahren und in der Durchführung zellbasierter Bioassays
sehr strukturiertes, zielorientiertes und sorgfältiges Arbeiten unter Einhaltung enger Zeitlinien
Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Kundenorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel, Powerpoint) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung
eine intensive Einarbeitung mit Onboarding Programm
kostenfreie Parkplätze / Fahrkostenzuschuss
Fortbildungsmöglichkeiten
Engagement Programm

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 227478 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Vorangehen - Wir gehen voran, wenn wir unsere Absichten und Werte entwickeln und unsere Kompetenz teilen, wenn wir für die Zukunft planen und Wandlungsfähigkeit und Flexibilität zeigen, wenn wir Innovation ermöglichen und die großartige Arbeit anderer schätzen.

Sorgfalt - Wir beweisen Sorgfalt, wenn wir einander, unsere Tiere und das gesellschaftliche Umfeld, in dem wir arbeiten und leben, respektieren, wenn wir einen positiven, gesunden Arbeitsplatz schaffen, wenn wir unsere Compliance-Standards einhalten, und wenn wir stets das Richtige tun.

Zusammenarbeit - Wir arbeiten zusammen, wenn wir klar und effizient in unserem direkten Umfeld ebenso wie weltweit kommunizieren, andere einbeziehen und unterschiedliche Ideen schätzen, wenn wir unseren Kunden zum Erfolg verhelfen und das Teamwork fördern und wenn wir allumfassend und ganzheitlich denken und handeln.

Verantwortung - Wir handeln wie Eigentümer, wenn wir Verantwortung für unsere Handlungen übernehmen, wenn wir auf interne und externe Kunden mit Geschwindigkeit und Genauigkeit reagieren, wenn wir sinnvolle Ziele setzen und erreichen und wenn wir nach kontinuierlicher Verbesserung streben.

Biologics Testing Solutions

Mit über 50 Jahren Erfahrung und bewährter regulatorischer Kompetenz kann die Charles River Biologics-Gruppe sich den Herausforderungen von Biotech- und Pharma-Unternehmen weltweit stellen. Wir unterstützen mit Dienstleistungen wie Kontaminations- und Verunreinigungstests, Proteincharakterisierung, Bioassays, virale Clearance-Studien sowie Stabilitäts- und Chargenfreigabeprogrammen Kunden während des gesamten biologischen Entwicklungszyklus, von der Einrichtung und Charakterisierung von Zellbanken bis hin zu präklinischen und klinischen Studien und der Markteinführung von Produkten. Ganz gleich, ob Kunden eigenständige Dienstleistungen, ein maßgeschneidertes Testpaket oder In-house-Support benötigen, unsere Biologics-Gruppe kann für jeden Bedarf eine maßgeschneiderte Lösung entwickeln. Jedes Jahr werden mehr als 20.000 biologische Testberichte und über 200 lizenzierte Produkte von unserem Biologics-Team ausgesendet.

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

Automation Engineer I (Charleston, SC, US, 29407)

Job Summary

This position will work with both hardware and software aspects of automation to determine the best way to implement the Microbial Solutions automation roadmap, including conceptual design, capital expenditure approval, management of integration and suppliers, testing, and validation. This role will monitor existing automation for end of life/replacement/repair and identify, justify, and implement technology and equipment upgrades, process technologies, and process improvements. Additionally, the Automation and Controls Engineer will provide project leadership and support for assigned automation, equipment, and software projects.

Essential Duties and Responsibilities

Investigates, analyze, and prepare justification for the purchase of automation equipment and other capital equipment purchases
Identify, lead, and support continuous improvement/new projects, developing detailed specifications, electrical drawings, implementation plans, and other appropriate documentation
Collaborate with functional experts, operations personnel, and site management to shape the future state of the manufacturing facility and the plant software architecture that adheres to automation standards and regulations
Review, quality check, and provide final approval for all control system hardware drawings, including network architecture, panel drawings, communications wiring diagrams, etc.
Troubleshoot existing hardware and software and provide programming assistance to maintain current equipment and software/control systems.
Validation, Qualification and FAT/SAT experience a plus
Perform all other related duties as assigned

Qualifications

Education:
⦁ B.S or equivalent in Mechatronics, Industrial Engineering, Mechanical Engineering, Electrical Engineering, Computer/Computer Systems Engineering, Electronics

Experience:
⦁ At least 3 years in a cGMP environment
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above

Skills and Abilities:
Working knowledge and experience with PLC, HMI, and SCADA; working knowledge of vision systems (Cognex, Keyence, etc.); ability to work on multiple projects simultaneously, good interpersonal skills, quality mindset with focus on risk management and mitigation; technical writing and communication

WORK ENVIRONMENT:
⦁ Office and production environment.

Comments:
⦁ Occasional Travel may be required

Compensation Data

The pay range for this position is $80,000 to $100,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Equal Employment Opportunity

Animal Care Technologist - EG (Wilmington, MA, US, 01887)

Job Summary

We are seeking an Animal Care Technologist for our GEMS-Breed Department located in Wilmington, MA.

The Technologist performs specialized production duties to maintain and monitor the health, production and physical environment of animals within isolators, micro-isolator cages or barrier rooms. Provides training to departmental staff on all technical skills and Standard Operating Procedures (SOPs).

This is temporary opportunity with the potential to become a regular Charles River Labs employee.

Some benefits include:

Paid sick time
401K participation with a company match
Paid volunteer time off
Use of our onsite gym

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Has substantial understanding and knowledge to perform husbandry tasks, including supplying food, bedding, water and environmental enrichment.
Proficient at maintaining rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals, processing samples and other technical tasks as required.
Proficient at handling rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Has substantial understanding and knowledge to observe animals for any abnormalities or common health issues.
Has substantial understanding and knowledge to identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Learn, understand, and comply with all Standard Operating Procedures (SOPs). Able to complete new processes/tasks with minimal instruction.
Strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.
Workload contains complex projects and requires judgement in resolving issues and/or in making recommendations. Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).
Ensure compliance with all local, state and federal laws governing the use of research animals.
Ability to collaborate with others to train and mentor on knowledge and skills learned.
Ability to self-organize, plan and execute daily tasks.
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
Has substantial understanding of using general computer skills and ability to quickly learn and master required computer programs, databases and other applications (i.e. ICM and Microsoft Office)
Engage in studies, special projects, efficiency improvements, engagement opportunities, etc.
Identify issues and recommend potential solutions to management.
Able to effectively apply and incorporate CRL DNA into day-to-day work.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

High school graduation diploma or General Education Degree (G.E.D.), higher educational experience preferred.
Two (2) to four (4) years related experience and/or training.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds is required.
The ability to communicate clearly and effectively is required.
Must possess a high level of initiative and ability to work with minimal supervision
Proficient in computers (IE: MS Office Suite).

PREFERRED QUALIFICATIONS

AALAS certification at the ALATG.

The hourly pay rate for this position is $21.25. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Clinical Veterinarian I (Ashland, OH, US, 44805)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Responsible for providing professional veterinary services and assisting with the management of all phases of health care for the animal colony.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Provide clinical care for the animal colony.
•   Perform veterinary rounds as scheduled, and provide clinical care and preventive medicine support.
•   Perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice to facilitate protocol development.
•   Assist in the development and deliver training for staff. Training may include veterinary diagnostics, techniques and minor surgical procedures.
•   Provide animal health care guidance for veterinary services personnel as required.
•   Ensure that reports and other materials are prepared and submitted as required.
•   May participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
•   Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
•   Write, review and update veterinary care and/or necropsy SOPs as required.
•   Perform literature searches relating to veterinary subject matters.
•   Ensure facility is in compliance with all applicable regulations, guidelines and standards that relate to animal care and use (e.g. USDA, FDA, AAALAC).
•   Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
•   May use controlled substances and be responsible for maintaining appropriate records.
•   May develop new or innovative surgical techniques or other procedural improvements appropriate to research studies.
•   May assist in management of the activities of assigned section, including providing direction to junior employees, scheduling activities, and personnel development of veterinary technical team and husbandry staff.
•   Perform special projects and assist with administrative efforts as needed.
•   Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
•   Education: Veterinary degree (D.V.M./V.M.D.).
•   Experience: Zero to two years related experience with animal care and surgical techniques. Strong preference for experience in a research/lab animal/GLP environment.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable. USDA accreditation or application submitted within 1 month of hire.
•   Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

PHYSICAL DEMANDS:
•   While performing the duties of this job, the employee is regularly required to stand, crouch, bend, climb, reach overhead, kneel, push/pull and use hands to manipulate objects of varying size and with varying degrees of precision.
•   While performing the duties of this job, the employee is regularly required to discern animal health and well-being through visual and physical assessment.
•   Employees must be able to lift, move and/or hold up to 40 pounds; this includes equipment and animals.

Compensation Data

The pay range for this position starts at $120,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Note: A sign-on bonus and a retention bonus will be part of the compensation package.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

For more information, please visit www.criver.com.

Quality Operations Supervisor (Rockville, MD, US, 20850)

Job Summary

This leadership role is responsible for a team of Quality Operations Specialists, which will require providing oversight of quality documentation and operations in adherence to cGMPs and SOP regulations. QOps Supervisors will represent Quality at cross-functional meetings, providing Quality input and decision making in Quality events and deviations. They will provide training to groups and departments when needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Assume supervisory responsibility for a team of Quality Operations (QOps) Specialists, including scheduling, work assignment, and productivity monitoring
• Coordinate review of manufacturing Batch Production Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc.
• Support Internal Management System by engagement in Work Center Team activities
• Serve as owner of assigned nonconformances, CAPA, change controls, or other quality system documents and collaborate to drive completion
• Create, review and approve documents in electronic document management systems
• Serve as QOps representative for client project teams as assigned by management
• Coordinate performance of key QOps functions by team members, including line clearances, general manufacturing support, product shipment, raw material receipt and release, etc.
• Participate in departmental and cross-functional continuous improvement efforts
• Train and mentor assigned QOps Specialists and Leads
• Consistently set a high standard for quality of work
• Promote a safety mindset through daily actions and communication with team members
• Manage risk and escalate issues to QOps management in a timely manner
• Communicate professionally, effectively, and efficiently with all clients, internal and external
• Demonstrate flexibility when confronted with high stress/emergency situations, shifting
• Perform all other duties as necessary

Job Qualifications

• Bachelors degree in a life science or related field preferred
• Minimum of 5 year GMP related experience in biopharmaceutical/pharmaceutical or related industry or a combination of 5 years of education and related work experience required
• Demonstrated leadership capability
• Experience with GMP regulatory requirements
• Ability to multi-task effectively
• Excellent written and verbal communication skills
• Ability to prioritize daily activities in order to meet client needs on time of established time lines in a fast-paced environment
• Proficient in computer system use, including but not limited to Microsoft Office (Word, Excel, Power Point)

Compensation Data

The pay range for this position is $83,380 to $105,200. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Senior Immunoassay Analyst (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Senior Immunoassay Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Immunoassay Supervisor and the main duties & responsibilities shall be:
• Project Management of routine batch release testing in the Analytical Services Department (client correspondence, /weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
• Generation of GMP compliant SOPs, Protocols and reports.
• Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
• Receipt and processing of test samples in LIMS
• Carry out data calculations, basic statistics and trending. Provide additional information at the clients request as required.
• Assist in internal, regulatory and client visits/audits and respond to findings.
• Assist in the development and validation of different immunoassays (ELISA, Western Blot, ELISPot, etc.) and activity based assays.
• Safe and compliant disposal of all laboratory generated waste.

Job Qualifications

The following are minimum requirements related to the Senior Immunoassay Analyst position:

• A minimum of 3-5 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
• Experience in project management essential.
• BSc/M.Sc. in a relevant science discipline
• Experience in analytical techniques/immunoassays desirable but not essential.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Animal Care Technician I (Reno, NV, US, 89511)

Job Summary

The Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support study conduct which may include cage change out, animal handling, husbandry, observations, basic physiological indices, and data collection/recoding to support each skill.

Essential Functions (The fundamental Duties & Responsibilities of the role products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cage manipulation, and movement, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Vivarium PPE stocking, and facility cleaning.
Use and maintain instrumentation and equipment.
Skill plan completed for this role based on department training plan.
Perform all other related duties as assigned.

The pay for this position is $19.00 USD per hour.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High School Diploma, General Education Degree (G.E.D) preferred, but not required.
Experience: No previous experience required
An equivalent combination of education and experience may be accepted as a satisfactory
substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.

Preferred Qualifications:

Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evening, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sample Manager - F/H - CDI (Saint-Nazaire, FR, 44600)

Le poste

Notre site de St Nazaire (44) est spécialisé dans la mise en place de tests de bioanalyses pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération.

Intégré(e) au service Supply Chain, nous recrutons un Sample Manager - F/H en CDI afin de gérer l'intégralité des échantillons reçus et envoyés sur le site.

En partenariat avec le Sample Officier, les responsables d'études et sous la supervision du Supply Chain Manager, vous garantirez la bonne mise à disposition des échantillons pour le laboratoire.

Les missions

Participer à l’optimisation du process de gestion des échantillons
Assurer la préparation de la documentation relative à la gestion des échantillons (DDPP, CITES…)
Participer à la bonne réception des échantillons en termes de quantité, délais et documentation associée, si nécessaire
Participer à la création des design/import des listings d’échantillons dans les logiciels et outils utilisés par le site conformément aux plans d’étude ou protocoles et selon les procédures en vigueur
Participer à l’élaboration des DTA/DTS cliniques
Être le point de contact des clients et/ou sites d’expédition ainsi que des responsables d’études sur la gestion des échantillons de leurs études (réceptions, gestions des anomalies à réception, destruction, …)
Initier toutes déviations aux plans d’études ou protocoles concernant la gestion des échantillons et communique au responsable d’études
Participer aux réconciliations relatives à l’identification des échantillons dans le cas des études cliniques
Assurer le suivi des échantillons en fin d’étude ou de période d’archivage : transmission des formulaires de devenir des échantillons auprès des clients (demande de destruction/transfert, relance, attestation de destruction…)

Qualifications attendues

De formation Bac + 2 minimum, vous disposez d'une première expérience probante en gestion d'échantillons de bioanalyse dans un contexte BPL/BPC.

Vous avez de bonnes connaissances des normes BPL/BPC ou du travail en contexte qualité/réglementaire (suivi et respect de procédures et consignes).

Force de proposition et autonome, vous êtes reconnu(e) pour votre orientation solutions. Votre esprit d'analyse et votre capacité à gérer vos priorités vous permettent d'identifier et résoudre les problèmes rapidement.

Vous savez communiquer avec des acteurs internes comme externes (relation clients).

Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI cadre (forfaits jours, RTT)
Salaire : Environ 34 000 € bruts/an, sur 12 mois, selon expérience
Prise en charge de la mutuelle à 60% et tickets restaurants

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Scientist - Electrophysiology (Groningen, NL)

Does Neuroscience / CNS research interest you?

Have you got experience with patch clamp measurements?

Could you be our next ex vivo Electrophysiologist?

Our site:

Our Groningen CNS specialised site is a dedicated group where we perform discovery level research. We focus on non-GLP DMPK (drug metabolism and pharmacokinetics) and pharmacology studies to better understand neuroscience disease pathophysiology. including but not limited to, microdialysis, electrophysiology, pharmacokinetic screening and bioanalysis.

Your role:

In this position you will be responsible for designing, planning, performing and reporting of sponsor requested electrophysiology studies. Studies are based on ex vivo single cell or slice recordings. Manual Patch-Clamp and Multi Electrode Array are the techniques you will be using to conduct your studies with. The hands on work is often more individual, but for the entire study you will be collaborating together with scientific staff and animal technicians. You will bring in hands-on expertise to transfer and establish methods and to obtain high quality data.

Responsibilities:

Your responsibilities will include data collection and analysis as well as data interpretation and communication of results internally and externally. You ensure that study aims are reached and work follows relevant protocols, guidelines and legislation. CRL is committed to support the 3Rs and you have an equally strong sense of applying this to the research.

Qualifications:

Advanced academic degree in the life sciences;
Understanding of neuroscience on the cellular and systems level;
Experience with patch clamp measurements in cultured cells and/or acute slices and/or experience with multi electrode array measurements in acute slices;
Programming skills and understanding of principles of electronics;
Fluency in English, oral and written;
Ability to coordinate and prioritize;
Excellent communication, loves a scientific challenge and positive attitude.

Desirables:

Experience with ex vivo extracellular electrophysiology will be an asset
Knowledge of neuropharmacology and / or drug development processes will be an asset
Article 9 (Laboratory Animal Science)

What We Offer You:

Working at our organisation means working in a dynamic international organisation. In addition, we offer excellent primary and secondary working conditions including:

25 vacation days
Possibility to purchase 10 additional vacation days per year;
Annual one-time 8% vacation pay of your gross annual salary;
Annual one-time payment based on company results;
Travel allowance at € 0.23 cents per kilometer with a maximum of € 250 net per month,
Collective Aegon Capitall pension with a personal contribution of 2.9%;
Collective health insurance with CZ or VGZ. 10 to 12% discount on any supplementary insurance.

For more information, please visit www.criver.com.

Security Officer - Wilmington/Shrewsbury, MA (Sat & Sun, 6p-6a) (Wilmington, MA, US, 01887)

Job Summary

Charles River Laboratories is seeking a PART TIME (24 hrs. per week, benefit eligible) Security Officer for their Wilmington and Shrewsbury, MA sites.

Shift is overnights, Saturday & Sunday, 6pm-6am (12hrs) + 15% Differential

Following established procedures and guidelines, monitor and ensure compliance with company security and safety policies. Monitor all access activities to the facility by checking and issuing security badges. Monitor security, safety and integrity of buildings and environs and respond to any unusual circumstances. Protect facility from unwanted actions or espionage. Provide a safe and secure environment for employees, clients, visitors and animals.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
Monitor security systems and/or environmental systems and investigate and/or report any incidents.
Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physcial security measures; and monitors the critical building systems.
Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
Document all security department activity and generates incident reports as necessary.
Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
Contact emergency personnel as required and in accordance with adherence to pertinent departmental policies, practices, and procedures.
Assist in directing appropriate emergency response efforts when required.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Must be willing to work on a Part time schedule – 24hrs per week (position will be Benefits Eligible)
Shift: Sat & Sun 6pm-6am (12hrs) + 15% Differential.

Compensation Data

The base pay for this position is $22/hr. + 15% shift differential. Please note that salaries vary within the range (if applicable) based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Shipping Technician I (Charleston, SC, US, 29407)

Job Summary

Pack and ship products to customers and complete all associated paperwork.
Check orders prepared by others for shipment to customers; monitor for accuracy of lot numbers, quantities, certificate of analysis, and agreement between customer order and content of package.
Move finished goods to released storage area after QA release.
Perform inspection of final product as necessary; verify count, package insert, that label and vial meets standards described in SOPs and product specs.\
Perform Kit production: assemble packaging, components and necessary paperwork for Kit release.
Maintain retention storage area, retrieve samples for QC testing, and fill out appropriate paperwork.
Maintain customer returns by inspecting and quarantining the product until QA release.Create freight shipping labels; must perform measurement and weighing and document shipping specifications.
Maintain documentation as required by FDA, company policy, and cGMP.Share responsibility for inventory control to prevent stock-out situations.
Clean and maintain work and storage areas and adhere to established safety procedures.
Perform seasonal duties associated with processing crude LAL, as needed.
Assist other areas of the facility when needed.
Remain proficient in all SOPs in areas of responsibility.
Perform all other related duties as assigned.

Job Qualifications

• Education: High school diploma or General Education Degree (G.E.D.).
• Experience: Zero to twelve months related experience in and/or training in a GMP manufacturing environment.

PHYSICAL DEMANDS:
•   Tasks require full range of motion of arms.
•   While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel objects, tools, or controls.
•   The employee is frequently required to stand while performing duties; sit; reach with hands and arms; and stoop, kneel, crouch, or crawl.
•   The employee is occasionally required to work/type at a computer.
•   The employee must frequently lift and/or move up to 50 pounds.
•   Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
•   While performing the duties of this job, the employee regularly wears protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots)
•   The employee occasionally works near moving mechanical parts, works with sharp objects, works with or near toxic or caustic chemicals, works with biohazards, works with live animals (small, medium, large) with risk of exposure to allergens, is exposed to fumes or airborne particles, is exposed to unpleasant odors, is exposed to wet, humid and/or extreme temperature conditions, is exposed to vibration.
•   The noise level in the work environment is usually low / moderate

Compensation Data

The pay for this position is $19.25 hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Hamilton, MT.

As the Animal Care Technician I, you will be working in ABSL 4 facility environments to perform a variety of duties, including cleaning, sanitizing, routine preventative maintenance, and repair of caging materials and autoclaves.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD per hour.

