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

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

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.

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 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

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.

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

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 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.

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.

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.

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

Technicien de laboratoire en Immuno-Histo-Chimie - F/H - 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 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

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

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.

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.

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)

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.

Pour plus d'information, consultez 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.

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.

Equal Employment Opportunity

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

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.

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, 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.

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.

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

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.

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.

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 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.

Mitarbeiter für den internen Produktions- und Logistikbereich (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.

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

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 rund 80% der von der FDA in den letzten fünf Jahren zugelassenen Arzneimittel 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.

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

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。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.

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 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.

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

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.

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

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.

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.

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.

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.

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.

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

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.

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.

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.

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.

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

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

Animal Care Technician II (Baltimore, MD, US, 21224)

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

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.

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 ~85% of the drugs approved by the FDA in 2018.

Equal Employment Opportunity

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

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.

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.

Testreq - Italy Walkthrough (Ahmedabad, IN)

Job Summary

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Job Qualifications

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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

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.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

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.

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。

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。

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.

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.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

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

Testreq - Training Req (Parma, IT, 43122)

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

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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.

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.

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.

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.

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.

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.

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.

Equal Employment Opportunity

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

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, 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.

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.

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.

Equal Employment Opportunity

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.

Equal Employment Opportunity

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.

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.

Zootecnia de vivarios de investigación - Colaborador 1 1 1 (Barcelona, B, ES, 08003)

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

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 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.

Cuidador/a Animalario BCN (Barcelona, B, ES, 08003)

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 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

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.

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.

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。

QA Specialist II - Shift is 12pm - 10:30pm, Wed - Sat (Rockville, MD, US, 20850)

Job Summary

The QA Specialist II 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 QA Specialist II will compile the batch record review records and batch disposition documents 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
• Support Manufacturing and quality control departments in performing, and documenting deviations and failure investigations, including root cause analysis, evaluating product/facility impacts, and identifying/implementing effective corrective and preventive actions (CAPAs)
• Track and evaluate any non-conformances that occur during the manufacture of drug product and evaluate change controls as they impact the project
• 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.
• Compile batch disposition documentation timely for the final disposition of finished products
• 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 raw materials review and disposition following approved internal procedure
• Receive and issue Batch Production Records and labels to manufacturing departments by verifying the accuracy and completeness from QA Document Control
• Ensure SOPs are current and effective, and staff performs routine tasks according to SOP through direct observation
• Review quality control test reports related to the execution of the batch processing
• Train Level 1 QA Specialists as required
• 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
• Evening and weekend hours may be needed to support production operations
• 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 or related industry
• Previous knowledge and experience with the practical implementation of FDA, EMA and ICH regulations and guidelines
• Previous experience in TrackWise Digital and Pilgrim is a plus
• 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)
• Able to follow instructions and Standard Operating Procedures

Compensation Data

The pay range for this position is $87,733 - $116,978 annually. 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.

Senior Electrician - Featuring a $5000 sign on bonus (Ashland, OH, US, 44805)

Job Summary

We are seeking a Senior Electrician for our Maintenance & Facilities team at our Safety Assessment site located in Ashland, OH.

A Senior Electrician will perform a variety of master-level skilled electrical tasks to repair, install and replace equipment and materials. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing electrical projects.

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

Install and repair electrical materials, equipment, and machinery working from blueprints, drawings, lay-outs, or other specifications.
Inspect, isolate problems, and repair defects in lighting, electrical wiring and equipment using motorized machinery, hand tools, and electrical testing equipment. May require calculation of electrical loads and feeds.
Dismantle equipment/fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
Oversee electrical tasks being performed by other department personnel.
Inspect completed electrical 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.
Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
Perform all other related duties as assigned.

The pay range for this position is $32-42/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:

Education: High school diploma or General Education Degree (G.E.D.) and trade school diploma preferred.
Experience: Four to six 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 Master Electrician’s license (where required by state). Valid driver’s license required.
Other: Basic experience with Microsoft Office Suite

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to stoop, kneel, crouch, or crawl and talk or hear.
The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move more than 100 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.

WORK ENVIRONMENT:

While performing the duties of this job, the employee frequently works near moving mechanical parts and in outside weather conditions.
While performing the duties of this job, the employee occasionally works in high, precarious places and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, risk of electrical shock, risk of radiation, and vibration.
The noise level in the work environment is usually moderate.

Equal Employment Opportunity

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

Electrician - Featuring a $5000 sign on bonus (Ashland, OH, US, 44805)

Job Summary

Perform a variety of skilled electrical tasks to repair, install and replace equipment and materials. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing electrical projects.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Install and repair electrical materials, equipment, and machinery working from blueprints, drawings, lay-outs, or other specifications.Inspect, isolate problems, and repair defects in lighting, electrical wiring and equipment using motorized machinery, hand tools, and electrical testing equipment.
May require calculation of electrical loads and feeds.
Dismantle equipment/fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
Oversee electrical tasks being performed by other department personnel.
Inspect completed electrical 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.
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 (G.E.D.) and trade school diploma preferred.
Experience: Four to six 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.
Valid driver’s license required.
Certification/Licensure: Valid Journeyman Electrician’s license (where required by state).Other: Basic experience with Microsoft Office Suite

Compensation Data

The pay range for this position is $28.00 - $35.00 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

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

Assistant Administratif - F/H - CDD 12 mois (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 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. Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Dans le cadre d'un remplacement, nous recrutons un Assistant Administratif - F/H pour un CDD de 12 mois.

Rattaché(e) à notre Directrice de Site, ce poste central vise à apporter tout le support nécessaire à la vie de l'entreprise.

Les missions

1/ Accueil

Assurer l'accueil téléphonique et physique des visiteurs
Préparer les salles de réunion
Commander les repas en cas de visite

2/ Administratif

Gérer l'envoi et la réception du courrier
Planifier et organiser les réunions générales de Direction
Gérer l'agenda de la Directrice du Site
Organiser les voyages et déplacements
Gérer les stocks des encas du site
Gérer les demandes d'achats
Traduire des documents en anglais

3/ Support aux Archives et Laboratoires

Distribuer et scanner les cahiers de laboratoire
Assurer la préparation documentaire de nos études

4/ Communication interne

Informer le site des actualités via des mails internes
Mettre à jour l'intranet local

5/ Réception

Participer à la réception des colis au magasin

Qualifications attendues

De formation Bac à Bac +2 en gestion administrative ou commerciale, vous disposez d'une première expérience dans l'assistanat de direction.
Vous êtes organisé(e), autonome et rigoureux(se).
Vous maitrisez parfaitement les outils informatiques (Excel, ERP,...).
Vous êtes reconnu(e) pour vos qualités de communication, écrites comme orales.
Vous disposez d'un excellent relationnel, savez être à l'écoute et interagir avec diplomatie, quelque soit l'interlocuteur.
Notre groupe étant international, un bon niveau d'anglais (lu, écrit, parlé) est indispensable pour ce poste.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 3
Contrat : CDD de 12 mois non-cadre (36h/semaine, 6 RTT)
Salaire : A partir de 24 000 € 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.

Auditeur Qualité - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Nous recherchons un Auditeur en AQ pour rejoindre une équipe d’environ 15 personnes sur le site.
Rattaché(e) au Directeur du service Qualité et affaires réglementaires, vous aurez la responsabilité de garantir la bonne application des Bonnes Pratiques de Laboratoire (BPL) et des procédures par le biais des audits que vous réaliserez sur les études précliniques.
 

Les missions

Effectuer en autonomie des inspections et audits d’évaluation (processus, installations, équipements, personnel, matériaux, méthodes, pratiques, les enregistrements et les contrôles),
Assurer la conformité des activités de recherche à la réglementation internationale (GxP, BPL),
Contrôler l’exactitude, la clarté et la précision des plans d’étude et des rapports finaux,
Participer aux audits des sous-traitants, des vendeurs et des fournisseurs de produits et services,
Participer à la formation réglementaire du personnel assurance qualité et des opérations,
Participer à la planification et au suivi des audits, inspections et activités AQ,
Participer à la collecte et à la communication d’indicateurs concernant la qualité,
Conseiller les équipes scientifiques et la direction, être force de proposition.

Conditions spécifiques du poste 

Amplitude horaire : 8h/18h avec planning partiel à la semaine
Interventions de week-end ponctuelles sur la base du volontariat
Interventions en animaleries dans le cadre des audits
 

Qualifications souhaitées

Vous êtes titulaire d'un diplôme Bac+3 dans le domaine de la biologie, ou gestion de la qualité.
Vous avez une première expérience en gestion de la qualité dans l’industrie pharmaceutique.
Vous avez le sens de l’écoute, le souci du détail et travaillez avec rigueur et organisation.
Des connaissances des techniques d'audits dans un environnement (GxP BPL) sont un atout.
Vous êtes à l’aise avec l’anglais écrit et oral.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 4
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 28 184 € 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.

Laboratory Instrument Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As an Instrument Specialist for our Safety Assessment team at the Senneville location, you will be helping with issues related to the support of the equipment and instruments used, and will be a resource to the technical group.

In this role, primary responsibilities include:

Perform routine system maintenance and verification of laboratory instruments in compliance with SOP’s, safety procedures and biosafety protocols, and GLP regulations;
Perform trouble shooting and repair of laboratory instruments;
Participate in the set up, configuration and qualification of the instrumentation necessary to implement the tests in the laboratory;
Understand the interactions between the different components that make up the instrument in order to target the cause of a problem;
Perform or participate in the creation of IQ/OQ/PQ procedures for equipment and instruments.

Key Elements

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

College diploma in analytical chemistry or in laboratory sciences;
One year of experience require in laboratory sciences;
Able to take initiative and solve problems autonomously;
Able to work physically occasionally (lift up to 20 kg, walk, stand, stoop, etc.).

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: Monday to Friday during the day;
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.

Equal Employment Opportunity

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

Spécialiste d'instrumentation de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Spécialiste d’instrumentation pour notre équipe de Sciences de laboratoire située au site de Senneville, vous aurez à répondre aux questions liées au soutien de l’équipement et des instruments utilisés et serez une ressource pour le groupe technique.

Dans ce poste, les principales responsabilités incluront:

S'assurer que le système d’entretien et de vérification d’archives des données des équipements fonctionne selon les PNO, les procédures de sécurité et de biosécurité et les normes BPL;
Participer à la mise en place, configuration et qualification de l’instrumentation nécessaire afin de mettre en œuvre les essais dans le laboratoire;
Comprendre les interactions entre les différentes composantes qui constituent l’instrument afin de pouvoir cibler la cause d’un problème;
Effectuer ou participer à la création des procédures IQ/OQ/PQ pour les équipements et les instruments.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études collégiales en chimie analytique ou en sciences de laboratoire;
Un an d’expérience requis en tant qu’analyste de laboratoire;
Capacité à prendre des initiatives et de résoudre des problèmes de manière autonome;
Apte à travailler physiquement occasionnellement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X ICI;
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: Lundi au Vendredi de jour;
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.

Spécialiste d'équipement (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Spécialiste d’équipement pour notre équipe de Sciences de laboratoire située au site de Senneville, vous supporterez la division et autre secteur de la compagnie avec la gestion des équipements qui serviront sur les études.

Dans ce poste, les principales responsabilités incluront:

Exécuter et planifier la vérification, calibration, ou réparation des équipements;
Supporter la gestion des demandes d’équipement ou de matériel pour les études;
S’assurer qu’un environnement de travail sécuritaire est maintenu en respectant toutes les procédures et méthodes de travail, en faisant un usage approprié des vêtements et de l’équipement de protection, et en lisant, en comprenant et en suivant tous les documents de sécurité délivrés;
S‘assurer que le système d’entretien et de réparation des équipements fonctionne selon les PNO, les procédures de sécurité et de biosécurité et les normes BPL.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme d’études secondaire;
Capacité à prendre des initiatives et de résoudre des problèmes de manière autonome;
Apte à travailler physiquement occasionnellement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

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. Selon les besoins de l’entreprise vous devez être disponible à travailler occasionnellement de soir et la fin de semaine;
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.

Equipment Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As an Equipment Specialist for our Safety Assessment team at the Senneville location, you will be support the division and other areas of the company by managing the equipment to be used on studies.

In this role, primary responsibilities include:

Execute and schedule the verification, calibration, and maintenance of equipment;
Support the management of requests for equipment or supplies for studies with minimal supervision;
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;
Ensure that system maintenance and repair equipment data are performed in compliance with SOP’s, safety procedures and biosafety protocols, and GLP regulations.

Key Elements

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

High School Diploma;
Able to take initiative and solve problems autonomously;
Able to work physically occasionally (lift up to 20 kg, walk, stand, stoop, etc.).

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 shift from Monday to Friday. Depending on business needs, you must be available to work evening and occasional weekends;
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.

Equal Employment Opportunity

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

Quality Control Associate I - Sun - Wed 12pm to 10:30pm (Rockville, MD, US, 20850)

Job Summary

Note: Shift for this position is as follows: Sun-Wed 12:00pm - 10:30pm

The QC Associate I is responsible for performing in-process, release and stability testing in a GMP environment. The Associate may also contribute to testing as part of test method optimization, trouble shooting, and development/qualification studies.

Key Responsibilities and Duties:

• Perform routine testing in a quality control laboratory to support in-process, lot release and stability testing
• Experience performing some of the following in a QC laboratory setting: qPCR / ddPCR, cell-based assays, ELISA, other QC methods (pH, osmolality, endotoxin and appearance)
• Perform sample receipt and log-in procedures as required
• Contribute to generating SOP’s and qualification/validation/transfer protocols and reports
• Responsible for cross training on multiple QC assays
• Responsible for participation in method development/qualification studies
• May train other associates on methods as appropriate
• Perform general lab upkeep, order of lab supplies and maintenance of logbooks as required.
• Other responsibilities as required

Job Qualifications

• B.S. or M.S. and 1-2 years of experience in biology, virology, molecular biology, cell biology, biochemistry, or related field in a quality control testing laboratory
• Team-player
• Develop proficiency in compendial methods, molecular biology, cell culture, and ELISA techniques
• Able to work in a GMP environment to execute testing
• Able to support multiple projects and strong organizational skills
• Able to learn data analysis and interpretation experimental data
• Complete On-The-Job Training before executing the QC lab responsibilities
• Develop communication skills with ability to present information to the internal QC team
• Must be able to lift up to 40 lbs.
• Standing, sitting, pushing, pulling, walking

• Amenable to occasional off hours and weekend work

The pay range for this position is $22.24 - $28.17. Please note that salaries vary within the range based on factors but not limited to experience, skills, education and location.

Equal Employment Opportunity

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

Production Supervisor 1st Shift (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 seeking a Production Supervisor for our Microbial Solution site in Charleston, SC. This is a 1st shift supervisory role for our PTS production team.

The primary functions of the Production Supervisor role is to 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.

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.
Interview and select qualified non-exempt personnel. Recommend personnel actions, including hiring, promotions and raises; Partner with Human Resources and departmental management to assist in employee relations.
Identify training and development needs of direct reports; Assist in the development, implementation and delivery of departmental training programs; ensure that direct reports receive departmental orientation and necessary on-the-job training.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
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.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in life sciences or related discipline.
Experience: 4-6 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:
Other: Effective communication and interpersonal skills required. Demonstrated computer skills (data input, word processing) required.

Compensation Data

The pay range for this position is $78,000 to $85,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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.

Equal Employment Opportunity

Auxiliar Técnico Laboratorio (Tres Cantos, M, ES, 28760)

Requisitos del puesto:

Formación: ciclo formativo grado medio Técnico de laboratorio

Tareas principales a realizar:

Preparación de medios de cultivo y soluciones.
Control del stock de los medios ya preparados y su disponibilidad.
Limpieza, preparación y esterilización de material de laboratorio (material quirúrgico, tubos de ensayo, etc)
Rotulado de tubos y botellas.
Gestionar las existencias de material, realizando pedidos cuando se precisen.
Organizar y limpiar el laboratorio. Eliminar los residuos de laboratorio.
Análisis ambiental y microbiológico de las instalaciones.
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

Job Qualifications

Requisitos del puesto:

Formación: ciclo formativo grado medio Técnico de laboratorio

Tareas principales a realizar:

Preparación de medios de cultivo y soluciones.
Control del stock de los medios ya preparados y su disponibilidad.
Limpieza, preparación y esterilización de material de laboratorio (material quirúrgico, tubos de ensayo, etc)
Rotulado de tubos y botellas.
Gestionar las existencias de material, realizando pedidos cuando se precisen.
Organizar y limpiar el laboratorio. Eliminar los residuos de laboratorio.
Análisis ambiental y microbiológico de las instalaciones.

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.

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 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.

Technician I - Second Shift Toxicology (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician 1 for our Second Shift Operations at our Safety Assessment site located Mattawan, MI.

A Technician 1 – Technical Operations 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 animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, and/or biological specimen collections for analysis. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Essential Duties and Responsibilities

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 handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, and/or biological specimen collections for analysis. 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.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, 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. 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.

Equal Employment Opportunity

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

Sr. Supply Chain Coordinator (Hanover, MD, US, 21076)

Job Summary

As a Senior Supply Chain Coordinator for Charles River, your role involves efficiently managing materials to support testing and meet client demands. Responsible for updating the Supply Chain Database or any other Warehouse Management System, documenting raw material movements and contributing to the completion of raw material request and submission of purchase requisitions. Your attention to detail and analytical skills contribute to Charles River’s operational efficiency and success in delivering high-quality products. This position reports onsite to the facility director.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Support Receiving, Shipping & Purchasing operations as needed.
Analyze and manage current inventory needs and levels, replenishment schedules, and order quantities.
Maintain accurate records of inventory levels, track material consumption and generate reports to provide insights into material usage patterns and identify areas for improvement.
Contribute to Raw Material Request completion and Purchase requisition submission.
Coordinate physical material movements for the picking of material and supply to testing.
Issue materials to testing by completing goods issue to material requisitions in inventory database.
Coordinate physical material movements for the picking of material and supply to testing
Maintain accurate daily records of good receipts and shipments made.
Manages and maintains inventory system; facilities upgrade to related database and/or software under the direction of the purchasing or inventory manager.
Conduct cycle counts as needed.
Execute timely inventory adjustments.
Reconcile and conduct root cause analysis to determine reasons for needed inventory adjustments and transactions.
Ensure materials meet specifications, standards, cost-efficient, with adequate supply for testing.
Document inventory properly and communicate any issues with upper management immediately
Ensures adherence to Approved Supplier List for all cGMP purchases.
Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing samples and product for the facility.
Create and process purchase requisitions.
Process invoices for payment in ERP SAP for the facility.
Create and assign material part numbers.
Develops/updates facility specific standard operating procedures and internal policies for material movement and delivery flow activities and documentation requirements.
Establishes inventory categorization and storage locations within facility.
Support negotiations and problem resolution with internal and external customers to ensure all issues are addressed and countermeasures are implemented and tracked.
Optimize inbound freight routes and timing to achieve company/client expectations.
Monitor and report performance metrics including (but not limited to) misses associated with on-time deliveries, quality metrics, and cost (including overtime).

Job Qualifications

Bachelor’s degree required
Minimum 3 to 4 years of experience performing Enterprise Resource Planning (ERP) inventory transactions.
Enterprise Resource Planning (ERP) or Warehouse Management System (WMS) experience required; SAP preferred
4+ years working around manufacturing and warehousing environments including logistics, materials handling, inventory control, and shipping/receiving in a lead or senior position.
3 years working in a GMP environment including transacting inventory in ERP system preferred
Demonstrated attention to detail and accuracy
Experience with ERP cycle counting
Familiarity with inventory batch management
Experience with Quality System/Standard (ISO, TQM, Six Sigma) Good Manufacturing Practices (cGMP) preferred.
Experience with Scheduling International shipments and drafting of Pro Forma Invoices
Experience with revising or creating Standard Operating Procedures
Proficiency with office technology including Microsoft Office Applications (Outlook, Excel, Word)
Strong written and verbal communication skills
Ability to lift 35 pounds without assistance.
Ability to read, analyze, and interpret documentation.
Ability to work independently, with a team, and different departments to improve processes for improved performance.
Adaptable and able to work within a fast-paced, changing environment.

The pay range for this position is $64,700 - $71,500. 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 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 Staff Veterinarian (Reno, NV, US, 89511)

Job Summary

Oversee and perform veterinary procedures that support all studies. Assist the Director in oversight of the animal care and use program. May supervise or oversee veterinary staff and manage the activities of assigned section to ensure effective performance. Assist the Director in department management functions as required and serve as acting department head in Director's absence.

