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.

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

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

Le poste

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

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

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

Responsabilités principales

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

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

Profil recherché

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

Modalités

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

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.

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.

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

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

Riepilogo del lavoro

Di cosa si occupa la Charles River

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

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

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

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

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

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

Job Summary

Per cliente sito in Perugia ricerchiamo un operaio stabularista

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

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

Job Qualifications

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

Di cosa si occupa la Charles River

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

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

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

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

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

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

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

• Jornada laboral de 40 h de lunes a viernes.

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

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

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

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

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

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

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

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

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

Requisitos

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

Acerca de Charles River

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

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

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

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

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

Para más información, visite www.criver.com.

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

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

Resumen de trabajo

Acerca de Microbial Solutions

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

Acerca de Charles River

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

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

Para más información, visite www.criver.com.

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

Qui sommes-nous ?

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

L’équipe

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

Votre quotidien

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

Pourquoi nous rejoindre ?

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

Les Modalités

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

À propos de Safety Assessment

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.

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

Scheduler I (Reno, NV, US, 89511)

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

Job Summary

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

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

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

The following are minimum requirements related to the Scheduler position.

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

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

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

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

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

Qui sommes-nous ?

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

Le poste

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

Les missions 

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

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

Qualifications souhaitées

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

Vous maitrisez l’anglais scientifique (compréhension écrite)

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

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

Conditions spécifiques du poste

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

Les modalités

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

À propos de Safety Assessment

À propos de Charles River

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

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

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.

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.

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.

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.

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.

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

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

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

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

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

Missions principales

Gestion d'élevage (rongeurs)

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

Entretien, soin et surveillance des animaux

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

Profil recherché

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

Modalités

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

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

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

Job Summary

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

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

Job Qualifications

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

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

Equal Employment Opportunity

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

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

Job Summary

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

Job Qualifications

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

Compensation Data

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

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

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

Job Summary

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

Basic Summary:

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

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:

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

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

Job Qualifications

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

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

Physical Demands:

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

Work Environment:

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

Equal Employment Opportunity

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

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

Job Summary

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

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

Job Qualifications

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

PHYSICAL DEMANDS:

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

WORK ENVIRONMENT:

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

COMMENTS:

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

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

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.

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

Job Summary

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

In this role, primary responsibilities include:

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

Key Elements

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

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

Role Specific Information:

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

Why Charles River ?

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

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

Equal Employment Opportunity

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

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

Job Summary

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

The following are responsibilities related to the Clinical Pathology Assistant:

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

Job Qualifications

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

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

Equal Employment Opportunity

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

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

Sommaire de l'emploi

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

Dans ce poste, les principales responsabilités incluront:

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

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

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

Informations spécifiques au poste:

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

Pourquoi Charles River?

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

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

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

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

Job Summary

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

In this role, primary responsibilities include:

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

Key Elements

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

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

Role Specific Information:

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

Why Charles River ?

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

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

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.

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

Sommaire de l’emploi

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

Dans ce poste, les principales responsabilités incluront:

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

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

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

Informations spécifiques au poste:

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

Pourquoi Charles River?

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

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

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

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

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

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

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

Missions principales

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

Gestion d'élevage transgénique (rongeurs)

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

Participation aux suivis des projets expérimentaux

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

Entretien, soin et surveillance des animaux

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

Profil recherché

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

Modalités

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

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

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

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

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

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

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

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

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

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

Job Summary

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

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

QUALIFICATIONS:

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

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

Comments:
• May require occasional domestic or international travel.

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

At Charles River 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.

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

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.

Qui-sommes-nous ?

Le poste

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

Les missions

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

Conditions spécifiques du poste

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

Qualifications souhaitées

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

Modalités

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

À propos de Safety Assessment

À propos de Charles River

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

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

Qui-sommes-nous ?

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

Le poste

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

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

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

Les missions

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

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

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

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

Qualifications souhaitées

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

Modalités contractuelles

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

À propos de Safety Assessment

À propos de Charles River

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

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

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

Job Summary

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

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

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

Job Qualifications

Qualifications:

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

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

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.

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

Qui sommes-nous ?

Le poste

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

Les missions 

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

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

Conditions spécifiques du poste

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

Travail le WE.

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

Qualifications souhaitées

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

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

Vous maitrisez l’anglais

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

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

Les modalités

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

À propos de Safety Assessment

À propos de Charles River

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

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

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

Job Summary

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

In this role, primary responsibilities include:

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

Key Elements

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

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

Role Specific Information:

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

Why Charles River?

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

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

Equal Employment Opportunity

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

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

Sommaire de l’emploi

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

Dans ce rôle, les principales responsabilités sont les suivantes:

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

Éléments clés

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

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

Informations spécifiques au poste:

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

Pourquoi Charles River?

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

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

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

Junior Technical Service (Hyderabad, IN)

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

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

GENERAL REQUIRMENTS

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

Job Qualifications

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

At Charles River 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.

Clinical Veterinarian (Ashland, OH, US, 44805)

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

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

Job Summary

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

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

For successful hires we offer:

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

Job Qualifications

QUALIFICATIONS:

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

Compensation Information:

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

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

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.

Staff Veterinarian (Reno, NV, US, 89511)

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

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

Job Summary

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

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

Job Summary

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

Qualifications

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

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

Preferred:

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

Compensation information:

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

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

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

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

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

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

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

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

Qualifications

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

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

PHYSICAL DEMANDS:

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

WORK ENVIRONMENT:

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

COMMENTS:

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

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

Qui sommes-nous ?