For more information, please visit www.criver.com.

Data Coordinator - Reporting Services (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Coordinator for our Reporting Services team at the Senneville location, you will be responsible for providing the scientists with the information necessary for them to be able to write the summary and results sections of their reports, based on individual and summary data included in the appendices, tables and graphs customized to meet client specific reporting requirements.

In this role, primary responsibilities include:

Coordination of all pertinent data and scientific interpretation information in accordance with the Study Plan to enable the correct tabulation to be included in the report;
Transcribe data from hand-written data records and/or, process computer-generated data files, into formats suitable to meet sponsors’ needs;
Prepare finished reports, tables and/or graphs, that are clear and professionally presented as per Company requirements and guidelines;
Processing of reports or tabulated data, which are accessed either electronically or from hard copy sources following specific e-file management criteria involving the use of various software;
Ensure work is compliant with applicable guidelines and regulations.

Key Elements

We are looking for the following minimum qualifications for this role:

High School diploma;
Previous experience in Sciences or Information Technology;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
Ability to work under time constraints, in order to respect deadlines;
Ability to work in a team environment.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging;
Salary: 18.50$/hrs;
Annual bonus based on performance;
Schedule: Day shift from Monday to Friday, flexible schedule with possibility to work remotely;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Coordonnateur.trice des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Coordinateur.trice des données pour notre équipe de Services de rapport située au site de Senneville, vous serez responsable de fournir aux scientifiques l’information nécessaire pour qu’ils puissent écrire les sections de sommaire et résultats de leurs rapports basés sur les données individuelles et sommaires incluses dans les annexes, les tables et les graphiques adaptés afin de rencontrer les exigences spécifiques des clients.

Dans ce poste, les principales responsabilités incluront:

Coordination de toutes les données pertinentes et de l’interprétation scientifique des informations en fonction du plan d’étude pour permettre une tabulation adéquate pouvant être incluse dans un rapport;
Transcrire des données à partir d'enregistrements de données manuscrites et/ou traiter des fichiers de données générés par ordinateur dans des formats adaptés aux besoins des sponsors;
Préparer des rapports, des tableaux et/ou des graphiques finis, clairs et présentés de manière professionnelle conformément aux exigences et aux directives de l'entreprise;
Traitement des rapports ou de données tabulées, lesquels sont accessibles par sources électroniques ou par documents imprimés suivant les critères de gestion de l’e-file impliquant l’utilisation de divers logiciels;
S’assurer que le travail est conforme aux directives et réglementations applicables.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études secondaire;
Expérience précédente en sciences ou en technologie de l’information;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Maîtrise des compétences informatiques notamment des logiciels de la suite Microsoft Office (par exemple Word, Access, Excel);
Être en mesure de gérer son temps efficacement, afin de respecter les échéanciers;
Capacité à travailler en équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 18.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi, horaire flexible et possibilité de télétravail;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Quality Control - Associate (Rockville, MD, US, 20850)

Job Summary

The QC Associate I operates in the Materials Release department to ensure that inventory used for manufacturing is sufficient to support multiple manufacturing processes.

Key Responsibilities and Duties:

Release materials for production following SOP’s and GMP
Ensure sufficient quantity of materials are provided for production activities in a timely manner
Perform inventory assessments at multiple sites
Assist with data collection and analysis
Review process improvements that support the project
Read and review SOPs as they apply to QC group
Read and review test forms and associated documents
Read and review release forms and associated documents
Move materials within the building
Communication with vendors/other departments
Other responsibilities as needed

Job Qualifications

Bachelor’s degree preferred but not required with 0-2 years of experience, or high school diploma with 2-4 years of relevant experience
1+ year of general lab experience in material testing preferred
Experience in materials management, inventory control systems, and customer service desired
Team-player with excellent attention to detail
Good organizational skills
General computer skills including Microsoft Office software
General lab skills or science background desired

Compensation Data

The pay range for this position is $ 23 hr. –26 hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

In Vivo Technician I (Spencerville, OH, US, 45887)

Job Summary

We are seeking an In Vivo Technician I for our In Vivo Team at our Safety Assessment site located in Spencerville, OH.

A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, and restraint on multiple species as well as feeding, watering, husbandry of multiple species. Clinical observations, acclimation observations, and body weight determination on multiple species as well as qualitative and quantitative food consumption. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.) or equivalent in a biological science, desired.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician II (Bldg 35) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Animal Care Technician II to join our Insourcing Solutions team, located in Bethesda, MD.

As an Animal Care Technician II, you will perform daily animal health observations to maintain the quality and health of research animals in complex/high traffic rooms, cubicles, vertical vivarium rooms, and/or a satellite facility.

Additional responsibilities include:

Perform daily water bottle and cage checks, cage changing and/or cage cleaning as required; provide food and water; and record health concerns.
Maintain accurate records of animal breeding, housing, or support areas.
Receive, inspect, and house incoming animals.
Assist with restraint, handling, and manipulation of various animal species.
May become involved in breeding and weaning procedures.
Monitor personnel and equipment entry into various rooms.
Operate required equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician II position:

high school diploma or general education degree
minimum one year's experience performing basic animal care
ALAT eligibility required, ALAT certification preferred

The pay range for this position is $21.00 - 22.00 USD per hour.  Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Animal Care Attendant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Animal Care Attendant - No Experience needed

Have you always dreamed of working with animals in a company that participates in drug research to save lives? Good news! We are currently looking for a full-time Animal Care Attendant for our Senneville (QC) site. You don't need any previous experience because we have an exceptional training team who will teach you everything!

As an Animal Care Attendant for our Toxicology team at the Senneville (QC) site, you will be you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Handling animals.

Key Elements

If you have the following qualifications, we'll train you for the rest:

You like to work physically (lifting loads of 20-25 lbs);
You are able to follow precises instructions;
You like animals;

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $18.50 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Mostly days, weekend rotations and holidays with overtime on evenings or nights when needed;
Permanent position, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier.ière (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Animaler.ère - Aucune Experience requise

Tu as toujours rêvé de travailler avec les animaux dans une compagnie qui participe à la recherche de médicament pour sauver des vies? Bonne nouvelle! Nous cherchons actuellement un.e Animalier.ère à temps-plein pour notre site de Senneville (QC). Tu n’as pas besoin d’expérience préalable car nous avons une équipe de formation exceptionnelle qui va tout t’apprendre!

En tant qu’Animalier.ère pour notre équipe de Toxicologie situé au site de Senneville (QC), vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Tu aimes travailler physiquement (lever des charges de 20-25 lbs);
Tu es capable de suivre des instructions précises;
Tu aimes les animaux.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 18.50 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire: Majoritairement le jour, la fin de semaine en rotation et les jours fériés. Selon les besoins, il pourrait y avoir du temps supplémentaire de soir ou de nuit;
Poste permanent, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Animal Care Technician (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Animal Care Technician for our Insourcing Solutions site located in Baltimore, MD.

As the Animal Care Technician, you will provide husbandry and veterinary assistance in a laboratory for small animals, as well as monitor animal health and report findings.

Additional responsibilities include:

Prepare caging for cagewash.
Perform daily animal health observations and report any abnormal conditions or behavior. Monitor and report irregularities in environmental conditions that may affect animals.
Clean assigned animal rooms, facility and animal care equipment, and associated animal facility areas. Obtain weekly animal census.
Ensure logbooks, checklists and other records are completed accurately in a timely fashion.
Provide environmental enrichment feed and other enrichment stimuli and/ or provide behavioral assessments.

Job Qualifications
The following are minimum requirements related to the Animal Care Technician position:

High school diploma or GED preferred
AALAS certification at the ALAT level within one year of eligibility
1 year related experience in animal care
3 months working with lab animal species, most applicable rodents, preferred

The pay for this position is $18.47 USD per hour.

For more information, please visit www.criver.com.

Behavioral Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Behavioral Technician for our Safety Assessment site located Reno, Nevada.

The following are responsibilities related to the Behavioral Technician:

Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities. Monitor colony behavioral health and provide care to animals needing special attention and/or treatments as directed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist with providing appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.
•   Monitor colony behavioral health, and provide care for animals needing special attention and/or treatment as directed.
•   Observe animals and report behavioral abnormalities.
•   Assist in performing behavioral assessments in response to reports of behavioral abnormalities.
•   Assist with coordinating animal psychological/behavioral enrichment, including the acclimation and socialization of study animals.
•   Review animal approval documentation and submit approval forms to appropriate personnel.
•   Work with other Behavioral staff to precondition animals for study procedures.
•   Work closely with the veterinary and animal care staff to ensure proper animal care standards are maintained.
•   Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.
•   Assist with revisions to relevant SOPs as needed to ensure accordance with the Animal Welfare Act and accepted professional standards.
•   Routinely handle animals as required for duties.
•   Maintain and track data related to social housing, exemptions to social housing, and abnormal behavior.
•   Maintain documentation for the Behavioral Management Program.
•   Assist with training animal care staff and other site personnel on aspects of animal behavior and enrichment as needed.
•   May serve as IACUC committee member.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in animal or life sciences or related discipline.
•   Experience: 1-3 years experience in animal research and/or husbandry; multi-species experience preferred or must have fully satisfied technical and experience requirements for the previous level.
•   Certification/Licensure: AALAS certification at the LAT level preferred.
•   Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLP’s and other federal regulations and guidelines relating to the care of laboratory animals. Understanding of routine study design and protocols.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Director, Operations (Shrewsbury, MA, US, 01545)

Job Summary

Responsible for the administration and management of In-life Operations, Formulations, Necropsy, Histology, Sample Processing, Clinical Pathology, Quality Control, Training and Archives. Responsible for the financial aspect, in collaboration with Finances and the Managerial staff, for the control of expenses to meet the company budget. Incumbent will optimize resource utilization to maintain an occupancy level to meet revenue targets. Collaborate with clients and scientific staff for effective study design, problem solving, and delivery of high-quality study data. Foster a culture of continuous improvement in site operations and ensure successful audits by regulatory agencies. Duties also include delegated activities as per the individual’s Delegation of Authority memo of Test Facility/Testing Facility Management Functions.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Develop short- and long-range operating objectives, organizational structure, staffing requirements and succession plans.
• Direct activities of assigned group(s) to ensure optimum performance of the group/function.
• Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.
• Integrate activities with those of other major organizational units (e.g. businesses, departments, functions).
• Develop and recommend departmental budget and authorize expenditures.
• Develop and oversee the implementation of departmental training programs, including orientation.
• Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
• Represent the site to government, regulatory agencies, local, state and federal officials, industry groups, key customers as required.
• Work with senior leadership to identify new service offerings and/or business.
• Contribute to the development and presentation of major business proposals for key clients and represent the site and company.
• With the Managers and Supervisors, review processes to improve efficiency and efficacy, develop tools, strategies and plan of actions to meet budget, to meet our high-quality standards, to meet or exceed our capacity, to forecast the workload, to ensure that health and safety regulations, governmental regulations such as AAALAC, CCAC etc. are met.
• Responsible for identifying and implementing best practices across the groups, facilitating collaboration and resource sharing, and adherence to site, regional and global policies and initiatives.

The pay range for this position is between $$176,000 - $230,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in biological sciences or related discipline recommend. Master’s degree preferred.
• Experience: 8-10 years related management experience in research or pharmaceutical environment required. Experience in maintaining AAALAC International, Inc. certification is required.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: No specific certifications or licensure required
• Other: Knowledge of governmental regulations and guidelines applicable to the care and use of laboratory animals. Knowledge of GLP regulations and other FDA regulations applicable to non-clinical testing programs. Excellent organizational skills and the ability to meet deadlines. Excellent communication (both written and verbal), leadership and negotiation skills. Ability to interact appropriately with all levels of employees, while supporting the efforts of departmental teams.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

QA Specialist I - Quality Systems (Rockville, MD, US, 20850)

Job Summary

The QA Specialist I – Quality Systems is responsible for supporting Quality Systems, including investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control. This position will facilitate the compiling, trending (as required), and reporting key quality metrics for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products.

Key Responsibilities and Duties:

Establishes and maintains Investigation, Deviation, CAPA, EV systems, and internal and external audit. This task includes collaborating with cross-functional departments to ensure timely implementation and closure of quality records
Provides guidance and advice on methods, procedures, standardization, and requirements associated with these systems
Responsible for tracking and trending (as required) aspects of the Quality System and provide reports to management identifying risks and trends on a routine basis
Performs CAPA effectiveness evaluation based on quantitative and qualitative measurements
Administers the Change Control process for the site and conduct effectiveness verification for changes implemented
Maintains tracking mechanisms to support various Quality Systems elements and ensures visibility throughout the organization
Continuously monitors and review systems and procedures for adherence to regulatory compliance, quality improvements, efficiency, and industry best practices. Provide compliance support and expertise for QA department
Compiles and reports site monthly corporate Quality metrics
Supports the Quarterly Management Review (QMR)
Supports Deviation system and ensure proper investigation and root cause analysis are performed
Supports CAPA/EV system to ensure proper corrective actions are implemented and effective
Supports Change Control system to ensure proper change and impact assessments are performed and tasks are implemented
Develops, implements, and delivers training content for Deviation, CAPA, EV and Change Control processes and procedures
Responsible for procedure reviews and facilitating procedure updates for the Deviation, CAPA, EV and Change Control systems
Assures that personnel are adequately trained in the principles, policies, and procedures of the Deviation, CAPA, EV and Change Control systems
Identifies and escalates compliance gaps across quality systems
Maintains customer complaint and suspect sample management system and ensure its implementation
Prepares the quarterly compliance report for management review
Actively participates in all recruiting efforts to secure, onboard, and develop new staff members
Additional duties as assigned

Job Qualifications

BS/ BA in life sciences or related fields.
Minimum 5 years of experience in GMP related experience in biopharmaceutical/ pharmaceutical
Strong knowledge of GMP, SOPs and quality system processes.
Excellent organizational skills and ability to review and update processes or procedures.
Proficient in MS Word, Excel, Power Point, Adobe Pro, and electronic quality management systems. Previous experience in TrackWise, Pilgrim is preferable
Strong written and verbal communication skills.
Experience in pharmaceutical or bio-pharmaceutical field.
Education or training in cell culture and gene therapy manufacturing environment is a plus.
Proficient in drafting and completing technical documents and presentations.
Expertise in document management processes.
Works on multiple assignments in collaboration with various department system owners.
Quality systems demonstrated knowledge in areas such as Deviation, CAPA, EV and Change Control system management practices/strategies.
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211/600/820, ICH and EMA).
Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities.
Demonstrates basic understanding of training, instructional design, communication and/or education.
Demonstrates knowledge and understanding of pharmaceutical manufacturing and quality assurance, aseptic and packaging processes, and product transfer.
Demonstrates presentation skills with the ability to conduct training sessions.
Proven organizational skills, planning skills and ability to work effectively within teams.
Demonstrates ability to lead cross-functional project teams.

Compensation Data

The pay range for this position is $65,387-80,183. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Molecular Technologist-1 Sequencing (Newark, DE, US, 19711)

Job Summary

Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE.
This position is Monday - Friday 8:30am to 5:00pm.

The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance.

Roles and Responsibilities:

•    Conduct accurate processing of customer samples in accordance with current SOPs.
•    Receive, unpack, log, and subculture customer samples according to current SOPs.
•    Aliquot and prepare reagents.
•    Perform test streaks for isolation, PCR, sequencing of customer samples and other laboratory processes including but not limited to mass spectrometry and ribotyping.
•    Perform continual maintenance, repair and cleaning of all laboratory equipment.
•    Perform pipette verification.
•    Operate and maintain laser cutter.
•    Provide backup for all laboratory functions when needed.
•    Dispose of microbe cultures, chemicals and glass in proper waste containers.
•    Collaborate with technical support to resolve discrepancies with customer samples.
•    Comply with all aspects of laboratory safety, safety stations, safety manuals, safety SOP, and MSDS sheets.
•    Suggest process improvements.
•    Perform or support special projects in the lab when needed.
•    Perform all other related duties as assigned.

Job Qualifications

•    Education: Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred.
•    Experience:  0-2 years related experience in a laboratory setting or academic setting.
•    Other: Must have working knowledge of the Quality System and Laboratory Information System. Must have ability to work in a fast paced and team oriented work environment. Strong attention to detail and accuracy required.

Compensation Data
The compensation range for this position is $21- $22 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Animal Care Technician II (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Care Technician II to join our Insourcing Solutions team located in Baltimore, MD

As the Animal Care Technician II, you will provide husbandry and technical support to the investigative staff in the production and maintenance of required animal models.

Additional responsibilities include:

Perform daily animal husbandry duties to maintain quality and health of research animals, including: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning. Accurately document animal health concerns.
Monitor environmental parameters and maintain written records.
Assist with restraint and handling of various animal species. Safely transfer non-human primates from cage to cage.
Provide support to rodent breeding program, including setting up mating pairs, weaning, recordkeeping, and performing associated technical procedures, including phenotype observations.
Ensures that cages are identified correctly with information regarding strain or lineage, sex and sexual status.
Maintain detailed breeding records indicating the birth date, animal age, and fertility data of each animal. Responsible for computerized or manual breeding records to maintain pedigree information on each animal. Cares for potential transgenic births, determines sex, and weans when appropriate.
Provide animal identification, i.e. ear notching, ear tagging, and toe clipping.
Assist with specialized care of animals including preparation of special diets, medicated water, care of immature, aged, and special study animals. Administer drugs or treatments to animals as directed.
Assist research staff with logistics and scheduling of projects, and conduct research and laboratory support services.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician II position:

High school diploma or GED
1 year of experience working with research animals
AALAS certification at the ALAT level required; LAT certification or equivalent training and experience preferred

The pay for this position is $20.70 USD per hour.

With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

Animal Care Technician I (BLDG 35) (Bethesda, MD, US, 20892)

Job Summary

We are looking for an Animal Care Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The responsibilities of the Animal Care Technician I are to perform daily animal health observations, animal husbandry duties, to maintain the quality and health of research animals, to include performing daily water bottle and cage checks, cage changing and/or cage cleaning as required; providing food and water; and recording health concerns.

In addition:

Maintain accurate records of animal breeding, housing, or support areas.
Receive, inspect, and house incoming animals.
Assist with restraint, handling, and manipulation of various animal species.
May become involved in breeding and weaning procedures.
Monitor personnel and equipment entry into various rooms.
Operate required equipment and performs general housekeeping.

Job Qualifications

A candidate that possesses a high school diploma or general education degree is preferred; experience performing basic animal care desired. Interest in achieving ALAT certification upon eligibility.

The pay for this position is $18.50 USD per hour.

For more information, please visit www.criver.com.

Commis aux soins des animaux (Laval, Quebec, CA, H7V 4B3)

En tant que Commis aux soins des animaux pour notre site de quarantaine situé à Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

AEP en soins animalier (atout);
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
À l’aise pour suivre des instructions précises;
Passion pour les animaux.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation : 531 Boul. des Prairies, Laval, QC, H7V 1B7;
Transport: Stationnement gratuit. Près du métro Montmorency;
Salaire : 19$/hrs;
Bonus annuel basé sur la performance;
Primes: Fin de semaine ($2.75), temps supplémentaires (temps et demi), jours fériés (temps double);
Horaire : De jour en semaine du lundi au vendredi, 7h00 à 15h15. Selon les besoins de l’entreprise vous pourriez avoir à effectuer des rotations de fin de semaine ainsi que du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances ainsi que 5 journées personnelles;
De nombreuses activités sociales!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Animal Care Clerk (Laval, Quebec, CA, H7V 4B3)

As an Animal Care Clerk for our Quarantine facility located in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Animals handling.

Key Elements

If you possess the following qualifications, we will train you in the rest:

AEP in Animal Care (asset);
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Able to follow precises instructions;
Passion for animals.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 531 Boul. des Prairies, Laval, QC, H7V 1B7;
Transportation: Free parking. Near the Montmorency Subway;
Salary: $19/hrs;
Annual bonus based on performance;
Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
Schedule: Weekdays, between Monday to Friday 7am to 3:15pm. Depending on the needs, you will have to do overtime and weekend rotations;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive health and dental benefits as of day 1. We pay up to 85% of premiums;
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal days;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Caretaker (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker to join our Insourcing Solutions team located in Baltimore, MD

As the Animal Caretaker, you will provide basic husbandry to rodents and lagomorphs, monitor environmental parameters for abnormalities and provide customer assistance to the investigative staff.

Additional responsibilities include:

- Perform daily animal husbandry duties to maintain quality and health of research animals, including: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning.

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $18.47 USD per hour.

For more information, please visit www.criver.com.