ESSENTIAL DUTIES AND RESPONSIBILITES:

Oversee daily animal health assessment program
Perform veterinary rounds as scheduled, and provide clinical care and preventive medicine support
May perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice to facilitate protocol development
May assist in sentinel animal monitoring and other monitoring programs
Responsible for the overall training program for veterinary technicians/staff. Ensure that training is properly documented and regularly updated as necessary
Provide animal health care guidance for veterinary services personnel as required
Ensure that internal and external applications, reports and other materials are prepared and submitted as required
Oversee responses to internal/external inspections and quality assurance audits of veterinary or animal welfare type content
Participate in the design and implementation of programs to assess vendors for animals and critical animal related suppliers. Monitor a Biosecurity program appropriate to the sites needs.
Serve as advisor to management in technical matters as they relate to the site including application of new technology, the use of alternatives, new animal models, and any changes in national policies, procedures, guidelines or regulations affecting animal care and use
Assist Director in oversight of quarantine and conditioning program which includes participation in vendor management, e.g. conducting site visits, reviewing vendor health information, communicating specific issues related to shipments to them, and tracking overall vendor performance
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
Assist Director as a consultant to Study Directors and/or sponsors regarding study design prior to IACUC submission and as part of the veterinarian review and IACUC monitoring
Ensure all study related in-life procedures and processes are accomplished in accordance with the study protocol as it relates to animal welfare and veterinary issues
Oversee long-term improvement projects such as redesign of SOPs and basic research procedures
Perform expert veterinary research support to Study Directors and Sponsors
Maintain compliance with all applicable laws and regulations including the Animal Welfare Act
Ensure that all animal care related activities are conducted in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC), United States Department of Agriculture (USDA), and Food and Drug Administration (FDA) standards and regulations
Oversee and administer the Veterinary Care Program as outlined in the AAALAC Program Description. Write updated Program for the Veterinary Care section of the AAALAC re-certification.
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 supervising employees, scheduling, personnel actions (hiring, promotions, raises), discipline, personnel development and performance monitoring

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: Veterinary degree (D.V.M./V.M.D.) or international equivalent.
Experience: Minimum of 6 years related experience in 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: Licensure to practice veterinary medicine in at least one U.S. state required.
Other: Computer literacy (Windows PC) WordPerfect and Excel. Good communication, interpersonal, and organizational skills. 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.

PREFERRED QUALIFICATIONS:

Experience: Two years supervisory/ management experience preferred.
Certification/Licensure: Ability to practice veterinary medicine in the work state highly desirable. ACLAM eligibility or accreditation is highly desired.

Compensation Data

The pay range for this position is $180,000 - $200,000 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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.

Study Coordinator I (Reno, NV, US, 89511)

Job Summary

We are seeking a Study Coordinator for our Safety Assessment site located in Reno, NV.

The following are responsibilities related to the Study Coordinator:

*Coordinate shipping or study related activities to ensure compliance with the protocol, applicable study documentation and applicable SOPs.
*Serve as lead/primary technician on assigned studies to assure activities are performed in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols or Sponsor guidance documents and company policies/practices.
*Read study protocols or Sponsor guidance documents and extract pertinent information related to required action items.
*Assist the various stakeholders in the execution of study-related activities required.
*Perform all tasks related to preparation and documentation of materials in support of sample collection, processing, management, and shipping. Includes entry of relevant information into LIMS systems or current database and may include scheduling shipments in the shipping database.
*Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
*May work in conjunction with other departments to coordinate assignments to facilitate scheduling of study-related processes on assigned studies to ensure protocol or study requirements are met.
*Prepare and review department calendars using protocols and other study documents to ensure all activities are appropriately scheduled.
*May communicate with Sponsor representatives on protocol-driven, study-related activities conducted by Pathology Services (e.g., shipment of biological samples in support of assigned studies).
*Assist in preparing responses to both internal and external quality assurance audits.
*Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).

Job Qualifications

The following are minimum qualifications related to the Study Coordnator position:

Education: High school diploma or General Education Degree (G.E.D.) required. Associate’s (A.A./A.S.) degree in a scientific field preferred.
Experience: Minimum of 3-5 years related experience, including GLP experience required, or must have demonstrated full knowledge of competencies and positive performance at 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: None.
Other: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database). Ability to work on assignments that are extremely complex in nature where independent action and a high degree of initiative are required in resolving problems and developing recommendations. Acts independently to determine processes and procedures on new assignments and may provide guidance and oversee the activities of other support personnel.

Equal Employment Opportunity

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

Maintenance Technician 2 (Sign On Bonus!) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Maintenance Technician 2 to perform routine and moderately complex daily and preventative maintenance, repair machinery, and assist in construction and refurbishment at our Production Site in Raleigh, NC.

SIGN ON BONUS UP TO $3000! (current CRL employees not eligible)

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform a wide variety of semi-skilled and skilled tasks to assist in the daily repair, preventative maintenance and construction of machinery and physical plant and expansion projects, including routine carpentry, masonry, electrical, heating/air-conditioning, plumbing, painting, mechanical and floor/wall coating installation.
Operate construction and maintenance equipment and power tools; maintain hand tools and assigned equipment; perform preventative maintenance on equipment.
Perform scheduled inspections/repairs on all facilities systems.
Examine machinery and equipment to diagnose trouble using basic mechanical tools and equipment. Disassemble machines and equipment and adjust, replace or repair broken or defective parts and pieces.
Inspect completed mechanical repairs for quality, safety, and proper operation.
Perform equipment calibration and preventative maintenance procedures as directed.
Perform supply, delivery, distribution, and acquisition tasks as directed.
May perform waste vacuum maintenance.
Participate in snow removal and ice remediation activities such as shoveling and spreading de- icing agents on walkways and parking lots, where site weather conditions necessitate.
Assist in moving office contents within site, including furniture, files, etc. as needed.
Maintain accurate records of maintenance repairs and services.
Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation.
May provide guidance to less experienced/skilled utility workers.
May operate yard equipment such as forklift and pickup truck including attaching and removing equipment such as snowplow blade.
Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

High school diploma or General Education Degree (G.E.D.)
Valid Drivers License
3+ years of experience in general building maintenance with mechanical, industrial, and construction background.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms.
The employee is occasionally required to stoop, kneel, crouch, or crawl and talk or hear.
The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move more than 100 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.

The pay range for this position is $23.00 - $30.00 / 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Behavioral Management Technician II (Frederick, MD, US, 21701)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Provide 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.

· Observe animals and report behavioral abnormalities.

· Assist in performing behavioral assessments in response to reports of behavioral abnormalities.

· Work with other departments to coordinate 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.

· Order fruit, enrichment foodstuffs and enrichment devices for the animals.

· Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.

· Research and review current literature regarding animal behavior and environmental enrichment as assigned.

· 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.

Job Qualifications

· Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.

· Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment or must have fully satisfied technical and experience requirements for the previous level. 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.

· Certification/Licensure: AALAS certification at the LAT level strongly preferred.

· Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in 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 required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet and database programs.

The pay range for this position is $31-$36/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

Equal Employment Opportunity

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

Assistant vétérinaire - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Au sein du département Vétérinaires, vous aurez pour objectif d'assurer le support aux Vétérinaires Cliniciens, dans le respect des réglementations.

Les missions

Agir en tant qu'accueil du service et hierarchiser les demandes pour optimiser les visites vétérinaires, en fonction des urgences,
Assurer les soins des animaux aux côtés du vétérinaire,
Réaliser les visites de suivis,
Participer à différents projets en soutien de l'équipe vétérinaire (amélioration des process, commandes, gestion des salles d'opérations),
Gérer la pharmacie des médicaments vétérinaires,
Maintenir le respect de la documentation et des données acquises, en appliquant rigouresement les procédures réglementaires.

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 dans le domaine des soins vétérinaires.

Vous possédez une première expérience sur ce type de poste, idéalement en CRO.

Vous êtes reconnu(e) pour votre organisation, votre assiduité et votre esprit d'équipe.

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.

Senior BI & Data Analyst (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

Senior BI & Data Analyst

We are seeking an experienced Senior Business Intelligence (BI) & Data Analyst for our Enterprise Data Analytics Team.

There’s never been a more exciting time to be on the Enterprise Data Analytics team at Charles River Labs! We are on a mission to make the Enterprise Data Analytics team the backbone of today’s business, as data-driven decision-making enables business leaders to make informed choices quickly to boost revenue, improve productivity, and stay a step ahead of the market. We have already launched our own Enterprise Data Hub, the digital backbone of this company, and we need more experts and leaders in the data analytics discipline who are forward-thinking, self-guided, and innovative to continue to build out the hub across our lines of business, integrating all of our data, mastering data and focusing on data quality to fundamentally shift the way Charles River operates through data science and advanced analytics.

You will be joining a team with an unyielding dedication to the company's purpose; Together We Create Healthier Lives. This laser focus on the patient makes the broader Global Technology Team so exciting. We are taking Charles River to a place where the Enterprise Data Analytics team will be applying the techniques of AI, Generative BI, data management, data engineering, and strategy development, as well as the use of analytics techniques that range from forecasting and simulation to linear programming and optimization and we want you to join us.

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.

Responsibilities:

• Engage Business Stakeholders at all levels to identify requirements for current and future products through ongoing interaction
• Data Profiling, mining, and data validation to ensure data is fit for use by the business
• Ability to see the big picture and then identify key areas for deep analysis to support sound solutions
• Perform ad-hoc analysis and present results in a clear and user-friendly manner
• Perform testing, resolve issues, and work with developers to automate testing/data validation
• Design and create analytics solutions utilizing Power-BI and Copilot
• Lead requirements workshops and User Acceptance Testing for new data and analytics solutions
• Build strong business relationships that foster a collaborative and trusting approach and partnership
• Act as scrum master for the team and prepare detailed stories for developers.

Job Qualifications:

• Bachelor’s degree in Business Management, Computer Science (or related field), MBA Preferred
• 3+ years of experience with Data Visualization tools such as Power BI, SSRS, or Tableau
• 1-2 years of experience with data analysis and profiling for Data Science Modelling
• 5+ years of experience in writing SQL queries, data mining, data profiling, and data validation/testing
• 5+ years of experience as a Business Systems Analyst / Data Analyst specializing in the Data & Analytics discipline
• Experienced in Microsoft Fabric and Copilot Power BI components
• 5+ years of experience organizing and running User Acceptance Testing cycles and training with business users and stakeholders
• Strong business mindset with an ability to collaborate with business partners to identify needs and opportunities for improved data management and delivery.

Previous experience in the Life Sciences Industry is required

Equal Employment Opportunity

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

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

Data 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

There has never been a more exciting time to be part of the Enterprise Data Analytics team at Charles River Labs. We are on a mission to position data as the core driver of our business, empowering leaders to make informed, data-driven decisions that accelerate revenue, enhance productivity, and keep us ahead of the competition. Our recently launched Enterprise Data Hub serves as the company's digital backbone, and we are looking for visionary people in data analytics to help us further expand and refine this hub.

Your role will be key in integrating, mastering, and ensuring the quality of our data across all business functions, ultimately transforming how Charles River operates through data science and advanced analytics. You will be joining a team that is deeply committed to our purpose: Together We Create Healthier Lives. This unwavering focus on patients makes our global technology team uniquely inspiring. As we look to the future, we reimagine how we do business through our Digital Journey.

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 Qualifications:

•    Bachelor’s degree in computer engineering, Computer Science, or a related discipline (Master’s degree preferred)
•    3+ years of experience in ETL design, development, and performance tuning using the Microsoft BI Stack in a multi-dimensional data warehousing environment.
•    3+ years of advanced SQL programming expertise (PL/SQL, T-SQL)
•    1+ years of experience in Enterprise Data & Analytics solution architecture
•    1+ years of experience in Python Programming
•    1+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions.
•    1+ years of experience with key Azure services: Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps, and Functions.

Preferred Skills:

•    Experience with Big Data technologies, such as Hadoop, Sqoop, Hive, Kafka, Spark, Pyspark, Python, Scala, or Pig
•    Experience managing both relational and non-relational data using Big Data Management (BDM) techniques (formats like JSON, XML, Avro, Parquet, etc.)
•    Experience setting up and operating data pipelines using Python or SQL
•    Familiarity with DevOps processes (CI/CD) and infrastructure as code
•    Knowledge of Master Data Management (MDM) and Data Quality tools
•    Experience developing REST APIs using Java Spring Boot
•    Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming)
•    Experience in data and analytics within the Life Sciences industry is a plus.

Equal Employment Opportunity

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

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

Senior Data 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

This journey is central to advancing our position in the market, unlocking new growth opportunities, and positioning us as a leading, digitally powered Contract Research Organization (CRO) that enables our clients to deliver innovative, safe, and effective treatments to patients faster and more efficiently than ever before.

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 Qualifications:

•   Bachelor’s degree in computer engineering, Computer Science, or a related discipline (Master’s degree preferred)
•   7+ years of experience in ETL design, development, and performance tuning using the Microsoft BI Stack in a multi-dimensional data warehousing environment.
•   7+ years of advanced SQL programming expertise (PL/SQL, T-SQL)
•   5+ years of experience in Enterprise Data & Analytics solution architecture
•   3+ years of experience in Python Programming
•   3+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions.
•   3+ years of experience with key Azure services: Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps, and Functions
•   2+ years of experience designing data models aligning with business requirements and analytics needs.

Preferred Skills:

•   2+ years of experience with Big Data technologies, such as Hadoop, Sqoop, Hive, Kafka, Spark, Pyspark, Python, Scala, or Pig
•   2+ years of experience managing both relational and non-relational data using Big Data Management (BDM) techniques (formats like JSON, XML, Avro, Parquet, etc.)
•   2+ years of experience setting up and operating data pipelines using Python or SQL
•   Familiarity with DevOps processes (CI/CD) and infrastructure as code
•   Knowledge of Master Data Management (MDM) and Data Quality tools
•   Experience developing REST APIs using Java Spring Boot
•   Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming)
•   Experience with API integrations (RESTful, SOAP) for both internal and external systems to enhance data flow and automation.
•   Experience in data and analytics within the Life Sciences industry is a plus.

Equal Employment Opportunity

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

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

Relief Veterinarian (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

The Relief (Clinical) Veterinarian is a flexible schedule based on scope of work up to full-time. This role is 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.

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.
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.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment.
May assist in sentinel animal monitoring and other monitoring programs.
Review 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.
Perform special projects and assist with administrative efforts as needed.

Job Qualifications

Education: Veterinary degree (D.V.M./V.M.D.) required.
Experience: Zero plus years related experience with animal care and surgical techniques. Strong preference for experience in a research/lab animal/GLP environment.
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 Data

The pay range for this position is $120/hour - $150/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

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.

Cagewash Technician (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Poolesville, MD.

Why work at Charles River?

We offer an excellent onboarding program for our new employees, internal career development, and competitive benefits.

What you will do!

In this role, 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:

Operates equipment and uses supplies according to safety guidelines; performs general housekeeping and adheres to safety procedures.
Sanitizes, maintains, and repairs caging materials as needed. Maintains cagewash and animal holding facilities in a clean and organized manner, in adherence with all SOP and facility requirements.
Disposes of waste materials in a safe and thorough manner as required.
Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Assists with the receipt, stocking and maintenance of supply inventories.
Assist with animal care activities to include, but not limited to; animal health observations, cage cleaning, water/feed checks, providing water/feed/enrichment.
Prepares and submits required written records, charts, logs and inventories.
Actively interacts with customers as required to resolve customer requests, inquiries, and complaints and to provide technical assistance.
Maintains consistent practice of general company and safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances. Performs all duties in compliance with local, state, and federal regulations.

Job Qualifications

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

Education: High school diploma or general education degree (GED) preferred.
Experience: Experience and/or training working with mechanical equipment preferred.
Certification/Licensure: none required.

The pay rate for this position is $20 USD per hour. 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 supported the development of ~85% of the drugs approved by the FDA in 2018.

Equal Employment Opportunity

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

Soigneur animalier / Assistant vétérinaire - F/H - Missions temporaires (Paris, FR)

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.

Notre société, de dimension internationale, partenaire de l’industrie pharmaceutique, est leader dans la vente de produits et services précliniques.

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.

Au sein de plusieurs animaleries de laboratoire, implantées dans plusieurs départements, principale à Paris et Marseille (75, 91, 92, 13, 34, 33), nous recherchons des Animaliers / ASV - F/H pour renforcer nos équipes dans le cadre de missions intérimaires de remplacement de courte durée.

Missions principales

Réception des animaux (rongeurs)

Vérification des animaux à l’arrivée
Installation des animaux dans les cages
Etiquetage des cages, suivi journalier des mouvements de cages et de leur nombre

Entretien et soins des animaux

Observation des animaux et vérification de l’état clinique, application du programme d’enrichissement
Distribution de l’aliment, vérification de l’abreuvement
Préparation des animaux et du matériel (cages, biberons, couvercles) pour les transferts
Opérations de change des litières et nettoyage des cages, distribution de l’alimentation et de la boisson

Entretien du matériel et des locaux

Désinfection du matériel et des produits
Nettoyage des locaux en respectant les règles de prophylaxie et de biosécurité

Votre profil

De formation ASV ou équivalent, vous possédez une expérience dans ce domaine ou dans une activité en lien avec les rongeurs.
Vous aimez les animaux, êtes rigoureux, autonome et assidu(e) et appréciez le travail en équipe.

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.

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

Veterinary Technician Assistant I (Reno, NV, US, 89511)

Job Summary

We are seeking a Veterinary Technician Assistant for our Safety Assessment site located in Reno, Nevada.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases In addition, this individual will may also perform technical in-life procedures.

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: High School Diploma or G.E.D.
Experience: 1-2 years related experience in a laboratory animal facility. related experience working with animals in pre-clinical laboratory or clinical setting; experience working with 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.
Certification/Licensure: ALAT preferred
Other: None.

PREFERRED QUALIFICATIONS:

LVT license or CVT/RVT certification.
AALAS certification.

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

Equal Employment Opportunity

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

Expert en Pharmacologie de Sécurité - F/H- CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Au sein du Département de Toxicologie, agir en tant qu’Expert de la pharmacologie de sécurité auprès de nos équipes et de nos clients, auprès du site d’Evreux et de Lyon.

Les missions

En tant qu’Expert Scientifique :

-   Agir comme un mentor auprès de l’équipe de Directeurs d’études, et assurer de la formation,
-   Participer à la rédaction d’articles, de posters, intervenir lors de congrès,
-   Conseiller nos clients sur les aspects scientifiques.

En tant que Directeur d’Etudes :

- Être responsable de la rédaction des plans d’études et modifications qui peuvent y être apportées,
-   Assurer le suivi, le respect du plan, en lien avec les services qui sont concernés. Apporter des corrections sur certaines procédures si besoin,
-   Veiller à la bonne réception et enregistrement des données d’études,
-   Réaliser l’interprétation des résultats et rédiger le rapport d’études,
-   Maintenir le lien avec le client pendant tout le suivi de l’étude,
-   Dans le cas d’études multisites, assurer le lien avec les différents services et responsables impactés (Pourra être nommé Responsable Principal d’Essai dans le cas d’études multisites).

Qualifications souhaitées

Vous êtes titulaire d’un Doctorat en Pharmacologie et avez idéalement 5 années d’expérience en pharmacologie de sécurité ou en toxicologie.
Avoir travaillé sur des études cardiovasculaires serait un atout pour ce poste.
Vous êtes bilingue en anglais, à l’écrit comme à l’oral.
Vous êtes reconnu pour votre relationnel, notamment clients ainsi que votre capacité de gestion de crises.

Modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 7
•   Contrat : Cadre forfait jours
•   Salaire : A compter de 50 000 € bruts / an sur 13 mois
•   Prise en charge de la mutuelle à 100%, restaurant d’entreprise, CSE
•   Primes de transport, d’intéressement/participation, accord de télétravail,...
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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.
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.

Spécialiste Senior en Santé et Sécurité (Laval, Quebec, CA, H7V 4B3)

Sommaire du Poste

Nous sommes à la recherche d'un.e Spécialiste en Santé et Sécurité d'expérience pour notre site de Laval (QC).

Dans ce poste, les principales responsabilités incluront:

Être un agent mobilisateur de changement, assurer un leadership interactif et pratique pour assurer la transformation de la culture S&S;
Participer à la standardisation des programmes et procédures en s'assurant du respect des lois, normes et standards des autorités gouvernementales locales et des directives corporatives ;
Collaborer à l'élaboration et à la présentation de formations S&S pour le personnel de la région;
Aider au développement des communications et des présentations S&S;
Soutenir le processus d'enquête et d'analyse des incidents afin d'identifier les causes profondes, les actions correctives et les suivis;
Réaliser/participer à des analyses de risques, recommander des mesures d'atténuation des risques appropriées et assurer la mise en place de méthodes de travail sécuritaires (approche pratique/à la base);
Participer aux comités/gouvernances Santé & Sécurité;
Classer les différents rapports et fournir des statistiques et des résultats de performance en santé et sécurité;
Améliorer le niveau d'excellence et de performance des programmes S&S du site.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Un minimum de 5 à 10 ans d'expérience en tant que spécialiste en santé et sécurité ;
Baccalauréat ou certificat en santé et sécurité;
Excellentes habiletés interpersonnelles, diplomatie, travail d'équipe et esprit de collaboration;
Autonomie et souci du détail;
Bilingue (anglais et français, écrit et parlé).

Informations spécifiques au poste:

Localisation: 445 Boul.Armand-Frappier,Laval, Québec H7V 4B3
Horaire: Lundi au Vendredi

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;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 10 jours personnels;
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.

Operaio stabularista - Firenze (Roma, IT, 00 100)

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

Attività aviaria

La nostra attività aviaria offre a ricercatori e produttori di vaccini la sicurezza che deriva dalla consapevolezza che i materiali impiegati per il loro processo di produzione sono esenti da agenti estranei. Charles River ha stabilito procedure per la manipolazione degli uccelli e la produzione di uova che hanno fissato lo standard d’industria a livello mondiale.

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 stabularista - Firenze (Roma, IT, 00 100)

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 nostro cliente sito in Firenze ricerchiamo uno stabularista.

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

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time e trasferta a Milano per un periodo iniziale di training

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

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.