Le poste

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

Les missions 

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

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

Qualifications souhaitées

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

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

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

Conditions spécifiques du poste

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

Les modalités

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

À propos de Safety Assessment

À propos de Charles River

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

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

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

Qui sommes-nous ?

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

Le poste

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

Missions :

1/ Responsabilités générales :

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

2/ Hygiène et Sécurité :

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

3/ Environnement :

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

Qualifications requises :

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

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

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

Modalités contractuelles :

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

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

À propos de Microbial Solutions

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

À propos de Charles River

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

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

Job Summary

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

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

Additional responsibilities include:

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

Job Qualifications

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

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

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

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

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

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

Job Summary

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

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

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

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

Job Qualifications

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

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

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

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

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

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.

Laboratory Animal Technician I (14BS) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Laboratory Animal Technician to join our Insourcing Solutions team located in Bethesda, MD.

As the Laboratory Animal Technician, you will maintain and monitor the health, technical, and physical environments within the animal care facility. You'll work closely with the Clinical Veterinarians and Veterinary support staff to perform daily health assessments, clinical observations and providing treatments to the lab animals.  

Additional responsibilities include:

Technical support: animal handling and restraint, weaning, timed mating, tail snips, ear tagging, injections (Sub-Q, IP, tail vein), blood/tissue collections (mandibular, tail vein, term bleed: IC or RO), treatments, microinjections, surgical preparations, and post-operative observations. 
Familiarity with and ability to use various forms of anesthetic (Gas/Injectable). '
Provide environmental enrichment feed, other enrichment stimuli as well as behavioral assessments.
Provide quality assurance to include animal health surveillance, HVAC, animal shipments, facility sanitation and other procedures.
Maintain accurate records of animal importations, breeding, and health checks. 
Assist in assessing training needs; develop and present to staff and PIs. 
Prepare and submit written reports, charts, logs, and inventories.

Job Qualifications

The following are minimum requirements for the Lab Animal Technician:

High school diploma or GED.
A minimum of 3 years' lab animal facility experience performing animal husbandry and clinical support.
Must have LAT certification.  
Schedule: Monday through Friday: 7AM-3:30PM, weekends and holidays if necessary.

The pay range for this position is $27 to $30 USD per hour.  Please note that salaries vary within the range based on factors including skills, and location.

Equal Employment Opportunity

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

Technicien de laboratoire en Immuno-Histo-Chimie - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service d'Immunohistochimie recrute un Technicien pour intégrer son équipe composée de 10 techniciens.

Les missions 

Au sein du service d'Immunohistochimie, vous aurez pour principales missions sous la responsabilité de la responsable d’équipe :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsable, conformément aux bonnes pratiques de laboratoire, aux procédures standards et aux protocoles d’études,
Réaliser progressivement certaines techniques de laboratoire en histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
S’assurer de la conformité des résultats obtenus,
Lire les protocoles, avenants et notices en anglais,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,

En contact avec notre équipe de Vétérinaires Pathologistes :

Effectuer la digitalisation des lames : digitalisation, mise à disposition aux pathologistes et archivage,
Réaliser la digitalisation en fluorescence,
Préparer et envoyer des disques durs,
Réaliser de l’analyse d’images (développement & validation & application algorithmes, compilation des résultats, mise en forme et partage),
Construire des banques de lames pour de l'analyse d’images.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique (type BUT Génie Biologique).

Vous possédez idéalement une première expérience professionnelle dans le domaine.

Vous possédez une aisance relationnelle et un sens du contact et du service.

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

Votre anglais est opérationnel ; vous êtes à l’aise à l’écrit et à la compréhension scientifique.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail, ...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

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

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

Chef de Projet Junior - F/H - Alternance (Saint Germain Nuelles, FR, 69210)

Le poste :

Au sein de l’équipe Excellence Opérationnelle, en tant que Junior Project Manager en Alternance , vous participez au développement de l’amélioration continue, le suivi des programmes de projets et la réalisation de ces derniers.

Véritable acteur du changement, vous accompagnez les opérationnels dans la réalisation des projets et changements nécessaires pour garantir l’efficacité et la rentabilité des activités en collaboration avec la direction du site, l’équipe Finance et vos homologues des autres sites du groupe Charles River.

Les missions proposées au cours de votre alternance :

Recueillir, comprendre et construire le cahier des charges les besoins fonctionnels exprimés,
Concevoir et développer des solutions à l'aide de la suite Office (Power Platform : Power BI, Automate, etc.),
Accompagner le développement et suivre la gestion du projet : suivi de planning, charte projet, analyse de risques, clôture et retour d'expérience.
Assurer la documentation de votre travail,
Maintenir et supporter les solutions développées dans un esprit d'amélioration continue.

Profil recherché :

De formation supérieure Master ou formation Ingénieur,
Vous avez une réelle appétence pour les technologies Low-Code/No-code,
Vous êtes reconnu(e) pour votre curiosité, votre adaptabilité et votre relationnel
Vous appréciez le travail en équipe et transverse,
Les + : vous avez de bonnes connaissances des outils de développement No Code de la suite Office 365 et le domaine de l'amélioration continue

Modalités:

Restaurant d’entreprise, CSE
Primes de transport
Site non-accessible en transport en commun – Moyen de locomotion indispensable (Saint-Germain-Nuelles)

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

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.

Biomanufacturing Manager, Cell & Gene Therapy (Memphis, TN, US, 38118)

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

The Biomanufacturing Manager is responsible for leading all manufacturing activities related to the start-up and GMP production of novel cellular products for new and existing clients in compliance with regulatory agencies and associated guidelines. The Manager will also schedule appropriate resources to meet production schedules and maintain a state of safety, compliance, and control within manufacturing.