QA Specialist I (Rockville, MD, US, 20850)

Job Summary

The QA Specialist I is responsible to ensure that production process is client focused, results oriented, performance driven, and in compliance with all applicable internal and external requirements. The Quality Specialist I will release critical materials required for GMP operation on timely basis.

Key Responsibilities and Duties:

• Provide QA oversight and support to client projects while working closely with QA Management to ensure QA support for GMP operations for the manufacture of master/working cell banks, bulk drug substance, plasmid products and/or final drug product used for human consumption
• Perform audits and/ or walkthrough of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and industry best practices
• Review executed batch production records and associated supporting documentation including logbooks, QC test reports, Environmental monitoring reports, cleaning records, etc.
• Perform QA on the floor activities supporting client projects, including line clearance and room release, observing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing
• Support in-process and raw materials review and disposition following approved internal procedure
• Ensure SOPs are current and effective, and staff performs routine tasks according to SOP through direct observation
• Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes and systems and instilling strong ownership and accountability
• Actively participate in all recruiting efforts to secure, onboard, and develop new staff members
• Additional duties as assigned

Job Qualifications

• BS/ BA in life sciences or related fields
• Minimum 3 years of experience in GMP related experience in biopharmaceutical/ pharmaceutical or related industry, preferably 2 years of experience in batch record review process
• Previous knowledge and experience with the practical implementation of FDA, EMA and ICH regulations and guidelines
• Exceptional interpersonal skills including the ability to influence behaviors and negotiate and resolve challenges with poise, tact, and diplomacy
• Strong verbal and written communication skills
• Strong organizational skills; able to prioritize and manage through complex processes/projects
• Ability to define problems, collect data, and draw valid conclusions
• Ability to organize and disseminate information efficiently and multi-task in a fast-paced environment
• Organized, responsible, creative, pays attention to detail
• Knowledge of Microsoft suite (Word, Excel, Access, Vizio and PowerPoint).
• The ability to follow instructions and Standard Operating procedures
• Ability to always maintain a professional and pleasant demeanor

Compensation Data

Pay rate for this role is $65,387 - $80,183 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Recrutements de talents - Administratif (Ahmedabad, IN)

Job Summary

About RightSource (Biologics Testing)

The biopharmaceutical industry is growing at an unprecedented pace which is simultaneously changing current testing methodologies. To keep up with the demand, we offer a flexible testing platform which can be deployed on-site at the client site to their exact needs. Our biologics testing lab...in a box…at the client site. RightSource℠ is completely managed and operated using our quality management system, SOP’s, methods, and best practices. It’s as if you shipped your samples to an outsourced lab but walked down the hall instead.

Our Biologics Testing Solutions offers a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

For more information, please visit www.criver.com.

Testreq - Italy Walkthrough (Ahmedabad, IN)

Job Summary

test test test test

Job Qualifications

test test test

Equal Employment Opportunity

For more information, please visit www.criver.com.

Facilities Technician I (Rockville, MD, US, 20850)

Job Summary

The Facilities Technician I is responsible for maintaining the facility in good operating and physical condition, as well as responding to normal and emergency service calls, and taking corrective action via diagnosis and repairs. As directed, conducts/oversees preventive maintenance. The Facilities Technician I will be required to perform a wide range of repair, maintenance, and escorting tasks.

Key Responsibilities and Duties:

· Perform routine GMP spaces cleaning

· Maintain stock of consumables (HVAC filters, cleaning supplies, etc)

· Perform routine simple maintenance and repair throughout the facilities, such as repairing cosmetic damage

· Oversee building utility systems equipment maintenance to ensure expected conditions in the facility. This may include HVAC, electrical, water (domestic and DI), compressed gasses, and controlled temperature storage systems.

· Recognize and correct potential safety hazards to avoid injuries

· Support building personnel by insuring the availability of water, gasses, and electrical, as well as furniture requests, office relocations, and general accommodations to assist employees with their work duties

· Paint & caulk small areas when paint or wall surface has become damaged

· Support general cleaning & housekeeping efforts as required. Pallet removal as needed from building

· Maintain relationship and coordination with janitorial contractor for non-lab domestic cleaning of facility

· Process/Manufacturing equipment support, ensuring written record keeping, and forms are completed as required

· Conduct systems rounds as required

· Check and confirm process gasses are at service pressure daily

· Move/relocate laboratory equipment as directed

· Work with the engineering personnel to handle process equipment needs

· Required to review relevant documentation for accuracy and completeness i.e., suite cleaning documentation

· Replace light bulbs as required

· Employ safe work practices

· Engage and inspire others

· Comprehends all duties assigned and performs responsibilities in absence of Manager when needed

· Other responsibilities as needed

Job Qualifications

· Associate degree in science preferred, or High School Diploma or GED with 0-3 years of prior work experience in the Biotechnology Industry in a GMP Facilities setting

· Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams. Maintain Calendar(s)

· Possess the willingness to learn new concepts to fully understand aseptic techniques and demonstrate proper clean-room behavior

· Excellent interpersonal and communication skills

· Detail-oriented and demonstrate the ability to perform highly detailed work

· Excellent organizational, multitasking, and problem-solving skills

· Able to accurately perform basic math calculations, including time conversion, fractions, decimals, and percentages

· Availability - Overtime work and schedule changes are required to meet business needs. Holiday, weekend, and night work will also be required based on manufacturing schedule. On-call as business needs arise

· Reliable mode of transportation to travel between sites in the Rockville area

· Able to work standing, bending, stooping, pulling, pushing, sitting, and reaching overhead for long periods of time

· Able to work around various cleaning chemicals that produce non-hazardous odors like bleach and vinegar

· Able to wear appropriate gowning covering most parts of the body and face. (Gowning Qualification)

· Able to lift, push, and pull 50 lbs.

· Use of basic hand tools

· Use multimeter

· Work from height not to exceed 10’

· Confined spaces could be encountered

· Work in heat and cold as required

· Climb ladders

Compensation Data

The pay range for this position is $22.00 - $24.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Medical Technologist I (Shrewsbury, MA, US, 01545)

Job Summary

Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain, and perform basic troubleshooting procedures on analyzers. Biological sample processing. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Perform all tasks in compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations.
Read study protocols and extract pertinent information with guidance.
Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and fecal analysis.
Operate, maintain, and troubleshoot clinical pathology analyzers with guidance.
Perform basic medical technology procedures such as blood slide differentials, reticulocyte counts and urinalysis with guidance.
Perform all specialized processing under supervision.
Prepare materials needed: labeling tubes, study books and appropriate paperwork prior to bleeding days.
Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
Manual entry of raw data into the computerized systems and review of data as needed.
Perform all other related duties as assigned.

The pay range for this position is between $30.00 - $35.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) preferred.
Experience: 0-2 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is required. GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Associate Imaging (Cambridge, MA, US, 02139)

Job Summary

We are seeking a Research Associate to join our Insourcing Solutions team, located in Cambridge, MA.

As the Research Associate, you will be responsible for performing multi-modality imaging studies, especially performing preclinical imaging data acquisition, image data processing and analysis, may also work with other scientists for in vivo and ex vivo imaging experiments.

Additional responsibilities include:

Perform laboratory tasks in support of in vivo studies
Preparation and administration of therapeutic agents through differing routes of administration (e.g. IP, IV, SC, or oral gavage).
Weighing of animals prior to dosing with test substances
Blood and tissue sample collection
Accurate collection of customer data and input into customer database
Read basic study protocols and extract pertinent information
Ability to plan and organize studies effectively
Record project data in accordance with SOPs and/or applicable regulations
Perform data collection using. whole-body optical imaging, high-field MRI, micro-CT, mouse-PET, intravital confocal microscopy, and ultrasound micro-imaging systems as well as digital image analysis workstations.
Performing preclinical imaging data acquisition, image data processing and analysis, may also work with other scientists for in vivo and ex vivo imaging experiments.
Perform other related responsibilities as assigned.

Job Qualifications

To qualify for this role, candidates must have one of the following combinations of education and experience.

B.S/B.A. degree in Biological Sciences or related field plus 0-6 months of experience in biopharmaceutical experiences.
Associates degree in Animal Science or equivalent college level program plus 1 year experience in biopharmaceutical experiences.
HS Diploma with two years experience in biopharmaceutical experiences.

The pay range for this position is $45 to $47 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Director - Lab Sciences (Shrewsbury, MA, US, 01545)

Job Summary

This is a senior management position within the company with overall responsibilities for the operations and management of all Lab Sciences group within Charles River Massachusetts Shrewsbury facility. Scope includes both regulated and non-regulated work (nGLP; GLP; Clinical).
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Management
•Manage capacity, flexibility, organizational structure and scalability of assigned services including personnel, instrumentation and laboratory space
•Manage allocation of resources to satisfy and exceed client expectations and requirements while also meeting company objectives
•Identify required resources, functional roles and organizational structure necessary to meet site and enterprise objectives
Commercial
•Lead as appropriate client interactions with SHR Lab Sciences clients, consultants and CRL colleagues, Including onsite visitations.
•Responsible for establishing pricing and ensuring alignment with that of other CRL locations as appropriate. Lead person responsible for all material decisions and negotiations regarding pricing discounts as applicable
•Responsible for monitoring financial performance versus plan, including commercial revenue; intercompany revenue; and operating income. Working with CRL colleagues, provide financial forecasting information for the assigned services and communicating and collaborating with colleagues to develop plans when necessary to address material shortfalls
Regulatory
•Ensure that processes fully satisfy regulatory requirements as applicable with company policies
•Serve as Test Facility/Site management
•Serve as Lab Sciences representative in regulatory agency visits and audits
Technical
•Provide scientific direction, oversight, and guidance to staff
•Ensure that new technologies and processes, applications, software, equipment and other initiatives are evaluated to improve the quality and/or value of the service to our clients
•Lead in the evaluation of new technologies in adjacent areas to assigned responsibilities with the objective of expanding service offerings to our clients
Personnel
•Develop and maintain a positive work environment supported by effective communication to inform employees of plans and progress
•Responsible for the development of all direct reports, providing regular coaching and feedback
•Ensuring that all staff have adequate training and education to do their jobs and when necessary
•Ensure the recruitment and retention of personnel necessary to meet departmental objective

The pay range for this position is between $219,000.00 and $245,000.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: Master’s degree in chemistry, biochemistry or a related scientific discipline required. PhD preferred.

Experience: 10 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP) standards. 5 years management experience, including staff management and development, and financial responsibility including budgets.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other Computer proficiency in MS Office suite. Excellent verbal and written communication and organizational skills required. Demonstrated independent analytical and problem-solving abilities. Knowledge of GLP regulations. Ability to develop and maintain productive vendor, site, and company relationships. Ability to interact appropriately with all levels of employees and work effectively as a member of a team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate (Raleigh, NC, US, 27610)

JOB SUMMARY

As an Animal Care Associate for our production site in Raleigh, NC, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world. You will perform routine animal husbandry and other production duties. You will also maintain supplies and environment of environmentally-controlled work area(s).

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

No experience required. On the job training will be provided.

ROLE SPECIFIC INFORMATION:

Location: Raleigh, NC
Pay: $17.75 - $19.00 / hour
Schedule: Start times fall between 4:00am - 6:00 am, working 9 hour shifts Monday - Thursday and a 4 hour shift on Friday. Weekend rotation is required.

PHYSICAL DEMANDS

Regularly required to utilize a computer/tablet.
Regularly required to stand, use hands to finger, handle or feel objects, tools or controls; and reach with hands and arms.
Regularly required to stand and ascend/descend rolling platform ladder (up to six steps) to perform all tasks and procedures related to the job.
Regularly transports supplies, removes waste, and/or laboratory equipment while ascending/descending rolling platform stairs (up to six steps).
Regularly positions self (stoop, crouch, squat, sit, reach) to access and inspect small models and be able to assess their conditions and environment from various distances.
Regularly lifts and/or moves materials weighing up to 10 pounds and occasionally lifts and/or moves materials weighing up to 50 pounds.
May occasionally lift and/or move equipment and materials weighing 30-50 pounds, and equipment and materials weighing over 50 pounds with assistance.
Specific vision abilities required by this job include close vision, depth perception, and the ability to differentiate colors.
Regularly works with chemicals that require the use of respirators. Medical clearance is required prior to using respirators.

The pay range for this position is $17.75-$19.00 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien de Toxicologie Non-Rongeurs - F/H - CDD 09 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service Toxicologie recrute un Technicien en Toxicologie pour intégrer son équipe de Techniciens (Non-Rongeurs).

Les missions 

Au sein des services de Toxicologie In Vivo, vous aurez pour principales missions sous la responsabilité de votre supérieur :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
Procéder à des prélèvements sanguins, d’urine ou de fécès,
Saisir l’intégralité des actes réalisés sur informatique,
Assurer la qualité des données recueillies et de résultats,
Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Conditions spécifiques du poste

Travail en milieu confiné avec port obligatoire d’équipements de protection individuelle.

Travail le WE.

Retours et horaires décalés possibles (Discutés en amont avec le Responsable).

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique.

Vous êtes à l’aise au contact des animaux.

Vous maitrisez l’anglais.

Vous possédez une aisance relationnelle et un sens du contact et du service.

Vous êtes organisé(e), vous appréciez de travailler en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDD de 09 mois | Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 400 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté ...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animalier d'élevage - F/H - Alternance (Chatillon sur Chalaronne, 01, FR, 01400)

Pour cette rentrée 2025, notre service de production recherche son futur(e) Animalier en alternance sur notre site de Châtillon sur Chalaronne dans l'Ain (01).
L'animalier contribue à la réalisation, en quantité et qualité, des objectifs de production définis par le responsable d’unité.
L’élevage des animaux est à haut statut sanitaire et génétique en zones protégées (cages ouvertes).

Vos missions principales seront les suivantes :

Entretenir les lieux d’hébergement des animaux et les espaces d’élevage:

Vérifier le fonctionnement du réseau d’eau ou nettoyer et remplir les biberons selon le planning
Alimenter les animaux
Vider, nettoyer et changer les lieux d’hébergement des animaux
Relever et vérifier les paramètres environnementaux
Entretenir le matériel d’élevage de manière autonome

Elevage:

Accoupler les animaux selon le schéma défini
Contrôler et suivre la mise-bas
Identifier, trier, sexer, équilibrer et sevrer les petits
Observer, contrôler l’état des animaux et déceler une anomalie ou souffrance
Renseigner les documents de suivi de production et d’assurance qualité
Faire remonter toute situation anormale (HSE, Qualité, Sûreté, Biosécurité et Ethique)

Profil recherché

Actuellement en formation Bac+2 en biologie , vous rechercher une alternance pour votre Bac+3,
Respecter strictement les règles éthiques et de sécurité.
Être observateur, minutieux, rigoureux et assidu.

Autres

Indemnités de transport
Châtillon-sur-Chalaronne – Moyen de locomotion indispensable, site non-accessible en transport en commun.

Pour plus d'information, consultez www.criver.com.

Scientific Associate 1 (Tranent, GB, EH33 2NE)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

We are seeking a Scientific Associate for our Clinical Pathology Laboratory department site located in Elphinstone, Tranent. This is a 12 month fixed term contract opportunity.

About Clinical Pathology Laboratory Services

Clinical Pathology is responsible for analysing biological samples, mostly blood and urine, taken from animals on toxicology and other regulatory studies. Training will be provided for instrument operation, use of our Laboratory Information Management System and working in a GLP environment.

Key responsibilities include the following:

To operate automated systems currently in use in clinical chemistry and haematology undertaking routine and specialised analyses.
To assess and report Clinical Pathology Data.

To be responsible for planning and scheduling of work assigned.
To be responsible for the production of tables, reports and data extracts.
To participate in the development of new techniques and services.

The following are minimum requirements related to the Scientific Associate position:

Life Sciences degree.
Strong organisational skills with the ability to pay attention to detail.
Good communication skills.
IT literate with experience of Microsoft packages.

The closing date is 16 July 2025.

Salary for this position is £27,951.22 per annum.

Profile and Requirements

For more information, please visit www.criver.com.

Assistant Technician 1 (Tranent, GB, EH33 2NE)

The Biosciences division currently has an exciting career opportunity for an Assistant Technician 1 to join our new and evolving BioSciences Lab Services group. Please note this is a 12 month fixed term contract opportunity.

The successful candidate will work within the team which provides support across a variety of operational areas to the pharmaceutical, veterinary pharmaceutical and chemical/agrochemical industries by evaluating the absorption, distribution, metabolism and excretion of new chemical and biological entities both in vitro and in vivo in a variety of test systems (cells, animals, plants and soils).

You will be required to take responsibility for the following activities (for which full training will be given):

Provide laboratory support to Study Directors in the day to day running of studies.
Horticultural tasks include growing and monitoring plants, crop maintenance, implementing fertiliser and pest prevention regimes, and assisting with horticultural aspects of the scientific research.
Provide assistance with study set-up, sample collection and data generation.
Conduct laboratory work in accordance with Standard Operating Procedures and the principles of Good Laboratory Practice.
Undertake routine tasks of laboratory and equipment maintenance as may be delegated.
Ensuring that a safe working environment is maintained by observing all safety procedures and working methods and by making proper use of protective clothing and equipment.

The following are minimum requirements related to the Assistant Technician 1 position:

National 5 qualifications (Assistant Technician) or HNC (or higher) or relevant on-job experience (Technician)
A positive and constructive approach to working in a busy laboratory environment and the ability to pay close attention to detail is essential.
Good level of computer literacy for Microsoft word and excel.

Please note this role is a 12 month Fixed Term Contract role.

Salary will be £23,842.35 per annum.

The closing date is 16 July 2025

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

With over 11,000 employees within 70 facilities in 18 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015.

For more information, please visit www.criver.com.

Assistant Technician 1 - Formulation Services (Tranent, GB, EH33 2NE)

Job Summary

We are seeking an Assistant Technician 1 for our Formulation Services Department located in Elphinstone, Tranent.

Working as an Assistant Technician 1 you’ll join a team responsible for the storage and control of test items and the preparation of formulations supporting toxicology studies.

Duties and responsibilities include:

Lab preparation and housekeeping
Stock control, ordering, organisation and replenishment
Calibration and maintenance of routine lab equipment
Preparation of Vehicles, general reagents used to prepare formulations
Disposals
Glassware preparation
Delivery of Formulations
Taking archive samples, test item weighings

Applicants should have:

At least 3 NAT5s including Maths, English
A good attention to detail
IT skills
Good communication skills

What you can expect from us:

A clear career progression
A structured Training programme
Pension scheme including 8% employer contribution
Access to private medical cover and employee assistance programme
Employee discount scheme – discounts across hundreds of retailers!
Paid opportunity to volunteer for 12.5 hours each year
Free onsite fitness suite and fitness lessons
Staff canteen
Free onsite parking

The salary for this position is £23,842.35 per annum. In exceptional circumstances where the candidate has relevant equivalent experience, this will be taken into consideration.

The closing date for applications is Wednesday, 16 July 2025.

Histology Technician I (Tranent, GB, EH33 2NE)

Job Summary

At our world class facility just a short drive from Edinburgh, due to our continued growth and success, we are looking to recruit a Histology Technician.

NO EXPERIENCE REQUIRED, FULL AND COMPREHENSIVE TRAINING PROVIDED TO THE SUCCESSFUL CANDIDATES

Duties and responsibilities include:

Carrying out laboratory procedures within Histology on all routine laboratory models.
Tissue Sampling and sample preparation post fixation for all tissues received from necropsy.
Wax Embedding manual and automated of processed tissue samples.
Sectioning of wax blocks using a microtome and mounting sections on glass slides.
Staining of tissues collected onto the glass slides, in preparation for presentation to the Pathologist.
General housekeeping of the Laboratory and the care and maintenance of all equipment.

Candidates are required to have the following:

A minimum of four Nat 5 (or equivalent).
Flexible approach to suit the needs of the business.
Commitment to quality and meeting deadlines.
Willingness to join the weekend Rota and provide overtime to suit the needs of the business.
Ability to sustain bench working conditions for long periods of time.

The following are attributes desirable for this Technician position:

Passion for animal welfare.
The desire for improving the quality of life for patients, people, and animals.
Hard working and committed.

The salary for this position is £23,842.35 per annum.

The closing date for applications: 15 July 2025

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Gestionnaire en Logistique Import-Export - H/F - Alternance 1 (Saint Germain Nuelles, FR, 69210)

Job Qualifications

Vous suiviez une formation dans le domaine de la logistique ou du développement international ? Vous recherchez un contrat en alternance opérationnel et polyvalent ? Vous avez envie d’intégrer un groupe innovant, en plein développement, au service de la recherche et de la santé humaine ? Cette offre au sein de notre service clients va vous intéresser.