Senior Health & Safety Specialist (Laval, Quebec, CA, H7V 4B3)

Job Summary

We are seeking an experienced Health and Safety Specialist for our Laval (QC) location.

In this role, primary responsibilities include:

Be a mobilizing agent of change, provide interactive and practical leadership to ensure the transformation of the H & S culture;
Participate in the standardization of programs and procedures by ensuring compliance with the laws, norms and standards of local government authorities and corporate directives;
Collaborate in the development and delivery of H & S training for staff in the region;
Assist in the development of H & S communications and presentations;
Support the incident investigation and analysis process in order to identify root causes, corrective actions and follow-ups;
Carry out / participate in risk analyses, recommend appropriate risk mitigation measures and ensure the implementation of safe work methods (hands-on / ground-up approach);
Participate in the Health & Safety committees/governances;
File the different reports and provide statistics and performance results on health and safety;
Improve the level of excellence and performance of the site's H & S programs;
Perform any other related tasks, as assigned.

Key Elements

We are looking for the following minimum qualifications for this role

A minimum 5-10 years experience as a Health and Safety Specialist;
Bachelor’s degree or Certificate in Health and Safety;
Excellent interpersonal skills, diplomacy, teamwork and collaborative spirit;
Autonomy and attention to detail;
Bilingual (English & French, Written & Spoken).

Role Specific Information:

Location: 445 Boul.Armand-Frappier, Laval, Québec H7V 4B3
Schedule: Monday to Friday

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;
Access to a doctor and various health professionals (telemedicine);
3 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Research Analyst I -Formulations 1 (Reno, NV, US, 89511)

Job Summary

***note this position is Sunday-Thursday 8-5pm"

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.

Equal Employment Opportunity

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

Technician in Clinical Laboratories (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Technician – Clinical Laboratories

As a Technician for our Clinical Laboratories team at the Senneville location, you will perform technical activities and follows directives from the study/phase plan and the SOP.

In this role, primary responsibilities include:

Perform the preparation and the analysis of samples;
Perform the quality control procedure and maintenances on the different instruments;
Perform the activities in a timely fashion by adhering to preset schedules;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules.

Key Elements

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

College diploma in science;
Relevant experience is an asset;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Reading and writing English is required. Bilingualism is preferred;
Ability to work under time constraint and adapt to change;
Demonstrate flexibility and ability to work independently.

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: 20$/per hour, evening premiums and opportunity to start at higher level and higher salary with specific research experience;
Schedule: Monday to Friday (3h PM-11h15PM) after 3-6 months of training from (8h AM-4h15 PM);
Annual bonus based on performance;
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.

Competencies

Equal Employment Opportunity

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

Technicien.ne en Laboratoires Cliniques (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Technicien.ne – Laboratoires cliniques

En tant que Technicien.ne pour notre équipe de Laboratoires cliniques située au site de Senneville, vous devrez accomplir les tâches techniques et suivre les directives des plans d’étude/phase et des PNO.

Dans ce poste, les principales responsabilités incluront:

Effectue les préparations ainsi que les analyses des échantillons;
Effectue le control de qualité ainsi que les maintenances sur les différents instruments;
Accomplis les activités en temps opportun en suivant les horaires établis;
Assure l’intégrité des études et satisfait les exigences des agences réglementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de Laboratoires (BPL), aux Procédures Normalisées d’Opération (PNO) et aux règles de santé sécurité.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études collégiales en sciences;
Une expérience connexe est un atout;
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;
Avoir la capacité de travailler sous la contrainte de temps et de s'adapter aux changements;
Lire et écrire en anglais est requis. Le bilinguisme est préférable;
Faire preuve de flexibilité et être capable de travailler de manière autonome.

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: 20$/hrs avec prime de soir et possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de 3h PM à 11h15 PM après la formation de 3 à 6 mois de 8 AM à 4h15 PM;
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.

Scientifique de recherche - Immunogénicité (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique de recherche pour notre équipe d’Immunogénicité située au site de Senneville, vous agirez en tant que chercheur principal responsable de la conception, de la réalisation et du rapport des études en sciences de laboratoire de manière efficace, rentable et avec la meilleure qualité scientifique.

Dans ce poste, les principales responsabilités incluront:

Concevoir, rédiger, revoir et modifier des plans d'études, des amendements et des calendriers d'études qui définissent et planifient toutes les activités d'études;
Superviser et coordonner tous les aspects des procédures de Sciences de laboratoire liées à l'étude;
Rédiger, revoir et modifier des rapports préliminaires et/ou finaux des scientifiques contributeurs qui documentent toutes les procédures et résultats liés à l'étude;
Assurer l'exactitude et l'exhaustivité des estimations de coûts du projet;
Réviser et approuver les données brutes.

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 ans d'expérience dans un poste Scientifique;
Doctorat en Immunologie ou dans toute discipline biologique connexe;
Expérience dans le développement et l'optimisation d'essais de liaison de ligand (ELISAs, ECLs) et/ou d'essais basés sur des cellules;
Expérience de travail dans un environnement de bonnes pratiques de laboratoire (BPL) est un atout;
Capacité à travailler sous contraintes de temps et à s'adapter au changement;
Bonnes compétences en résolution de problèmes;
Excellentes compétences interpersonnelles et de communication;
Capacité à diriger le travail dans un environnement 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 ;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour;
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.

Research Scientist - Immunogenicity (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Research Scientist for our Immunogenicity team at the Senneville location, you will serve as a Principal Investigator responsible for the design, conduct and reporting of Laboratory Science 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;
Write, review and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
Ensure the accuracy and completeness of project cost estimates;
Review and approve raw data.

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 years’ experience working in a Scientific position;
PhD in Immunology or any biological related discipline;
Experience in the development, optimization of Ligand Binding assays (ELISAs, ECLs) and/or cell based assays;
Experience working in a Good Laboratory Practices (GLP) environment is an asset;
Ability to work under time constraints and adapt to change;
Good problem-solving skills;
Strong interpersonal and communication skills;
Ability to lead 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 station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime schedule;
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.

Equal Employment Opportunity

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

Director, Microbiology and Sterility Assurance (Memphis, TN, US, 38118)

Job Summary

The Director Microbiology and Sterility Assurance be responsible for all strategy, process, compliance, and execution of critical activities to assure sterile processes, controlled environments, and biocontamination controls are maintained for the site. This includes but is not limited to: sterility assurance, environmental monitoring of the faciity, quality control microbial testing, utility monitoring, and site contamination control strategy. This position reports to the Site Head of Quality for the Memphis site. This person will be responsible to partner with Global Quality stakeholders for development, implementation, and continuous improvement of microbial control and sterility assurance standards. The person filling this role will be responsible for the leadership, development and training of team members within their oversight as well as providing supportive leadership and strategic direction to operate with and maintain compliance to regulatory and industry quality standards in support of existing and new cellular therapy production.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Responsible for microbiological testing and monitoring functions to support the manufacturing and release of products within the Memphis Laboratories. Ensure that these activities are timely, efficient and productive while adhering to client’s requirements and operational and quality parameters.
• Will liaise with the Manufacturing, Quality Assurance, Supply Chain, Project Management, Facilities, and other GMP Quality Control units to ensure contamination control and sterility assurance standards are maintained across all site operations.
• Preparation of Revenue and Capex Budget as per spent analysis project. Ensure financial prudence in resource planning, allocation and manage within approved budgets while building best in class quality processes and systems at site.
• Maintain quality system controls for area of oversight to ensure no critical and major market complaints or audit findings.
• Ensure that all statutory and regulatory compliance standards are regularly monitored and in a state of compliance for area of oversight, as applicable.
• Responsibile to oversee all PQ requirements for Environment and Utilities systems as well as routine monitoring and trending of systems.
• Take appropriate steps to reduce waste and losses in the microbiology and contamination control processes and improve efficiency in ways of working.
• Ensure timely sampling, analysis, release and trending of environmental and utility system samples.
• Ensure completion and adherence to training of subordinates in area of oversight as per the job requirement.
• Provide leadership to and ensure necessary Quality oversight to areas within span of control.
• Effectively model, demonstrate and live an employee-focused leadership style that prioritizes compliance, respectful and professional cross departmental collaboration, accountability, and the well-being, personal, and career development of each employee.
• Effectively model, demonstrate and live the Charles River core values of Care, Lead, Own, and Collaborate
• Lead, coach and mentor individuals from all parts of the organization with varying levels of experience. Be a valued resource for the site in all matters related quality and compliance.
• Perform all other related duties as assigned.

Job Qualifications

• Minimum Bachelors degree in life sciences or related field. An advanced degree in the life sciences is preferred, but not essential, based on experience
• Minimum 10 years of experience in a biologics, pharmaceutical, medical device, or related industry.
• Minimum 5 years as a Leader with direct reports
• ISO Lead Auditor training, desirable.
• Certified Quality Engineer (ASQ), desirable
• Experience working in a GMP Biologics environment required.
• Experience preferred with a CDMO business and/or gene-modification modalities, cell-based gene therapies, and strong scientific background in QC testing required for such products.
• Complete competency with electronic document managements systems and other information management systems (QMS, ERP, LIMS,MES etc)
• Familiarity preferred with applicable regulatory requirements and compendia concerning cGMP manufacturing and testing of human cells (21CFR210, 211, 820 and 1271; Eudralex, USP, EP and ICH).
• Understanding of analytical method qualification and validation per USP, EP and ICH guidelines.
• Ability to maintain a high degree of accuracy and attention to detail.
• Ability to handle a fast-paced, multi-tasking environment, and prioritize effectively.
• Outstanding verbal and written communication skills.
• Proficiency in Microsoft Office (Word, Excel, Outlook, etc.) is essential.

The pay range for this position is $176,500 - $207,680. Please note that salaries vary within the range based on factors but not limited to experience, skills, education and location.

Equal Employment Opportunity

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

Cagewash Attendant I (14BS) (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.

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.

Equal Employment Opportunity

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

Equal Employment Opportunity

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

Animal Caretaker - contratto a chiamata (AVIANO) (Aviano, IT, 33081)

Job Summary

Per nostro cliente sito ad Aviano 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 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

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro a chiamata in settimana e 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.

Animal Caretaker - contratto a chiamata (AVIANO) (Aviano, IT, 33081)

Riepilogo del lavoro

Di cosa si occupa la Charles River

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

Commis au lave-cage (Laval, Quebec, CA, H7V 4B3)

Sommaire de l’emploi

En tant que Commis au lave-cage pour notre équipe de Toxicologie à notre site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche en gardant leur habitation propre. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Faire fonctionner et effectuer les vérifications quotidiennes des lave-cages;
Surveiller l’utilisation des savons et les différents besoins des lave-cages;
Nettoyer tous types d’habitation d’animaux ainsi que leurs accessoires;
Effectuer l’entretien de base et les réparations mineures sur toutes les cages et accessoires afin de s’assurer que tout est sécuritaire pour les animaux;
Au besoin, effectuer des tâches de manutention dans le vivarium.

Éléments clés

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

Posséder un bon esprit d’équipe;
Polyvalence;
Bonnes aptitudes de communication et d’observation;
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 : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport : Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : 18.25$/hrs;
Primes : Soirée (2.50$), fin de semaine (2.75$), heure supplémentaire (temps et demi), fériés (temps double);
Bonus annuel basé sur la performance;
Horaire : Horaire flexible, vous devez être disponible de jour et de soir. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaires ainsi que des fins de semaine;
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 & 5 jours de congé personnel/maladie par année;
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.

Cage-Wash Clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Cage-Wash Clerk for our Toxicology team located in Laval, you will be responsible for the well-being of our laboratory animals by keeping their living space clean. 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:

Operate and perform daily checks on cage washer machines;
Monitor the use of soap and various needs of the cage washers;
Clean all type of animal housing and accessories;
Perform basic maintenance and minor repairs on cages and accessories;
Perform manutention tasks in the vivarium as required.

Key Elements

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

Be a good team player;
Polyvalence;
Good observations and communications skills;
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: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $18.25/hrs;
Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
Annual bonus based on performance plan;
Schedule: Flexible schedule, you must be available days and evenings. Depending on the needs, you may have to do overtime and weekends;
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/Sick day 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.

Equal Employment Opportunity

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

Supervisor QC Operations (Memphis, TN, US, 38118)

Job Summary

This is a leadership role that is responsible for a team of Quality Operations Specialist, 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 group 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.
• Prepare lot packages for disposition by management
• 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 MasterControl
• 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
• 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)

The pay range for this position is $ 85,900 - $96,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Compensation Data

Equal Employment Opportunity

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

Animal Packer (Kingston, NY, US, 12401)

Job Summary

We are seeking an Animal Packer to join our team at our Production facility at our Stone Ridge, NY location.

Work schedule: Monday 5:30 am to 3:30 pm, Tuesday and Wednesday, 6:00 am to 3:30 pm, Thursday, 6:00 am to 2:30pm. Friday and Sunday will be a 4 hour shift, on a rotational basis.

This is a temp to perm opportunity.

Benefits include: Paid sick time / Volunteer paid time / 401K Participation

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Pack and ship containers per standard operating procedures according to appropriate packing/shipping documentation.
Complete paperwork related to packing and shipping.
Unload delivery trucks and place supplies in appropriate areas.
Operate fork lift to transport supplies within the warehouse area.
Prepare and submit written records, charts, logs and inventories as requested.
Perform physical environment housekeeping and sanitizing of all support work areas.
Perform humane chemical and physical euthanasia in accordance with the Guide for Care and Use of Laboratory Animals, the AVMA Guide on Euthanasia, and under the direction of the attending veterinarian, or designee.
Check live traps each weekday morning and report all findings in accordance with site biosecurity procedures.
Perform research model production activities as needed.
May provide other support services, including materials delivery and housekeeping, as assigned.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

Must have a valid driver's license
No experience necessary, we will train you.

PREFERRED QUALIFICATIONS:

One to two years of related experience.
One to two years warehouse or stockroom experience.
Forklift experience.

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.

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

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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Animal Technician I (Stilwell, KS, US, 66085)

Job Summary

Charles River Laboratories (CRL) is seeking an Animal Technician to join our Integrated Toxicology (ITox) team at the Kansas City (CR-KAN) Site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join, you will have a significant impact on the health and well-being of people across the globe. The technician is learning basic skills required to conduct a study, which include animal husbandry needs, animal handling/restraint, housing maintenance, feeding procedures; collecting data, observing the animals for health status, body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals, using gentle and positive human-animal interactions.
Perform basic skills of the department including animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. 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 pay range for this position is $20/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, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required. Experience working with/around animals is preferred. Experience in a role requiring physical labor a plus.
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 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 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:

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.

COMMENTS:

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

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

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

Executive Director DSA Commercial Finance (Remote) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

The Executive Director DSA Commercial Finance is accountable for establishing sustainable and accurate forecasting and reporting, STRAT, budget development and delivery, and financial analysis, in addition to providing financial leadership, direction, and advice to the DSA Commercial team. The role requires leadership, strategic mindset, team performance management, along with strong influencing and negotiating skills.

In this role, primary responsibilities include:

Build, develop and lead a high-performing team.
Focus on customer centricity and work closely with internal business partners, providing financial expertise and value-added services to support them in achieving their objectives.
Initiate and maintain positive business partnerships and collaboration across operations, business finance and corporate accounting teams.
Ensure data integrity and quality in both internal and external reporting/analysis.
Drive the development of management reporting and planning systems and tools.
Promote standardization and simplification.

Commercial Finance

Partner in developing and implementing commercial strategies, ensuring alignment with overall business and financial strategies.
Work alongside the commercial team, supporting and advising strategic and operational decision making resulting in better business performance.
Interpret, explain and drive performance in the industry, competitor and economic context.
Support and influence key commercial and strategic decisions.
Advise on key commercial planning opportunities.
Perform commercial analytics, such as pricing, customer segmentation, service line profitability and price/volume/mix.
Prepare and present financials and key indicators for business reviews, management reporting, budget and strategic planning.
Prepare analysis of monthly, quarterly and annual financials compared to forecast, budget and prior year, including market impacts, currency fluctuations, etc.
Perform complex analyses including year-to-year comparisons and margins on new services for forecasting and pricing purposes.
Analyze appropriate key performance indicators optimally to improve commercial performance.

Job Qualifications

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

Bachelor’s degree (B.A./B.S.) or equivalent required.
20+ years related experience in accounting or finance, with a minimum of 10 years’ experience in financial analysis.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MBA, CPA or CMA designation preferred.
Comprehensive understanding of operational, sales and financial issues for business unit required.
This position may require domestic and international travel.

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.

Animal Care Taker (Dingcheng Hainan , CN)

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

关于安全评估
Charles River致力于帮助我们的合作伙伴加快临床前药物开发，我们提供卓越的安全评估服务、先进的设施和专家监管指导。从单独的专业毒理学研究和试验性新药（IND）相关研究，到定制的服务组合和全套实验室支持，我们经验丰富的团队可以设计和执行相应计划，能够预期可能遇到的挑战并避免问题，以协助您顺利、高效地将药物推向市场。我们的安全评估设施每年都开展大约300项试验性新药（IND）计划。

欲了解更多信息，请访问www.criver.com。

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

Job Summary

We are seeking a Technician I for our Necropsy 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 animal handling, euthanasia and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. 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, euthanasia and sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions . 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.

The pay for this position is $19/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:

Education: High school diploma or General Education Degree (G.E.D.) preferred. Associates degree (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.

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.

Research Analyst I -Bioanalytical Sciences 1 (Reno, NV, US, 89511)

Job Summary

We are seeking a Research Analyst I for our Safety Assessment site located in Reno, NV.

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.

Equal Employment Opportunity

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

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

Job Summary

Responsible for managing the Environmental, Health & Safety (EH&S) Program for adherence to local, state, and federal regulations at CRADL facilities. Assist in program development unique to CRADL facilities, staff and client needs and participate in growing site expansion portfolio for the CRADL business. Provide EHS&S support for NY RMS Production Model site as needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Establish, administer, and update specific EH&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 and CRADL clients as required and advise management on safety and environmental issues. Review new regulatory standards and make compliance recommendations.
• Inspect the facilities for compliance with OSHA and EPA regulations as applicable. Recommend solutions to management that address deficiencies in EH&S compliance.
• Periodic observations of CRADL clients performing work with hazards to ensure post-IACUC approval compliance. Liaise with clients for work consultations and recommendations for studies.
• Implement and maintain EH&S programs and metrics.
• Perform documented risk assessments for the CRADL business.
• Oversee maintenance of group training manual, in-person training, and training records for CRADL clients and staff.
• Develop and ensure adherence to pertinent regulatory requirements and to departmental policies, practices, and procedures (SOPs, safety procedures, biosafety protocols, biohazard, and medical waste).
• Serve as an EHS pre-reviewer for all CRADL IACUC protocols.
• Assist in CRADL AAALAC Accreditation process for all existing and new sites.
• 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 EH&S Emergency Coordinator for 24-hour incident response.
• 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 EH&S issues to all staff.
• Available to clients and federal and state investigators to explain procedures and produce written documentation as proof of compliance.
• Manage and maintain necessary facility permit, licenses, and compliance reports to federal, local, and state regulatory authorities for all CRADL sites and ensure new sites are permitted and in compliance appropriate for the region.
• Assist in the basis of design of new CRADL facilities including but not limited to, oxygen depletion assessments, monitoring and alarm requirements for hazardous gases, and waste systems.
• Coordinate communications to regulatory agencies and client inspections on EH&S related matters.
• May assist in development of departmental budget.
• Support the policy of equal employment opportunity through affirmative action in personnel actions.
• Attend and participate in on-the-job and classroom training sessions and complete all assigned computer-based safety and professional development training by predetermined due dates.
• Maintain required attendance level and adherence to work schedule in accordance with required staffing levels to ensure that assigned duties are completed.
• Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in Environmental Science, Environmental Engineering, or related discipline.
Experience: Minimum of four (4) years related experience in Environmental Health & Safety. Experience supporting laboratory animal facilities preferred. Experience in multiple state regulations, including Massachusetts, preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

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.

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

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

Sommaire de l'emploi

Emploi étudiant - 15hrs par semaine lors de la période scolaire et 40hrs par semaine cet été

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:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux avec soins.

Éléments clés

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

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 : Tous les samedis et dimanches, horaire entre 6h00 et 14h15;
Poste temps partiel, 15 heures par semaine – 40hrs par semaine cet été.

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.

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

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

Job Summary

Student job - 15hrs per week during school term and 40hrs per week this summer

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:

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:

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: Saturday and Sunday, schedule between 6:00 am to 2:15 pm;
Part-time position, 15 hours per week – 40hrs per week this summer.

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.

Equal Employment Opportunity

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

Directeur.trice exécutif.tive - DSA Financement des entreprises commerciales (Télétravail) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que directeur.trice exécutif.tive - DSA Financement des entreprises commerciales vous serez responsable de l’établissement de prévisions et de rapports durables et précis, des stratégies, de l’élaboration et de la livraison du budget et de l’analyse financière. En plus de fournir un leadership financier, de l'orientation et des conseils à l’équipe commerciale de DSA. Le rôle exige du leadership, un état d’esprit stratégique, la gestion du rendement de l’équipe, ainsi que de solides compétences en matière d’influence et de négociation.