Oversee all activities related to the start-up and production of new and existing client processes in accordance with Charles River quality and production timelines and agreements.
Schedule and manage manufacturing staff ensuring adherence to production schedules; coordinate with relevant functions to ensure schedule adherence.
Ensure a safe and compliant working environment by enforcing safety and quality policies and practices.
Serve as manufacturing representative on cross-functional teams ensuring on-time completion of deliverables related to technology transfer, operations, production, and disposition.
Advise and inform site and company leadership of issues with the potential to impact production timelines or Critical Quality Attributes of client products.
Participate in Regulatory, Quality, and Customer inspections and audits as manufacturing systems and production process SME.
Work closely with clients and internal functions to troubleshoot and solve issues related to client processes and production.
Build, train, and develop highly skilled production teams capable of producing cell therapy products in accordance with regulatory guidelines and Cognate quality standards.
Oversee the drafting, review, and approval of process specific and Internal Quality System documents.
Foster a culture of continuous improvement; identify opportunities and lead implementation of improvement activities, as required.

Job Qualifications

BS or MS in a scientific field.
Minimum of 3 years or equivalent applicable experience
Minimum of 2 years demonstrated success in a supervisory role
Exhibits exceptional leadership skills and deep knowledge of GMP
Must be detail oriented and have excellent organizational skills
Must possess effective written and oral communication skills
Must display a high degree of professionalism and confidentiality
Must demonstrate initiative to remain apprised of relevant industry and regulatory trends

Compensation Data

The pay range for this position is $94,000 - $120,000. Please note that salaries vary within the range based on factors but not limited to experience, skills, education and location.

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

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.

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.

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.

Administratieve Projectondersteuner (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Al bijna 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u over gepassioneerd kunt voelen.

Zou jij als Administratief Projectondersteuner graag willen bijdragen aan onderzoek naar de veiligheid van bestaande en nieuwe stoffen?
Ben jij oplossingsgericht, nauwkeurig, flexibel en ben je communicatief vaardig?
Heb je affiniteit met softwareprogramma’s?

Heb je alle bovenstaande vragen met ja beantwoord, dan zijn wij op zoek naar jou!

Administratief Projectondersteuner voor de afdeling Toxicologie

Afdeling:
Met meer dan 240 medewerkers voert de afdeling Toxicologie onderzoek uit naar de veiligheid van bestaande/nieuwe medicijnen en chemische stoffen. Kenmerkend voor het werk is de grote diversiteit aan projecten, teststoffen en opdrachtgevers.

Over jouw rol:

Als administratief projectondersteuner fungeer je als assistent, ben je een energiek steun- en schakelpunt voor de afdeling Toxicologie en werk je nauw samen met de huidige drie administratieve projectondersteuners en de Lead Electronic File Processing. Je ondersteunt op dagelijkse basis een team van ca. 30 studie directors en zorgt ervoor dat alle processen soepel en efficiënt verlopen.

Primaire werkzaamheden:
•   Projectadministratie (o.a. het omzetten van studieplannen, amendementen en rapporten in PDF format met behulp van Adobe; het versturen van deze documenten; het verzamelen en opslaan van digitale handtekeningen met behulp van Docusign);
•   Voorbereiden van studieplannen en draft rapporten voor projecten en het monitoren van deze projecten;
•   Genereren van wetenschappelijke electronische rapporten en rapportonderdelen (publishen) via M-Files/AdLib volgens de regels van de geldende autoriteiten en verzoeken van klanten;
•   Vergunning gerelateerde werkzaamheden (controleren en registreren van data voor indiening bij de NVWA);
•   Onboarding van nieuwe collega’s;
•   Algemene werkzaamheden zoals het verwerken van emailcorrespondentie; het onderhouden van in- en externe contacten en overige voorkomende (ad-hoc) werkzaamheden.

Wat is vereist:
•   MBO-4/HBO werk- en denkniveau;
•   32 - 36 uur per week; mogelijkheid om 1x per week vanuit huis te werken;
•   Je bent communicatief sterk en kunt onder druk van deadlines werken;
•   Je beschikt over goede computervaardigheden en hebt affiniteit met het jezelf eigen maken van verschillende software;
•   Ervaring met MS office (Ecxel, Word, Outlook) en Adobe is een pré;
•   Je staat organisatorisch sterk in je schoenen;
•   Je kunt zelfstandig en in teamverband werken;
•   Je fungeert als aanspreekpunt voor interne partijen en bent in staat om problemen met een oplossingsgerichte houding af te handelen;
•   Draagt actief bij aan procesverbeteringen;
•   Je hebt uitstekende communicatieve vaardigheden, zowel mondeling als schriftelijk in Nederlands en Engels;
•   Je kunt omgaan met vertrouwelijke informatie;
•   Je bent accuraat, kunt prioriteiten stellen, structuur aanbrengen en het overzicht behouden;
•   Je hebt een flexibele, proactieve en servicegerichte houding.

Wij bieden:
Werken bij onze organisatie betekent werken in een dynamische internationale organisatie met een modern laboratorium en een grote diversiteit aan apparatuur en technieken tot je beschikking.
Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

•   27,5 vakantiedagen en 2 collectieve dagen per jaar;
•   Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
•   Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
•   Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
•   Reiskostenvergoeding á 0,23 cent per kilometer met een max. van 250 netto per maand, of een NS-Businesscard;
•   Fiets(lease)plan;
•   Collectief pensioen met een eigen bijdrage van 2.9%;
•   Bedrijfsfitness;
•   De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
•   De mogelijkheid tot een consult van onze in house ergonoom;
•   Elke dag gratis vers fruit.