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport, Restaurant d'entreprise
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Gestionnaire en Logistique Import-Export - F/H - Alternance (Saint Germain Nuelles, FR, 69210)

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport, Restaurant d'entreprise
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

Pour plus d'information, consultez www.criver.com.

QA System Specialist (m/w/d) (Erkrath, NW, DE, 40699)

Für die Abteilung Quality Assurance am Standort Erkrath suchen wir ab sofort und unbefristet eine/n

QA Specialist (m/w/d) Schwerpunkt computergestützte Systeme & GxP

Ihre Aufgaben:

Sicherstellung der Compliance computergestützter Systeme (lokal, bereichs- und funktionsübergreifend) mit globalen regulatorischen Anforderungen sowie den internen CRL-Standards
Freigabe und Überwachung der Implementierung und Instandhaltung dieser Systeme gemäß aktueller regulatorischer Vorgaben
Unterstützung bei der Validierung von Computersystemen (CSV) sowie bei Qualifizierungsprojekten für technisches Equipment
Mitwirkung bei der Einführung elektronischer Dokumentations- und Managementtools für Gerätequalifizierungen
Organisation und Durchführung risikobasierter Inspektionen von Laboren, Anlagen und Systemen; Erstellung von Auditberichten und Verfolgung von CAPAs
Analyse und Berichterstattung qualitätsrelevanter KPIs sowie Unterstützung der vierteljährlichen Management Reviews (QMR)
Kontinuierliche Optimierung bestehender Systeme und Prozesse im Hinblick auf regulatorische Anforderungen, Effizienz und Best Practices
Eskalation identifizierter Compliance-Lücken und aktive Mitwirkung bei der Entwicklung bzw. Überarbeitung von Richtlinien und SOPs
Unterstützung des QA-Teams bei regulatorischen und qualitätsbezogenen Fragestellungen
Review und Freigabe studienbezogener Dokumentation mit Fokus auf Prozessoptimierung

Ihr Profil:

Abgeschlossenes naturwissenschaftliches, technisches oder vergleichbares Studium
1–5 Jahre Berufserfahrung im Qualitätsmanagement innerhalb eines GxP-regulierten Umfelds (z. B. Pharma, Biotech, Auftragsforschung)
Erfahrung im Umgang mit computergestützten Qualitätssystemen (z. B. TrackWise, Veeva oder vergleichbar) und Kenntnisse in der Computer System Validation (CSV)
Vertraut mit regulatorischen Anforderungen (FDA, EMA, GxP) und Qualitätssystemen
Strukturierte, proaktive Arbeitsweise sowie ausgeprägte Team- und Kommunikationsfähigkeiten
Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift

Wir bieten Ihnen:

Eine verantwortungsvolle Position in einem weltweit agierenden Life-Science-Unternehmen
Kollegiales Arbeitsumfeld mit flachen Hierarchien und kurzen Entscheidungswegen
Individuelle Weiterbildungs- und Entwicklungsmöglichkeiten
Flexible Arbeitszeiten und attraktive Sozialleistungen

Haben wir Ihr Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 228245 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath
Email: RecruitBPS@crl.com

For more information, please visit www.criver.com.

Technicien.ne en santé animale (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Technicien(ne) en santé animale pour notre équipe de Toxicologie à notre site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Collecte d’échantillons biologiques (sang, urine, etc.);
Prise de données (prise de poids, consommation de nourriture, signes cliniques, etc.) ;
Injections (sous-cutanée, intramusculaire, etc.);
Manipulation des animaux;
Nettoyage des salles d’animaux.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Santé animale, en Bioécologie ou toutes autres disciplines en lien avec la Science animale;
Baccalauréat en Biologie ou l’équivalent;
Bon sens de l’observation;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
La compréhension de la lecture en anglais est obligatoire. Le bilinguisme français et anglais est préférable.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation:445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 ;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: à partir de 23.50$/hrs. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Primes: Fin de semaine ($2.75), temps supplémentaires (temps et demi), jours fériés (temps double);
Bonus annuel basé sur la performance;
Horaire: Horaire flexible, le candidat doit être disponible de jour, de soir et de fin de semaine. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire, des jours fériés et des horaires de nuit;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine)
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Animal Health Technician (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Animal Health Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include: 

Collection of biological samples (blood, urine, etc.);
Data collection (body weight, food consumption, clinical signs, etc.);
Injections (subcutaneous, intramuscular, etc.);
Animal contention;
Animal room cleaning.

Key Elements

We are looking for the following minimum qualifications for this role: 

Minimum a College Diploma in Animal Health, Bioecology or any related Animal Science discipline; 
Bachelor's degree in Biology or equivalent;
Good observation skills;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Reading comprehension in English is required. Bilingualism in French and English is preferred.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information: 

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: Starting at 23.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience;
Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
Annual bonus based on performance;
Schedule: Flexible schedule, the candidate must be available during the day, evenings and weekends. Depending on the needs of the company, you may be required to work overtime, holidays and night shifts;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Biotechnicus (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Baan Samenvatting

Voor de afdeling Toxicologie zoeken wij een enthousiaste

Biotechnicus/Proefdierverzorger in het bezit van artikel 13F.

Afdeling:
Met meer dan 200 medewerkers voert de afdeling Toxicologie onderzoek uit naar de veiligheid van bestaande en nieuwe medicijnen en chemische stoffen. Kenmerkend voor het werk is de grote diversiteit aan projecten, teststoffen en opdrachtgevers.

Team:
We bestaan uit 2 gezellige en hardwerkende afdelingen voor grote en kleine dieren, onderverdeeld in teams van 10-30 medewerkers per team onder leiding van een teamleider, in Den Bosch en Schaijk. Alle teams zijn dynamisch en betrokken bij de afdeling en elk lid draagt op zijn/haar manier een steentje bij aan de werkzaamheden en de goede sfeer op de afdeling.
Op de afdeling zijn er trainers die o.a. de voortgang van de opleiding voor nieuwe medewerkers en nieuwe technieken faciliteren. Ook heeft ieder teamlid het beheer over een aantal neventaken die zij min of meer zelfstandig uitvoert, onder leiding van de teamleiders/TSH.
Binnen de teams werken de teamleden intensief met elkaar samen en verzorgen gezamenlijk het diverse scala aan type studies, aanwezig in de faciliteit, van begin tot einde.

Over je rol:
Als beginnend biotechnicus bij Charles River verzorg je samen met je collega’s alle onderdelen die een dierstudie met zich meebrengt. Een belangrijk onderdeel hiervan is de dagelijkse verzorging en het verzorgen van het algemeen welzijn van alle dieren onder jouw verantwoordelijkheid. Daarnaast besteed je ook veel tijd en aandacht aan het aanleren van alle veel voorkomende handelingen, technieken en metingen die uitgevoerd worden binnen iedere studie. Hierbij sta je ook in nauw contact met studieleiders, dierenartsen en andere afdelingen.

Na een terdege, interne opleiding in alle basisvaardigheden, word je opgeleid tot coördinerend biotechnicus. Je bent medeverantwoordelijk voor meerdere, soms complexe studies die lopen op de afdeling en andere neventaken. Samen met je collega’s zorg je voor het dierwelzijn en een correcte uitvoer van alle werkzaamheden op de afdeling.

Weekenddiensten zijn een vast onderdeel van je werk en zal je elke paar weken ingedeeld worden hiervoor.

Primaire verantwoordelijkheden:
•   Je werkt op een prettige en constructieve manier samen met je directe collega’s, TSH, teamleiders en trainers. Je houdt je aan de gestelde regels.
•   Je werkt onder GLP (Good Laboratory Practice) en bewaakt de kwaliteit van je werk.
•   Je bewaakt de kwaliteit van dierwelzijn, en voldoet hiermee aan de AAALAC eisen en wet- en regelgeving rondom het gebruik van proefdieren.

Wat is vereist:

MBO of HBO werk- en denkniveau en een artikel 13F;
Beschikbaarheid van 32-40 uur per week, hiernaast werk je ook elke maand een aantal uren in weekenddienst en ben je ook bereid tot af en toe overwerk.
Je bent prettig in de omgang, durft je uit te spreken en bent een echte teamspeler.
Daarnaast kun je ook goed zelfstandig werken en je verantwoordelijkheden nemen voor je eigen werk.
Je zorgt dat alle processen soepel verlopen, je kan inspelen op veranderingen, vragen van collega's en andere afdelingen.
Je kunt snel schakelen tussen diverse werkzaamheden en prioriteiten stellen binnen het team en alle studies.
Je wil graag proactief meedenken in procedures en verbeteringen doorvoeren.
Flexibiliteit en stressbestendigheid is een pre.

Wat bieden we jou:
Wij bieden uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

27,5 vakantiedagen en 2 collectieve dagen per jaar;
Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
Reiskostenvergoeding á 0,23 cent per kilometer met een max. van 250 netto per maand, of een NS-Businesscard;
Fiets(lease)plan;
Collectief pensioen met een eigen bijdrage van 2.9%;
Bedrijfsfitness;
De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
De mogelijkheid tot een consult van onze in house ergonoom;
Elke dag gratis vers fruit.

Heb je vragen over deze vacature?

Voor verdere informatie over de functie kun je contact opnemen met Maaike Verrijt via her-recruitment@crl.com of reageer direct via onze werken bij website: Charles River Laboratories, Inc. Jobs (criver.com)  

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld  

Over Safety Assessment

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogt zodat producten eerder op de markt gebracht kunnen worden.

Meer informatie vindt u op www.criver.com.

Proposal Manager - Gene Therapy Manufacturing CDMO (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

The Proposal Manager will be responsible for creating customized proposal documents for prospective and existing clients. The Proposal Manager works alongside commercial operations, business development, and technical professionals to respond to inbound requests for proposal (RFPs), requests for information (RFIs), and other proposal services support requests.

Position will support Gene Therapy Manufacturing at the CRL Rockville, MD site.

Role can work from remote home office.

Key Responsibilities and Duties:

• Assist all aspects of proposal development while adhering to agreed-upon proposal and pricing processes
• Design, generate, and amend standard proposal materials in order to fulfill specific client requirements, ensuring legal documentation is in place
• Coordinate and collaborate with key internal stakeholders on areas such FTE’s, timeline, etc., to allow the program design, proposal generation, resource and timeline estimates, and pricing required for a robust and strategic project proposal
• Qualify bids and scopes of work with sponsors to ensure appropriate service is provided
• Support sales & revenue growth through the completion of RFPs, RFIs, etc.
• Answer, edit, and complete sales proposals, client reports, consultant databases, and ad hoc questionnaires with accuracy and meet client’s expectations/timelines
• Proactively Assist or lead proposal process improvement projects/initiatives
• Coordinate all aspects of the sales proposal document production process to ensure the overall quality meets company and client standards
• Research appropriate responses through supplied databases as well as any other identified sources
• Interact with reviewers and obtain approvals on all terms of references relevant to an RFP
• Provide coverage for peers during high volume periods (cross-site) and supporting multi-site proposal generation
• Peer review proposals and ensure they are all consistent and to a high standard with no mistakes
• Strive to achieve proposal KPIs including timeliness and accuracy
• Collaborate cross-site within CDMO as well as the CRL network (test houses)
• Creatively identify ways to secure open proposals by working with scientific staff, finance, management and others.
• Interact with scheduling or project management groups to identify the dates for study or service initiation and assist with scheduling needs.
• Assist with updating and maintaining applicable databases and department files (inc SFDC)
• Ensuring all aspects of the role are followed while incorporating CRL DNA values (Care, Lead, Own, Collaborate)
• Perform historic price analysis and margins analysis on large programs
• Support client calls and visits with BD team
• Participate in overtime as is reasonably required for the successful completion of your role
• Actively performs all administrative activities on time (ie SFDC) and proposal processing
• Other responsibilities as needed

Job Qualifications

• B.S. in relevant scientific discipline is required, M.S. is preferred
• A minimum of 8 years’ experience in a CDMO with understanding of gene therapy processes from process development to GMP. Broad understanding of program flow from development, QC/QA, logistics and GMP. 1 – 3 years of cGMP industry experience required
• Previous CDMO Technical Writing experience preferred
• Previous biologics contract manufacturing organization and proposal writing experience preferred
• Ability to work effectively with a diverse range of people who possess a variety of skills and experience
• Acute attention to detail with excellent organization and project management skills
• Strong experience with writing and reviewing technical documentation/proposals preferred. Line management experience would be advantageous.
• Ability to coordinate multiple projects/tasks while still delivering high quality skills and escalate issues to leaders
• Self-motivated with the ability to prioritize and execute tasks to meet strict deadlines
• An entrepreneurial spirit along with a keen sense of ownership
• Excellent verbal and written communication skills
• Demonstrated emotional intelligence when interacting with peers, clients, and leadership
• Microsoft Office experience (Word, Excel, PowerPoint, etc.)
• Standing, sitting, pushing, pulling, and lifting up to 10lbs.

Compensation Data

The pay range for this position is $79,758 - 106,344K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Animal Care Technician – On site training

As an Animal Care Technician for our Toxicology team for our site located in the city of Sherbrooke (QC), you will be responsible of ensuring the welfare of the animals and the integrity of our pre-clinical studies.

In this role, key responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry.
Assist the technicians in their daily tasks .
Handle animals.
Participate in the physical/social activities of the animals.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Able to follow precises instructions.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.
Passionate about animals.
High School Diploma (DES) required - Having an AEP in Animal Care is an asset.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Job specific information:

Location: 1580 Ida Métivier, Sherbrooke (Qc), J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Salary: Starting at 19.00$/hrs. Opportunity to start at higher level and higher salary with specific research experience.
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
Access to a doctor and various health professionals (telemedicine).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. This is Your Moment!

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier.ière (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire du poste

Technicien.ne en Soins aux Animaux – Formation sur place

En tant que Technicien.ne en Soins aux Animaux pour notre équipe de Toxicologie à notre site situé dans la ville de Sherbrooke (QC), vous aurez la charge de veiller au bien-être de tous nos animaux ainsi qu’à intégrité de nos études pré-cliniques.

Dans ce rôle, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie
Assister les techniciens dans leurs tâches quotidiennes
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Capable de suivre des instructions précises.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.
Diplôme d'étude Secondaire (DES) requis - Diplôme AEP en soins animaliers est un atout.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation : 1580 Rue Ida-Métivier, Sherbrooke (Qc), J1E 0B5.
Transport: Facilement accessible par le transport en commun (Rabais avec la Société des Transport de Sherbrooke). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 19.00$/HR. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/HR).

Pourquoi Charles River?

3 semaines de vacances et des congés personnels.
Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire).
Accès à un programme d’épargne et de retraite qui comprend une contribution de l’employeur.
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne.
Gym gratuit sur place.
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine).

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe.C'est Votre Moment!

Pour plus d'information, consultez www.criver.com.

Research Analyst I - Analytical Chemistry 1 (Reno, NV, US, 89511)

Job Summary

We are seeking a Research Analyst I for our Safety Assessment site located in Reno, NV.

This position will be responsible for handling and processing samples and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies.

Job Qualifications

The following are minimum requirements related to the Research Analyst 1 position.

Associate's degree (A.A. / A.S) or equivalent in biological science or related discipline required. Bachelor’s degree (B.A. / B.S.) preferred.
6 Months minimum related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Proficient in basic technical skills and the operation of data collection equipment.
Knowledge of GLPs and other federal regulations and guidelines.
Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information.
Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.
Able to quickly learn and utilize computer programs as needed.

The pay for this position starts at $24/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Receiving Clerk (Rockville, MD, US, 20850)

Job Summary

The Receiving Clerk will maintain inventory of controlled materials and gowning supplies. This person will maintain records and track GMP materials required for various client projects under the guidance of the Associate Director Materials Management. They will also interact with Charles River Laboratories raw material suppliers and manufacturers and request required documentation for GMP materials release.

Key Responsibilities and Duties:

• Assist in receiving of controlled materials following established procedures. Ensure all materials are received and stored in controlled materials storage locations to ensure cGMP compliance.
• Check and maintain sufficient inventory of common materials required at Rockville and submit request in ordering system if inventory is low.
• Follow Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs) in daily activities.
• Complete (MSD’s) and (MOS) or any other QC required forms
• Track overdue materials and component shortages for various client projects in BOM excel sheet and work with purchasing to successfully resolve the documentation required and request Certificates or any other required documentation with Charles River Laboratories suppliers.
• Serve as a contributor to cross-functional project teams for problem solving issues within the supply chain operations.
• Review multiple data inputs and understand how to actively support digitization through the implementation of automation with the use of industry specific tools (including Microsoft Excel and Access).
• Effectively utilize key processes and tools (i.e. BOM excel sheet for Projects) to pull data in order to build a deeper understanding of our operations.
• Work on mini projects assigned in supply chain department (e.g., tracking of materials, numbering of shelves for GMP materials storage)
• Drive Charles River Laboratories truck and transport GMP materials between sites.
• Other responsibilities as needed

Job Qualifications

• High School Diploma required with some GMP experience preferred
• MUST possess a valid driver’s license (non CDL)
• Excellent organizational, multitasking, and problem-solving skills
• Must be able to drive company vehicle between sites in the Rockville area with valid driver’s license and will sometimes also need an alternative reliable mode of transportation to travel between sites in the Rockville area
• Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer
• Must regularly communicate with employees and suppliers; must be able to exchange accurate information
• Must occasionally move about inside the office to access file cabinets, office machinery, etc.

Compensation Data

Pay rate for this role is $17.75 - $22.85 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Technician Assistant (Reno, NV, US, 89511)

Job Summary

We are seeking an experienced Research Technician Assistant for our Safety Assessment site located in Reno, Nevada.

The following are minimum requirements related to the Research Technician Assistant position.

High School Diploma or General Education Degree (G.E.D.)
0-6 months related experience in animal research and/or husbandry preferred.
Ability to handle common laboratory animal species.
Basic knowledge of Good Laboratory Practice regulations preferred.

Job Qualifications

If you possess the following qualities, we will train you in the rest:

Enjoys working within a team
Has the ability to work in a fast-paced and challenging environment
Pays attention to detail
Dependable
Ability to work independently
Ability to multitask
Ability to think on your feet

With plenty of room for growth, you can enjoy a long and meaningful career in a positive work environment. Take your first step, patients are waiting.

The pay range for this position is $22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

饲养员-DIRECT LABOR (Chengdu City, SC, CN, 610213)

工作总结

欲了解更多信息，请访问www.criver.com。

饲养员-DIRECT LABOR (Chengdu City, SC, CN, 610213)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融， IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

欲了解更多信息，请访问www.criver.com。

Apheresis Registered Nurse - $5000 Sign on bonus included (Northridge, CA, US, 91325)

For over 40 years, HemaCare, a Charles River company, has worked to making a positive impact on the world by providing the highest quality cellular material and services to biotech and
pharmaceutical companies and research organizations that are performing innovative research and developing novel cell-based therapies.

We recognize that our success depends on the vision and passion of our employees; that is why we are devoted to making HemaCare a rewarding and valuable place to work. We believe in making a difference, and at HemaCare, you will make a difference every day.

Job Summary

The Registered Nurse will assume responsibility for the daily activities involved in the collection of plateletpheresis, leukapheresis, and whole blood. Partner with other donor room staff to ensure a smooth operation and efficient production of blood products. Must be able to interact with various departments to ensure integrity and quality of daily processes.

Essential Responsibilities

Utilize applicable aseptic techniques to plan, perform, and chart the following procedures in accordance with Hema Care Donor Center policies and procedures.
Automated plateletpheresis and leukapheresis including set-up, run, quality control, troubleshooting and routine maintenance.
White blood cell collections and other special procedures as required.
Whole blood procedures.
Make appropriate adjustments to apheresis machines based on product integrity and physical status of donor
Expertise in venous access, identification and treatment of donor reactions.
Expertise in blood donor medical history.
Expertise in assessment of laboratory reports.
Appropriate handling of information regarding positive test results.
Work cohesively as a team member and at times in a non-verbal manner while under pressure and time constraints.
Consistently manage self in ways that express professionalism.
Demonstrate warmth and compassion in a meaningful manner.
Understand and correctly use the Blood Establishment Computer Software (BECS).
Responsible for the evaluation, management, and documentation of donor reactions, post donation reports, risk management reports and customer complaint forms.
Provide technical and clinical guidance to staff as needed.
Preparation of all paperwork related to daily production.
Maintain positive communication with interacting departments.
Ensure satisfactory completion of all donor records.
Rigid adherence to all safety and quality protocols and regulation.
Other duties as assigned.

Job Qualifications

Minimum of 2 years acute care nursing experience.
3 years previous blood banking, apheresis and phlebotomy experience preferred.
Associates degree in healthcare required, BSN preferred.
Must have current state RN licensure.
Current BLS certification.