Dans ce poste, les responsabilités principales incluront:

Bâtir, développer et diriger une équipe performante.
Se concentrer sur l’orientation client et travailler en étroite collaboration avec les partenaires commerciaux internes, en leur fournissant une expertise financière et des services à valeur ajoutée pour les aider à atteindre leurs objectifs.
Initier et maintenir des partenariats d’affaires positifs et une collaboration entre les équipes des opérations, des finances d’entreprise et de la comptabilité d’entreprise.
Garantir l’intégrité et la qualité des données dans les rapports/analyses internes et externes.
Diriger l’élaboration de systèmes de rapports de gestion et de planification et d’outils.
Promouvoir la normalisation et la simplification.

Financement Commercial

Collaborer à l’élaboration et à la mise en œuvre de stratégies commerciales, en veillant à ce qu’elles s’alignent sur les stratégies commerciales et financières globales.
Travailler aux côtés de l’équipe commerciale, soutenir et conseiller la prise de décisions stratégiques et opérationnelles pour améliorer la performance de l’entreprise.
Interpréter, expliquer et stimuler la performance dans le contexte industriel, concurrentiel et économique.
Soutenir et influencer les décisions commerciales et stratégiques clés.
Conseiller sur les principales opportunités de planification commerciale.
Effectuer des analyses commerciales, telles que les prix, la segmentation de la clientèle, la rentabilité de la gamme de services et le prix/volume/mix.
Préparer et présenter des états financiers et des indicateurs clés pour les revues d’entreprise, les rapports de gestion, le budget et la planification stratégique.
Préparer l’analyse des données financières mensuelles, trimestrielles et annuelles par rapport aux prévisions, au budget et à l’année précédente, y compris les impacts sur le marché, les fluctuations des devises, etc.
Effectuer des analyses complexes, y compris des comparaisons d’une année à l’autre et des marges sur de nouveaux services à des fins de prévision et de tarification.
Analyser de manière optimale les indicateurs clés de performance appropriés pour améliorer la performance commerciale.

Qualifications

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Baccalauréat (B.A./B.S.) ou l’équivalent requis.
20+ ans d’expérience connexe en comptabilité ou en finance, avec un minimum de 10 ans d’expérience en analyse financière.
Une combinaison équivalente d’études et d’expérience peut être acceptée comme substitut satisfaisant à la formation et à l’expérience spécifiques énumérées ci-dessus.
Certification/Permis d’exercice : MBA, CPA ou CMA de préférence.
Compréhension approfondie des questions opérationnelles, commerciales et financières de l’unité commerciale requise.
Ce poste peut nécessiter des déplacements nationaux et internationaux.

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.

Technician 1 - Necropsy (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician 1 – Necropsy for our Pathology Services Team in Mattawan MI.

A Technician 1 – Necropsy 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 animal handling, sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The work schedule for this role is: Monday - Friday 8:00AM to 4:30PM with a weekend/holiday rotation and overtime, as necessary.

Essential Duties and Responsibilities

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 handling, sedation; animal procedures including dissection; collection of samples and weights; laboratory preparation, set up and cleaning; preparation of laboratory solutions. 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.
Learn and know anatomic terms
Receive, track, and prepare samples or materials, as required for department.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
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 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 Requirements

The functions of this role require to be able to physically:

lift/move up to 60 pounds regularly, possibly over the head
stand for extended periods of time
walk long distances across the facility, possibly up to 10 miles per day on concrete floors
remain seated for extended periods of time
utilize meticulous fine-motor skills
work while wearing personal protective equipment (PPE)
work in close proximity to rodents and rabbits that may result in sensitization to allergens or exacerbate preexisting allergies

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.

Animal Care Technician I (Boston, MA, US, 02215)

Job Summary

We are seeking an Animal Care Technician to join our Insourcing Solutions team, located in Boston, MA.

As the Animal Care Technician, you will perform routine animal husbandry tasks to include the cleaning, feeding, and watering of laboratory animals; the cleaning of cages, related ancillary equipment; and the maintenance of animal care environments within the Charles River Accelerator & Development Labs (CRADL) animal facility.

Additional responsibilities include:

• Handle, transfer, and deliver animals, supplies (caging, gases, dry ice, liquid nitrogen), and waste as needed to and from work area(s).
• Perform daily cage duties including recycling and scheduled sanitation procedures.
• Monitor daily animal health and welfare while performing daily animal health observations.
• Operate a washer and autoclave machines to sterilize caging equipment and instruments for the animals.
• Maintain documentation for QA including but not limited to temperature strips, room environmental reports and logs, dish washer and/or autoclaving logs.
• Perform animal husbandry duties to maintain quality and health of research animals, to include performing daily water bottle and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning as required; record animal health concerns per SOP and/or specified protocols.
• Communicate procedural questions and self-identified training deficiencies to team lead or Facility Supervisor.
• Perform humane euthanasia in accordance with the Guide for Care and Use of Laboratory Animals.
• May monitor client row assignments in shared animal holding room to ensure rack/row is labelled and assigned correctly per facility needs.
• Maintain an organized and clean work environment including but not limited to animal rooms, common areas such as corridors, cage washrooms, procedure rooms, anterooms, storage areas and grounds by cleaning at prescribed intervals following established procedures.

Job Qualifications

Required:
• High school diploma, General Education Degree (G.E.D.) or equivalent required.

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.

Vaccine Mandate

Equal Employment Opportunity

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.

Equal Employment Opportunity

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

QA Specialist II - Shift is 12pm - 10:30pm, Sun - Wed (Rockville, MD, US, 20850)

Job Summary

Key Responsibilities and Duties:

Job Qualifications

Compensation Data

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

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

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

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.

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.

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.

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.

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 Associate Scientist, Disc Bioanalytical (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Senior Associate Scientist for our Discovery Bioanalytical team at our Mattawan, MI site.

The Senior Associate Scientist in Discovery Bioanalytical is responsible for quantitative analysis of drug in body fluids and tissue from non-regulated and regulated safety evaluation, pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation & reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques 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.

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

Efficiently perform and document all procedures and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.
Assist with laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues with minimal oversight.
Effectively develop and validate quantitative/qualitative LC/MS-MS methods/procedures with limited complexity/scope in one operational area with minimal oversight.
Independently perform data analysis in appropriate software for at least one analytical platform with minimal oversight.
Independently operate laboratory instruments including their respective software applications for 1-2 analytical platforms 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.
Able to recognize method and/or data issues and communicate them to management to minimize study impact with minimal oversight.
Independently prepare summary of method development data
Write both study and non-study deviations with minimal oversight.
Full understanding of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Independently lead the lab staff in the completion of method validation studies
Provide support to staff members as required by operational area as needed.
Actively participate in internal process improvements, presentations, and harmonization efforts
Performs all other related duties as assigned.

The pay for this position is $75,000 annually USD. 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 the minimum requirements related to the Senior Associate Scientist position.

Bachelor's degree (BS) with 5-7 years of relevant working experience or Master's degree (MS) with 2-4 years of relevant work experience or Doctorate degree (PhD) with 1-2 year of relevant experience
An equivalent combination of relevant education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
LCMS Experience Required
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.
This is an onsite position (no remote options) requires no travel.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Vétérinaire clinicien - F/H - CDI (Evreux, FR, 27930)

Qui-sommes-nous ?

Le poste

Nous recherchons un Vétérinaire Clinicien (F/H) pour intégrer notre équipe de 4 vétérinaires en CDI.
Sous la responsabilité de notre vétérinaire désigné et dans un cadre règlementaire strict (BPL), vous assurerez les suivis cliniques, médicaux et sanitaires de l’ensemble des animaux au sein du laboratoire (toutes espèces, rongeurs et non rongeurs).
Vous jouerez un rôle de conseil technique et scientifique en animalerie et veillerez à la santé et au bien-être des animaux.
Vous participerez aux chirurgies expérimentales de routine et au développement de nouvelles techniques chirurgicales sur les principales espèces animales du laboratoire.
Cette prise de poste s'accompagnera d'un véritable parcours d'intégration et de formation, dispensé par des experts techniques et scientifiques.

Les missions

• Assurer les examens vétérinaires des animaux, prescription des soins et traitements, y compris les chirurgies standards
• Participer aux chirurgies expérimentales de routine et développer de nouvelles techniques pour répondre aux demandes des clients
• Apporter l’expertise technique et scientifique du vétérinaire au sein des animaleries en lien avec les techniciens et les directeurs d’études
• Appliquer la politique de contrôle sanitaire des animaux de laboratoire et de contrôle des aliments, des litières et de l’eau
• Participer activement au développement et à la mise au point de nouvelles méthodes (techniques de prélèvement, d'administration,...)
• Intervenir dans des phases spécifiques de certaines études nécessitant une expertise vétérinaire (examens neurologiques,...)
• Participer activement à la SBEA (Structure chargée du Bien-être Animal)
• Participer activement aux groupes de travail de l’entreprise en lien avec le bien-être animal et les 3R
• Participer aux audits clients et aux inspections réglementaires (DDPP, ANSM, AAALAC)

Conditions spécifiques

Des astreintes sont à prévoir pour les soirs et week-ends (astreintes par semaine complète, 1 toutes les 5 semaines, environ).

Qualifications souhaitées

Vous êtes titulaire d'un diplôme vétérinaire reconnu en France et vous êtes impérativement inscrit(e) à l’Ordre Vétérinaire.
Une expérience et une appétence pour la chirurgie vétérinaire sont attendues.
Une première expérience auprès d'animaux utilisés à des fins scientifiques serait un atout, sans être indispensable.
Vous avez une maîtrise du français et de l'anglais courant, oral et écrit.
Vous avez d'excellentes qualités relationnelles et de bonnes capacités à travailler en équipe.

Modalités

Convention collective de l’industrie pharmaceutique
Contrat : CDI cadre forfait Jours (RTT)
Salaire : A compter de 45 000 € bruts / an sur 13 mois, selon profil et expérience
Prise en charge de la mutuelle à 100%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement et de participation, accord de télétravail,...
Site non accessible en transport en commun, un moyen de locomotion est 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.

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.

Equal Employment Opportunity

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

Senior Associate Scientist - Bioanalytical Method Development 1 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Senior Associate Scientist for our Bioanalytical Team site located in Mattawan, MI.

The following are responsibilities related to the Senior Associate Scientist:

An Senior Associate Scientist in Laboratory Sciences is responsible for developing and validating methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The individual in this role is proficient in the use of instrumentation and laboratory techniques and in the execution of method development and validation procedures. An Senior Associate Scientist is expected to work independently, participate in process improvement initiatives, and may function as a Principal Investigator or Study Director.

Job Qualifications

The following are minimum qualifications related to the Senior Associate Scientist position:

Bachelors 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 some relevant experience and CRO is preferred.
LCMS Experience Required
Proficient using laboratory software applications (i.e., LIMS and data acquisition software).
Working knowledge of GxPs and industry guidance documents.
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.
Familiarity with Microsoft Office Suite.
Ability to work under specific time constraints.

The pay range for this position is $70 - 75,000 k/year. 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.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Wissenschaftler (m/w/d) als Scientific Officer - GTS (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort unbefristet eine/n

Wissenschaftler*in als Scientific Officer (m/w/d)

Unterstütze uns bei:

der Durchführung von molekularbiologischen Analysen (Routine)
der eigenständigen Einleitung, Durchführung und Betreuung von Transfer & Validation Aufträgen
der Verbesserung der bestehenden Methoden und Ablaufe
die Etablierung von neuen Methoden und Verfahren
den Laborarbeiten mit GVOs und Biostoffen bis hin zur Risikogruppe S1
der Unterstützung der Scientific Officer bei der Bearbeitung von internen Dokumenten wie BOPs und Laborablaufplänen
der Erstellung von Auswertungs- und Trackingsheets mit Hilfe von Excel oder Smartsheet,
der eigenständigen Überprüfung von Labordokumentation sowie der Auswertung und Zusammenfassung von Analyseergebnissen
der Organisation und Pflege der Analysendaten in einer Datenbank in Verbindung dem LTM (Laboratory Testing Management) System
Betreuung des technischen Personals bei der Durchführung von Analysen
Zusammenarbeit mit in- und ausländischen Kunden
Bearbeitung von wissenschaftlichen Fragestellungen, Kundenanfragen sowie Freigabe von Analysenergebnissen

Überzeuge uns durch:

Ein abgeschlossenes Studium der Naturwissenschaften oder vergleichbare Qualifikation
Wissenschaftliche Expertise (praktisch und theoretisch) im Molekularbiologischem Bereich speziell im Bereich PCR und real time PCR
Sehr strukturiertes, detailorientiertes und zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien
Wünschenswert wären Erfahrungen mit Tiermodellen
Service und Kundenorientierung
Sehr gute Kenntnisse von Microsoft Office sowie gute Deutsch- und Englischkenntnisse

Wir bieten Dir:

Eine Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
Eine intensive Einarbeitung
Flexible Arbeitszeiten
Eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
Eine angemessene Vergütung

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 228685 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
Phone: 0211 9255-356 (Michaela Klein)

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.

Vivarium Support Technician - Cagewash (Stilwell, KS, US, 66085)

Job Summary

We are seeking a Vivarium Support Technician at our Safety Assessment site located in Stilwell. The pay for this position is $19/hour plus benefits.

A Vivarium Support Technician is responsible for assisting in vivarium operations activities which facilitate clean housing and care for laboratory animals. Also responsible for helping assist in the preparation of materials which enable study activity completion.

Essential Duties and Responsibilities:

Clean and sanitize animal cages and related environmental items.
Perform daily routine maintenance checks on the automated cage wash machines.
Prepares appropriate housing for receipt of new animals; may assist with receiving animals.
Report the need for equipment repair (cages, racks, cagewash machines, etc.) to the appropriate personnel.
Sanitize floors, walls and other surfaces in the automatic cage wash area and in other areas of the lab.
Maintain a clean cage wash area.
Maintain storage area in an organized fashion.
Complete animal care technical duties such as changing liners and sanitizing animal room walls and floors.
Receive, store, and distribute animal husbandry supplies.
Perform limited troubleshooting and calibration of instruments as appropriate for assigned area.
Prepare environmental enrichment items (edible and durable).
Operate basic lab equipment and perform routine maintenance as needed.
Prepare study and colony supplies as needed.

Job Qualifications

Education: High School diploma or General Education Degree (G.E.D) preferred.
Experience: No experience necessary
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
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

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.

Technician IV - Surgery, Advanced Functions Team 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician 4 for our Surgery OR, Advanced Functions Team at our Safety Assessment site located in Mattawan, MI.

A Technician 4 – Technical Operations has substantial knowledge in the basic skills and able to perform the intermediate skills and procedures of the department training plan. The technician is assigned to work on study, performing skills independently which may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering more intermediate/specialized doses by various methods, and/or biological specimen collections for analysis. The technician assists with more advanced skills that may include working with additional species, and/or specialized procedures to support the study needs.

Essential Duties and Responsibilities:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Perform basic and intermediate skills of the department, with little to no supervision. Skills may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering more intermediate/specialized doses by various methods, and/or biological specimen collections for analysis. Specific skills will be based on each area’s training plan and business needs.
Assist with advanced skills of the department.
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, maintain, and troubleshoot instrumentation and equipment.
Perform all other related duties as assigned.

The pay for this position is $24/hr USD. 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.) required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: 2 years of relevant 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: Functional certification preferred. Others may be required by local government.
Skill plan completed for this role based on department training plan.
Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data.
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 exercise independent decision-making and self-manage under the direction of a technical supervisor.
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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Veterinary Technician I (Poolesville, MD, US, 20837)

Job Summary

We are looking for a Veterinary Technician (Levels I, II, III) to join our Insourcing Solutions team located in Poolesville, MD. (See qualifications for each level)

What you will do!

In the Veterinary Technician I, II, and III role, you will assist will all activities required for supporting and maintaining the site animal colonies and Animal Study Protocols in support of the research program. Care for and maintain lab animals in accordance with all guidelines, policies, and regulations to ensure their health and welfare.

You will perform the following duties:

Prepare and distribute animal diets, enrichment, and clinical treatments; collect and record physiological data (pulse, respiration, heart rate, body temperature, etc.).
Perform technical procedures including femoral blood collection, IV catheterization, aseptic tissue collection and processing, anesthesia, food or liquid consumption, drug dosage calculation and administration (Topical, PO, IM, SQ, IV and ID), TB testing, weighing, physical examinations, restraint and handling of animals, radiographs, and other technical procedures as needed.
Understand basic animal behavior for training techniques; including positive reinforcement and cognitive testing; assist in on-going behavioral testing and data collection.
Assist veterinarian or investigators with surgeries or specialized procedures.
Perform animal health surveillance checks and report any abnormal findings.
Maintain electronic medical records, update treatment plans, send daily emails regarding clinical and experimental information vet staff and client.
Collect, preserve, and prepare blood, urine, stool, and tissue samples.
Participate in study related necropsies and tissue harvest.
Perform weekly mid-day health checks and daily pm health checks of all animals in the colony (including geriatric rhesus monkeys).
Daily, weekly, and monthly cleaning and sanitization of prep areas and procedure rooms. Set-up procedure areas and prepare supplies and equipment for procedures.
Ability to maintain freezer organization and sample inventory.
Participate in all required training (topics may include animal specific information and technical procedures, medical care, OSHA, regulatory, ASP support, and standard operating procedures).

Job Qualifications

Candidate must possess one of the following: combination of education/experience.

Education: All levels- a high school diploma or GED is required; a BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred
Experience: Level I – 2-3 years’ experience working with animals in biomedical research, of which 1 year must be with non-human primates. Veterinary Hospital technical experience will be considered.
Level II-III a minimum of 5 years’ experience of same. Supervisory experience preferred for Level III. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education/experience listed above for these levels.
Certification: Level I- Eligibility to take the AALAS certification at the LAT level required. Level II-III LATG eligibility required.

The pay range for this position is $27.00 to $33.00 USD per hour.  Please note the range covers level I-III, salary will depend on level, in addition to factors such as experience, skills, and certification.

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.

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 10:00 am to 6:30pm.

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.

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 ~85% of the drugs approved by the FDA in 2019.

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

Principal Scientific Advisor (Wilmington, MA, US, 01887)

Job Summary

We are seeking an experienced nonclinical drug development professional to serve as a Senior Principal Scientific Advisor within our Discovery and Safety Assessment business units.

The Scientific Advisory Services team is hiring an experienced professional with expertise in establishing effective scientific and regulatory strategies to advance new medicines through the various stages of the development process. This position provides opportunity for independent scientific guidance and leadership roles within project teams and functional areas across the organization, with an emphasis on providing innovative advice on nonclinical (pharmacology and toxicology) drug development programs across a broad spectrum of drug modalities and therapeutic indications.

This individual will work closely with current and potential clients and internal Charles River functional groups to design robust and scientifically sound nonclinical drug development programs. The person may act as the scientific leader for cross-functional teams for integrated discovery and safety programs. When appropriate, the individual may perform gap analyses, support due diligence procedures, and perform scientific review of discovery and/or safety assessment data or reports. This role provides for recognition throughout the company as a subject matter expert in one or more therapeutic area(s) or class(es) of therapeutic products. Successful individuals have knowledge of domestic and international regulatory expectations and requirements; and can provide intellectual input in determining the appropriate discovery and nonclinical safety assessment strategy for complex and novel products, including advanced medicinal products. There will be opportunities to support department leadership regarding strategy and recruitment. More broadly, one will work closely with Business Development, Client Services, Account Management, Marketing, and Operations by ensuring that clients’ business and scientific needs are understood and efficiently addressed.

In addition to providing scientific and regulatory support in client interactions, the individual will have the ability to an expanded breadth of experience in covering multiple drug modalities and be able to contribute solutions to complex scientific and regulatory issues when situations occur during the conduct of a drug development program. They will be able to lend support to multiple divisions of CRL and assume leadership roles in multidisciplinary teams when required. Within Charles River, the individual will be able to provide pivotal leadership and guidance to internal working groups, projects, and/or marketing activities when requested.

This position will mainly support potential clients generally located in the Eastern Time Zone.

Job Qualifications

The following are minimum requirements related to the Senior Principal Scientific Advisor position.

• Education: master’s degree or PhD in relevant discipline (toxicology, pharmacology, biology, immunology, etc.).
• Experience: Minimum 20 years’ experience in pharmaceutical/biotech sector, nonclinical contract research or consulting including at least 12 years nonclinical drug development experience. Must have direct experience in regulated toxicology and drug development. Prior direct experience in interacting with regulatory agencies is preferable. Prior experience in program management and/or Pharm/Tox Program Leadership is considered useful.
• Certification/Licensure: DABT, DACVP or European Registered Toxicologist preferred.
• Other: Applied understanding of regulatory requirements for the conduct of nonclinical safety assessment studies including Testing Facility SOPs and the Good Laboratory Practices (GLPs). Deep understanding of relevant regulatory guidance documents is essential. Demonstrated leadership skills in support of intra- and interdepartmental initiatives, client/external interactions, and business development. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and standard laboratory calculations.

Equal Employment Opportunity

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

Veterinary Technician I (Poolesville, MD, US, 20837)

Job Summary

We are looking for a Veterinary Technician (Levels I, II, III) to join our Insourcing Solutions team located in Poolesville, MD. (See qualifications for each level)

What you will do!