Over Safety Assessment

Charles River helpt zijn partners bij het versneld uitvoeren van preklinische geneesmiddelontwikkeling dankzij uitstekende programma's voor veiligheidsbeoordeling, de allernieuwste voorzieningen en deskundig advies op het gebied van wet- en regelgeving. Van individuele gespecialiseerde toxicologie- en “IND enabling”-onderzoeken tot pakketten op maat en complete laboratoriumondersteuning: ons ervaren team kan programma's ontwerpen en uitvoeren die anticiperen op problemen en obstakels uit de weg gaan, voor een probleemloze en efficiënte ontwikkelingsgang naar de markt. Bij onze Safety Assessment-vestigingen lopen jaarlijks zo'n 300 programma's voor experimentele nieuwe geneesmiddelen (investigational new drugs [IND's]).

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogt zodat producten eerder op de markt gebracht kunnen worden.

Meer informatie vindt u op www.criver.com.

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.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.

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.

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.

Elektriker / Elektroniker (m/w/d) - allgemeine Gebäudetechnik (Erkrath, NW, DE, 40699)

Am Standort Erkrath suchen wir ab sofort und unbefristet
eine/n

Elektriker / Elektroniker (m/w/d) für das Management der allgemeinen Gebäudetechnik

(Equipment, Safety &-Facility Management Specialisten (m/w/d)

Zu Deinen Aufgaben zählen:

Elektrotechnische Arbeiten
- Installationen, Reparaturen, Wartungen & Prüfungen von z.B. Lüftungs- & Klimaanlagen, Lampen etc.
das Management der allgemeinen Gebäudetechnik
die Verantwortlichkeit für (Labor)-Geräte nach der Einarbeitung
- Gerätewartungen & Gerätequalifizierungen
Dokumentation nach GMP-Richtlinien:
- Erstellung und Revision von SOPs
- Erstellung von einheitlichen Vorlagen für die Gerätedokumentation
Beratung von Mitarbeitenden in Hinblick auf
- Gerätequalifizierung und die Auswahl neuer Geräte

Überzeuge uns durch:

eine erfolgreiche abgeschlossene Ausbildung als Elektriker, Elektroniker, Betriebstechniker o.ä.
Erfahrung im Bereich der Instandhaltung und / oder Qualifizierung von technischen Anlagen und Geräten wünschenswert
Erfahrung im zertifizierten oder GMP-regulierten Umfeld wünschenswert
idealerweise Erfahrung im Bereich der Erstellung und Pflege von technischer Dokumentation
schnelles Erfassen und grundlegendes Verständnis von Arbeitsabläufen und Netzwerken sowie diplomatisches Geschick
hohes Maß an interdisziplinärem Denken und der Bereitschaft auch Arbeiten in angrenzenden Arbeitsgebieten durchzuführen
lösungsorientiertes Arbeiten und flexibler Umgang mit ungeplanten Situationen
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung
eine intensive Einarbeitung mit Onboarding Programm
kostenfreie Parkplätze / Fahrkostenzuschuss
Fortbildungsmöglichkeiten
Engagement Programm

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb Dich bitte unter der Job-ID 227053 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath

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

Clinical Veterinarian II (Stilwell, KS, US, 66085)

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

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

Job Summary

A Clinical Veterinarian II is responsible for providing consultation, oversight, and direct support of veterinary care activities for all animals used by Charles River Laboratories; supporting the IACUC to ensure compliance with animal welfare standards and regulations by AAALAC, Int., USDA, and PHS-OLAW; and supporting the evaluation of test article effects by performing examinations and making assessments to interpret study effects on animals.

Essential Duties and Responsibilities:

Oversee daily animal health assessment program including both routine stock and study examinations which support research.
Respond to requests for veterinary care, planned or emergency, by examining the animal, communicating with staff, and following the case until resolution, and address veterinary concerns.
May perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice.
Functions as departmental representative for interdepartmental communications and initiatives as required.
Supports and contributes to occupational health and safety program.
Support the overall training program for veterinary techniques/treatments performed by veterinary technicians/technical staff and ensure that training is properly documented and regularly updated. Contributes to training others in research animal techniques and other aspects of vivarium operations.
May assist in the development of operating objectives and Standard Operating Procedures (SOP's).
May serve as a full or ad-hoc member of the Institutional Animal Care and Use Committee (IACUC), assisting in protocol review and other efforts as identified.
Develop understanding of animal welfare regulations and standards and their application.
Development of understanding of the 3Rs and considers where refinements may be applied within the animal care program. Works with cross-site team members to implement refinements.
In consultation with the Study Director is a contact for Sponsor discussion on veterinary care and animal responses to the test article as well as review study plans as needed.
Actively engages with internal and external customers and demonstrates understanding of customers’ needs, requirements, and expectations.
Other duties as assigned

Job Qualifications

Education: DVM or equivalent degree required
Experience: 2+ years of experience in veterinary medicine required; experience in laboratory animal medicine or relevant area/education preferred
Licensure to practice veterinary medicine in at least 1 U.S. state required
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Must be able to obtain a veterinary license, controlled substances license, and USDA accreditation in state of employment.
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions and including ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively, and lead/manage staff in a growing, changing environment

Compensation Data

The starting salary for this opportunity is $155,000 USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Note: Relocation assistance, sign-on bonus and a retention bonus will be part of the overall compensation package as well.