Compensation Data

The pay range for this position is $41.35 - $51.06 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About HemaCare

HemaCare, a Charles River company, is a global leader and trusted brand in the customization of human-derived biological products and services for biomedical research, drug discovery, and cell and gene therapy development. HemaCare’s vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.

In January 2020, HemaCare was acquired by Charles River Laboratories, an early-stage contract research organization (CRO). Combined with Charles River’s integrated, early-stage portfolio of discovery, safety assessment, and manufacturing support services, the acquisition creates a unique, comprehensive solution for researchers and cell therapy developers and manufacturers worldwide to help accelerate their critical programs from basic research and proof-of-concept to regulatory approval and commercialization. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs and enhances their productivity and effectiveness to increase speed to market. We work closely with our clients throughout the clinical process to maximize success and drive positive clinical outcomes.

Together, with over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical and biotechnology companies, government agencies, and hospitals and academic institutions around the world.

At HemaCare, we are passionate about our role in improving the quality of people’s lives. We have proudly supported the development of 100% of the current commercially available FDA-approved immunocellular therapies. Our mission is to provide a best-in-class portfolio of high quality, customizable human cellular material and services to support drug discovery, scientific research, and cell therapy. This resonates from our employees and impacts our customers because we know that every day is an opportunity to advance discoveries and make a difference in someone’s life.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com and www.hemacare.com.

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

Equal Employment Opportunity

For more information, please visit www.criver.com.

Veterinary Pathologist II (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Anatomic Veterinary Pathologist for our Safety Assessment Team at our Mattawan, Michigan facility.

Our Veterinary Pathologists are responsible for independently performing gross and microscopic evaluation of tissues, recording results, preparing reports delineating pathological findings, and assisting with necropsy supervision. With minimal supervision, work with customers as needed to market company services and to assure customer satisfaction.

Essential Duties and Responsibilities:

• With minimal supervision, interact with clients to assure satisfaction, provide scientific support and input, and to market services.

• Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.

• Assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation.

• Enter pathology findings in data capturing system(s).

• Write comprehensive report narratives detailing all test article effects. As needed, work with study directors to ensure data is accurately integrated into study reports.

• Provide training, technical guidance and leadership to laboratory staff, pathology trainees, and less experienced pathologist.

• May provide scientific expertise for experimental design and other aspects of research studies as needed.

• May serve as a consultant in pathology-related issues.

• May serve as a study director or principal investigator.

• May function as a peer review pathologist or may participate in a pathology working group (PWG).

Job Qualifications

Qualifications:

Education: Doctoral degree (D.V.M./V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.
Experience: 3 or more years of pathology experience post-D.V.M.; specialized training and/or experience in toxicologic pathology preferred. Compensation commensurate with experience and qualifications.
Certification/Licensure: American College of Veterinary Pathologists (A.C.V.P.) board-eligibility required. ACVP board certification strongly preferred and required to enter the grade at the minimum experience level.
Other: Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Computer literacy in word processing, spreadsheet and database software.

Compensation Data

The salary for this position is $170,000 - $180,000 USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

CSV Specialist I (Memphis, TN, US, 38118)

Job Summary

BASIC SUMMARY:
Responsible for computerized system validation activities within CRL Manufacturing Operations, including, but not limited to, equipment and software. Responsible for maintaining all documentation pertaining to validation activities. Serve as an information resource for validation team members, contractors, and vendors.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage the full lifecycle of validation projects, ensuring timely delivery, meeting specifications, and maintaining quality throughout.
• Prepare clear and concise validation deliverables for computerized systems, including Validation Plans, Requirement Specifications, Configuration Specifications, Risk Assessments, Test Scripts, Traceability Matrices, and Summary Reports.
• Assist system SMEs in the preparation of test scripts comprising formal testing of functional, system and regulatory requirements in conjunction with computerized system validation. Oversee test script execution.
• Manage validation project, ensuring timely completion and effective communication of project timelines and milestones.
• Adhere to pertinent regulatory requirements and departmental policies and procedures [SOPs, safety procedures and biosafety protocols].
• Write or assist in the writing of SOPs as they pertain to computer system validation and data integrity.
• Collaborate with cross functional teams involved in the validation and maintenance of computerized system (e.g. System Owner, IT, QA, Departmental Managers, vendors, etc).
• Provide guidance and support on Computer System Validation (CSV) practices, helping others develop skills and knowledge in regulatory compliance, validation processes, and industry best practices.
• Identify, schedule and track validation project tasks and timelines using appropriate tools.
• Effectively communicate project expectations to team members and stakeholders in a timely and clear manner.
• Schedule validation project team meetings to ensure project milestone schedules are maintained and deliverables satisfy requirements.
• Contribute to the development of corrective actions, as needed, for deficiencies that may be uncovered/observed during validation efforts to ensure compliance with applicable regulatory requirements, guidelines, procedures, and policies.
• Proactively identify opportunities for process enhancements and implement innovative solutions to drive efficiency, quality, and effectiveness, fostering a culture of continuous improvement.
• Serve as the primary point of contact for client and regulatory audits related to computer system validation, resolving or mitigating audit findings related to system validation.
• Assist, as needed, during client and regulatory audits and help to resolve or mitigate audit findings related to system qualification/validation.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s degree (B.A./B.S.) or equivalent in Computer Science, Information Technology, Engineering, Life Sciences, or related field.
• Experience: 2-5 years of experience in computer system validation within a regulated industry (pharmaceutical, medical device, biotechnology).
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: Certifications like Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or specialized CSV training can be advantageous.
• Other: Comprehensive knowledge of regulatory requirements, including GxPs, 21 CFR Part 11, and Annex 11 as they pertain to computerized systems, is preferred.
• Excellent organizational and analytical skills and demonstrated ability to shift priorities to meet a constantly changing environment.
• Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.
• Working knowledge and experience in Microsoft Office products (Outlook, Word, Excel, Power Point, Teams, SharePoint).
• Understanding of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity, ALCOA++.

The pay range for this position is $ 75K-85K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technical Trainer I (Poolesville, MD, US, 20837)

Job Summary

We are seeking an experienced Technical Trainer I to join our Insourcing Solutions team, located in Poolesville, Maryland.

As the Technical Trainer I, you will develop, deliver, document, and report technical skills training programs involving both small and large laboratory animal species in accordance with client’s facility SOPs, Charles River policy and applicable Federal regulations.

Additional responsibilities include:

Direct, schedule, perform and document all relevant Task-specific technical, husbandry and administrative training for all contract positions in coordination with management and supervisors.
Perform continuing education and training to maintain and enhance employee skills and capabilities, including SOP or ASP revisions, animal welfare topics, operations and maintenance, and technical advancements.
Conduct AALAS certification training, monthly health & safety training; conduct and/or coordinate ASP-directed training.
Select or develop teaching aids such as training handbooks, demonstration models, multimedia visual aids, computer tutorials, and reference works.
Conduct training sessions covering specified areas such as on-the-job training, refresher training, in laboratory animal techniques.
Test trainees to measure progress and to evaluate effectiveness of technical training.
Provide didactic and hands-on technical training on SOPs Monitor technical methods used by employees and make on the spot corrections.
Perform quality assurance responsibilities for the contract site, including:
- Inspecting procedures, reports, facilities, equipment and data for on-going administrative, husbandry and technical-related functions relevant to contract performance and research mission support for adherence to CDC protocols and SOPs.
- Scheduling and conducting phase inspections and personnel performance audits to determine compliance with internal SOPs and study protocols.
Actively interact with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance.
Occasionally provide technical support, animal husbandry, and assist with research procedures as necessary to respond to surge in work load or personnel shortages.

Job Qualifications

The following are minimum requirements related to the Technical Trainer I position.

Associate degree or bachelor’s degree in animal science, veterinary technology or equivalent college level program required.
Minimum of three (3) years related animal care and handling experience required. One (1) year technical experience performing the duties and responsibilities detailed above preferred. Previous training and successful "hands -on" performance of animal care technical procedures required. Related technical experience includes, but not limited to:
- Rodents: Handling and restraint, identification methods, sexing, tissue collection (blood, tails, various organs), administration of medications and treatment.
- Non-human Primates: Utilization of squeeze cages, transferring, TB tests, blood collection, basic injections / administration of medications, treatments and anesthesia, identification (tattoo) proper use of bite/scratch kits.
- Farm Species: Handling and restrain, identification methods, blood collection, basic injections/administration of medications and treatment.
- General techniques: Surgical pack preparation, proper scrub-in technique, proper physical/physiological observation, gas and/or autoclave sterilization (use of machines and rationale for use of each type), drug dosage calculation, pre-surgical animal prep, gestation periods of various species, proper use of anesthesia machine (portable & fixed), anesthesia monitoring, safe handling and restraint techniques, proper use of PPE, euthanasia, blood collection and injection techniques - all species, all sites.
AALAS certification at the Laboratory Animal Technologist (LATG) level preferred.

The pay range for this position is $35-38 USD per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Testreq - Training Req (Parma, IT, 43122)

Job Summary

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Job Qualifications

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IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

For more information, please visit www.criver.com.

Senior Laboratory Analyst (Analytical Sciences) (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Senior Analytical Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Analytical Supervisor and the main duties & responsibilities shall be:

Carrying out analytical tests using different techniques like HPLC, Capillary Electrophoresis, UV-Vis spectroscopy, Ion Chromatography, GC, and wet chemistry.
Practical and theoretical knowledge on several analytical techniques, with capability of troubleshooting based on the specific request.
Strong knowledge of GMP regulation applied to a laboratory environment.
Assist in developing and/or verification/validation of analytical methods that use equipment like HPLC, Ion and Gas Chromatography, spectrophotometers as well as wet chemistry techniques and compendial methods.
Receipt and processing of test samples in LIMS.
Safe and compliant disposal of all laboratories generated waste.
Carry out data calculations and basic statistics.
Assist in internal, regulatory and client visits/audits and respond to findings.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.

Job Qualifications

The following are minimum requirements related to the Senior Analytical Analyst position:

BSc/MSc. in a relevant science discipline (e.g. chemistry, biochemistry, pharmacy, and biotechnology)
A minimum of 3 years relevant experience in Laboratory preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry.
Analytical techniques (HPLC, GC, MS and similar) experience essential.
Experience in development and validation of analytical methods according to ICH guideline required but not essential.
Experience in analytical techniques/immunoassays desirable but not essential.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Animal Technician - Milano (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Di cosa si occupa la Charles River

Per ulteriori informazioni, visita il sito www.criver.com.

Animal Technician - Milano (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano e Calco ricerchiamo un Animal Technician

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;
Effettuare attività e procedure tecniche sugli animali

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosamente ha collaborato allo sviluppo di ~85% dei farmaci approvati dalla FDA nel 2021.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Analist Genetische en in vitro toxicologie 1 (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Heb jij een afgeronde MLO/ HLO opleiding en wil jij als analist graag bijdragen aan onderzoek naar de veiligheid van bestaande en nieuwe stoffen? Ben jij analytisch, nauwkeurig en werk je graag in teamverband, dan zijn wij op zoek naar jou!

Voor onze afdeling Genetische en In Vitro Toxicologie zoeken wij een enthousiaste

Analist Genetische en In Vitro Toxicologie

Afdeling:

De afdeling Discovery & Environmental Sciences bestaat uit circa 90 medewerkers. Binnen deze afdeling wordt onderzoek uitgevoerd naar de veiligheid van bestaande en nieuwe stoffen. Kenmerkend voor het werk is de grote diversiteit aan testen, teststoffen, klanten en samenwerkingen.

Team:
Je komt te werken binnen een gezellig team van ongeveer 15 analisten. Als analist werk je in teamverband, onder leiding van de studieleider, aan de uitvoering van diverse in vitro toxiciteitstesten. In deze rol werk je vaak in duo’s en moet je goed samen kunnen werken. Geen dag is hetzelfde en vraagt om flexibiliteit. Elke dag kan dus anders zijn!

Over je rol:
Als analist bestaan je werkzaamheden voornamelijk uit het uitvoeren van verschillende in vitro en in vivo studies om de mogelijke mutagene werking van stoffen en/of hun metabolieten te onderzoeken. Er worden diverse in vitro studies uitgevoerd ter vervanging van in vivo testen. Wanneer de praktische kant van de studie is afgerond, moeten de resultaten worden verwerkt en gerapporteerd. Hierbij heb je een ondersteunende rol, waardoor je de test grotendeels meemaakt. Je werkt in deze rol ook veel samen met analisten van andere afdelingen. Alle werkzaamheden gebeuren in lijn met het kwaliteitssysteem GLP.

Primaire verantwoordelijkheden:

Laboratorium werkzaamheden; diverse in vitro testen waaronder oog- en huidirritatietesten, mutageniciteit, fototoxiciteit en DNA schade bepalingen;
Werken volgens Good Laboratory Practice (GLP) richtlijnen;
Verwerking van de resultaten; je verwerkt de resultaten van de analyses in de rapportages van de studies.

Wat is vereist?

Een afgeronde opleiding op MLO/ HLO-niveau; richting biologie, medische biochemie, moleculair life science;
Een oplossingsgerichte teamplayer met een proactieve houding;
Je bent accuraat, zelfstandig en flexibel;
Een goede beheersing van de Nederlandse taal in woord en geschrift.

Wat zou prettig zijn:

Laboratoriumervaring met celkweek en/ of bacteriekweek;
Bij voorkeur een goede beheersing van de Engelse taal.

Wij bieden: 
Werken bij onze organisatie betekent werken in een dynamische internationale organisatie met een modern laboratorium en een grote diversiteit aan apparatuur en technieken tot je beschikking. 

Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder: 

27,5 vakantiedagen en 2 collectieve dagen per jaar; 

Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar; 

Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris; 

Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat; 

Reiskostenvergoeding á 0,23 cent per kilometer met een max. van 250 netto per maand, of een NS-Businesscard; 

Fiets(lease)plan; 

Collectief pensioen met een eigen bijdrage van 2.9%;

Bedrijfsfitness;

De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;

De mogelijkheid tot een consult van onze in house ergonoom;

Elke dag gratis vers fruit.

Heb je vragen over deze vacature? 
Voor verdere informatie over de functie kun je contact opnemen met Janneke Basten +31638857962Heb je belangstelling voor deze functie, dan nodigen wij je uit te reageren via onze carreer site: Charles River Laboratories, Inc. Jobs (criver.com) 

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld 

Over Safety Assessment

Over Charles River

Meer informatie vindt u op www.criver.com.

Officier.e Biosécurité Régional (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant qu’ Officier.e Biosécurité Régional pour notre équipe de Santé et Sécurité, vous coordonnerez le programme régional de biosécurité pour garantir que notre programme répond aux exigences fédérales, locales et corporatives.

Dans ce poste, les principales responsabilités incluront:

Coordonner le réseau régional de biosécurité ; maintenir les adhésions et les licences appropriées, coordonner/gérer la fréquence des réunions, piloter les objectifs régionaux et tenir les dossiers à jours;
Favoriser et surveiller le respect de la législation applicable, des conditions de licence, des permis d'importation d'agents zoopathogènes, des normes de biosécurité et de biosûreté, du Manuel de biosécurité et des procédures opérationnelles normalisées;
Organiser et documenter la formation appropriée du personnel en matière de biosécurité et de biosûreté;
Élaborer et maintenir des systèmes et des outils de gestion des documents justificatifs pour soutenir le programme, notamment les évaluations des risques locaux et les inventaires de matières réglementées;
Effectuer des inspections et des audits de biosécurité périodiques. Signaler par écrit les constatations d'audit au titulaire de licence et au titulaire du permis d'importation d'agents zoopathogènes de toute non-conformité et met en œuvre les plans d'action qui en découlent jusqu'à leur résolution;
Communiquer avec l'Agence de la santé publique du Canada (ASPC) et l'Agence canadienne d'inspection des aliments (ACIA) au nom du titulaire de licence et du titulaire du permis d'importation d'agents zoopathogènes, le cas échéant.
Soutenir l'examen et l'approbation des projets de travaux de sécurité infectieuse et biologique menés sur site.
Collaborer avec l'équipe SST mondiale/régionale pour mettre en place des outils d'évaluation et d'inspection afin d'identifier les risques de biosécurité associés aux opérations et crée des solutions pour combler les lacunes ou améliorer les programmes.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

DEC ou BAC en sciences biologiques;
3-5 années d’expérience en de travail avec la biosécurité;
Experience de travail avec les NHP est un atout;
Capacité à inspirer confiance grâce à de solides compétences interpersonnelles et à une collaboration efficace ;
Capacité à gérer efficacement plusieurs projets simultanément;
Bilingue (français et anglais).

Informations spécifiques au poste:

Localisations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 (1-2x par semaine);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4 x par semaine);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x par mois);
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de jours, sur site;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Security Officer - Part Time (Reno, NV, US, 89511)

Job Summary

***This position covers weekends, Saturday - Sunday from 6:00pm to 6:00am****

We are seeking a Security Officer for our Safety Assessment site located in Reno, NV.

Ensures the protection of organizational personnel and company property against fire, theft, vandalism, illegal entry, and other hazards. Inspects credentials and facilities, and reports irregularities, alarm activation and tampering. Develops, implements and administers programs designed to protect organizational personnel and property. Ensures compliance with government and organization security policies and procedures and protects and safeguards intellectual property. Conducts investigations to identify and document instances of noncompliance and possible breaches in law.

The following are responsibilities related to the Security Officer:

•   Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
•   Monitor security systems and/or environmental systems and investigate and/or report any incidents.
•   Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
•   Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physical security measures; and monitors the critical building systems.
•   Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
•   Document all security department activity and generates incident reports as necessary.
•   Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
•   Contact emergency personnel as required and in accordance with
•   Assist in directing appropriate emergency response efforts when required.
•   Perform all other related duties as assigned.
•   We are also seeking an individual to work on the weekends but may be available to provide coverage for others during the week, during vacation, and sick leaves

Job Qualifications

The following are minimum qualifications related to the Security Officer position:

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least Six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Other: None

The pay for this position starts at $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Supervisor (Boston, MA, US, 02115)

For 75 years, Charles River employees have worked to advance the discovery, development, and safe manufacture of new drug therapies, making a profound impact on global health. Our 20-year partnership with Boston Children’s Hospital takes this mission to the next level, supporting groundbreaking innovations that directly impact patient care. At Boston Children’s, their commitment to diversity drives the exceptional quality of care provided to patients from local communities to over 160 countries worldwide. This is your moment to become part of a family where unique talents and perspectives unite to change lives, including your own. Together, we’re shaping a healthier future through compassion, innovation, and opportunity.

JOB SUMMARY

We are seeking a Supervisor to join our Insourcing Solutions team, located at Boston’s Children’s Hospital.  You will be working with multiple animal species.

Under the direction of the Manager, Animal Care, this position provides direction and leadership for the daily operations of Boston Children’s Hospital animal facilities and program. Maintains performance levels consistent with and according to Animal Resources Children’s Hospital (ARCH) standards and requirements. Collaborates with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines and regulations. Responsible for providing back up and assistance for the Manager, Animal Care.

ESSENTIAL DUTIES AND RESPONSIBILTIES

The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

Responsible for assisting in the training of animal care staff in the following: cage changing, microisolator cage changing techniques, room sanitation, autoclave operation, cagewash operations, waste disposal and other husbandry duties as required.
Outlines the job responsibilities of animal care staff, including Children's Hospital policies, procedures and the daily husbandry assignments of the animal care staff.
Collaborates with Animal Facility Manager and maintains necessary supply and equipment inventory to operate the day-to-day operation of the animal care program, including feed/bedding, sanitation supplies, office supplies, cage equipment, autoclave supplies and other supplies and equipment as needed.
Responsible for developing and maintaining animal records including, room logs, health reports, cage card labels, autoclave records, cagewash records, animal census and other records as required.
Ensures that all animal rooms are observed on a daily basis to monitor for sick, or dead animals, and reports findings to the veterinary staff or alternatively to the Animal Facility Manager.
Interviews and recommends selection of candidates for employment to the Animal Facility Manager. In consultation with the Animal Facility Manager and Human Resources Manager, this position performs personnel actions including but not limited to hiring, transferring, suspending, counseling, disciplining, discharging, assigning, rewarding or addressing employee concerns.
Supervises direct reports in their efforts to maintain quality performance of departmental and client objectives, including meeting/exceeding departmental standards with respect to animal health and welfare, facilities condition, sanitation levels.
Build competence among employees through conducting appropriate training activities and through appropriate supervision related activities (e.g. recruitment, separation, performance appraisal, disciplinary actions, etc.).
Supports and affirms the company policy of Equal Opportunity through Affirmative Action.
Conducts daily inspections of animal holding and support facilities to determine the degree to which established levels of animal health, facilities condition, sanitation levels, environmental parameters and security are being met/exceeded.
Participates in the development and implementation of site-specific standard operating procedures (SOP's), in compliance with all state, federal and industry requirements. Oversee adherence to site SOP's and all required documentation related to department. Coordinate operations with the assistance of staff support departments and personnel.
Coordinates repair and general up-keep of physical environment in areas of responsibility. Is available on site for assistance, coordinating during upkeep and repairs.
Participates as required in the development of projections for equipment, supplies and personnel needed to effectively operate the research facilities in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state and federal requirements.