You will perform the following duties:

Prepare and distribute animal diets, enrichment, and clinical treatments; collect and record physiological data (pulse, respiration, heart rate, body temperature, etc.).
Perform technical procedures including femoral blood collection, IV catheterization, aseptic tissue collection and processing, anesthesia, food or liquid consumption, drug dosage calculation and administration (Topical, PO, IM, SQ, IV and ID), TB testing, weighing, physical examinations, restraint and handling of animals, radiographs, and other technical procedures as needed.
Understand basic animal behavior for training techniques; including positive reinforcement and cognitive testing; assist in on-going behavioral testing and data collection.
Assist veterinarian or investigators with surgeries or specialized procedures.
Perform animal health surveillance checks and report any abnormal findings.
Maintain electronic medical records, update treatment plans, send daily emails regarding clinical and experimental information vet staff and client.
Collect, preserve, and prepare blood, urine, stool, and tissue samples.
Participate in study related necropsies and tissue harvest.
Perform weekly mid-day health checks and daily pm health checks of all animals in the colony (including geriatric rhesus monkeys).
Daily, weekly, and monthly cleaning and sanitization of prep areas and procedure rooms. Set-up procedure areas and prepare supplies and equipment for procedures.
Ability to maintain freezer organization and sample inventory.
Participate in all required training (topics may include animal specific information and technical procedures, medical care, OSHA, regulatory, ASP support, and standard operating procedures).

Job Qualifications

Candidate must possess one of the following: combination of education/experience.

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.

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

IMPORTANT: Afin d'être considéré pour ce poste, le CV doit être téléchargé et soumis lors du processus de candidature. Veuillez vous assurer que les antécédents de travail et de scolarité sont ajoutés correctement.

Sommaire de l'emploi

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.

IMPORTANT: Un CV est requis pour être considéré pour ce poste. Si vous n'avez pas téléchargé votre CV dans votre profil de candidat, veuillez retourner dans le champ de téléchargement et y joindre votre CV.

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

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

Job Summary

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.

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 20-25 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.

Equal Employment Opportunity

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

Responsable du Magasin - F/H - CDI (Saint-Nazaire, FR, 44600)

Le poste

Afin d’optimiser la gestion de notre service Supply Chain, nous recrutons un Responsable du Magasin 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. Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Les missions

1/ Gestion des stocks et du magasin :

Veiller à garantir la réception efficace des produits livrés
Veiller à l’organisation du stockage et la rationalisation des flux afin d’optimiser les mouvements et les livraisons
Veiller à gérer le bon niveau de réassort pour minimiser les niveaux de stocks sans risquer la rupture
Assurer l’enregistrement des produits dans l’ELN (cahier de laboratoire informatique) et le suivi informatique des stocks dans SAP, tout en garantissant la mise à jour informatique en temps réel des stocks physiques
Veiller à assurer la préparation des commandes
Veiller à assurer une distribution ponctuelle des produits stockés ou reçus vers les services destinataires
Assurer la libération des lots de matières premières reçus au magasin
Veiller à préparer les colis conformément aux exigences pour les expéditions
Planifier et coordonner les activités d’inventaires physiques et comptables
Mettre à jour les PSO en fonction des activités, des produits et des changements de réglementation
Etre force de proposition pour continuellement améliorer la performance du service

2/ Gestion du matériel de production stocké :

Veiller à stocker le matériel dans des conditions satisfaisantes de conservation, de sûreté et de sécurité
Veiller à assurer le transport de ce matériel à la demande des services de production
Tenir l’inventaire du matériel stocké

Conditions spécifiques

Horaires fixes du magasin : du lundi au vendredi, 9h – 12h / 13h30 – 17h
Activités impliquant des produits dangereux et/ou réglementés
Respect des procédures BPL et HSE

Qualifications attendues

A minima titulaire d’une formation de niveau bac+2/3 en logistique, vous savez justifier d’une première expérience dans la gestion des stocks et flux associés.
Vous disposez du sens du service et d’un bon niveau communication auprès de parties prenantes variées, internes comme externes.
Vous êtes autonome et savez prendre des initiatives. Votre esprit d’analyse vous permet de gérer les urgences et d’apporter rapidement des solutions aux problèmes rencontrés.
Vous êtes à l’aise sur les outils informatiques (Excel, Word, Smartsheet) et avez une première expérience avec un ERP (SAP, idéalement).

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.

Work Schedule Planner (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Work Schedule Planner for our Toxicology team in Laval, you will be responsible for the optimal planning of the working hours of our technical staff. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Efficiently plan the daily technical schedule implementing various work shifts to minimize overtime;
Balance individual employee workloads;
Plan the schedule according to individual skills and restrictions;
Plan the training depending on operational needs.

Key Elements

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

College Diploma in Administration or any related discipline;
Minimum of 1-2 years’ experience in work schedule planning;
Good attention to details;
Strong observation & organizational skills;
Good problem-solving skills;
Good stress management;
Team spirit.

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 27.50$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday weekdays. Possibility of having a condensed schedule of 4 days a week. You will also have to do a weekend rotation (1/2 or 1/3) and do overtime depending on the business needs;
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.

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

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

Research Analyst I, Bioanalytical Chemistry (Ashland, OH, US, 44805)

Job Summary

We are seeking a Research Analyst I (Bioanalytical Chemistry) for our Safety Assessment Group site located in Ashland, Ohio.

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. Perform laboratory tasks by various basic methods.

Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices.
Under supervision may act as lead/primary technician on basic studies.
Basic Understand/Knowledge LCMS
Input, print and edit computer entries (e.g., laboratory data).
Prepare materials and data for shipment and archiving.
Receive samples and complete tracking documentation.
Review documentation of functions performed as part of quality control requirements.
Perform study preparation activities including collection tube labeling and room setup.
Maintain clean work areas.
Perform all other related duties as assigned.

The following are miminum requirements related to the Research Assistant I position.

Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline 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 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 experiences preferred.

The pay range for this position is $21.00 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

For more information, please visit 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.

Equal Employment Opportunity

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.

Principal Scientist - Immunochemistry (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Principal Scientist for the Immunochemistry Department located in Ville Saint-Laurent, you will be supporting non-clinical and clinical studies requiring measurement of therapeutic oligonucleotides in biological matrix using hybridization ELISA technique.

In this role, primary responsibilities include:

Design, write, review and edit, as necessary, 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.
Ensure that relevant projects are performed according to standard operating procedures (SOPs) and Good Laboratory Practice (GLP) regulations, and are aware of regulations published by the FDA, EPA, JMHW and OECD.
Write, review and edit, as necessary, stand-alone and 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 Sponsors on study related business and generate and distribute Client Interaction Reports (CIRs) in a timely manner.
Ensure the accuracy and completeness of project cost estimates.
Review and approve raw data.
Attend scientific meetings, symposia or workshops at the discretion of the Executive Director, Laboratory Sciences North America and/or Principal Director, Laboratory Sciences and publish or present results of the research whenever possible.
Assist in the design of study packages and be able to provide advice to Study Directors and Sponsors on Laboratory Sciences issues.
Assist in maintaining laboratory documentation to a satisfactory standard, satisfying the requirement of GLP, as required. This includes preparing, reviewing, updating, issuing,SOPs and Guidance Documents.

Key Elements

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

Education: Ph.D., M.Sc. or B.Sc. in chemistry or a related discipline.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Role Specific Information:

Location: 7170 rue Frederick-Banting, Ville St-Laurent / Free Parking
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm;
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.

Equal Employment Opportunity

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

Scientifique principal - Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Scientifique principal en Immunochimie notre équipe située au site de Ville Saint-Laurent, vous soutiendrez des études non cliniques et cliniques nécessitant la mesure d'oligonucléotides thérapeutiques dans une matrice biologique à l'aide de la technique ELISA d'hybridation.

Dans ce poste, les principales responsabilités incluront:

Concevoir, rédiger, réviser et éditer, si nécessaire, les plans d'étude, les modifications et les calendriers qui définissent et planifient toutes les activités de l'étude.
Superviser et coordonner tous les aspects des procédures des sciences de laboratoire liées à l'étude, qu'elles soient réalisées au sein du département ou par les services.
S'assurer que les projets concernés sont réalisés conformément aux procédures opérationnelles normalisées (PON) et aux réglementations relatives aux bonnes pratiques de laboratoire (BPL), et qu'ils sont conformes aux réglementations publiées par la FDA, l'EPA, le JMHW et l'OCDE.
Rédiger, réviser et éditer, si nécessaire, les projets et/ou les rapports finaux des scientifiques, qu'ils soient autonomes ou contributeurs, qui documentent toutes les procédures et tous les résultats de l'étude.
Communiquer rapidement, verbalement ou par écrit, avec les directeurs d'étude et/ou les promoteurs sur les questions liées à l'étude, et générer et diffuser les rapports d'interaction client (CIR) dans les délais impartis.
S'assurer de l'exactitude et de l'exhaustivité des estimations de coûts des projets.
Examiner et approuver les données brutes.
Assister à des réunions scientifiques, des colloques ou des ateliers, à la discrétion du directeur exécutif, Sciences de laboratoire Amérique du Nord, et/ou du directeur principal, Sciences de laboratoire, et publier ou présenter les résultats de la recherche dans la mesure du possible.
Participer à la conception des programmes d'études et conseiller les directeurs d'études et les promoteurs sur les questions relatives aux sciences de laboratoire.
Contribuer au maintien de la documentation du laboratoire à un niveau satisfaisant, conformément aux exigences des BPL, le cas échéant. Cela comprend la préparation, la révision, la mise à jour et la publication, entre autres, de procédures opérationnelles normalisées (SOP) et de documents d'orientation.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Doctorat, maîtrise ou licence en chimie ou dans une discipline connexe.
Une combinaison équivalente de formation et d’expérience peut être acceptée comme substitut satisfaisant à la formation et à l’expérience spécifiques mentionnées ci-dessus.

Informations spécifiques au poste:

Localisation : 7170 rue Frederick-Banting, Ville St-Laurent / Stationnement gratuit
Bonus annuel basé sur la performance
Horaire : Du lundi au vendredi, de 8h à 16h15.
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.

Planificateur.trice d'horaire de travail (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Planificateur.trice d’horaire de travail pour notre équipe de Toxicologie à notre site de Laval, vous serez responsable de la planification optimale des heures de travail de notre personnel technique. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Établir efficacement les horaires de travail du personnel technique en mettant en place des quarts de travail afin de réduire les heures supplémentaires;
Équilibrer les charges de travail individuelle des employés;
Planifier les horaires selon les compétences et les restrictions individuelles;
Planifier les formations selon les besoins opérationnels.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme d’études collégiales en Administration ou toutes autres disciplines connexes;
Au minimum 1-2 ans d’expérience dans la planification des horaires de travail;
Bonne attention aux détails;
Bon sens de l’observation et bonne organisation;
Bonnes compétences en résolution de problèmes;
Bonne gestion du stress;
Esprit d'équipe.

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 27.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jours. Possibilité d’avoir un horaire condensé à 4 jours par semaine. Vous devrez également faire une rotation de fin de semaine (1/2 ou 1/3) et faire des heures supplémentaires selon les besoins de l'entreprise;
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.

À propos de l'évaluation de sécurité

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

Technical Service Research Supervisor (Cambridge, MA, US, 02142)

Job Summary

We are seeking an experienced Technical Services & Research Supervisor to join our Insourcing Solutions team, located in Cambridge, MA.

As the Technical Services & Research Supervisor, you will provide direct supervision of Charles River Accelerator & Development Labs (CRADL) in vivo technical service and research group. Provides supervision and training for employees. Maintains performance and service levels consistent with and according to company standards, the CRADL organization and client contractual requirements. Recommend new or innovative techniques to improve productivity, increase efficiencies, and maintain quality standards Prioritizes and completes on-going tasks independently following established policies and guidelines. Liaises with clients to ensure satisfaction with technical staff’s performance.   

Additional responsibilities include:

Supervises the daily activities of technical services and study team comprising of research associate/study technicians and study coordinators, ensuring all services meets organizational standards & client expectations.
Schedules, assign and balance workload among the technical staff for research and tech services.
Interacts with clients as required to address client inquiries and complaints.
Maintain an awareness of the financial status and impacts of ongoing studies.
Proactive resolution of operational and quality issues; continuously guiding and training staff to improve processes, and operational efficiencies. 
Ensure in vivo study applications are performed in accordance with currently defined protocols and in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state, and federal requirements. 
Ensure creation and maintenance of accurate study records, and delivery of study data to clients.
Partner with the veterinarians, veterinary technicians, trainers, and the IACUC office to ensure compliance with biosecurity policies and procedures, IACUC required training, IACUC non-compliance and/or animal welfare concerns.
Responsible for personnel management activities such as: mentorship, hiring, promotions, training & development.

Job Qualifications

The following are minimum requirements related to the Technical Services & Research Supervisor position.

Bachelor's degree (B.A./B.S.) or equivalent in animal or laboratory science, business, or related discipline.
Minimum 4 years in the laboratory animal industry of which 2 years is supervisory or lead technician experience.
AALAS certification at the Laboratory Animal Technologist level (LATG) preferred.

The pay range for this position is $100-103k USD annually Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

Vaccine Mandate

Equal Employment Opportunity

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

Technicien Animalier - 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 nos animaleries en charge de la bonne conduite de nos études de toxicologie, nous recherchons un Technicien Animalier (F/H) en CDI.

Vous rejoindrez un département d'environ 160 personnes, comportant une zone protégée (hébergeant souris, rats, lapins) et une zone conventionnelle (hébergeant chiens, porcs et primates).

En fonction de la charge fluctuante de notre activité, et après une formation dispensée en interne, vous serez amené(e) à réaliser les interventions techniques auprès de toutes nos différentes espèces.

Missions :

Participer au lancement des études en préparant les cahiers dont vous aurez la charge
Vérifier l'adéquation des conditions d'hébergement avec les procédures
Assurer l'ensemble des techniques de contentions, administrations, prélèvements et examens standards sur les animaux
Assurer tout ou partie des techniques spécifiques des études de reproduction et des études de perfusion
Contrôler l'état clinique (croissance, poids, comportement) des animaux en cours d'études et remonter les anomalies
Préparer quotidienne le matériel nécessaire à l'étude et assurer sa disponibilité
Acquérir les données selon nos plans d'études, assurer leur contrôle et leur enregistrement

Conditions spécifiques du poste :

Amplitude horaire hebdomadaire du département : 6h/18h
Permanences de weekend : 1 par mois environ

Qualifications souhaitées :

Titulaire d'un diplôme de niveau Bac (général ou professionnel), vous disposez d'une première expérience en tant que technicien de laboratoire ou technicien animalier.

Passionné(e) par les animaux, vous avez à coeur de réaliser les actes techniques dans le respect des procédures et de leur bien-être.

Votre première expérience ou votre formation vous a idéalement permis d'être titulaire de la formation à l’Expérimentation Animale de niveau A/II.

Vous savez prioriser, organiser vos tâches et communiquer auprès de vos coéquipiers.

Modalités contractuelles :

Convention collective de l'industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (accord de modulation - 35h)
Salaire : A compter de 25 800€ 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, etc.
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.

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

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

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 etwa 86% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Informationen finden Sie unter www.criver.com.

Maintenance Electrician (Tranent, GB, EH33 2NE)

Job Summary

An Electrician vacancy now exists within the Site Services Engineering department based in Tranent. This is a permanent full-time role. This role is to carry out Electrical Maintenance, repairs and installations under the direction of the Site Services Engineering Supervisor. Although based in Tranent, this role covers Electrical maintenance requirements for three sites across the Edinburgh area.

Applicants Must Have:

Qualified Electrician which must include 18th Edition Wiring Regulations and industry standard qualifications
You must have a full, clean driver’s license and your own transport
Previous experience working as an Electrician, ideally in an industrial context
To be able to participate in overtime as is reasonably required to ensure the smooth running of the department
To be able to participate on a rotational basis in the emergency out of hours on-call system (eligible upon successful completion of the probationary period)
Ability to interact with peers effectively
Ability to adopt a methodical approach to work, employing sound risk assessment techniques
Able to interact and communicate professionally with internal and external stakeholders
Able to collaborate effectively with colleagues across all levels of the organization
Ability to work effectively as part of a team as well as individually
Effective customer service skills
Ability to work to tight timescales
Adopt a flexible response to changing priorities
An ability to comfortably work at height
An ability to comfortably work in potentially confined spaces

Key Responsibilities:

To carry out an electrical repair and maintenance service to Charles River Laboratories sites
To carry out installation of electrical and computer wiring and systems to IEE regulations
To carry out portable appliance testing and maintenance of records
To maintain electrical equipment
The recording of data and management of work orders in the work order management system (Maximo)
To advise staff on use of electrical apparatus and systems
To alter room environmental controls settings as directed by operational departments
To participate in Generator Testing and restart equipment
To liaise and make themselves familiar with Plant maintenance requirements (for on-call duties)
To liaise with external vendor service engineers
To maintain necessary legible records of work carried out, both electronic and written
Fault finding and diagnostic testing
Work on high voltage equipment (if qualified)

Due to the nature of this role, you must also be able to work out with 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, own transport is essential for this.

Salary for this role £43,000 per annum. You will also be expected to participate in the rotational on-call system upon successful completion of the probationary period. You will receive an on-call allowance, and the details of this will be provided to you, once you commence in post. In the event that the on-call arrangement or your participation therein ceases for any reason, then the payment will be discontinued. The payment will not be included in your salary for pension purposes.

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 80% of the drugs approved by the FDA in the last 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.

Associate Director Biomanufacturing (Memphis, TN, US, 38118)

Job Summary

Reporting to the Site Director, the Associate Director, Biomanufacturing Operations is responsible for managing a cross functional work cell team that provides for the manufacture of drug substance and drug product. The Associate Director is responsible for ensuring that all staff is appropriately trained and follows the appropriate SOPs. This role will work closely with the Site Director and Manufacturing Leadership Team to ensure manufacturing activities are fully supported. This role will also work closely with Tech Transfer and Manufacturing Leadership to assess incoming processes and advise site leadership and business development on compatibility of incoming technologies and manufacturing facility.

Participate in overall account governance, facilitate leadership review as required.
Provide strategic context for objectives and decisions to team, senior leadership, and the broader organization as appropriate
Drive collaboration with internal cross-functional teams necessary for delivery on the project including Process Sciences, Manufacturing Sciences & Technologies, Quality Control, Quality Assurance, Supply Chain to ensuring alignment on project objectives and priorities.
Facilitate internal project team meetings and external client meetings including delivery and management of a project objectives, meeting agendas, integrated project schedules, key performance measures, risk registrar, timely meeting minutes & action items.
Assist in development of budget and budget planning, forecasting, etc
Assist in strategic planning and development of projections for business needs required to meet production goals
Advise and inform leadership of any potential impacts to production, production timelines, or CQA
Build, train, and develops highly skilled teams by identifying opportunities for improvement, coaching/mentoring reports towards growth, and provided goals and challenges to stretch capabilities
Oversees and approves nonconformance investigations, including root cause analysis, and CAPA development

Job Qualifications

A minimum of a BS in science or engineering or advanced degree (MS preferred), with at least 7 years of biologics manufacturing experience or equivalent cGMP experience is required
A minimum of 5 years cGMP manufacturing leadership experience required
Exhibits exceptional leadership skills and deep knowledge of GMP
Possess effective written and oral communication skills
Demonstrates initiative to remain apprise of relevant industry and regulatory trends

The pay range for this position is $165K - $185K. Please note that salaries vary within the range based on factors 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 supported the development of 86% of the drugs approved by the FDA in 2021.

For more information, please visit 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.

Equal Employment Opportunity

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

Microbiologist (Ballina, IE, F26D786)

We are seeking an experienced Microbiologist for our Biologics Department located in Ballina, Co. Mayo. You shall be reporting to the Microbiology Functional Manager.

The main duties & responsibilities shall be;

• GMP Compliance.
• Perform Endotoxin testing, Sterility testing, Efficacy of Antimicrobial Effectiveness test, Environmental Monitoring, Water testing, Microbial Limit testing, Bioburden testing.
• Qualification/Validation of test methods
• Carry out Quality Control Checks
• Assist in Laboratory Investigations
• Trending of Laboratory Data
• Update SOP's as required
• Provides training to other members of the Microbiology team as required.
• Proactively identifies and implements Laboratory process improvements.

The following are minimum requirements related to the Microbiologist position;
• BSc. in a relevant science discipline
• Some hands on work experience in a regulated Microbiology Laboratory would be beneficial.
• GMP experience
• Excellent communication skills, both verbal and written
• Collaboration and Teamwork. Maintains the highest standards of ethical behavior
• Results and performance driven
• Strong analytical ability and associated problem solving
• Good time management and attention to detail
• Knowledge and proficient in the use of Word, Excel etc.

Job Summary

Profile and Requirements

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.

Security Officer - 3rd Shift - Rotating Weekends (Mattawan, MI, US, 49071)

Compensation Data

This position offers $19.00/hr as a starting wage alongside a 10% shift differential for all hours worked on the weekends.

Job Summary

We are seeking an experienced full-time Security Officer for the 3rd Shift Security team in Mattawan, MI.

A Security Officer is responsible for: following established procedures and guidelines; monitoring and ensuring compliance with company security and safety policies; monitoring all access to the facility by checking and issuing security badges; monitoring security, safety and integrity of buildings and environs; responding to any unusual circumstances; protecting facility from unwanted actions or espionage; and providing a safe and secure environment for employees, clients, visitors and animals.

Job Qualifications

HS/GED degree with 2- 3 years of experience, with at least six to twelve months of related security experience and/or training; contract research organization experience preferred. Driver’s license is required.
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.

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

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

Job Summary

As an Student - 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.

Key Elements

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

At least have completed Secondary 4;
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;
Part-time position, 15hrs per week - 40hrs per week this summer.