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

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.

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

Scientist - Electrophysiology (Groningen, NL)

Does Neuroscience / CNS research interest you?

Have you got experience with patch clamp measurements?

Could you be our next ex vivo Electrophysiologist?

Our site:

Our Groningen CNS specialised site is a dedicated group where we perform discovery level research. We focus on non-GLP DMPK (drug metabolism and pharmacokinetics) and pharmacology studies to better understand neuroscience disease pathophysiology. including but not limited to, microdialysis, electrophysiology, pharmacokinetic screening and bioanalysis.

Your role:

In this position you will be responsible for designing, planning, performing and reporting of sponsor requested electrophysiology studies. Studies are based on ex vivo single cell or slice recordings. Manual Patch-Clamp and Multi Electrode Array are the techniques you will be using to conduct your studies with. The hands on work is often more individual, but for the entire study you will be collaborating together with scientific staff and animal technicians. You will bring in hands-on expertise to transfer and establish methods and to obtain high quality data.

Responsibilities:

Your responsibilities will include data collection and analysis as well as data interpretation and communication of results internally and externally. You ensure that study aims are reached and work follows relevant protocols, guidelines and legislation. CRL is committed to support the 3Rs and you have an equally strong sense of applying this to the research.

Qualifications:

Advanced academic degree in the life sciences;
Understanding of neuroscience on the cellular and systems level;
Experience with patch clamp measurements in cultured cells and/or acute slices and/or experience with multi electrode array measurements in acute slices;
Programming skills and understanding of principles of electronics;
Fluency in English, oral and written;
Ability to coordinate and prioritize;
Excellent communication, loves a scientific challenge and positive attitude.

Desirables:

Experience with ex vivo extracellular electrophysiology will be an asset
Knowledge of neuropharmacology and / or drug development processes will be an asset
Article 9 (Laboratory Animal Science)

What We Offer You:

Working at our organisation means working in a dynamic international organisation. In addition, we offer excellent primary and secondary working conditions including:

25 vacation days
Possibility to purchase 10 additional vacation days per year;
Annual one-time 8% vacation pay of your gross annual salary;
Annual one-time payment based on company results;
Travel allowance at € 0.23 cents per kilometer with a maximum of € 250 net per month,
Collective Aegon Capitall pension with a personal contribution of 2.9%;
Collective health insurance with CZ or VGZ. 10 to 12% discount on any supplementary insurance.

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.

Data Coordinator - Reporting Services (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Coordinator for our Reporting Services team at the Senneville location, you will be responsible for providing the scientists with the information necessary for them to be able to write the summary and results sections of their reports, based on individual and summary data included in the appendices, tables and graphs customized to meet client specific reporting requirements.

In this role, primary responsibilities include:

Coordination of all pertinent data and scientific interpretation information in accordance with the Study Plan to enable the correct tabulation to be included in the report;
Transcribe data from hand-written data records and/or, process computer-generated data files, into formats suitable to meet sponsors’ needs;
Prepare finished reports, tables and/or graphs, that are clear and professionally presented as per Company requirements and guidelines;
Processing of reports or tabulated data, which are accessed either electronically or from hard copy sources following specific e-file management criteria involving the use of various software;
Ensure work is compliant with applicable guidelines and regulations.

Key Elements

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

High School diploma;
Previous experience in Sciences or Information Technology;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
Ability to work under time constraints, in order to respect deadlines;
Ability to work in a team environment.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging;
Salary: 18.50$/hrs;
Annual bonus based on performance;
Schedule: Day shift from Monday to Friday, flexible schedule with possibility to work remotely;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

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

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

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.

Coordonnateur.trice des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Coordinateur.trice des données pour notre équipe de Services de rapport située au site de Senneville, vous serez responsable de fournir aux scientifiques l’information nécessaire pour qu’ils puissent écrire les sections de sommaire et résultats de leurs rapports basés sur les données individuelles et sommaires incluses dans les annexes, les tables et les graphiques adaptés afin de rencontrer les exigences spécifiques des clients.

Dans ce poste, les principales responsabilités incluront:

Coordination de toutes les données pertinentes et de l’interprétation scientifique des informations en fonction du plan d’étude pour permettre une tabulation adéquate pouvant être incluse dans un rapport;
Transcrire des données à partir d'enregistrements de données manuscrites et/ou traiter des fichiers de données générés par ordinateur dans des formats adaptés aux besoins des sponsors;
Préparer des rapports, des tableaux et/ou des graphiques finis, clairs et présentés de manière professionnelle conformément aux exigences et aux directives de l'entreprise;
Traitement des rapports ou de données tabulées, lesquels sont accessibles par sources électroniques ou par documents imprimés suivant les critères de gestion de l’e-file impliquant l’utilisation de divers logiciels;
S’assurer que le travail est conforme aux directives et réglementations applicables.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études secondaire;
Expérience précédente en sciences ou en technologie de l’information;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Maîtrise des compétences informatiques notamment des logiciels de la suite Microsoft Office (par exemple Word, Access, Excel);
Être en mesure de gérer son temps efficacement, afin de respecter les échéanciers;
Capacité à travailler en équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 18.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi, horaire flexible et possibilité de télétravail;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

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

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

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.

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)

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

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.

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

test test test test

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.

Facilities Technician I (Rockville, MD, US, 20850)

Job Summary

The Facilities Technician I is responsible for maintaining the facility in good operating and physical condition, as well as responding to normal and emergency service calls, and taking corrective action via diagnosis and repairs. As directed, conducts/oversees preventive maintenance. The Facilities Technician I will be required to perform a wide range of repair, maintenance, and escorting tasks.