.

Actively interacts with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance. Act as liaison between scientific staff and support personnel.
Trains and oversees consistent practice of general Children's Hospital safety policies and procedures, including those related to biohazards and radioactive substances. Supervises in compliance with local, state, and federal regulations.
In coordination with Human Resources Manager, investigates personnel problems and to employees in accordance with company policies and procedures.
Maintains required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Assists in any contract related activity, as assigned by Supervisor, to complete the required work.
Performs all other related duties as assigned.

MINIMUM QUALIFICATIONS

To qualify for this role, you must have one of the following combinations of education/experience:

- High school diploma/General education development plus six plus years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.
- Bachelor or Associate degree plus two-four years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.

Certification/Licensure: AALAS Certification at the ALAT level preferred.

The pay range for this position is $90,000-$95,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Data Privacy Analyst (Bangalore, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

As a Senior Data Privacy Analyst, you have to be a subject matter expert across (Data Privacy) IT compliance areas, including privacy and compliance, to ensure appropriate processes, procedures, and controls are in place and adhered to. Collaborate with business groups and internal/external auditors to ensure that statutory and regulatory controls are adequately designed, implemented, and/or remediated to meet audit and compliance requirements. Steward improvement and/or remediation efforts associated with statutory and regulatory compliance.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Privacy & Data Protection experience is a mandatory experience for this role. e.g and not limited to India Digital Personal Data Protection Act, 2023 (DPDP Act) and GDPR

• Privacy Third-Party Risk Management: Conduct and manage end-to-end vendor privacy risk assessments

• Audit & Client Support: Coordinate with internal and external auditors during Privacy compliance reviews. Complete Privacy questionnaires for prospective and existing clients

• DSARs: Respond to data subject access requests (DSARs) and support ongoing data protection processes

• RoPA Management: Own and manage the Record of Processing Activities process, and continuous improvement of RoPA by leveraging the privacy management platform (TrustArc)

• Carrying out Data Privacy Impact Assessments

• Supporting, informing, and advising the business on the use of personal data (Privacy by Default and Design)

• Policy, Training & Awareness: Assist in developing and updating privacy and compliance policies, procedures, and training materials.

• Contribute to IT risk and controls program strategies, design, development, implementation, and communication.

• Ensure compliance with the CRL Global Privacy Framework by collecting and reviewing evidence

QUALIFICATIONS:

• Education: Bachelor's degree (B.A./B.S.) or equivalent in Computer Science, Information Systems Management, or related field.

• 5 plus years of related experience in a data privacy support and Compliance role.

• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Skills And Abilities:

Strong understanding of privacy laws e.g., DPDP Act, GDPR, CCPA, CPRA, UK-GDPR, China Data Privacy regulatory and internal control regulations and frameworks as they relate to IT processes. High desirable
Experience in Privacy Management Tools, such as TrustArc Desirable
Fluency in English

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Project Manager I (Cagewash Manager) (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Manager to join our Insourcing Solutions team, located in Bethesda, MD.

In the CWM role, you can do that by planning, organizing, and directing the activities of the cagewash program, which directly contributes to the integrity of the research.

Additional responsibilities include:

Use existing SOPs and quality assurance standards to provide daily direction and supervision to cagewash technicians to maintain facility operation, condition, security, and sanitation levels, as well as coordinate personnel scheduling.
Ensure staff operates and maintains equipment and supplies; develop projections for equipment, personnel
Conduct routine inspections to determine if standards are being met.
Evaluate and adjust the workflow to ensure efficiency and effectiveness of cagewash operations
Conduct/participate in training activities and ongoing learning, including improvement planning.
Develop and implement new or updated SOPs. Additional duties include coordinating and communicating special projects/procedures, supervising record maintenance, as well as generating/submitting reports to management on operations-related issues.
Coordinate preventative maintenance on all cagewash machinery, equipment, and materials; in addition to organization and up-keep of physical environments.
Troubleshooting equipment issues, performing minor repairs, and coordinating service visits would also be a responsibility of this position.
Identify, document, and/or report environmental or cagewash abnormalities.
Use of computer programs to maintain data and reporting is required; in addition to actively interacting with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

The following are minimum requirements related to the Cagewash Manager position:

A.A. in Animal Science or a related field plus 4 years lab animal experience or
B.A./B.S. degree or higher in Animal Science or related field plus 3 years lab animal experience
Minimum of 1 year supervisory experience in a multi-labor category rodent facility
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

Additional requirements

Customer service experience preferred
Cagewash equipment maintenance experience preferred

The pay range for this position is $38.00 - 42.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate

This position services client(s) that requires us to ensure our employees are fully vaccinated against COVID-19. We will require proof of vaccination from all employees servicing client(s) with COVID-19 Vaccination requirements.

For more information, please visit www.criver.com.

Senior Salesforce Developer (Bangalore, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

We are hiring a Senior Salesforce Developer to lead the design, development, and optimization of our Salesforce ecosystem (Sales Cloud, Service Cloud, Experience Cloud, Apttus CPQ/CLM). You will leverage Apex, LWC, Flows and integrations to build scalable solutions, enforce best practices and enhance system performance while collaborating with architects and business leaders.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•   Salesforce Development & Architecture: Lead the design and development of Apex, LWC, and Salesforce Flow solutions.
•   Automation & Customization: Implement scalable automation, custom objects and advanced trigger logic to streamline business processes.
•   Apttus CPQ Customization: Configure and customize Salesforce Apttus CPQ to enhance quoting efficiency and integrate Apttus CPQ with other modules.
•   Integrations & APIs: Develop robust integrations using REST/SOAP APIs, Platform Events, CDC, and middleware tools such as MuleSoft, SAP CPI, etc.
•   Performance Optimization: Optimize data architecture, performance tuning, and governor limit handling for system efficiency.
•   AI & Bot Automation: Design and enhance Salesforce Einstein Bots and Enhanced Bots to improve customer service.
•   Technical Troubleshooting: Diagnose and resolve complex Salesforce and Apttus CPQ issues.
•   Collaboration & Best Practices: Work with Solution Architects and DevOps teams to implement best practices and CI/CD automation.
•   Documentation & Code Quality: Maintain technical documentation, conduct code reviews, and mentor junior developers.
•   Continuous Learning & Innovation: Stay updated on Salesforce releases, security best practices, and emerging technologies to drive innovation.

QUALIFICATIONS:

•   Education: Bachelor’s degree in IT or Computer Science is preferred
•   Experience: Five or more year’s related SFDC implementation, configuration, and administration experience, including Sales Cloud, Service Cloud, Apttus CPQ/CLM, Pardot/Einstein, Live Agent and Integrations.
•   Technical Expertise: Strong hands-on experience with Apttus CPQ & CLM (required) and a deep understanding of Quoting, Opportunity Management and Order Management processes.
•   Certifications: Salesforce Administrator, Platform Developer I, and JavaScript Developer I (CPQ Specialist or Platform Developer II is a plus).
•   Development & Troubleshooting: Proficiency in Apex, LWC, Flow, SOQL, triggers and Salesforce design patterns & testing frameworks, with strong problem-solving and debugging skills.
•   Agile & Collaboration: Experience in Agile environments with excellent communication, teamwork and business acumen to develop effective solutions.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Director Regulatory Compliance (Wayne, PA, US, 19087)

Job Summary

Responsible for managing the Quality Assurance program(s) at one or more Charles River operations and serves as a member of the Regulatory Affairs and Compliance management team. Provides direction in implementing the Charles River Compliance Program and may lead corporate quality initiatives to improve the program.

Essential Duties

⦁ Communicate all identified compliance and quality risks to his/her supervisor.
⦁ Develop departmental policies and procedures and assure their consistency with Quality Assurance programs at other Charles River sites/operations.
⦁ Identify the need for Corporate Quality and Compliance Policies and lead development and implementation efforts.
⦁ Direct site/operation Quality Assurance program to assure inspections and audits are accurate, thorough, timely, and provide the correct interpretation of regulatory requirements and corporate policies.
⦁ Maintain a close working relationship with site/operation management to assure a cohesive approach to regulatory compliance.
⦁ Assure staff receives appropriate regulatory and management training, and mentoring to enable the execution of regulatory and management responsibilities.
⦁ Assume a lead role in the development and presentation of regulatory training for Quality Assurance and operations staff.
⦁ Manage site/operation Quality Assurance inspection and audit programs and schedule resources to assure efficient and effective operation of the site/operation Quality Assurance organization. Align Quality Assurance staffing level and expertise with identified business needs.
⦁ Monitor the effectiveness of subordinate Quality Assurance managers in reviewing Quality Assurance reports of audits and inspections to assure proper and consistent interpretation of regulatory requirements and corporate policies. Identify and resolve inconsistencies between Quality Assurance audit teams should they occur.
⦁ Assure that all records and reports are prepared, communicated, and retained in accordance with applicable regulatory requirements.
⦁ Serves as the principal liaison with site operations managers to identify regulatory deficiencies, explain audit findings, resolve escalated conflicts, and consult on corrective and preventative actions.
⦁ Assemble, evaluate, and report site metrics measuring compliance and quality key performance indicators.
⦁ Serve as the principal site representative for scheduling and management of regulatory and client inspections/audits.
⦁ Interact, as appropriate, with regulatory agencies in developing a positive working relationship.

Responsibilities:

⦁ Train site/operation personnel and management on interacting with client and regulatory auditors prepare appropriate summaries and reports of such audits.
⦁ Review and endorse regulatory and client audit responses and corrective action commitments.
⦁ Monitor site/operation corrective actions commitments and communicate “at risk” commitments to management with recommendations for their timely resolution.
⦁ Identify practices, methods, and processes for improvement and assist other operations on related compliance issues.
⦁ Provide regulatory guidance to internal departments for the development of new products, test methodology, new facility construction, and new processes.
⦁ Participate in development and revision of regulatory submissions, e.g., license applications, supplements, annual reports, and master files.
⦁ Participate in the review and development of quality agreements with clients and contract service providers.
⦁ Assure vendors and suppliers identified/designated by Charles River are assessed for the compliance with applicable regulatory requirements.
⦁ Assume a key role in designated Regulatory Affairs and Compliance projects and programs.
⦁ Participate in Corporate Quality Meetings, Regulatory Affairs and Compliance meetings, intranet communications, and relevant strategic planning sessions.
⦁ Assure that Corporate Quality and Compliance Policies are implemented and administered at the site/operation.
⦁ Direct activities of assigned group(s) to ensure optimum performance of the group/function.
⦁ Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.
⦁ Develop short- and long-range operating objectives, organizational structure, staffing requirements and succession plans.
⦁ Integrate activities with those of other major organizational units (e.g. segments, departments, functions).
⦁ Develop and recommend departmental budget and authorize expenditures.
⦁ Develop and oversee the implementation of departmental training programs, including orientation.
⦁ Support the policy of equal employment opportunity through affirmative action in personnel actions.
⦁ Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
⦁ Communicate all identified compliance and quality risks to his/her supervisor.
⦁ Perform all other related duties as assigned.

Job Qualifications

⦁ Education: Bachelor's degree (B.A. /B.S.) or equivalent. Advanced degree in biological sciences, pharmaceutical sciences, or computer sciences preferred.
⦁ Experience: Ten to twelve years related experience in the pharmaceutical, and/or biotechnology based industry.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
⦁ Other: Strong experience and direct responsibility for management of Quality Assurance programs. Extensive experience with management of government regulatory inspections and preparing/reviewing responses to any inspectional findings. Excellent knowledge of pertinent national and international regulations pertaining to the pharmaceutical and biotechnology industries. Excellent leadership and communication skills.

PHYSICAL DEMANDS:
⦁ Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁ Must regularly communicate with employees/customers; must be able to exchange accurate information.
⦁ Must occasionally move about inside the office to access file cabinets, office machinery, etc.

WORK ENVIRONMENT:
⦁ General office working conditions; the noise level is usually quiet.

COMMENTS:
⦁ Requires regular domestic and international travel.

Compensation Data

The pay range for this position is 170K-190K Base and equity eligible (RSUs). Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Company Secretary 1 (Bangalore, IN)

Job Summary

Roles and Responsibilities

Handling entire Secretarial compliances of Charles River under the Companies Act and to ensure that Company’s interests are protected at all times

Handling entire Secretarial compliances of Charles River under the Companies Act 2013 and Secretarial Standards including but not limited to;
Ensuring the company complies with all legal and statutory requirements, including internal policies, external regulations, and corporate governance requirements.
Handling other statutory compliances required under the Shop & establishment Act, labour laws and other State & Central Government Acts applicable to Charles River Laboratories Pvt Ltd. from time to time.
Maintenance and safe keeping of Register of members/ Share holders, Directors, Minute books of General and Directors meeting.
Submission of returns to Registrar of Companies.
Under directive of board, to issue notices for Board & General meeting, Coordinating board / general Meeting and follow up activities thereon. .
To conduct Correspondence with members w.r.t Share capital matters and Share Transfer Matters.
Assisting legal department in preparing legal documents and Maintenance of Agreement Copies. Review of general contracts including engagement letters, lease agreements, no objection certificates, non-disclosure agreements.
Sending out alerts on the respective due dates Compliance with the clauses mentioned in the agreement.
Required to carry out related duties and responsibilities and any other assignments entrusted to from time to time
Updating of various Statutory Registers.
Filing of various Forms with RBI.
Providing legal guidance /advice to the management
Liaising with external agencies and advocates on legal aspects
Drafting and reviewing Policies and terms of reference of committees on an annual basis implementing processes or systems to help and ensure good management and compliance with Law

Job Qualifications

Desired Candidate Profile:

Education PG : CS

Experience: 2 to 5 years

Salary: INR 7 to 9 lakhs per annum.

Must be presentable, knowledgeable and good in secretarial compliances.

Qualified CS with ability to join as full time CS Role.

Must possess excellent communication skills

Must possess a positive attitude and a team player.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Research Scientist 1 - Immunochemistry (Shrewsbury, MA, US, 01545)

Job Summary

Charles River Laboratories is seeking a Research Scientist to join our Laboratory Sciences group within our Safety Assessment site located in Shrewsbury, MA. The incumbent will serve as a scientific team member in the conduct of preclinical and clinical research studies at all levels of complexity. Responsibilities include study management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include serving as a Principal Investigator for the development and validation of biomarker, PK and ADA assays (eg: ligand binding assays, enzymatic assays, Luminex, Bioplex, MSD, Quanterix, ProteinSimple). This individual would be responsible for the composition and execution of validation and sample analysis protocols/plan in accordance with company standard operating procedures and industry regulatory guidelines. This position will serve as the primary scientific contact for key clients and the on-site support of their programs.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Function independently as a Project Scientist, Principal Investigator, Contributing Scientist in the direction and execution of assigned studies in compliance with regulations as they apply to the conduct of preclinical and clinical research. Provide scientific expertise in study conduct, design, and interpretation.
•   Participate in and coordinate all phases of the study planning process with appropriate departments.
•   Develop assays, generate high-quality laboratory method, protocols, amendments, reports, and facilitate appropriate changes to study design for assigned projects and programs.
•   Review, interpret, integrate, and present data on assigned studies.
•   Writes and edits draft or final reports that document all study related procedures and results.
•   Analyze scientific problems, troubleshoot analytical methods and technical issues.
•   Function independently as the point of contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
•   Provide prompt verbal or written communication with Sponsors on study related business.
•   Mentor technical staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and execution of validation studies.
•   Provide technical and scientific guidance to the research staff.
•   Contribute to testing of new biomarker technologies or introduce improvements in existing technologies.

The pay range for this position is between $100,000 to $110,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
• Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD/DVM preferred.
Experience: Minimum of 6 years related experience in the development and/or validation of biomarker, PK and ADA assays is preferred (eg: ligand binding assays, enzymatic assays, Luminex, Bioplex, MSD, Quanterix Simoa, ProteinSimple Ella). Experience in a contract research organization is preferred.
• Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Experience with Watson LIMS (preferred).

PHYSICAL DEMANDS:
• While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
• Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:
•   General office working conditions, the noise level in the work environment is usually quiet.
•   While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near
toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
•   The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

COMMENTS:
• This position may require occasional travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Environmental Health, Safety and Sustainability Manager (Hollister, CA, US, 95023)

JOB SUMMARY

We are seeking an experienced Environment, Health, Safety, and Sustainability (EHS&S) Manager to lead the integration of safety and sustainability practices across multiple operational sites. This role will be based at our Hollister, CA facility and will also support several CRADL locations in South San Francisco and San Diego. The position requires a minimum of 2.5 days per week on-site in Hollister, with the remaining 2.5 days dedicated to CRADL site support, either on-site or remote, as agreed upon with your manager and in alignment with each location’s needs. Time allocation may vary based on project priorities and operational requirements. In this role, you will be responsible for developing, implementing, and promoting EHS&S procedures and programs that align with our organizational framework, and embedding a culture of safety to ensure a safe and sustainable workplace.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Develop and implement policies and procedures targeted toward increasing the safety and protection of the environment for the businesses.
Ensure facility compliance with applicable environment health and safety regulations.
Implement site audit program of the EHS&S compliance of the site, track and report status of corrective actions, and alerting senior management to developing problems where intervention or oversight is required.
Participate in site leadership as a member of the site Leadership Team and conduct reviews at appropriate intervals with facility senior management.
Consult with site management and employees on Federal, State, and Local regulatory compliance related issues. Work with site facility management to ensure proper training programs are established with regards to environmental and health and safety compliance.
Responsible for timely submission of environmental reports and permits to local, state and federal regulatory agencies.
Work with site Leadership and Site/Global Procurement to develop cost savings initiatives to ensure business continuity and best in class service pricing.
Provide lead support and formal response to EHS agency inspections conducted by local, state and federal regulatory bodies.
Manage moderate size capital infrastructure projects from inception to completion including regulated areas.
Develop program budgets and schedules in support of EHS&S initiatives including platform tools (e.g. Enablon).
Monitor and drive progress of EHS&S projects and programs, maintaining budgets and schedules.
Lead the selection process for hiring third party service firms, evaluating proposals, conducting interviews and making recommendations to senior management, in partnership with site Procurement and Management
Provide supervision and development of EHS Site staff. Ensure appropriate communication takes place around EHS issues.
Consult with Corporate Engineering, Company management and workplace staff to identify and resolve potential EHS&S issues through engineering design changes or other means necessary, such as Facilities controls, risk assessments.
Clarify, define, and assist in enforcement and application of Agency and Company policies and practices.
Support and affirm the Company policy of Equal Opportunity through Affirmative Action.
Partner with site leadership to address audit findings from clients, regulatory agencies, or internal CRL audits.
Develop and provide EHS&S training to staff and contractors including SOP and EHS&S policy training.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

- Candidate will possess one of the following:
  - Master's degree (M.A. / M.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 5 years of related experience
  - Bachelor’s degree (B.A. / B.S.) in a life science (biology, chemistry), environmental engineering, or environmental health and safety with 7 years of related experience
  - Associate degree (A.A. / A.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 10 years of related experience
- Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs) and government regulatory requirements and guidelines, including California OSHA regulations. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in MS Office suite including Excel, Word, Power point and Project. In- depth knowledge of environment, health and safety regulations required.
- Ability to communicate and influence senior management on EHS compliance initiatives.

Compensation Data

The pay range for this position is $125,000 - $155,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Assistant Facility Manager (14DNR) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Assistant Facility Manager to join our Insourcing Solutions team, located in Bethesda, MD.As the Assistant Facility Manager, you will use existing SOPs and quality assurance standards to oversee and coordinate the daily activities of the animal facility, to include scheduling of staff.