Why Charles River ?

No experience needed;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Guaranteed hours - The research field is in high demand;
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.

Equal Employment Opportunity

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

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

Sommaire de l'emploi

En tant qu'Étudiant.e - 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:

Au minimum avoir terminé son secondaire 4;
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, QC, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Tous les samedis et dimanches, horaire entre 6h00 et 14h15;
Poste temps partiel, 15 heures par semaine – 40hrs par semaine cette été.

Pourquoi Charles River?

Aucune expérience préalable requise;
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;
Des heures garanties, car le milieu de la recherche est très en demande;
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.

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

Research Analyst I - Analytical Chemistry (Ashland, OH, US, 44805)

Job Summary

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

Basic Summary:

Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices.
Under supervision may act as lead/primary technician on basic studies.
Input, print and edit computer entries (e.g., laboratory data).
Prepare materials and data for shipment and archiving.
Receive samples and complete tracking documentation.
Review documentation of functions performed as part of quality control requirements.
Perform study preparation activities including collection tube labeling and room setup.
Maintain clean work areas.
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: Associate’s degree or equivalent two-year college, preferred. Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline, recommended.
Experience: Zero to two years 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.
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.

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 supplies.
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 hold and manipulate work materials 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, working at noise levels ranging from moderate to loud.
The employee is occasionally exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to moderate depending upon the task being performed.

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.

Technician I-Histology-1st shift (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our 1st shift Histology Team located in Ashland, OH.

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. 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.

Analytical Chemistry - Associate (Tranent, GB, EH33 2NE)

Job Summary

At our world class facility in Elphinstone, Tranent (close to Edinburgh), our Analytical Chemistry Department currently has exciting career opportunities for a Scientific Associate.

Department Information

Analytical Chemistry Services provide formulation and analytical methodology as well as analytical support to external clients and internal customers.

Key Responsibilities:

Working on analytical method development and GLP validation studies
Sample analysis on major GLP toxicology programmes
Data recording to GLP
Reporting and Quality control checking of data
Communicating and working effectively as part of a team
Liaising with internal and external customers
Working to agreed deadlines
Applicants should have:
Honours degree (or equivalent) in Chemistry or a Chemistry related subject
Relevant Laboratory experience with HPLC/UHPLC/GC
Effective organizational skills and time management
Good problem solving skills

Salary for this role is £27,951.22 and this role closes Wednesday, 30 July 2025.

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.

Profile and Requirements

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 80% of the drugs approved by the FDA in the last 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.

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

Qui sommes-nous ?

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

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

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

Weitere Informationen finden Sie unter 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.

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.

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.

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 >80% of the drugs approved by the FDA for the past 3 years.

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

Lab Assistant I - Analytical Chemistry (Ashland, OH, US, 44805)

Job Summary

We are seeking a Lab Assistant I for our Analytical Chemistry group for our Safety Assessment site located in Ashland, OH. A Laboratory Assistant will perform basic laboratory and record-keeping tasks.

Wash and dry glassware and distribute to appropriate locations within the laboratory. Keep glass-washing area clean and organized. May sterilize glassware and other items using an autoclave.
Label tubes, devices and containers and perform laboratory set-up/clean-up.
Assist technical personnel with clerical duties (e.g., filing, making copies, etc.).
Monitor inventory and stock assigned areas.
May record observations and measurements for basic lab/research tasks.
Operate basic lab equipment and perform routine maintenance as needed.
Perform limited troubleshooting and calibration of instruments as appropriate for assigned area.
May be responsible for preparing simple lab solutions (e.g., buffers, media/common vehicles).
May generate reports, data, and forms.
Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
Perform all other related duties as assigned.

The pay for this position is $18/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:

Education: High school diploma or General Education Degree (G.E.D.) preferred.
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 communication skills required. Basic computer skills; familiarity with Microsoft Office software.

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 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 is occasionally exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to moderate 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

For more information, please visit 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.

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.

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.

Equal Employment Opportunity

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

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

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.

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.

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.

Equal Employment Opportunity

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

Associate Director Production Quality (Rockville, MD, US, 20850)

Job Summary

This position reports to the Site Head of Quality, and the person filling this role is responsible for partnering with functional stakeholders at the site level to ensure Quality performance and Compliance is designed into, and maintained, across all strategic initiatives, Operations, functional support organizations, and execution of GMP activities at the Rockville site. This position interacts regularly with key clients as well as interfaces with regulatory agencies during inspections. This position is responsible for overseeing all quality operations functions, including execution of environmental monitoring, sterility assurance, routine QC testing and deliver to stability testing, and the overall oversight and operation of the Quality Testing Lab. This position will also oversee timely batch lot disposition, timely investigation and CAPA related to deviations. The person filling this role will be responsible for the leadership, development and training of team members within their oversight as well as providing supportive leadership and strategic direction to operate with and maintain compliance to regulatory and industry quality standards in support of existing and new production processes.

Key Responsibilities and Duties:

• Conceptualize, create and implement all Quality Production strategy and tactics for the site, in collaboration with other Quality, Operations, and Functional groups.
• Develop and oversee the quality on the floor operations, including timely identification of deviations and corrective actions, and line clearances.
• Develop and execute training and Management briefings at any technical or compliance level required on updates and regulatory requirements.
• Regularly communicate with clients and participate in the Client quality reviews and other steering committees as required.
• Guide Environmental Monitoring and Quality Lab Manager in identifying and maintaining services and timeframes to all internal and external clients.
• Develop metrics and dashboard to show the effect Quality is having on the floor and in Production.
• Supervise the QA Program leads, who are responsible for client communications during the production process, to ensure customer service and program KPIs are met successfully.
• Provide leadership to and ensure necessary Quality oversight to areas within span of control.
• Effectively model, demonstrate and live an employee-focused leadership style that prioritizes compliance, respectful and professional cross departmental collaboration, accountability, and the well-being, personal, and career development of each employee.
• Effectively demonstrate and live the Charles River core values of Care, Lead, Own, and Collaborate.
• Lead, coach and mentor individuals from all parts of the organization with varying levels of experience. Be a valued resource for the site in all matters related quality and compliance.
• Perform all other related duties as assigned.

Job Qualifications

• Minimum BS/BA Life Sciences or related field. An advanced degree in the life sciences is
preferred, but not essential, based on experience
• Minimum 8 years of experience in a biologics, pharmaceutical, medical device, or related industry. 10 years of experience is preferred
• Minimum 5 years of experience with Environmental Monitoring and Assay Testing
• Minimum 7 years of managerial and supervisory experience
• Ability to maintain a high degree of accuracy and attention to detail
• Ability to handle a fast-paced, multi-tasking environment, and prioritize effectively
• Demonstrated project management skills
• Demonstrated management and collaboration skills
• Outstanding verbal and written communication skills
• Complete competency with electronic document managements systems and other information management systems
• Complete competency with electronic document managements systems and other information management systems
• Proficiency in Microsoft Office (Word, Excel, Outlook, etc.) is essential
• Understanding/familiarity with relevant FDA, EMA, ICH, USP and EP guidelines and regulations associated with the quality control of biologic/cell therapies
• Experience preferred with CDMO business and/or gene-modification modalities, cell-based gene therapies.
• ISO Lead Auditor training, desirable
• Certified Quality Engineer (ASQ), desirable

Compensation Data

The pay rate for this role is $150,000 - $176,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Equal Employment Opportunity

For more information, please visit 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.

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.

Technician I - Surgery and Efficacy - Surgery OR (Mattawan, MI, US, 49071)

Job Summary

**1st Shift Mon-Fri 700am-330pm**

We are seeking an experienced Technician 1 for our Surgery (OR) Team at our Safety Assessment site located in Mattawan, MI.

A Technician 1 is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives.

The pay for this position is $20/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The following are minimum Qualifications related to the Technician 1 position.

HS/GED/Bachelor's degree (preferred, not required) with no experience; contract research organization experience 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 communicate verbally and in writing.
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.
Ability to lift/move up to 30 pounds regularly and up to 60 pounds frequently.
Physically able to wear personal protective equipment (PPE) to include properly fitted respirator.

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 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 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.

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

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

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

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

Associate Scientist - Histology (IHC) 1 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Associate Scientist - Histology (IHC) for our Histology department in our Mattawan, MI location.

An Associate Scientist is responsible for supporting the pathology services departments by performing necropsy and histology procedures, study development procedures, and providing mentorship and training to staff. The individual in this role may also function in the role of a Contributing Scientist, responsible for the development of methods and study specific procedures in accordance with applicable protocols/plans, company standard operating procedures (SOPs), industry regulatory guidelines, and budgetary guidelines as business and scientific needs require.

The pay range for this position is $75,000-84,000/year USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Essential Functions

Performs advanced histology and/or necropsy preparation procedures on a variety of biological specimens using requisite instrumentation and techniques; performs microscopic review on a variety of specimens.
Develops, validates, implements, and/or evaluates methods and techniques for production environment and process improvement; documents procedures and materials.
Reviews study protocols, attends the pre-initiation meetings for related studies, assists with analyzing study needs, and provides expertise to study directors, sponsor representatives, QA personnel and management; serves as project lead for studies that require advanced techniques.
Consults with internal and external customers regarding scientific issues.
Assists in laboratory investigations, procedural troubleshooting, quality observations, and improvements in good laboratory practices, non-GLP practices, and departmental processes.
Assists management with presentation of scientific information.
Mentors and trains less experienced staff.
Collects, documents, analyzes, reviews, and verifies data on forms or in electronic data capture systems; recognizes method and data issues and communicates them to management to minimize study impact, collates data into the study book for archiving and study reports.
Performs quality control procedures, calibrates, maintains, cleans, and troubleshoots laboratory instrumentation and equipment.
Receives, inspects, processes, stores, and maintains documentation for biological specimens.
Other duties as assigned.

Job Qualifications

HS/GED in relevant field, with 7 or more years of relevant experience; Histotechnician (HT)/ Histotechnologist (HTL) certification required; or, Bachelor’s/Master’s degree with 5 or more years of relevant experience; HT/HTL certification required.
Two or more years IHC experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated ability to perform minor necropsy and histology techniques.
Demonstrated ability to explain scientific relevance of necropsy or histology techniques as it relates to the purpose of a study.
Ability to troubleshoot necropsy or histology techniques to preserve the integrity of a study.
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.

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.

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.

Necropsy Lab Assistant I (Reno, NV, US, 89511)

Job Summary

The pay range for this position is $17.00 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.

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

The following are responsibilities related to the Necropsy Technician 1 position:

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist in data recording.
•   Ensure the laboratory is clean and orderly.
•   Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties.
•   Receive, label and store laboratory supplies
•   Perform basic necropsy and histology support procedures (documentation, solution preparation, labeling, sample container preparation, cassette labeling, slide/block match, block sealing and tissue bagging, etc.)
•   Assist in receipt of samples, in completion of tracking documentation, and in preparation of pathology materials and data for shipment and archiving.
•   Assist in ordering supplies.
•   Perform all other related duties as assigned.

Job Qualifications

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 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 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 supported the development of ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

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

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

Laboratory Assistant I (Reno, NV, US, 89511)

Job Summary

We are seeking a Laboratory Assistant 1 for our Safety Assessment site located in Reno, NV.

This position will be responsible for performing basic laboratory and record keeping tasks

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Wash and dry glassware and distribute to appropriate locations within the laboratory. Keep glass-washing area clean and organized. May sterilize glassware and other items using an autoclave.
•   Label tubes, devices and containers and perform laboratory set-up/clean-up.
•   Assist technical personnel with clerical duties (e.g., filing, making copies, etc.).
•   Monitor inventory and stock assigned areas.
•   May record observations and measurements for basic lab/research tasks.
•   Operate basic lab equipment and perform routine maintenance as needed.
•   Perform limited troubleshooting and calibration of instruments as appropriate for assigned area.
•   May be responsible for preparing simple lab solutions (e.g., buffers, media/common vehicles).
•   May generate reports, data, and forms.
•   Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (G.E.D.).
•   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 communication skills required. Basic computer skills; familiarity with Microsoft Office software.

Equal Employment Opportunity

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

BTA / Biologielaborant /BSc als Technical Officer (m/w/d) - Genetic Testing Services (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services 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:

Laborarbeiten mit Prüfmaterialien und -Substanzen
selbständige Durchführung und Dokumentation bioanalytischer Methoden
die Auswertung der Ergebnisse nach Kapillargelelektrophorese mit Hilfe entsprechender Software, sowie Ergebnisauswertung nach real time PCR.
Erstellung von prüfungsbezogenen und übergreifenden Dokumente über das LTM (laboratory testing management) System
Durchführung aller Arbeiten unter Einhaltung von Sicherheitsstandards und internen Vorschriften.
Allgemeine Labororganisatorische Aufgaben wie Erstellen von Business Operation Standard (BOB) – Arbeitsanweisungen, Pflege von Laborgeräten und Bestellung von Laborreagenzien/-materialien
der Kommunikation mit internen / externen Kunden (GTS).

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein erfolgreich abgeschlossenes Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
strukturiertes, zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien, Verantwortungsbewusstsein, Verlässlichkeit, hohes Sicherheitsempfinden und Teamfähigkeit
hohe Lernbereitschaft zur Weiterbildung
hohe Leistungsbereitschaft
fähig Entscheidungen zu treffen
fähig zur kritischen Selbstreflexion
ausgeprägtes Informations- und Kommunikationsverhalten (intern und extern)
fähig Konflikte zu lösen
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 229274 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

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.

Weitere Informationen finden Sie unter www.criver.com.

Associate Technical Specialist (Q28T1) 12 month FTC (Portishead, GB, BS20 7AW)

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

Do you have lab experience in the biotech or pharma industry?

Are you ready for your next laboratory position?

Our In Vitro Biology team in Portishead are recruiting, could you be the next team member in our lab?

As an Associate Technical Specialist, you’ll be applying a defined technical knowledge base and skillset to independently execute routine tasks. These tasks aim to support the sites experimental and lab operations. You’ll work in accordance with the Charles River Values at all times.

Main Tasks

Accountable for delivering specialised practical support that positively impacts the day-day lab operations for immediate team and wider division.

Able to contribute to the development of robust routine technical procedures under some supervision, can present own work effectively to peers within the team and wider division.

Resolve relatively complex technical issues with some confidence, utilising support from line manager within specialism.

Demonstrate clear ownership of tasks, consistently meeting project deliverables in line with client requirements.

Independent Technical support:

Blood and Ex Vivo Sample processing

Maintenance of cell lines across projects

Isolation of subsets of immune cells from blood (MACS)

Phenotype purity assessments by flow cytometry

Following training, other standardly used techniques used within in vitro/ex vivo Biology

Continuous improvement – ensure that any “just do it” actions are carried out in order to enhance efficiency and productivity. Focus on cost-saving initiatives both hard and soft savings.

Health and Safety – support H&S initiatives that ensure laboratories and buildings comply with CRL site-based guidelines – Proactively seek improvements and aid the implementation of new processes.

Stock control – ensure consumables stocks are kept to the required level, procuring best alternatives and finding cost savings where possible.

Maximo - continued operation and update of Maximo and ensuring all servicing reports are saved in the correct place. Work orders are completed/acted within a week (earlier depending on the urgency).

Skills and Experience

Significant lab-based experience in academia and / or industry

Strong communication skills, both written and verbal.

Excellent problem-solving skills, able to approach problems with sound logic and judgement.

Able to collate complex scientific data effectively.

Training is provided for all scientific tasks and processing.

Advantageous but NOT essential:

Educated to BSc level.

MSc preferred within a relevant scientific discipline.

Relevant CRO / Biotech / Pharma industry in specialism.

General cell biology and in vivo processing support.

What We Offer You

A very comprehensive benefits package from day one, including a generous pension contribution, private medical for you (and can add family members), private dental care, critical illness cover, bonus and more!

Access to great discounts via our CREDS discount scheme.

Global opportunities and strong career progression.

The chance to work on several varied projects and liaise globally and nationally with other business areas.

To be able make a difference to health and wellbeing of people.

To continue your own career growth.

Flexible and hybrid working.

Parental leave.

Group Life Assurance and Group Income Protection.

Remote GP access 24/7.

Well-being support and initiatives.

Cycle to work scheme.

Well-being support and initiatives.

Cycle to work scheme.

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.

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.

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.

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

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.

Marketing Specialist (Zhanjiang, GD, CN)

Job Summary

Job Qualifications

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.

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.

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

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 ~85% of the drugs approved by the FDA in 2019.

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

Veterinary Pathology Certified (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Veterinary Pathologist for our team at the Laval location, 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 Histopathology findings in data capturing system;
Prepare complex reports delineating pathological findings and detailing all test article effects;
Interact with clients to assure satisfaction and to market services;
Assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation;
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;
Provide advanced scientific expertise for experimental design and other aspects of research studies;
Collaborate with other units within the Pathology teams and other departments within the site.

Key Elements

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

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;
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;
Special interest in digital Pathology & Molecular Pathology as well as digital image analysis is preferred;
Bilingualism in French and English is mandatory. Good communication skills in both languages is required.

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;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
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 ACVP / ECVP yearly license;
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.

Equal Employment Opportunity

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

Pathologiste vétérinaire avec certification (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Pathologiste Vétérinaire pour notre équipe située au site de Laval, 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 poste, les principales responsabilités incluront:

Effectuer l'évaluation et l'interprétation macroscopes et microscopiques des tissus des études assignées;
Enregistrer les résultats d'histopathologie dans le système de capture de données;
Préparer des rapports complexes décrivant les résultats pathologiques et détaillant tous les effets des articles de test;
Interagir avec les clients pour assurer leur satisfaction et promouvoir les services;
Aider à la supervision des nécropsies et peut réaliser des nécropsies, y compris l'interprétation de la pathologie macroscopique, la collecte et la fixation des échantillons;
Travailler avec les directeurs d'études pour s'assurer que les données sont intégrées avec précision dans les rapports d'études;
Fournir formation, orientation technique et leadership au personnel de laboratoire et aux pathologistes moins expérimentés;
Apporter une expertise scientifique avancée pour la conception expérimentale et d'autres aspects des études de recherche;
Collaborer avec d'autres unités au sein des équipes de Pathologie et d'autres départements sur le site.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme de doctorat (D.V.M/V.M.D.) d'une école vétérinaire accréditée, ou équivalent international acceptable en médecine vétérinaire;
Connaissance pratique de la pathologie clinique préférée;
Certification par le American College of Veterinary Pathologists (A.C.V.P.) ou le European College of Veterinary Pathologists (E.C.V.P) requise pour accéder au grade de niveau;
Succès démontré en compétence technique, créativité scientifique, collaboration avec les autres et pensée indépendante;
Capacité à travailler sur des problèmes de portée diverse où l'analyse des données nécessite une évaluation de multiples facteurs;
Capacité à exercer un jugement dans le cadre de pratiques et politiques généralement définies lors de la sélection des méthodes ou techniques pour obtenir des solutions;
Connaissance pratique des applications informatiques connexes;
Un intérêt particulier pour la Pathologie numérique et la Pathologie moléculaire ainsi que l'analyse d'image numérique est préféré;
Le bilinguisme en français et en anglais est obligatoire. De bonnes compétences en communication dans les deux langues sont requises.

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: 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;
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);
Licence annuelle ACVP / ECVP payée;
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.

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

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.

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

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

Microbiologist 1 (Dublin, IE, D09)

Job Summary

Full-time Scientific Research In-Vitro Associate 1 (Microbiologist) required to operate under the Technical Services Department for our Microbial Solution Site in Dublin.

The successful candidate will be responsible for processing microbial and LAL testing samples in our CELSIS laboratory utilising various technology platforms.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform LAL testing for different studies as assigned encompassing a full range of LAL techniques, gel-clot, kinetic and PTS.
Perform IQ, OQ, PQ of lab equipment such as Biotek, PTS and maintain appropriate documents.
Perform contract testing laboratories for Celsis and LAL including method development studies, method validation studies, accessory release, CSE/RSE, LAL water etc as required.
Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria.
Perform and manage bioburden testing, membrane filtration and, cleaning validations.
Ensure adherence to pertinent regulatory requirements (cGMP, FDA, ISO) and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
Collaborate with inventory check of laboratory consumables and assist with general housekeeping of the laboratory, performing equipment maintenance and scheduling instrument calibrations.
Assist management with development and revision of departmental standard operating procedures and qualification documents.
Perform all other related duties as assigned.

Job Qualifications

Education: Degree in Microbiology, Biology or a related discipline.
Experience: Established and demonstrable track record of related experience in a microbiology laboratory setting. Experience in cGMP pharmaceutical microbiology environment is preferred.
Other: Knowledge of windows based programs such as word and excel and a minimum knowledge of algebra.

PHYSICAL DEMANDS:

Requires colour vision, close vision and the ability to adjust focus.
Regularly works in a stationary position; occasionally moves about the lab/office to access supplies and equipment.
Regularly communicates with other employees/customers and must be able to exchange accurate information verbally and in written form.
Occasionally operates a computer.
Occasionally must perform manual handling.
Must be able to wear personal protective equipment (PPE) according to company standards.

WORK ENVIRONMENT:

Working in a lab environment. May work with sharp objects, near toxic or caustic chemicals, with biohazards, may be exposed to fumes or airborne particles, unpleasant odors and may be exposed to the risk of radiation.
The noise level in the work environment is usually quiet to moderate.
While performing the duties of this job, the employee regularly wears protective clothing and equipment (lab coat and safety glasses) when exposed to the laboratory area

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.