Key Responsibilities and Duties:

· Perform routine GMP spaces cleaning

· Maintain stock of consumables (HVAC filters, cleaning supplies, etc)

· Perform routine simple maintenance and repair throughout the facilities, such as repairing cosmetic damage

· Oversee building utility systems equipment maintenance to ensure expected conditions in the facility. This may include HVAC, electrical, water (domestic and DI), compressed gasses, and controlled temperature storage systems.

· Recognize and correct potential safety hazards to avoid injuries

· Support building personnel by insuring the availability of water, gasses, and electrical, as well as furniture requests, office relocations, and general accommodations to assist employees with their work duties

· Paint & caulk small areas when paint or wall surface has become damaged

· Support general cleaning & housekeeping efforts as required. Pallet removal as needed from building

· Maintain relationship and coordination with janitorial contractor for non-lab domestic cleaning of facility

· Process/Manufacturing equipment support, ensuring written record keeping, and forms are completed as required

· Conduct systems rounds as required

· Check and confirm process gasses are at service pressure daily

· Move/relocate laboratory equipment as directed

· Work with the engineering personnel to handle process equipment needs

· Required to review relevant documentation for accuracy and completeness i.e., suite cleaning documentation

· Replace light bulbs as required

· Employ safe work practices

· Engage and inspire others

· Comprehends all duties assigned and performs responsibilities in absence of Manager when needed

· Other responsibilities as needed

Job Qualifications

· Associate degree in science preferred, or High School Diploma or GED with 0-3 years of prior work experience in the Biotechnology Industry in a GMP Facilities setting

· Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams. Maintain Calendar(s)

· Possess the willingness to learn new concepts to fully understand aseptic techniques and demonstrate proper clean-room behavior

· Excellent interpersonal and communication skills

· Detail-oriented and demonstrate the ability to perform highly detailed work

· Excellent organizational, multitasking, and problem-solving skills

· Able to accurately perform basic math calculations, including time conversion, fractions, decimals, and percentages

· Availability - Overtime work and schedule changes are required to meet business needs. Holiday, weekend, and night work will also be required based on manufacturing schedule. On-call as business needs arise

· Reliable mode of transportation to travel between sites in the Rockville area

· Able to work standing, bending, stooping, pulling, pushing, sitting, and reaching overhead for long periods of time

· Able to work around various cleaning chemicals that produce non-hazardous odors like bleach and vinegar

· Able to wear appropriate gowning covering most parts of the body and face. (Gowning Qualification)

· Able to lift, push, and pull 50 lbs.

· Use of basic hand tools

· Use multimeter

· Work from height not to exceed 10’

· Confined spaces could be encountered

· Work in heat and cold as required

· Climb ladders

Compensation Data

The pay range for this position is $22.00 - $24.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Gestionnaire en Logistique Import-Export - H/F - Alternance 1 (Saint Germain Nuelles, FR, 69210)

Job Qualifications

Vous suiviez une formation dans le domaine de la logistique ou du développement international ? Vous recherchez un contrat en alternance opérationnel et polyvalent ? Vous avez envie d’intégrer un groupe innovant, en plein développement, au service de la recherche et de la santé humaine ? Cette offre au sein de notre service clients va vous intéresser.

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport, Restaurant d'entreprise
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

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.

Gestionnaire en Logistique Import-Export - F/H - Alternance (Saint Germain Nuelles, FR, 69210)

Rattaché(e) au Responsable Service Clients et Logistique, vous participez aux activités du service et vous aurez la responsabilité des missions suivantes :

Assister le Responsable Logistique dans la gestion cette activité.
Organiser avec nos partenaires des dossiers d’import et/ou export.
Accompagner le suivi et la mise à jour des systèmes de management de la qualité et de conformité réglementaire.
Accompagner le service dans les nouveaux projets de digitalisation en lien avec les livraisons clients et/ou les aspects réglementaires.
Participer aux projets de mise en performance des activités logistiques et de la gestion administrative (arbre décisionnel du transport en fonction de la commande client par exemple)

Profil recherché :

Vous êtes de formation BAC+2 / BAC+4
Vous avez des connaissances en relation clients, gestion de projets logistique, INCOTERM, douanes, et en processus d’innovation.
Vous avez des qualités relationnelles, une bonne communication orale et écrite, vous êtes organisé(e), méthodique et force de proposition.
Langues : Anglais

Autres :

Indemnité de transport, Restaurant d'entreprise
Poste localisé à St Germain-Nuelles (35 min de Lyon centre).Moyen de locomotion indispensable, site non accessible en transport en commun.

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

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.

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)

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.

Animal Technician - Milano (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Di cosa si occupa la Charles River

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

Animal Technician - Milano (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano e Calco ricerchiamo un Animal Technician

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

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;
Effettuare attività e procedure tecniche sugli animali

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

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

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

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

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

Job Summary

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

We are seeking a Security Officer for our Safety Assessment site located in Reno, NV.

Ensures the protection of organizational personnel and company property against fire, theft, vandalism, illegal entry, and other hazards. Inspects credentials and facilities, and reports irregularities, alarm activation and tampering. Develops, implements and administers programs designed to protect organizational personnel and property. Ensures compliance with government and organization security policies and procedures and protects and safeguards intellectual property. Conducts investigations to identify and document instances of noncompliance and possible breaches in law.