Operates and maintains equipment and supplies
Oversees all aspects of husbandry support, to include related paperwork, cage change scheduling, and supplies
Actively interacts with Project Officers, facility veterinarian(s) and investigators to solve customer requests, inquiries, and complaints
Ensure that all work is performed according to the task Statement of Work
Participates in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations
Assist in assessing, developing, and presenting training for staff and investigators
Performs daily clinical observations, preliminary health exam of sick animals prior to reporting to the Clinical Veterinarian.
Oversees the animal surveillance program related to the husbandry staff.
Occasionally provides technical support (e.g., restraining animals, collecting blood, collecting tissues, performing injections, treatments, surgical preparation, assisting with research procedures).
Occasionally provides animal husbandry and environmental enrichment for colony animals
Provides quality assurance to include animal health surveillance, monitoring of the effectiveness of facility sanitation, cage washing and autoclaving procedures, monitoring of incoming animal shipments for container integrity and animal health, monitor the HVAC, internal facility reports for monitoring deviations from pre-established parameters, other quality assurance services
Provides data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements
Prepares and submits written records, charts, logs, and inventories

Job Qualifications

The following are minimum requirements related to the Assistant Facility Manager position:

High school diploma or GED
A minimum four years’ experience working in an animal facility, two (2) of which in a supervisory capacity, must have experience with rodents and rabbits
Current AALAS certification at the LAT level; successful achievement of LATG within one year of eligibility

The pay range for this position is $40.00 to $43.00 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Caretaker (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker to join our Insourcing Solutions team located in Baltimore, MD

Additional responsibilities include:

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $18.47 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (50) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician I, you will work with our research animals to ensure they are well cared for.

Additional responsibilities include:
•   Providing food & water.
•   Ensuring cages are clean.
•   Performing and recording daily animal health checks.
•   Handing & restraining animals for injections
•   Learning & applying quality assurance standards
•   Examining new animals that arrive at the site & helping them to settle in
•   Learn & become involved in breeding of multiple animal species.

Job Qualifications 
The following are minimum requirements related to the Animal Care Technician I position:
•   Six months of animal experience (e.g., dog walking, pet sitting, kennel attendant, vet assistant, farm hand, 4-H background, pet store worker)
•   Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1-2 years of eligibility

• High school diploma/GED preferred
 
The pay for this position is $20-22/hour USD per hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations. Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekend and holidays if necessary

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Facility Manager II (33) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Facility Manager II to join our Insourcing Solutions team, located in Bethesda, MD.

As the Facility Manager II, you will be the primary point of contact for the facility, utilizing existing SOPs and quality assurance standards to oversee and coordinate the daily activities of the facility within varied animal care environments, including scheduling of staff.

Additional responsibilities include:

Oversee the animal surveillance program and all aspects of husbandry, including technical and cage wash support.
Provide quality assurance to include animal health surveillance; monitoring of the effectiveness of facility sanitation, cage washing and autoclaving procedures; monitoring of incoming animal shipments for container integrity and animal health; monitor the heating, ventilation, and air conditioning (HVAC); internal facility reports for monitoring deviations from pre-established parameters; and other quality assurance services as deemed necessary (e.g., water cultures).
Participate in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations.
Assist in assessing, developing, and presenting training for staff and investigators.
Participate in QC/QA, and ensure CAPA development, implementation, and adherence.
Occasionally provide technical support (e.g., restraining animals, collecting blood, collecting tissues, performing injections, treatments, surgical preparation, assisting with research procedures).
Occasionally provide animal husbandry and environmental enrichment.
Provide data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements.
Prepare and submit written records, charts, logs, and inventories.
Actively interact with Project Officers, facility veterinarian(s) and investigators to solve customer requests, inquiries, and complaints.

Job Qualifications

The following are minimum requirements related to the Facility Manager II position:

High school diploma or GED required.
Bachelor’s degree in animal science or related preferred
Minimum of 6 years’ experience in a research vivarium facility, with at least 2 years’ experience in an ABSL3 environment, and 3 years of supervisory experience
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

The pay range for this position is $45.00 to $50.00 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Senior In-Vitro Bioassay Analyst (Ballina, IE, F26D786)

Job Summary

This role shall report to the Biosafety & Cell Based Assay Supervisor and the main duties & responsibilities shall be to assist the Department Manager and/or the Scientist in the following:

Leading the execution of routine cell-based potency assays
Support technical transfer, qualification and validation of new cell-based assays
Maintenance and propagation of antibiotic free cell cultures.
Evaluation of mammalian cells / Generation and maintenance of mammalian cell banks.
Establishment of Test Method SOPs and validation of methods

Core duties shall include:

Maintenance and propagation of antibiotic free cell cultures.
Competent in microscopic evaluation of mammalian cells (e.g. cell morphology, count and viability)
Provide technical training to team as required.
Receipt and processing of test samples in LIMS.
Update current standard operating procedures.
Assist in laboratory investigations where necessary.
Responsible for reporting progress information to Management.
Assist in internal, regulatory and client visits/audits and respond to findings.
Complete understanding off all regulatory guidelines.
Liaise with the Quality Department for the generation of all departmental quality documents including audit responses, facility replies and deviation reports.
Generation of GMP compliant SOPs, Protocols and reports
Generate risk assessments for laboratory and test items as required.
Maintain Laboratory Data Integrity and compliance

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Necropsy Technician I (Horsham, PA, US, 19044)

Job Summary

Full Time - 40 hours/week. Day Shift

As a Necropsy Tech I, you will have the opportunity to learn and perform necropsy functions and generate data on various types of studies. You will prepare and review documentation and perform quality control review of study data. You will contribute to department operations improvement in areas such as process development, SOP revisions, department inspections and equipment maintenance.

Essential Duties:
-Perform necropsies/autopsies on rodents and rabbits
-Collect/evaluate organs/tissues from rodents and rabbits
-Perform c-sections and related maternal/pup evaluations on rodents and rabbits
-Perform blood collections via vena cava, aorta, etc. on laboratory animals
-Perform specialized techniques such as whole body perfusions, neuro-dissections, etc on laboratory animals

The training and development offered to our Technicians is state of the art and designed to help you succeed. The work you will be doing will impact the lives of patients and animals across the world.

The pay rate for this position is $21.70 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

Education: Bachelor’s degree B.S. or equivalent in a biological science or a High School diploma or G.E.D.
Experience: Minimum of 1-year laboratory experience strongly preferred

Charles River, offers a comprehensive benefit package including
-Group insurance (medical, dental, vision, disability, Life insurance and employee assistance program)
-3 weeks Paid vacation
-Tuition Reimbursement
-401k with employer match
-Opportunity for career advancement

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Data & DevOps Engineer (Ahmedabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Sr. Data & DevOps Engineer

About the Job: There’s never been a more exciting time to be on the Analytics team at Charles River Labs!

Charles River Labs is on an exciting journey to modernize the data landscape, building a Customer 360, implementing new data standards, bringing to life the ‘art of the possible’ to our business partners, integrating with several new data sources, and ultimately building a brand-new Modern Data Warehouse in Azure. If you are an engineer who enjoys cloud technologies, data warehousing, data analytics, and designing innovative analytical solutions, this job may be for you! This role will work collaboratively, in a consultative way, across the business units and IT, supporting and mentoring engineering teams and advising on the best approaches to leveraging Azure most effectively and efficiently.

The team is seeking top-notch talent in the Microsoft Azure full data stack and modern data toolset. If you are interested in using your leadership, expertise, and innovative skills to build something brand new, enjoy making architectural decisions, are a thought leader in the data space, have a passion for data and analytics, and like to mentor others, then we want to talk to you! A truly exciting and unique opportunity awaits you!

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Basic Qualifications:

• Strong and extensive hands-on Experience with Azure cloud big data architecture
• Good understanding of Microsoft Azure security, privacy, and compliance.
• Implement best practices for Azure services authentication using service principals and managed identities.
• Familiarity with Azure resources service level agreements (SLA), and pricing for planning and cost management.
• Configure and manage Azure virtual network, define Inbound and outbound rules.
• Manage source control with GitHub best practices and define standards for the pull request (PR) process.
• Define and manage a release workflow to update the latest code to the corresponding environments.
• Build continuous integration (CI) pipelines with GitHub actions.

Requirements:

• Bachelor’s degree in Computer Engineering, Computer Science, or related discipline, Master’s Degree preferred
• 4+ years of Microsoft Azure experience or equivalent with AWS or GPC.
• 3+ years of experience implementing automated deployments with GitHub integration and CI/CD pipelines.
• 5+ years of experience in defining GitHub branching strategy for Dev, TEST, PROD, and Hotfix deployments.
• 2+ years of experience automating infrastructure as code using Terraform templates.
• 5+ years of experience in scripting with bash, PowerShell, and Azure CLI.
• 3+ years of experience supporting Azure resources by monitoring diagnostics logs and alerts.
• 2+ years of experience in defining security strategy for Azure resources with networking and firewall rules.
• 2+ years of experience in defining and managing access control strategy for Azure resources.
• Understand different types of storage (filesystem, relation, MPP, NoSQL) and work with various kinds of data (structured, unstructured, metrics, logs, etc.)
• 6+ years of experience working with SQL.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Cagewash Technician (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Baltimore, MD.

As the Cagewash Technician, you will Provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas under minimal supervision. Provide quality assurance to the cagewash area.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position.

Experience and/or training working with animal husbandry preferred
High school diploma/GED preferred

The pay for this position is $18.47 per hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

APAC Distributor Manager (Singapore, SG)

Job Summary

The APAC Distributor Manager is responsible for supporting the Microbial Solutions Distributor Network in the region of Asia Pacific. This goal of this role is to provide support to the APAC Channel Partners that will drive revenue, strengthen channel partner relationships, and assist in the growth of CRL Business in APAC territory. This individual works closely with the Microbial Solutions Commercial team to meet and exceed sales quotas for a specific territory.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Developing and Executing Channel Strategy: Defining the overall approach for working with partners in the APAC region, including recruitment, onboarding, management, and enablement. Goals need to be outlined in quarterly business reviews with partners and internal stakeholders.
Managing and Nurturing Partner Relationships: Building strong relationships with partners is essential for driving sales and ensuring partner success. This is accomplished through co-travel, support at trade shows, seminars, workshops, and in person and remote support on opportunities with customers.
Driving Revenue through Channel Partners: This is the core responsibility, and it involves setting sales targets for partners, providing them with necessary resources and support, and tracking their performance. Recognizing where partners can expand market share and the company’s reach, tracking opportunities through Sales Force.
Providing Training and Support to Partners: Ensuring partners are knowledgeable about Charles River’s products and services. Creating new and using existing tools and resources to sell effectively.
Analyzing and Optimizing Partner Performance: Tracking key metrics, identifying areas for improvement, and adjusting the channel strategy as needed to achieve company goals.

Job Qualifications

Experience: A minimum of 8-10 years of experience in channel sales, business development, or related fields, including experience in CRM software
Leadership skills: The ability to lead and motivate channel partners and their teams, as well as influence and collaborate with cross-functional teams, both internal and within channel partner’s teams.
Strategic thinking: The ability to develop and execute channel strategies that align with overall business objectives.
Relationship-building skills: The ability to build strong relationships with partners and stakeholders.
Communication skills: The ability to communicate effectively with partners and internal teams.
Data analysis skills: The ability to track and analyze partner performance data to identify areas for improvement.
Travel: Expected to travel around 50% of the time

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Research Support Specialist I -Veterinary Technicians encouraged to apply (Poolesville) (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Research Support Specialist I for our Insourcing Solutions site located in Poolesville, MD.

Prepare and administer research treatments; collect and record physiological data (weight, temperature, pulse, respiration)
Perform technical procedures as needed associated with the Animal Study Proposals in relation to NHP retroviral, human respiratory and flavivirus studies to include but not limited to blood collection, IV catheterization, intubation, broncho-alveolar lavage, tracheal and nasal lavages, documented research observations, and administration of research treatments
Must have a basic understanding of aseptic technique, anesthesia induction, monitoring, and recovery as well as drug dosage calculations and administration
Assist Veterinarian & Sr. RSS staff with surgeries and specialized procedures
Perform daily animal health observations and report any abnormal findings to veterinarian
Maintain electronic medical records, send daily emails regarding animal health information to vet staff
Collect, preserve, and prepare blood, urine, stool, and tissue samples
Participate in study related necropsies/tissue harvest
Set-up for procedures and prepare supplies and equipment
Ability to maintain freezer organization and sample inventory
Practice universal precautions appropriate to different levels of ABSL. Work safely with animal / human pathogen biohazards and help to maintain the research animal facility as a safe work environment / operation
Report any animal health, care, and / or wellbeing concerns to the appropriate facility management staff
Report any facility infrastructure issues, relative to the animal care and support areas to the appropriate facility management

Job Qualifications

The following are the minimum requirements related to Research Support Specialist I:

- High school diploma or general education degree (GED) required. BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred.

- 2-3 years’ experience working with non-human primates in biomedical research or 2-3 years Veterinary Hospital technical experience preferred.

- Must have computer program proficiency such as MS Word / Access / Excel. Must have a proficient technical vocabulary.

- RVT/CVT/LVT or LAT certification preferred

The hourly range for this position is between $28/hour and $30/hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Cuisinier.ère de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Cuisinier.ère de laboratoire pour notre équipe de Formulation située au site de Senneville, serez responsable de préparer les différentes formulations requises pour le dosage, en solution, suspension ou mélange de poudre, pour nos équipes de recherche.

Dans ce poste, les principales responsabilités incluront:

Préparer des formulations pour le dosage, en solution, suspension ou mélange de poudre en utilisant différentes techniques tout en respectant les règles des BPL;
Utiliser différents programmes informatiques et équipements tels que PH mètre, appareil d’homogénéisation, balance, osmomètre, densimètre et boîte à gants;
Manipuler des échantillons sous la hotte en utilisant une méthode aseptique;
Préparer le matériel de l’étude selon le protocole.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

AEC/DEC en sciences de laboratoire;
À l’aise de suivre des procédures strictes ;
Personne motivée, autonome et minutieuse ;
Attitude positive et un bon esprit d’équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 23$ de l’heure;
Bonus annuel basé sur la performance;
Horaire:
- Lundi au vendredi avec 1 fin de semaine sur 2 en rotation;
- Heure de début entre 6 et 9 heures du matin;
- Journées fériées;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Documentation Data Reviewer 1 1 1 (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay for this position is $23.50/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

SCHEDULE: Monday - Friday 8:00am - 4:30pm (must be onsite 5 days a week)

We are currently seeking a Data Analyst II for our Quality Control team located at our Mattawan, MI site.

Quality Control supports the review and archival of analysis performed and provides administrative support to the Project Scientists in Laboratory Science disciplines that may include dose formulations, large and small molecule analysis, molecular and cell-based assays, Biomarker, and flow cytometry-based lab work. Staff participate in the review of methods; equipment records and the creation of report tables. Staff participate in the tracking and managing study related materials, providing requested data/information to the Project Scientist or Sponsor as required. Staff are knowledgeable in the application of GxP’s and applicable SOPs, protocols and ensuring adherence to regulatory documents.

Essential Duties and Responsibilities

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Accurately identify and effectively communicates any issues with data
Effectively support administrative tasks including but not limited to, filing, ordering, distribution of documents and study related materials as needed
Independently compile and archive data books and departmental records
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational area
Review and issue data sets in adherence to established timelines
Accurately review departmental and study specific data to ensure adherence to SOPs, methods/protocols, industry standards, and regulatory requirements as applicable in timely manner
Oversee and maintain responsibility for one operational area with minimal oversight
Identify data discrepancies involving collection and analyses compared to study plan by working with appropriate personnel with oversight
Ensure sample analysis data collected is accurate against study plans, methods/type of analysis conducted and subjects' collection time points with oversight
Create and compile report tables with oversight
Review methods for accuracy, consistency and formatting with oversight
Review and monitor study schedules to ensure timelines are met with oversight
Ensure documents align with requirements indicated in Client Information Database (CID)
Attend study and/or department related meetings to assure understanding of assigned projects
Attain CRL personnel and Sponsor signature/approval for study documents and distribute documents when necessary
Assist in preparation, review and/or processing of specialty data shared with Sponsors
Independently generate and maintain standard and complex draft study plans/protocols/amendments and reporting templates in accordance with CRL or Sponsor specific requirements within one operational area
Review laboratory study data to provide financial information for Unit Based Invoicing
Perform all other related duties as assigned

Job Qualifications

Bachelor’s degree (BA/BS) or equivalent in a relevant field with no previous work experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Regional Biosafety Officer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Regional Biosafety Officer for our Health and Safety team, you will be coordinating the Regional Biosafety Program to ensure our program meets federal, local and corporate requirements.

In this role, primary responsibilities include:

Coordinates the Regional Biosafety network; maintains appropriate memberships and licenses, coordinates/manages a regular meeting cadence, drives regional objectives, and maintains records.
Promotes and monitors compliance with applicable legislation, conditions of license, animal pathogen import permits, biosafety and biosecurity standards, the Biosafety Manual and standard operating procedures;
Arrange and document appropriate biosafety and biosecurity training for personnel
Develop/maintain supporting document management systems and tools to support the program including local risks assessments and inventories of regulated material.
Conduct periodic inspections and biosafety audits. Report audit findings to the license holder and animal pathogen import holder in writing of any non-compliance and drive resulting action plans to closure
Communicate with the Public Health Agency of Canada (PHAC) and the Canadian Food Inspection Agency (CFIA) on behalf of the license holder and animal pathogen import permit holder, as applicable.
Supports the review and approval of proposed work involving infectious and biological safety work conducted at site level
Collaborates with Global/ Regional EHS&S team to establish assessment and inspection tools to identify Biosafety risks associated with operations and creates solutions for gaps or opportunities for program improvement.

Key Elements

We are looking for the following minimum qualifications for this role:

Technical or Bachelor’s degree in biological sciences;
3-5 years experience in biosafety work;
Experience working with NHP and asset;
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Ability to effectively manage multiple projects simultaneously;
Bilingual (French & English).

Role Specific Information:

Locations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3(1-2x per week);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4x per week);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x per month);
Annual bonus based on performance;
Schedule: Monday to Friday, Day schedule, On site;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Senior HVAC Technician (Reno, NV, US, 89511)

Job Summary

We are seeking a Senior HVAC Technician for our Safety Assessment site located in Reno, Nevada.

Perform a variety of master-level mechanical and pressure/temperature equipment repairs and maintenance requiring close interface with other trade/craft functions. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing HVAC projects.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Monitor and maintain HVAC systems including high/low temperature, water and electricity. Isolate and identify malfunctioning equipment for repair, adjustment, and replacement. Interpret instructions as required
•   Observe and interpret readings on gauges, meters, and charts to ensure correct functioning of systems. May calibrate equipment.
•   Perform adjustments, repairs and replacement of parts and equipment following written specifications such as blueprints, drawings and schematics.
•   Dismantle equipment fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
•   Oversee HVAC-related tasks being performed by other department personnel.
•   Inspect completed work for quality, safety, and proper operation.
•   Coordinate maintenance work with other departments and divisions; maintain accurate records of maintenance and repair work.
•   Periodically perform preventative maintenance programs as required.
•   Perform other semi-skilled tasks as assigned to assist in the general maintenance of the physical plant.
•   Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation
•   May perform waste vacuum maintenance.
•   Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (GE.D.). Completion of trade school or formal apprenticeship program.
•   Experience: Five or more related experience.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: Valid EPA 608 certification.
•   Other: None

The pay range for this position starts at $39.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Laboratory cook (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a laboratory cook for our formulation team located at the Senneville site, you will be responsible of preparing different formulations required for dosing, in solution, suspension or powder mix , for our research teams.

In this role, primary responsibilities include:

Prepare formulations for dosing, in solution, suspension or powder mix using various techniques while adhering to GLP regulations;
Operate various computer programs and equipment such as PH meter, homogenizer, balance, osmometer, densimeter and glove box;
Handle samples in a fume hood using aseptic method;
Prepare study materials according to protocol.

Key Elements

We are looking for the following minimum qualifications for this role:

AEC/DEC in Laboratory Sciences;
Comfortable following strict procedures;
Motivated, autonomous, and meticulous person;
Positive attitude and good team spirit.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 23$/hour;
Annual bonus based on performance;
Schedule:
- Monday to Friday & 1 weekend out of 2 in rotation;
- Start time between 6AM and 9AM;
- Holidays;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Laborhilfe (m/w/d) - Quereinsteiger Willkommen (Erkrath, NW, DE, 40699)

Für die Abteilung Molecular & Analytical Testing am Standort Erkrath suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet
eine/n

Laborhilfe / Lab Assistant (m/w/d)

WIR FREUEN UNS AUSDRÜCKLICH AUCH ÜBER BEWERBUNGEN VON BERUFSEINSTEIGERN, BERUFSRÜCKKEHRERN ODER QUEREINSTEIGERN!