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, 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.

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.

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.

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

Manager Biobanques - F/H - CDI (Saint-Nazaire, FR, 44600)

Le poste

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.

Production Technician 1st Shift (Charleston, SC, US, 29407)

Job Summary

Assist with seasonal cell collection. Perform all PTS production related activities with general supervision. Shift hours 6:00 AM - 2:00 PM Monday - Friday

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Assist with seasonal crude lysate production.
Perform all PTS production related activities.
Responsible for cleaning and preparation of clean rooms, stocking fill supplies, performing pre-fill potency test and preparing reusable supplies for autoclaving/depyrogenation.
Perform Class 100 fill operations using automated and manual equipment.
Responsible for printing and inspection of final PTS products and sustain general environmental upkeep.
Responsible for proficiency in all SOPs in areas of responsibility.
Responsible for documentation as required by company policy, cGMP and FDA.
Perform 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.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

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.

Equal Employment Opportunity

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.

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.

Equal Employment Opportunity

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

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.

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.

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!

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

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.

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!

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

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

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.

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

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

Team Leader - Animal Care (Shrewsbury, MA, US, 01545)

Job Summary

We are seeking an experienced Team Leader, Animal Care for our Safety Assessment site located in Shrewsbury, MA.

The Team Leader Animal care is 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, administration of prescribe treatments, handling and restraint and related tasks.

The following are minimum responsibilities related to the Team Leader, Animal Care position:

Serve as lead/primary technician and perform technical duties.
Provide leadership and technical guidance and serve as a mentor to less experienced staff.

The following are minimum requirements related to the Team Leader, Animal Care position.

Education: High school diploma or General Education Degree (G.E.D.) required. Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline preferred.
Experience: Min of 2-3 years related experience in animal research and/or husbandry required. 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 LAT level required; LATG preferred. LVT/RVT 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.

The pay for this position is between $34.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Formulations Technician I (Horsham, PA, US, 19044)

Job Summary

Full Time – 40 Hours/Week - Must be able to start within one month

Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Prepare bulk vehicles and test article formulations utilizing various mixing methods and apparatus.

· Prepare dosing aliquots and formulation samples for solutions, suspensions and dispensations under supervision.

· Ensure accurate recording of test article and vehicles/reagents to maintain accountability and inventory.

· Calibrate, operate and assist in maintenance of basic laboratory equipment.

· Collect, record data and perform all tasks in accordance with Good Laboratory Practices Regulations (GLPs), study protocols and Standard Operating Procedures (SOPs).

· Perform daily verification of formulation calculations and data quality control checks.

· Perform study preparation activities including labelling aliquot and sample tubes, study book set-up and laboratory set-up/clean-up.

· Assist with glassware washing and maintain cleanliness and general appearance of the Formulations Laboratory.

· Perform other related duties as assigned

The pay range for this position is $21.70/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: Bachelor’ degree (B.S.) preferred

· Experience: Minimum of 0 to 1 years laboratory 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: Must have valid, state-issued, driver’s license.

· Other: Must be detail-oriented and have good verbal and written communication skills. Must have good computer skills and experience with Microsoft Office software.

PHYSICAL DEMANDS:
•   While performing the duties of this job, the employee is regularly required to talk, hear and lift.
•   Must be able to regularly wear safety equipment and clothing in compliance with OSHA regulations and company SOPs.
•   Specific vision abilities required by this job include close vision and the ability to adjust focus.
•   Must be able to regularly measure and combine chemicals in order to prepare test article for use in the laboratory.
•   Regularly record data by hand or on a computer terminal.
•   Must be able to regularly stand approximately 6 to 8 hours a day.
•   Must be able to regularly measure and combine chemicals in order to prepare test article for use in the laboratory.
•   Must be able to regularly communicate with other personnel and sponsors regarding all aspects of the day to day operations of the Formulations Laboratory.
•   Must be able to regularly read and follow Standard Operating Procedures.

WORK ENVIRONMENT:
•   General research laboratory working conditions.
•   The noise level in the work environment is usually moderate.
•   Works with or near caustic chemicals and with chemical compounds with unknown levels of toxicity.

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

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.

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.

Research Technician I (Shrewsbury, MA, US, 01545)

Job Summary

Charles River Laboratories is seeking a Research Technician I for our In Vivo (In Life) Team within our Safety Assessment site located in Shrewsbury, MA.

The Research Technician 1 will 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.

The following are minimum 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 to 1 year 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 GLPs and other federal regulations and guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay range for this position is $24.50 an 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.

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 supported the development of 86% of the drugs approved by the FDA in 2021.

For more information, please visit www.criver.com. #LI-LH1

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 2-3 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:

ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred
High school diploma OR GED preferred

The pay for this position is $22.00 USD 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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.

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.

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.

Animalier contrôle de production - F/H - CDI Week-end (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.

Nous recherchons un Animalier contrôle de production (F/H) pour un contrat en CDI week-end et jours fériés pour un contrat de 8h/semaine à raison de 4h par jour (samedi, dimanche et jours fériés) sur l'un de nos site client basé à Paris 13ème.
Vous contribuerez au respect du bien-être animal et au maintien des meilleures conditions d'hébergement pour les animaux (poissons).

Missions principales

Contrôle du bien-être des animaux selon les consignes préalablement transmises
Vérifier l'abreuvement, l'alimentation et l'enrichissement
Vérification et relevé des paramètres d'ambiance
Respect des consignes transmises
Garantir la mise à jour des registres de suivi.

Profil recherché

Vous êtes étudiant dans des études scientifiques, motivé, rigoureux, passionné par le travail des animaux et vous voulez acquérir une expérience en contact avec les animaux de laboratoire:

Formation initiale: étudiant en étude vétérinaire, biologie ou en cours d'obtention d'un diplôme dans un domaine scientifique ou animalier.
Expérience: une première expérience en contact avec les animaux et/ou en animalerie de laboratoire est un atout
Esprit d'équipe et capacité à collaborer avec les différents interlocuteurs
Organisation et rigueur au quotidien
Sens de l'observation et capacité à identifier des anomalies
Autonomie et proactivité

Modalités contractuelles

   • Convention collective de l’industrie pharmaceutique
   • Nous vous proposons un CDI avec le rythme de travail suivant : samedi, dimanche matin (4h/jour) et jours fériés
   • Prime de transport, 13e et 14e mois, Intéressement, participation, mutuelle et prévoyance, CE

À propos d'Insourcing Solutions
Insourcing Solutions℠ de Charles River peut rationaliser la recherche en favorisant l'efficacité opérationnelle et les économies de coût grâce à son processus stratégique de réalisation en interne pour les services de recherche GMP, GLP et hors GLP, depuis la découverte jusqu'à l'évaluation de l'innocuité. Insourcing Solutions℠ vous offre la possibilité de continuer à contrôler votre espace de travail et à rester maître de votre expertise tout en tirant le meilleur parti possible de l'espace disponible.

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

Senior HVAC Technician (Wayne, PA, US, 19087)

Job Summary

The Senior HVAC Technician is responsible to 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.

This position will work on-site at the Wayne, PA Charles River site. Position will also be responsible to travel to additional CRL sites located in Malvern and Philadelphia.

Position is scheduled to work Monday - Friday, from 9am - 5pm.

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

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) and trade school diploma.
• Experience: Four to six 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 HVAC license (where required by state).
• Valid Driver's License.

PHYSICAL DEMANDS:
• While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to stoop, kneel, crouch, or crawl and talk or hear.
• The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move more than 100 pounds.
• Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.

WORK ENVIRONMENT:
• While performing the duties of this job, the employee frequently works near moving mechanical parts and in outside weather conditions.
• While performing the duties of this job, the employee occasionally works in high, precarious places and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, risk of electrical shock, risk of radiation, and vibration.
• The noise level in the work environment is usually moderate.

Compensation Data

The pay range for this position is $35.63/hr. 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

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.

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

Qui sommes-nous ?

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.

Study Coordinator I (Horsham, PA, US, 19044)

Job Summary

Perform the collection, preparation and distribution of information necessary for protocol development and study initiation for studies on basic levels of studies under the supervision of a study director, principal investigator and/or supervisor of study coordination. Assist the Study Director during in- and post-life by providing and coordinating scientific and administrative support and in the production of a high quality, accurate and timely study report.

Essential Duties and Responsibilities
• Assist in preparation of study-specific protocols consistent with the requirements of the Sponsor, laboratory SOPs and applicable government and regulatory body guidelines and GLPs.
• Assist in the preparation of schedules for study-specific protocols; review schedules for consistency with lab scheduling system and update the schedule as required.
• Distribute draft protocols for internal/Sponsor review, coordinate protocol finalization process, and distribute and track distribution of final protocols and completed approval pages to the Sponsor, facility staff and subcontractors.
• Coordinate revision of draft protocols in response to Sponsor requests, QAU audits and internal review, and prepare response letters to Sponsors documenting draft protocol revisions.
• Generate study timelines for study reports.
• Assist in notifying departments of new information or design changes for upcoming studies
• Provide internal QC via peer review
• Assist SD in communicating study status to the Sponsor
• • Monitor key study events and notify study team members of upcoming events
• Assist in responding to audits of methodology, deviation and result report sections, and responding to or routing questions appropriately for audits of other report sections.
• Edit, format and compile assigned reports for final issue as assigned by Supervisor.
• Review Sponsor requests for changes to the draft or final reports and route tasks to appropriate personnel.
• Responsible for tracking and processing revised draft final reports for finalization.
• Responsible for updating Sponsors request files for staff’s use when preparing draft and final reports.
• Coordinate the generation and handling of electronic report format requests. Assist in evaluating new technologies for creating these formats.
• File correspondence and other documents in central filing system.
• Prepare historical control data summaries for specialized data.
• Prepare for and attend Protocol Meetings as required.
• Contact subcontractors as necessary to clarify study requirements or facilitate scheduling or revisions of reports.
• Gather data/information to fulfill special Sponsor requests.
• Prepare End of Study e-mail and distribute to study teams. Compile responses

The pay range for this position is between $26.00 and $28.00 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: Bachelor’s degree (BS/BA) or equivalent, preferably in a life science.
• Experience: One or more years experience in a GLP laboratory 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: None
• Other: None
Physical Demands:
• While performing the duties of this job, the employee is regularly required to talk and hear.
• Specific vision abilities required by this job include regular use of close vision and the ability to adjust focus.
• Must be able to regularly sit approximately six hours a day.
• Must be able to regularly read and transcribe typewritten or handwritten information into a personal computer and make edits on information therein.
• Regularly required to type for three to four hours at a time.
• Frequently files and retrieves information in four drawer file cabinets.
• Regularly operates all office equipment.
WORK ENVIRONMENT:
• General office working conditions. The noise level in the work environment is usually quiet.
• Occasionally works near toxic or caustic chemicals and test articles with unknown levels of toxicity.
• May occasionally be required to wear protective clothing and equipment.

Equal Employment Opportunity

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

Associate Instrument Specialist 1 (Tranent, GB, EH33 2NE)

Job Summary

We are currently recruiting for an Associate Application Specialist to work in the Computer System Validation team (CSV), based at our world class facility in Tranent, East Lothian.

The Computer System Validation (CSV) team support the departments conducting scientific studies by managing their computer systems (instrumentation/equipment and software) to meet regulatory requirements. This will involve working collaboratively with scientific staff, IT and quality assurance to ensure strict regulatory expectations are met regarding the capture, processing and secure storage of electronic data, whilst providing a practical and user friendly system for scientific staff to conduct their work efficiently, effectively and with full trust and confidence in the data they produce.

The successful candidate’s role will be to help maintain current active computer systems, implement user access control requirements, troubleshoot reported errors, liaise with vendors etc. They will also ensure systems remain relevant and fully compliant through regular reviews. Completion and administration of documentation is an active part of the regular duties. The successful candidate will be expected to keep modernising and improving the compliance and usability of systems through introduction of new features in a controlled manner involving testing.

The minimum requirements for this role are:

Ideally educated to a graduate level, preferably in a Scientific or Information Technology discipline but not essential.
Candidates must be enthusiastic, proactive, organised, customer focused and have an analytical approach to problem solving.
Experience of working in a regulated environment (GLP/GMP) preferred but not essential.
Excellent communication skills and working seamlessly with different groups of people.
Excellent computer system skills. (Excel, Word, etc.)

Project Management skills and attention to detail

Salary for this role is £27,951.22.

Closing date is 31 July 2025.

Profile and Requirements

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.

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.

Laboratory Animal Technician I (NHP) (Poolesville, MD, US, 20837)

Job Summary

We are looking for an Laboratory Animal Technician I to join our Insourcing Solutions team located in Poolesville, MD.

Why work at Charles River?
We adhere to strong values, share the same mission, that together, we create healthier lives. Our culture is one of endless opportunity, purpose and creating change. We are committed to empowering our employees with the tools and programs they need to develop rewarding careers. We offer competitive benefits and excellent training programs for all our employees.

What you will do!

In the Laboratory Animal Technician I role, you will maintain, monitor, and document the health, well-being, and physical environment of animals on-site.

You will also be tasked with the following:

Monitoring daily animal health and welfare while performing daily animal health observations.
Animal husbandry duties include daily water bottle /automatic water line and cage checks; provide appropriate food and water; environmental enrichment; perform cage changing and/or cage cleaning as required.
Maintain records related to the animal and facility functions; record animal health concerns and report as needed.
Assists with restraint, handling, and manipulation of various animal species.
Receive, inspect, and house incoming animals.
Other duties will include general housekeeping, in addition to reviewing, comprehending, and complying with all SOPs and quality assurance standards pertaining to specific area.

Who are we looking for?

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

A candidate that possesses a high school diploma or GED required.
Experience with lab animals, specifically non-human primates, or any animal experience preferred but not required.
Must be able to obtain the AALAS certification at the ALAT level within 6 months of eligibility.

The pay for this position is $21.00 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Laboratory Operations lead (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Laboratory Operations lead to work in our Biosafety and Cell Based Assay Laboratory located in Ballina, Co. Mayo, Ireland.
The preferred candidate will have demonstrable knowledge of laboratory safety and laboratory equipment in a GMP setting and will be instrumental in planning, directing and implementing improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory.

This role shall report to the Biosafety & Cell Based Assay Manager and the main duties & responsibilities shall be to:
• Manage the daily operation of the laboratory, ensuring efficient workflow, appropriate allocation of tasks, and maintenance of high operational standards
• Ensure the laboratory maintains compliance and adherence to Good Manufacturing Practices (GMP)
• Manage laboratory Health & Safety, including risk assessments, COSHH, internal safety audits, and promoting a culture of good laboratory practice and safe working
• Oversee stock maintenance, procurement and supplier approval
• Coordinate internal/client/regulatory audits of the laboratory area
• Liaise with the Quality Department on audit responses, facility replies and equipment OOL / deviation reports
• Oversee maintenance of all laboratory equipment in coordination with Calibration /Validation team
• Communicate with external engineers / contractors
• Generation of / Updating GMP compliant SOPs

Job Qualifications

The following are minimum requirements related to the Laboratory Operations Lead position.
• Bachelor’s degree in Pharmaceutical Science, Cell Biology / Molecular Biology or a related science
• 3+ years’ experience in a fast-paced GMP Lab
• Must be able to work as an integral part of a broader team with QA, QC, Validations, Procurement, etc
• Excellent communication skills and a good problem solver
• Experience of managing people is preferable
• Detail-oriented with a high level of accuracy
• Ability to deal with people at all levels including internal and external clients

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 supported the development of 80% of the drugs approved by the FDA in the last 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.

Research Analyst I - Bioanalytical Chemistry (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI.

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.

Essential Functions:

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
Assist with laboratory maintenance functions
Independently perform laboratory support functions such as labeling and solution preparations
Assist with maintaining study specific inventory of consumables with oversight
Write both study and non-study deviations with minimal oversight
Actively participate in process improvement initiatives with oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area
Assist in execution of routine sample analysis studies with oversight
Assist in execution of method validation projects with oversight as needed
Operate laboratory instruments with complete oversight
Assist with data analysis in appropriate software for at least one analytical platform

Job Qualifications

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

Minimum of a Bachelor’s degree (BA/BS) or equivalent experience. No previous work experience required
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.
Experience with LC/MS/MS preferred
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
Ability to wear proper PPE for the duration of the shift; which includes and is not limited to the following: Gloves, safety glasses, laboratory coat, cartridge respirator, dust/mist respirator, supplied air respirator, Tyvek suit, sleeve protectors.

The pay for this position is $23.50. 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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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

Security Officer - 2nd Shift - Rotating Weekends (Mattawan, MI, US, 49071)

Compensation Data

This position offers $19.00/hr as a starting wage alongside a 10% shift differential.

Job Summary

We are seeking an experienced full-time Security Officer for the 2nd Shift Security team in Mattawan, MI.

Job Qualifications

HS/GED degree with 2- 3 years of experience, with at least six to twelve months of related security experience and/or training; contract research organization experience preferred. Driver’s license is required.
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.

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 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 supported the development of 86% of the drugs approved by the FDA in 2021.

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

Technician I, Technical Operations (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I, Technical Operations for our Safety Assessment site located in Ashland, OH. This is a full-time position that requires 5-9 weeks of training Tuesday-Friday 6am-430pm at $19/hour. After training the WEEKDAY shift is Tues-Fri 6am-430pm; every 4th weekend, every other holiday. We also have weekend shifts available. The weekend schedules are Friday-Sunday or Saturday-Monday 6am-630pm, every other holiday after training. There is a 10% pay differential for Saturday/Sunday hours only.

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 support a study, which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. The technician may occasionally perform basic skills independently but continues working under supervision to gain proficiency on skills still in development.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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 handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. 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.
Ensure high levels of study quality to meet study goals.
Follow all PPE, safety, cleaning, and cross-contamination elimination practices.
Maintain appropriate communication with other personnel.
Support team-mates, technicians, and members of other departments.
Follow direction from team leaders, trainers, research associates and supervisors.
Use and maintain instrumentation and equipment according to SOPs.
Perform all tasks per SOP, BOP, and/or protocols.
Perform all other related duties as assigned

The starting pay for this position is 19.00 per hour. Please note that starting salaries vary 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.) 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.
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 Procedures (SOPS).

Equal Employment Opportunity

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.

Equal Employment Opportunity

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

Gestionnaire Senior, Conformité commerciale mondiale (À Distance) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Gestionnaire Senior de notre équipe à distance, Conformité Commerciale Mondiale, vous apporterez un soutien commercial et douanier en supervisant la gestion quotidienne du processus de dédouanement aux États-Unis et au Canada. Vous veillerez à ce que les transactions respectent les exigences réglementaires relatives au dépôt de déclarations d'exportation et d'importation complètes et exactes auprès des douanes locales et des autres autorités gouvernementales pour les expéditions internationales.

Dans ce poste, les principales responsabilités incluront:

Gérer l'administration de l'équipe Conformité des classifications HTS des États-Unis et du Canada, de l'applicabilité des tarifs, de la détermination de l'origine et de toutes les exigences des organismes gouvernementaux participants (p. ex. FDA, USDA/APHIS, FWS, CDC, EPA) ;
Superviser le processus d'examen après entrée des importations américaines et canadiennes et faciliter les ajustements sommaires après entrée ;
Communiquer avec le CBP et l'ASFC, les courtiers en douane, les organismes de réglementation des produits et les autres parties prenantes afin de faciliter la mainlevée des expéditions ;
Responsable de la qualification des demandes d'accords de libre-échange (p. ex. AEUMC) ;
Former, motiver et encadrer les équipes de conformité et d'expédition sur site afin d'atteindre les objectifs de conformité ;
Identifier les possibilités d'amélioration des processus opérationnels et des niveaux de service existants et gagner en efficacité ;
Travailler en étroite collaboration avec toutes les unités opérationnelles afin de comprendre leurs besoins spécifiques et les matières importées et exportées ;
Suivre les modifications réglementaires régionales et mondiales en matière de conformité douanière et commerciale ;
Tenir à jour les registres d'importation et d'exportation afin de garantir la conformité de l'entreprise à la réglementation douanière ;
Aider au contrôle des parties restreintes et assurer la conformité au contrôle des exportations.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Au minium 7 ans d'expérience professionnelle pertinente dans le domaine de la conformité douanière et commerciale, de préférence dans les secteurs pharmaceutique et des biosciences ;
Solide compréhension de la conformité douanière et commerciale à l'importation et à l'exportation ;
Capacité à gérer plusieurs problèmes simultanément avec de solides compétences en organisation et en priorisation ;
Courtier en douane agréé (LCB) ou spécialiste en douane certifié (CCS) de préférence ;
Expérience avec ACE et CARM.

Informations spécifiques au poste:

Localisation: À distance
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi, de jour;
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.

À propos des fonctions support

Les personnes exerçant des fonctions de gestion apportent un soutien opérationnel dans tous les domaines dans lesquels travaille Charles River, notamment dans les ressources humaines, les finances, l'informatique, les affaires juridiques, les ventes, l'assurance qualité, le marketing et le développement de l'entreprise. Elles collaborent avec leurs homologues dans toute l'entreprise pour élaborer et mettre en oeuvre des stratégies, et pour établir des normes mondiales. Ces fonctions sont essentielles dans la mesure où elles créent un lien entre la vision stratégique de l'entreprise et sa disponibilité opérationnelle afin de garantir une innovation fonctionnelle permanente et une amélioration continue de ses capacités.

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.