The following are responsibilities related to the Security Officer:

•   Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
•   Monitor security systems and/or environmental systems and investigate and/or report any incidents.
•   Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
•   Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physical security measures; and monitors the critical building systems.
•   Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
•   Document all security department activity and generates incident reports as necessary.
•   Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
•   Contact emergency personnel as required and in accordance with
•   Assist in directing appropriate emergency response efforts when required.
•   Perform all other related duties as assigned.
•   We are also seeking an individual to work on the weekends but may be available to provide coverage for others during the week, during vacation, and sick leaves

Job Qualifications

The following are minimum qualifications related to the Security Officer position:

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least Six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Other: None

The pay for this position starts at $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

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

Supervisor (Boston, MA, US, 02115)

For 75 years, Charles River employees have worked to advance the discovery, development, and safe manufacture of new drug therapies, making a profound impact on global health. Our 20-year partnership with Boston Children’s Hospital takes this mission to the next level, supporting groundbreaking innovations that directly impact patient care. At Boston Children’s, their commitment to diversity drives the exceptional quality of care provided to patients from local communities to over 160 countries worldwide. This is your moment to become part of a family where unique talents and perspectives unite to change lives, including your own. Together, we’re shaping a healthier future through compassion, innovation, and opportunity.

JOB SUMMARY

We are seeking a Supervisor to join our Insourcing Solutions team, located at Boston’s Children’s Hospital.  You will be working with multiple animal species.

Under the direction of the Manager, Animal Care, this position provides direction and leadership for the daily operations of Boston Children’s Hospital animal facilities and program. Maintains performance levels consistent with and according to Animal Resources Children’s Hospital (ARCH) standards and requirements. Collaborates with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines and regulations. Responsible for providing back up and assistance for the Manager, Animal Care.

ESSENTIAL DUTIES AND RESPONSIBILTIES

The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

Responsible for assisting in the training of animal care staff in the following: cage changing, microisolator cage changing techniques, room sanitation, autoclave operation, cagewash operations, waste disposal and other husbandry duties as required.
Outlines the job responsibilities of animal care staff, including Children's Hospital policies, procedures and the daily husbandry assignments of the animal care staff.
Collaborates with Animal Facility Manager and maintains necessary supply and equipment inventory to operate the day-to-day operation of the animal care program, including feed/bedding, sanitation supplies, office supplies, cage equipment, autoclave supplies and other supplies and equipment as needed.
Responsible for developing and maintaining animal records including, room logs, health reports, cage card labels, autoclave records, cagewash records, animal census and other records as required.
Ensures that all animal rooms are observed on a daily basis to monitor for sick, or dead animals, and reports findings to the veterinary staff or alternatively to the Animal Facility Manager.
Interviews and recommends selection of candidates for employment to the Animal Facility Manager. In consultation with the Animal Facility Manager and Human Resources Manager, this position performs personnel actions including but not limited to hiring, transferring, suspending, counseling, disciplining, discharging, assigning, rewarding or addressing employee concerns.
Supervises direct reports in their efforts to maintain quality performance of departmental and client objectives, including meeting/exceeding departmental standards with respect to animal health and welfare, facilities condition, sanitation levels.
Build competence among employees through conducting appropriate training activities and through appropriate supervision related activities (e.g. recruitment, separation, performance appraisal, disciplinary actions, etc.).
Supports and affirms the company policy of Equal Opportunity through Affirmative Action.
Conducts daily inspections of animal holding and support facilities to determine the degree to which established levels of animal health, facilities condition, sanitation levels, environmental parameters and security are being met/exceeded.
Participates in the development and implementation of site-specific standard operating procedures (SOP's), in compliance with all state, federal and industry requirements. Oversee adherence to site SOP's and all required documentation related to department. Coordinate operations with the assistance of staff support departments and personnel.
Coordinates repair and general up-keep of physical environment in areas of responsibility. Is available on site for assistance, coordinating during upkeep and repairs.
Participates as required in the development of projections for equipment, supplies and personnel needed to effectively operate the research facilities in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state and federal requirements.

.

Actively interacts with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance. Act as liaison between scientific staff and support personnel.
Trains and oversees consistent practice of general Children's Hospital safety policies and procedures, including those related to biohazards and radioactive substances. Supervises in compliance with local, state, and federal regulations.
In coordination with Human Resources Manager, investigates personnel problems and to employees in accordance with company policies and procedures.
Maintains required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Assists in any contract related activity, as assigned by Supervisor, to complete the required work.
Performs all other related duties as assigned.

MINIMUM QUALIFICATIONS

To qualify for this role, you must have one of the following combinations of education/experience:

- High school diploma/General education development plus six plus years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.
- Bachelor or Associate degree plus two-four years husbandry experience in a laboratory animal facility of which six to twelve months is leadership experience.

Certification/Licensure: AALAS Certification at the ALAT level preferred.

The pay range for this position is $90,000-$95,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

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.

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.

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.

Senior In-Vitro Bioassay Analyst (Ballina, IE, F26D786)

Job Summary

This role shall report to the Biosafety & Cell Based Assay Supervisor and the main duties & responsibilities shall be to assist the Department Manager and/or the Scientist in the following:

Leading the execution of routine cell-based potency assays
Support technical transfer, qualification and validation of new cell-based assays
Maintenance and propagation of antibiotic free cell cultures.
Evaluation of mammalian cells / Generation and maintenance of mammalian cell banks.
Establishment of Test Method SOPs and validation of methods

Core duties shall include:

Maintenance and propagation of antibiotic free cell cultures.
Competent in microscopic evaluation of mammalian cells (e.g. cell morphology, count and viability)
Provide technical training to team as required.
Receipt and processing of test samples in LIMS.
Update current standard operating procedures.
Assist in laboratory investigations where necessary.
Responsible for reporting progress information to Management.
Assist in internal, regulatory and client visits/audits and respond to findings.
Complete understanding off all regulatory guidelines.
Liaise with the Quality Department for the generation of all departmental quality documents including audit responses, facility replies and deviation reports.
Generation of GMP compliant SOPs, Protocols and reports
Generate risk assessments for laboratory and test items as required.
Maintain Laboratory Data Integrity and compliance

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

At Charles River, 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.