Unterstütze uns bei allgemeinen Laborarbeiten:

Organisation des Laboralltags in einem GMP-regulierten Umfeld
Auffüllen von Materialien und Reagenzien
Beschaffung und Verwaltung von Materialien und Reagenzien
Herstellung von Puffern
fachgerechte Entsorgung von Laborabfällen nach Inaktivierung
Pflege und Wartung von Labor-Geräten, insbesondere Pipetten
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des Qualitätssicherungs-Systems (GMP)
Routinemäßige Reinigung der Laborfußböden und Laboroberflächen
Reinigung von Laborgeräten, wie z.B. Kühlschränke, Tiefkühlschränke und weiteren
Überprüfung von Sicherheitseinrichtungen, wie z.B. Notduschen
Diverse weitere Tätigkeiten

Überzeuge uns durch:

Möchtest Du einen wichtigen Beitrag in der Entwicklung (und Freigabe) von Medikamenten leisten?
Hast Du erste Berufserfahrung, oder suchst einen Neu- oder Quereinstieg
Bist du an einem Arbeitsumfeld im Labor interessiert?
Bist du ordentlich, strukturiert und zielorientiert?
Hast du ein ausgeprägtes Verantwortungsbewusstsein, kannst dich gut organisieren und bist verlässlich und flexibel?
Arbeitest du gerne im Team?
Hast du Interesse an Computersystemen?

Wir bieten Dir:

Eine unbefristete Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
Flexible Arbeitszeiten
Eine angemessene Vergütung
Eine intensive Einarbeitung mit Onboarding Programm
Kostenfreie Parkplätze
Fortbildungsmöglichkeiten
Engagement Programm und attraktive Mitarbeiter-Benefits

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 227947 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

QC Officer (Ballina, IE, F26D786)

We are seeking an experienced QC Officer for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Biosafety and Cell Based Assay Department Manager and the main duties & responsibilities shall be:

Project Management of routine batch release testing in the Biosafety and Cell Based Assay Department (client correspondence,/weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
Generation and updating of GMP compliant SOPs, Protocols and reports.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
Receipt and processing of test samples in LIMS
Carry out data calculations ,basic statistics and trending. Provide additional information at the clients request as required.
Assist in internal, regulatory and client visits/audits and respond to findings.

The following are minimum requirements related to this Position;

A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
Experience in project management essential.
BSc/M.Sc. in a relevant science discipline (e.g. cell biology / Molecular Biology / Biomedical Science)
Experience in cell-based assays / molecular techniques desirable but not essential.

Job Summary

Job Qualifications

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Zootecnia de vivarios de investigación - Colaborador 1 1 1 (Barcelona, B, ES, 08003)

Resumen de trabajo

Acerca de Microbial Solutions

Acerca de Charles River

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo del 80% de los fármacos aprobados por la FDA en los últimos cinco años.

Para más información, visite www.criver.com.

Cuidador/a Animalario BCN (Barcelona, B, ES, 08003)

Charles River Laboratories España, S.A., empresa dedicada a la investigación y desarrollo experimental en biotecnología, necesita incorporar CUIDADORES/AS DE ANIMALARIO en Barcelona.

• Jornada laboral de 40 h de lunes a viernes.

• Contrato laboral temporal por suplencia. Duración en función de la suplencia a cubrir.

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

• Tareas de mantenimiento de animales con fines experimentales (cambio de jaula, rejilla y cobertor)

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

• Desinfecciones de material de estabulación (racks ventilados, cabinas de cambio, jaulas, cobertores, etc.)

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

• Mantenimiento de registros ambientales (Tª, humedad, ciclos de luz, etc.)

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

• Desinfección de salas de estabulación, pasillos, almacenes, zona de lavado, etc.

Requisitos

Experiencia 3 meses. Experiencia mínima de 3 meses, aunque formamos a nuestro propio personal.
Título CFGM
Técnico/a superior anatomía patológica y citodiagnóstico
Idioma español
Competencias / conocimientos: se valorará acreditación para funciones A y B o formación como ATV (asistente técnico veterinario)

Acerca de Charles River

Para más información, visite www.criver.com.

Production Supervisor (Small Animal) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Production Supervisor to support our Breed Operation in Raleigh, NC. As the Production Supervisor, you will provide daily supervision of personnel and operations to ensure achievement of departmental goals and levels. You will independently handle routine personnel-related issues; assist in the handling of complex personnel-related issues.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, SOPs, safety procedures and biosafety protocols. Schedule and prioritize workload of group members.
Assist in the coordination and scheduling of activities of the department through hands-on technical support, delegation of responsibility and/or authority to departmental subordinates.
Oversee production and shipping activities of assigned group, including SOPs and OORs. Ensure proper record-keeping and report preparation.
Review safety issues and Workers’ Compensation claims.
Actively interact with and provide technical assistance to customers as required to resolve customer requests, inquiries, and complaints.
Review customer complaints and participate in the development and implementation of any resulting procedural changes. Create and maintain complaint chart.
Audit production rooms and/or isolators.
Review and ensure appropriate inventory levels of departmental supplies.
Interview and select qualified non-exempt personnel. Recom¬mend personnel actions, including hiring, promotions and raises. Partner with Human Resources and departmental management to assist in the handling of disciplinary issues. Draft appropriate personnel action paperwork.
Identify training and development needs of direct reports. Assist in the development, implementa¬tion and delivery of depart¬mental training programs; ensure that direct reports receive departmental orien¬tation and necessary on-the-job training. Oversee main¬tenance of group training manual and training records.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
Schedule overtime as authorized. Review and approve timecards. Coordinate vacation/time off schedules.
Recommend short-range operating objectives, organizational structure of direct reports and staffing requirements. Assist in the development of a departmental plan for backup and succession of key technical personnel.
May assist in development of departmental budget.
Ensure optimum performance of group function. Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Assist in the development, maintenance and communication of departmental systems and SOPs. Assist in the development and communication of job descriptions for subordinate positions.
Ensure that departmental equipment is maintained in good working condition and that departmental area(s) are maintained in a clean and orderly condition. Ensure proper recycling and setup of cages in assigned area(s).
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s degree in life sciences or related discipline and 4 years of supervisory experience of a high-performing team to deliver complex initiatives and/or support operations, and assistance in cross-functional collaboration to drive successful business outcomes.
Associates degree in life sciences or related discipline and 6 years of supervisory experience
High school diploma or GED and 8 years of supervisory experience

ADDITIONAL QUALIFICATIONS:

Effective communication and interpersonal skills required. Demonstrated computer skills (data input, word processing) required.

PREFERRED QUALIFICATIONS:

ALAT certification

Salary Range

The pay range for this position is $70,000 - $80,000 / annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Animal Care Technician I (Cambridge, MA, US, 02139)

Job Summary

We are looking for an Animal Care Technician I to join our Insourcing Solutions team, located in Cambridge, MA.

In the Animal Care Technician 1 role, you will use existing SOPs and quality assurance standards to monitor, observe, and record animal health and welfare daily, as well as complete various standard animal husbandry duties.

Maintain accurate records of animal breeding, health, and housing.
Follow all procedures to maintain housing areas, including room or facility personnel entry; personnel protective equipment use, spraying in all equipment and materials into controlled areas.
Receive, inspect, and put away incoming animals; and operating equipment following all safety guidelines. 
 You may also be involved in the breeding and weaning program, performing various duties from weaning and sexing, to ensuring appropriate production levels are met.
Work cooperatively with the on-site supervisor and/or facility veterinarian to assist with restraint, handling and manipulation of various animal species to include mice, rats and other rodents and possibly rabbits.

Job Qualifications

High school diploma, General Education Degree (G.E.D.) or equivalent required.
Six (6) to twelve (12) months related experience in animal husbandry.
Interest in achieving ALAT certification upon eligibility

The pay range for this position is $23-25 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Vaccine Mandate

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Central Services Technician I (Cambridge, MA, US, 02139)

Job Summary

We are seeking an experienced Central Services Technician I to join our Insourcing Solutions team located in Cambridge, MA.

As the Central Services Technician I, you will provide cleaning and maintenance of laboratory animal caging, equipment, and cage preparation areas, as well as cleaning of animal support areas.

Additional responsibilities include:

Transport caging and equipment between animal areas and cage washrooms.
Receive and store feed, bedding, and supplies.
Provide quality assurance to the cagewash area.
Ensure that all logbooks, checklists, and other records are completed in a timely fashion.
Conduct and collect various aseptic sampling for the monitoring of water quality, sanitized animal racks, and equipment.
Inspect enrichment devices, cages, and other items, and perform all other related duties as assigned.

Job Qualifications

The following are minimum requirements related to the Central Services Technician I position:

High school diploma, general education degree (G.E.D.) or equivalent
Minimum of six months experience working in a laboratory animal facility performing cage wash duties, or working with glassware cleaning or a commercial dishwashing operation.

The pay range for this position is $20.00-22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Vaccine Mandate

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Lead Cagewash Technician (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Lead Cagewash Technician to join our Insourcing Solutions team, located in Bethesda, MD.

As the Lead Cagewash Technician, you will provide quality assurance and control, in addition to coordinating preventative maintenance of equipment, as well as prioritizing workload on the assigned side to ensure daily goals are met and the integrity of the research is maintained.

Additional responsibilities include:

Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Responsible for conducting trouble shooting on the equipment and reporting any problems to the Cagewash Supervisor. If necessary, communicating directly with the manufacturers on problems with the equipment.
In the absence of the Cagewash Supervisor, is responsible for scheduling the staff, ensuring work and all related paperwork is completed.
Sanitize, maintain, and repair animal caging materials as needed and ensure cagewash facilities are kept clean and organized
Other tasks may include assisting with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories.
Assist with training and redirection of workload as necessary to ensure a cohesive team and that daily goals are met.

Qualifications

The following are minimum requirements related to the Lead Cagewash Technician position:

High school diploma or GED
Minimum six months of successful performance in cagewash facility operations

The pay range for this position is $19.00 - $19.50 per hour.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Project Manager I (Animal Husbandry) Bldg 35 1 (Bethesda, MD, US, 20892)

Job Summary

We are seeking a Project Manager 1 (husbandry) Bldg 35 for our Insourcing Solutions site located in Bethesda, MD.

The following are responsibilities related to the Project Manager 1:

Review, comprehend and comply with all SOP's and quality assurance standards pertaining to specific area. Cares for and maintains laboratory animals
Oversees and coordinates the daily activities of the animal facility to include scheduling of staff for both workdays and weekends.
Oversees all aspects of husbandry support, to include related paperwork, cage change scheduling, and supplies.
Actively interacts with Project Officers, facility veterinarian(s) and investigators as required to solve customer requests, inquiries, and complaints.
Works with subordinate employees to ensure that all work is performed according the task Statement of Work.
Participates in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations.
Assists in assessing training needs, as well as, developing and presenting training for staff and investigators
Oversees the animal surveillance program related to the husbandry staff.
Occasionally provides technical support (e.g. restraining animals, weaning, etc.).
Provides animal husbandry and environmental enrichment for colony animals.
Provides quality assurance to include animal health surveillance, monitoring of the effectiveness of facility sanitation, autoclaving procedures, monitoring of incoming animal shipments for container integrity and animal health, monitor the heating, ventilation and air conditioning (HVAC), internal facility reports for monitoring deviations from pre-established parameters, other quality assurance services as deemed necessary (e.g., water cultures) by the Project Officer.
Provides data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements.
Assist training department and supervisors in the development of course content and materials for training and continuing education of the animal care staff to achieve AALAS certification. Assists in assessing training needs, as well as, developing and presenting training for staff and investigators.
Will be required to rotate weekend coverage.

Qualifications

The following are minimum qualifications related to the Project Manager 1 position:

Education: AA/AS degree in Animal Science or related field required plus four years lab animal experience. Or BA/BS degree or higher in Animal Science or related field and 3 years same experience.
Experience: Minimum of one (1) year of experience of supervisory experience in a multiple labor category rodent facility.
Certification/Licensure: AALAS certification at the Laboratory Animal Technologist level (LATG).

The pay range for this position $38.50 to $42.25 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021. Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees.

With over 18,000 employees within 100 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

For more information, please visit www.criver.com.

Animal Care Associate - (EG) (Kingston, NY, US, 12401)

Job Summary

As an Animal Care Associate for our production site in Stone Ridge, NY, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world.

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

* Up to $500 sign on bonus (CRL employees not eligible)

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

No experience required. On the job training will be provided.

Role Specific Information:

Location: Stone Ridge, NY
This is a temporary opportunity with the potential to be hired as a full-time, employee*
Schedule: Monday - Friday - 1st shift, some rotating weekends required. Early morning hours.
Up to $500 sign on bonus (CRL employees not eligible)
Benefits: 401K participation/Paid Sick Time and Paid Volunteer Time Off

The hourly pay rate for this position is $17.75. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Scientist - Immunology (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Research Scientist for our Immunology team at the Laval location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In this role, primary responsibilities include:

Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
Analyze scientific problems, troubleshoot analytical methods and technical issues;
Write scientific documents, review and interpret the raw data;
Write, review, and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
Ensure the accuracy and completeness of project cost estimates;
Notify the Principal Scientist and/or the Scientific Director of scientist or technical problems as soon as they become apparent.

Key Elements

We are looking for the following minimum qualifications for this role:

Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years’ experience working in a Scientific position;
PhD in Immunology or any biological related discipline;
3 to 5 years’ experience in the development, optimization and use of multi-parameter flow cytometry;
Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and cell-based assays (ELISpot, bioassays) is an asset;
Experience with the BD flow cytometer platforms; spectral flow cytometry experience is an asset;
Outstanding organizational skills;
Good interpersonal and communication skills;
Strong problem-solving skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime. Depending on the business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientifique de recherche - Immunologie (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Scientifique de recherche pour notre équipe d’Immunologie située au site de Laval, vous serez désigné comme Scientifique d'études ou Investigateur principal, responsable de la conception, de la réalisation et du rapport des études en sciences de laboratoire de manière efficace, rentable et avec un maximum de qualité scientifique.

Dans ce poste, les principales responsabilités incluront:

Concevoir, rédiger, examiner et éditer des plans d'étude, des modifications et des horaires d'étude qui définissent et programment toutes les activités d'étude;
Superviser et coordonner tous les aspects des procédures de Sciences de laboratoire liées à l'étude, qu'elles soient réalisées au sein du département ou par des départements de service;
Analyser des problèmes scientifiques, résoudre des méthodes analytiques et des problèmes techniques
Rédiger des documents scientifiques, examiner et interpréter les données brutes;
Rédiger, examiner et éditer des rapports préliminaires et/ou finaux qui documentent toutes les procédures et résultats liés à l'étude;
Établir une communication verbale ou écrite rapide avec les Directeurs d'étude et/ou les clients liées à l'étude en temps opportun;
Assurer l'exactitude et l'intégralité des estimations de coûts du projet;
Informer le Scientifique principal et/ou le Directeur scientifique des problèmes scientifiques ou techniques dès qu'ils deviennent apparents.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d'une Maîtrise en Immunologie ou dans toute autre discipline connexe avec un minimum de 3 à 5 ans d'expérience dans un poste scientifique;
Doctorat en immunologie ou dans toute discipline biologique connexe;
3 à 5 ans d'expérience dans le développement, l'optimisation et l'utilisation de la cytométrie en flux multi-paramétrique;
L'expérience avec les techniques d'immunodosage (ELISA, ECL, Luminex) et les tests cellulaires (ELISpot, bioessais) est un atout;
Expérience avec les plateformes de cytomètre en flux BD ; l'expérience en cytométrie en flux spectrale est un atout;
Excellentes compétences organisationnelles;
Bonnes compétences interpersonnelles et en communication;
Solides compétences en résolution de problèmes;
Travailler avec précision, prêter attention aux détails et s'efforcer d'obtenir un travail de qualité.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Research Technician II (Dixon, CA, US, 95620)

Job Summary

We are looking for a Research Technician II to join our Insourcing Solutions team located in Dixon, CA.

As the Research Technician II, you will join our high-throughput Animal Reproductive Technology Animal Care (ART-AC) team in Dixon, CA. The successful candidate will work closely with the ART-AC team to support custom mouse model creation, cryopreservation, rederivation, cross by microinjection and IVF, etc. Responsibilities include husbandry and other duties including lab support and work as assigned.

Additional responsibilities include:

Perform rodent husbandry duties, such as room sanitation, cage change, daily health checks, post-operative monitoring, breeder setup and takedown, tail biopsy for genotyping, cross-fostering, wean, etc. and specialized tasks such as hormone administration via intraperitoneal injection, estrus check, plug check, colony and room transfer, pseudopregnant and stud male colony management, stud male vasectomies and sterility testing, and other support tasks for the ART (Animal Reproductive Technology) and microinjection labs.
Exhibit professional and collegial behavior, communication skills, and expected to participate in discussions at unit meetings.
Serve as a mentor to less experienced staff, including periodic review of data processes and reports to the lab manager.
Review, comprehend and comply with all SOPs, guidelines/policies, and quality assurance standards pertaining to assigned responsibilities, and to the care and use of laboratory mice for research under the delegation and/or supervision of the ART (Animal Reproductive Technology) Lab manager.
Perform all other duties as assigned.

Job Qualifications

Education/Experience:

Master of Science (MS) degree in Animal Science or a related discipline and zero (0) to six (6) months' experience in animal research and/or husbandry; multi species preferred;

Associate of Science (AS) degree in Animal Science or a related discipline and three (3) years' experience in animal research and/or husbandry; multi species experience preferred;

Bachelor of Science (BS) degree in Animal Science or a related discipline, and one (1) to three (3) years' experience in animal research and/or husbandry; multi species experience preferred;

High School diploma/GED and a minimum of five (5) years' experience in animal research and/or husbandry; multi species experience preferred.

AALAS (American Association for Laboratory Animal Science) certification at the Assistant Laboratory Animal Technician (ALAT) level is preferred.
Must be proficient in mouse handling, sexing, and health assessment. Demonstrated experience with mouse reproductive technology and techniques required. Must have hands-on experience with daily operations such as hormone administration via intraperitoneal injection, estrus check, plug check, oviduct harvest/oocyte collection, colony and barrier room transfer.
Required to work evenings, weekends, and holidays as dictated by the lab schedules.
Excellent oral and written communication skills required. Demonstrated high level of attention to detail, responsiveness, adaptability and reliability needed. Proven ability to successfully work independently and collaboratively as a team. Excellent organizational and time management skills necessary. Must have experience with computers, mobile platforms, and accurate data management systems in a professional environment.

The pay for this position is $38.00 - 40.50 USD per hour. Schedule: The required work hours are 5 days a week, Monday - Friday from 8 am to 4:30 pm with one weekend and one evening shift required per week. The position is 100% onsite and the candidates must be available and willing to work evenings, weekends, and holidays.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

饲养员-DIRECT LABOR (Chengdu City, SC, CN, 610213)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融， IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

欲了解更多信息，请访问www.criver.com。

Senior Financial Analyst, Gene Therapy (Rockville, MD) (Rockville, MD, US, 20850)

Job Summary

Charles River Labs is seeking an experienced financial analyst to help support their growing Gene Therapy site in Rockville, Maryland. This position will be hybrid.

The Senior Financial Analyst will be responsible for supporting the Senior Finance Manager with activities related to monthly/quarterly financial close, forecasting & reporting, as well as participating in the preparation of the annual operating plan and any site improvement initiatives. The ideal candidate will have experience in a finance function in the life sciences or biotech industry and be comfortable working and building business relationships with both local and corporate business partners.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Partner with client project management and client services on Statements of Work and relevant SAP workflow as needed, including cost analysis used to develop pricing.
•   Analyze client unbilled and aging receivables and partner with CRL Credit and Collections, Project Coordination, Client Project Management, Business Development, and Site Operations to drive resolution.
•   Partner with site Operations and Quality to develop KPI’s and reporting to allow for relevant business decision making and measurement of the business operations and efficiency.
•   Utilize SAP, AFO and SAC applications to develop routine financial reporting tools for variance analysis and reporting.
•   Analyzes financial and operational performance, provides concise, relevant explanations, observations and/or recommendations to leadership and executive management.
•   Contribute to the development of monthly/quarterly forecasts, Annual Operating Plan, Strategic Plan, and analyze the variances.
•   Support monthly business reviews with senior management discussing operational and financial results, challenges, opportunities, strengths, and weaknesses.
•   Proactively partner with site leadership (Manufacturing, Operations, Quality, Sales, Human Resources, etc.) to address organizational needs and identify financial risk and opportunities to improve financial reporting.
•   Perform all other related duties as assigned.

Job Qualifications

•    Education: Bachelor’s degree (B.A./B.S.) or equivalent business or science degree.
•   Experience: 5 - 7+ years experience in financial analysis or business. Experience in Life Science industry strongly preferred.
•    Strong attention to detail, excellent analytical skills with recommendations grounded in data.
•    High proficiency in Microsoft Office applications.
•    Must be able to work with minimal supervision
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. 10 yrs experience as a Financial Analyst will be accepted in lieu of Bachelor's degree.

Compensation Data

The pay range for this position is $90,000 - $100,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.