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

Senior Manager Trade Compliance (Remote) (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Manager for our Global Trade Compliance remote team, you will provide trade and Customs support by overseeing the day-to-day management of the Customs clearance process in the US and Canada. You will
ensures that transactions satisfy regulatory requirements to file complete and accurate export and import declarations with local customs and other government authorities for international shipments.

In this role, primary responsibilities include:

Manage the Compliance team’s administration of US and Canada HTS classifications, tariff applicability, origin determination, and all participating government agency requirements (i.e. FDA, USDA/APHIS, FWS, CDC, EPA);
Oversee the Post Entry review process for US and Canada importations and facilitate post summary adjustments;
Communicate with CBP and CBSA, Customs brokers, PGA’s, and other stakeholders to facilitate release of shipments;
Responsible for qualification of free trade agreement claims (i.e. USMCA);
Train, motivate, and mentor compliance and site shipping teams to achieve compliance goals and objectives;
Identify improvement opportunities to existing business processes and service levels and gain efficiencies;
Work closely with all business units to understand their specific needs and the materials which are being imported and exported;
Monitor regional and global Customs and Trade Compliance Regulatory Changes;
Maintain import and export records to ensure company compliance with Customs regulations;
Assist with restricted party screening and ensure export control compliance.

Key Elements

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

Minimum 7 years of relevant working experience, within Customs and Trade Compliance, preferably in the pharmaceutical or bioscience industries;
Solid understanding of Customs and trade compliance for import and export;
Ability to handle multiple issues simultaneously with strong organizational and prioritization skills;
Licensed Customhouse Broker (LCB) or Certified Customs Specialist (CCS) preferred;
Experience with ACE and CARM.

Role Specific Information:

Location: Remote;
Annual bonus based on performance;
Schedule: Monday-Friday, Day;
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);
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.

Compensation Data

The pay range for this position is $120K - 140K USD annually. 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.

Animal Research Technician (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $20/hour plus benefits.

A Technician 1 – In Vivo Technical Operations 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 animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. The technician is working under close supervision to gain proficiency.

Successful Candidates will possess the 6 Cs of Success:

Character – Unquestionable integrity. Respect for all.
Coachable – Eager to receive feedback. Open to making improvements.
Commitment – Dedicated to our animals, our clients/studies, our team.
Collaborative – Team player. Eager to help.
Communicative – Proactively asks questions. Provide complete answers.
Competent – Continuously and proactively hones and expands skill sets.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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 handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. 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.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained 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.

Equal Employment Opportunity

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

Education & Experience: To qualify for this role, candidates must have one of the following combinations of education/experience:

High School Diploma or G.E.D. plus a minimum of six to twelve months experience working in a laboratory animal facility performing animal husbandry
Associates degree in animal science or related field plus a minimum of six months experience working in a laboratory animal facility performing animal husbandry.
Bachelors degree in animal science or related field plus zero to six months experience working in laboratory animal facility performing animal husbandry.
Certification/Licensure: None

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

Equal Employment Opportunity

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

Quality Control Associate I (Wed - Sat 8:00am - 6:30pm) 1 (Rockville, MD, US, 20850)

Job Summary

Note: Hours for this position: Wednesday thru Saturday 12pm - 10:30pm

Key Responsibilities and Duties:

Perform routine testing in a quality control laboratory to support in-process, lot release and stability testing
Experience performing some of the following in a QC laboratory setting: qPCR / ddPCR, cell-based assays, ELISA, other QC methods (pH, osmolality, endotoxin and appearance)
Perform sample receipt and log-in procedures as required
Contribute to generating SOP’s and qualification/validation/transfer protocols and reports
Responsible for cross training on multiple QC assays
Responsible for participation in method development/qualification studies
May train other associates on methods as appropriate
Perform general lab upkeep, order of lab supplies and maintenance of logbooks as required.
Other responsibilities as required

Job Qualifications

B.S. or M.S. and 1-2 years of experience in biology, virology, molecular biology, cell biology, biochemistry, or related field in a quality control testing laboratory
Team-player
Develop proficiency in compendial methods, molecular biology, cell culture, and ELISA techniques
Able to work in a GMP environment to execute testing
Able to support multiple projects and strong organizational skills
Able to learn data analysis and interpretation experimental data
Complete On-The-Job Training before executing the QC lab responsibilities
Develop communication skills with ability to present information to the internal QC team

Compensation Data

The pay range for this position is $22.24 - $28.17. 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.

Equal Employment Opportunity

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

Research Scientist - Safety Pharmacology (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Research Scientist in Safety Pharmacology in our Pharmacology team located at the Senneville site, you will be responsible for the design, execution, and interpretation of preclinical studies focused on cardiovascular safety, utilizing advanced telemetry and ECG technologies.

In this role, primary responsibilities include:

Plan, develop, and lead preclinical cardiovascular safety pharmacology studies, including ECG evaluations, telemetry,
Plan, develop and leads core battery safety pharmacology respiratory assessments, and neurobehavioral assessments.
Conduct ECG snapshot analysis and continuous telemetry monitoring to assess cardiovascular safety.
Perform qualitative and quantitative ECG data analysis, ensuring accurate interpretation of cardiovascular safety signals.
Analyze data from ECG, telemetry, and other safety pharmacology tests, and provide comprehensive reports and recommendations.
Ensure all studies are conducted following Good Laboratory Practice (GLP) and regulatory guidelines.
Oversee the integrity of scientific data, ensuring reproducibility and accuracy in results.
Work closely with multidisciplinary research teams, collaborating on study designs and contributing scientific expertise.
Innovate and implement improvements in testing protocols and data analysis techniques to enhance study efficiency and reliability.
Maintain accurate and detailed documentation of study protocols, procedures, and data in accordance with GLP standards.

Key Elements

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

M.Sc. or Ph.D. in Pharmacology, Physiology, or related scientific discipline with a strong emphasis on cardiovascular research or a closely related field;
Experience with cardiovascular research, Safety Pharmacology core battery testing.
Computer literate (Microsoft Word and Excel) and possess excellent communication, interpersonal and teamwork abilities;
Fluent in French and English. Bilingualism is preferred;
GLP knowledge (is an asset)

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);
3 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.

Equal Employment Opportunity

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

Scientifique de recherche - Pharmacologie de sécurité (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Scientifique de recherche au sein de notre équipe de pharmacologie de sécurité, située sur le site de Senneville, vous serez responsable de la conception, de la réalisation et de l'interprétation d'études précliniques axées sur la sécurité cardiovasculaire, en utilisant des technologies avancées de télémétrie et d'ECG.

Vos principales responsabilités incluent :

Planifier, développer et diriger des études précliniques de pharmacologie de sécurité cardiovasculaire, incluant des évaluations ECG, de télémétrie,
Planifier, développer et diriger des évaluations pharmacologiques de sécurité respiratoire et neurocomportementales.
Réaliser des analyses instantanées d'ECG et une surveillance télémétrique continue pour évaluer la sécurité cardiovasculaire.
Réaliser des analyses qualitatives et quantitatives des données ECG, garantissant une interprétation précise des signaux de sécurité cardiovasculaire.
Analyser les données d'ECG, de télémétrie et d'autres tests de pharmacologie de sécurité, et fournir des rapports et des recommandations complets.
S'assurer que toutes les études sont menées conformément aux Bonnes Pratiques de Laboratoire (BPL) et aux directives réglementaires.
Superviser l'intégrité des données scientifiques, en garantissant la reproductibilité et l'exactitude des résultats.
Travailler en étroite collaboration avec des équipes de recherche multidisciplinaires, en collaborant à la conception des études et en apportant son expertise scientifique. Innover et mettre en œuvre des améliorations dans les protocoles de test et les techniques d'analyse des données afin d'améliorer l'efficacité et la fiabilité des études. Tenir une documentation précise et détaillée des protocoles, procédures et données d'étude, conformément aux normes BPL.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Maîtrise ou doctorat en pharmacologie, physiologie ou discipline scientifique connexe, avec une forte concentration en recherche cardiovasculaire ou dans un domaine connexe ;
Expérience en recherche cardiovasculaire et en tests de batterie de tests de pharmacologie de sécurité.
Maîtrise de l'informatique (Microsoft Word et Excel) et excellentes aptitudes à la communication, aux relations interpersonnelles et au travail en équipe ;
Maîtrise du français et de l'anglais. Le bilinguisme est un atout ;
Connaissances en BPL (Bonnes pratiques de laboratoire) (un atout).

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);
3 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 Technologist / Team Lead (Chicago, IL, US, 60607)

JOB SUMMARY

We are seeking an Senior Technologist / Team Lead to support our GEMS site in Chicago, IL. The GEMS Senior Technologist / Team Lead is a highly skilled team leader who can work independently and within a team to maintain, monitor and help coordinate the health, production, and physical environment of client or Charles River Laboratories (CRL) animals housed at CRL facilities, as well as provide guidance. These environments may include isolators or individual ventilated cages (IVC).

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Highly skilled in techniques needed to perform basic husbandry tasks in a resourceful and efficient way, including supplying food, bedding, water and environmental enrichment.
Highly skilled in techniques and concepts of 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.
Highly skilled in techniques and concepts of handling rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Highly skilled in techniques and concepts of observing animals for any abnormalities or common health issues.
Highly skilled in techniques and concepts of identifying and selecting specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Understand and comply with all Standard Operating Procedures (SOPs). Acts independently to determine methods and procedures on new practices.
Often makes recommendations for revising or creating new procedures.
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 high-level responsibilities and requires independent action and a high degree of initiative to resolve issues. Must be highly effective, 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.
Often acts as a facilitator and team leader of department responsibilities.
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
Self-organize, plan and execute tasks independently. Ability to adapt and champion change.
Highly skilled in general computer skills and ability to quickly learn and master required computer programs, databases and other applications (i.e. ICM and Microsoft Office). Contributes to the development of new department concepts, programs and solutions.
Coordinates other operations personnel in department when Supervisor is absent.
Facilitates studies, special projects, efficiency improvements, engagement opportunities, etc.
Assist in providing leadership and motivation to department personnel.
Identify issues and owns implementation of solutions.
Champions and facilitates CRL DNA in day-to-day work.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidate must possess one of the following:

High School Diploma or GED and 4 years of leadership and/or animal care experience
Bachelor's Degree and 2 years of leadership and/or animal care experience
Masters Degree and 6 months of leadership and/or animal care experience

Other Required Qualifications:

Ability to communicate and follow verbal and written directions accurately
Ability to multi-task
Demonstrated organizational skills and close attention to detail

PREFERRED QUALIFICATIONS

AALAS certification at the ALAT or above
Experience using computers and peripheral hardware

Pay Transparency

The pay range for this position is $26.00 - $30.00 / 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.

Environmental Health & Safety - Management (Charleston, SC, US, 29407)

Job Summary

Responsible for the development and implementation of policies, procedures and programs to ensure the Environment Health, Safety, and Sustainability (EHS&S) compliance of the. facility

Collaborate on the development and support rollout of corporate programs as related to implementation at the facility. Lead and manage site EHS&S audits in collaboration with site management.

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, JHA job hazard analysis.
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.
Provide EHS&S training to staff and contractors including OEB, SOP, and EHS&S policy training.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in a life science (biology, chemistry), environmental engineering, or related discipline.
Experience: Seven to ten 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.
Other: Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs) and government regulatory requirements and guidelines. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in MS Office suite including Excel, Word, Powerpoint and Project. In- depth knowledge of environment, health and safety regulations required. Ability to communicate and influence senior management on EHS compliance initiatives.

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:

While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals.
General office working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

This position requires occasional domestic and international travel.

Compensation Data

The pay range for this position is $100,000 to $120,000. 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 supported the development of 80% of the drugs approved by the FDA in the last five years.

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

Veterinary Technician I (Horsham, PA, US, 19044)

Job Summary

Assist veterinary staff in the documentation and triage of all laboratory animal health cases. May also perform technical in-life procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
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 and husbandry skills which may include administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc., bandage/wrapping techniques, venipuncture techniques and other techniques.
Perform animal follow-up observations or new findings as required.
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.
May be responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.

The pay for this position is between $26.00 and $28.00 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: 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.
Experience: 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
Certification/Licensure: LVT license or CVT/RVT certification preferred.. AALAS certification desired.
Other: Demonstrate understanding of Standard Operating Procedures. Excellent organizational, time management and recordkeeping skills. Basic word processing skills required. Excellent communication skills both written and verbal. Must be proficient in routine veterinary technical and husbandry techniques.

Equal Employment Opportunity

For more information, please visit 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.

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.

Allevamento animali da ricerca - Collaboratore (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Attività aviaria

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.

BTA / Biologielaborant / BSc als Technical Officer (m/w/d) - Virology (Erkrath, NW, DE, 40699)

Für die Abteilung Virologie am Standort Erkrath suchen wir ab sofort unbefristet in Vollzeit eine/n

Biologisch-Technischen Assistenten (BTA) /

Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Technical Officer (m/w/d)

Zu Deinen Aufgaben zählen:

Laborarbeiten mit Zellkulturen, Mykoplasmen und Viren
der Nachweis von Viren und Mykoplasmen in biologischen Probenmaterialien
selbständige Durchführung und Dokumentation bioanalytischer Methoden
Erstellung von prüfungsbezogenen und übergreifenden Dokumenten
allgemeine Laborarbeiten, z.B. Gerätewartungen
Arbeiten und Dokumentation unter GMP-Bedingungen
Pflege und Aufrechterhaltung des GMP-Systems
Erstellen von Standardarbeitsanweisungen

Das bringst Du mit:

eine Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
Wünschenswert sind praktische Kenntnisse im Bereich Zellkultur, Virologie und / oder Mikrobiologie
Team- und Kommunikationsfähigkeit
Dienstleistungsorientierung
gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie gute Deutsch und Englischkenntnisse setzen wir voraus

Wir bieten Dir:

eine Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
eine intensive Einarbeitung
flexible Arbeitszeiten
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 229074 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

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.

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 229073 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

Biologics Testing Solutions

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 etwa 86% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Informationen finden Sie unter 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.

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.

Senior Manager Trade Compliance (REMOTE) (US)

Job Summary

The Sr. Manager, Global Trade Compliance, will provide trade and Customs support to CRL’s global business units. In this role you will report directly to the Director of Global Trade Compliance and will oversee the day-to-day management of the Customs clearance process in the US and Canada. You will support the various businesses in adhering to global worldwide trade compliance policies and governmental regulations and laws impacting imports and exports.

The Global Trade Compliance team ensures that CRL’s transactions satisfy regulatory requirements to file complete and accurate export and import declarations with local customs and other government authorities for international shipments. They are responsible for procedures for assigning and reporting correct and accurate import and export classifications, customs values, and country of origin.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage the Compliance team’s administration of US and Canada HTS classifications, tariff applicability, origin determination, and all participating government agency requirements (i.e. FDA, USDA/APHIS, FWS, CDC, EPA)
• Oversee the Post Entry review process for US and Canada importations and facilitate post summary adjustments
• Proactively monitor all daily activities of Customs brokers and respond to inquiries
• Communicate with CBP and CBSA, Customs brokers, PGA’s, and other stakeholders to facilitate release of shipments
• Responsible for qualification of free trade agreement claims (i.e. USMCA)
• Conduct QBR’s with Customs brokers to evaluate quality of services provided, review trends, and identify continuous improvement opportunities.
• Train, motivate, and mentor compliance and site shipping teams to achieve compliance goals and objectives
• Review and analyze existing business practices, procedures, and processes with goal of establishing benchmarks and standards
• Identify improvement opportunities to existing business processes and service levels and gain efficiencies
• Work closely with all business units to understand their specific needs and the materials which are being imported and exported
• Monitor regional and global Customs and Trade Compliance Regulatory Changes
• Maintain import and export records to ensure company compliance with Customs regulations
• Assist with restricted party screening and ensure export control compliance
• Creation and maintenance of SOPs and supporting documents
• Perform all other related duties as assigned

Skills:
o Ability to work remotely as part of a team
o Fluency in English is a must. Any additional language is a plus
o Strong written and oral communication skills in English to be able to express oneself clearly and in technical and non-technical terms
o Good working knowledge of MS Office, MS Outlook; MS Excel, MS PowerPoint
o Demonstrated experience using and potentially optimizing a Global Trade Management System (GTMS)
o Experienced ACE and CARM user
o Strong attention to details
o Ability to quickly analyze, document, and defend subjective matter
o Decision making aptitudes based on given guidelines and in ambiguous contexts
o Must be comfortable working with diverse business units
o Very good knowledge and experience in internet navigation and research
o Strong cross-functional collaboration skills and ability to influence others through demonstrated expertise
o Agile thinking mindset

Job Qualifications

• 7 – 10 years of relevant working experience, within Customs and Trade Compliance, preferably in the pharmaceutical or bioscience industries
• Solid understanding of Customs and trade compliance for import and export
• Ability to handle multiple issues simultaneously with strong organizational and prioritization skills
• Licensed Customhouse Broker (LCB) or Certified Customs Specialist (CCS) preferred
• University degree
• Experience leveraging technology to drive process improvements.

Compensation Data

Equal Employment Opportunity

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

Microbiology Data Analyst (Dublin, IE, D09)

Job Summary

An exciting new opportunity is being created to support our colleagues at the Dublin Endosafe/Celsis Technical Services laboratory.

The Data Analyst, under the guidance of the Laboratory Services Manager, will be required to support the collection, review and analysis of data associated with the testing and other activities related to the Technical Services Department.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Continue to perform aspects of the Microbiologist role as needed: LAL Testing (RSE/CSE, QC, customer testing, etc) and Celsis Testing (Consumer Care, Pharma, Adapt, AP etc).
Continue to develop efficient work procedures and processes that support company and departmental standards and procedures.
Work side by side with technical service personnel to complete projects and daily work-related items.
Ensure adherence to pertinent regulatory requirements (cGMP, FDA, ISO) and to departmental policies, practices, and procedures [SOPs, safety procedures and biosafety protocols].
Review/update SOPs, protocols and other controlled documents for Technical Service with all pertinent GMP regulations and internal policies.
Review laboratory testing reports for Celsis studies according to applicable testing proce-dures.
Review testing related to LAL QC and RSE/CSE determination.
May be responsible for Initiating, completing, or reviewing Quality documentation associated with change controls, deviations, CAPAs, OOS and lab investigations generated by Technical Service.
Assist in training as required.
May participate in inspections and audits.
Responsible for assisting with and processing product returns and customer complaints.
Compilation as well as presentation of metrics for processes associated with Technical Ser-vice such as contract testing, complaints, RSE/CSE testing, Service Cloud, quality manage-ment review sessions, tracking and trending meetings, etc. for management on designated frequencies.
Analyse and Interpret data in order to identify any ‘out of trend’ or early warning indicators. Recommend preventative or corrective action as appropriate.
Utilise best processes for data review and analysis (E.g. Statistical review, Minitab, PowerBI, etc). Training will be provided as needed.

This is a full time role which based on site primarily within the laboratory, involving the majority of working as part of a dedicated team of eight.

Job Qualifications

Education: Bachelor’s Degree (B.A. /B.S.) in Microbiology / Biology or a related discipline.

Experience: Established post graduation related experience as a Microbiologist supported by an additional track record of related experience in areas such as quality systems, data review, metrics collection and reporting, within a GMP/GLP environment. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other: Advanced computer literacy required. Proficient with Microsoft Excel. Attention to detail and organisation skills required. Fluency of written and spoken English Language is essential.

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.

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.

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 ~70% of the drugs approved by the FDA in 2016. For more information, please visit www.criver.com.

Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet

Equal Employment Opportunity

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

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.

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.

Equal Employment Opportunity

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 !

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.

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.

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 ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity

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

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

Security Officer - Part Time - Weekends (Reno, NV, US, 89511)

Job Summary

***This position covers weekends, Saturday - Sunday from 6:00am to 6:00pm****

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.

Equal Employment Opportunity

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

Candidate Experience Associate (Contract) (Reno, NV, US, 89511)

Job Summary

We are seeking an experienced Candidate Experience Associate (contract) for our global talent acquisition team, located in Reno, NV. This is a contract role that could develop into a permanant FTE position.

This unique entry level recruiting role ensures an excellent candidate experience for early talent or high-volume recruitment. From screening, phone interviewing to background checks, candidate care continues until the first day when our best in-class onboarding journey begins.

Job Qualifications

Collaborate with Talent Acquisition Partners, HR Business Partners and hiring managers to meet hiring needs.
Attract the right talent into our entry level roles by establishing productive relationships with local high schools, universities, and community colleges.
Pipeline talent, screen and launch selection assessments.
Conduct phone interviews and support for entry-level roles.
May support hiring managers as on-site point of contact to facilitate our Enhanced Interview Process.
May facilitate/support hiring events, same day offers and guide candidates through our expedited drug screen and background check process.
Act as a hiring ‘concierge’ to the candidate, from the moment they apply to the moment they start.
Partner with Talent Acquisition Coordinators or lead the process to monitor status of background checks and escalate as needed.
Track metrics of interviews and hires and report out monthly.
May support early career programming, including intern events and communications.
Assist with project work as needed.

Minimum requirements for the role:

Minimum 2 years related experience in Talent Acquisition.
Bachelor’s degree is preferred or a combination of a high school diploma with 4 years of applicable experience required.
Skilled at planning and prioritizing work activities; able to easily adapt as goals, priorities, and role responsibilities may change.

Compensation Data

The pay range for this position is $27.00/hr-$29.00/hr. 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.