Senior Data & DevOps Engineer (Ahmedabad, IN)

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

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

Job Summary

Sr. Data & DevOps Engineer

About the Job: There’s never been a more exciting time to be on the Analytics team at Charles River Labs!

Charles River Labs is on an exciting journey to modernize the data landscape, building a Customer 360, implementing new data standards, bringing to life the ‘art of the possible’ to our business partners, integrating with several new data sources, and ultimately building a brand-new Modern Data Warehouse in Azure. If you are an engineer who enjoys cloud technologies, data warehousing, data analytics, and designing innovative analytical solutions, this job may be for you! This role will work collaboratively, in a consultative way, across the business units and IT, supporting and mentoring engineering teams and advising on the best approaches to leveraging Azure most effectively and efficiently.

The team is seeking top-notch talent in the Microsoft Azure full data stack and modern data toolset. If you are interested in using your leadership, expertise, and innovative skills to build something brand new, enjoy making architectural decisions, are a thought leader in the data space, have a passion for data and analytics, and like to mentor others, then we want to talk to you! A truly exciting and unique opportunity awaits you!

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Basic Qualifications:

• Strong and extensive hands-on Experience with Azure cloud big data architecture
• Good understanding of Microsoft Azure security, privacy, and compliance.
• Implement best practices for Azure services authentication using service principals and managed identities.
• Familiarity with Azure resources service level agreements (SLA), and pricing for planning and cost management.
• Configure and manage Azure virtual network, define Inbound and outbound rules.
• Manage source control with GitHub best practices and define standards for the pull request (PR) process.
• Define and manage a release workflow to update the latest code to the corresponding environments.
• Build continuous integration (CI) pipelines with GitHub actions.

Requirements:

• Bachelor’s degree in Computer Engineering, Computer Science, or related discipline, Master’s Degree preferred
• 4+ years of Microsoft Azure experience or equivalent with AWS or GPC.
• 3+ years of experience implementing automated deployments with GitHub integration and CI/CD pipelines.
• 5+ years of experience in defining GitHub branching strategy for Dev, TEST, PROD, and Hotfix deployments.
• 2+ years of experience automating infrastructure as code using Terraform templates.
• 5+ years of experience in scripting with bash, PowerShell, and Azure CLI.
• 3+ years of experience supporting Azure resources by monitoring diagnostics logs and alerts.
• 2+ years of experience in defining security strategy for Azure resources with networking and firewall rules.
• 2+ years of experience in defining and managing access control strategy for Azure resources.
• Understand different types of storage (filesystem, relation, MPP, NoSQL) and work with various kinds of data (structured, unstructured, metrics, logs, etc.)
• 6+ years of experience working with SQL.

Equal Employment Opportunity

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

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

Cagewash Technician (Baltimore, MD, US, 21224)

Job Summary

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

As the Cagewash Technician, you will Provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas under minimal supervision. Provide quality assurance to the cagewash area.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

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

Experience and/or training working with animal husbandry preferred
High school diploma/GED preferred

The pay for this position is $18.47 per hour.

Equal Employment Opportunity

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

Research Support Specialist I -Veterinary Technicians encouraged to apply (Poolesville) (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Research Support Specialist I for our Insourcing Solutions site located in Poolesville, MD.

Prepare and administer research treatments; collect and record physiological data (weight, temperature, pulse, respiration)
Perform technical procedures as needed associated with the Animal Study Proposals in relation to NHP retroviral, human respiratory and flavivirus studies to include but not limited to blood collection, IV catheterization, intubation, broncho-alveolar lavage, tracheal and nasal lavages, documented research observations, and administration of research treatments
Must have a basic understanding of aseptic technique, anesthesia induction, monitoring, and recovery as well as drug dosage calculations and administration
Assist Veterinarian & Sr. RSS staff with surgeries and specialized procedures
Perform daily animal health observations and report any abnormal findings to veterinarian
Maintain electronic medical records, send daily emails regarding animal health information to vet staff
Collect, preserve, and prepare blood, urine, stool, and tissue samples
Participate in study related necropsies/tissue harvest
Set-up for procedures and prepare supplies and equipment
Ability to maintain freezer organization and sample inventory
Practice universal precautions appropriate to different levels of ABSL. Work safely with animal / human pathogen biohazards and help to maintain the research animal facility as a safe work environment / operation
Report any animal health, care, and / or wellbeing concerns to the appropriate facility management staff
Report any facility infrastructure issues, relative to the animal care and support areas to the appropriate facility management

Job Qualifications

The following are the minimum requirements related to Research Support Specialist I:

- High school diploma or general education degree (GED) required. BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred.

- 2-3 years’ experience working with non-human primates in biomedical research or 2-3 years Veterinary Hospital technical experience preferred.

- Must have computer program proficiency such as MS Word / Access / Excel. Must have a proficient technical vocabulary.

- RVT/CVT/LVT or LAT certification preferred

The hourly range for this position is between $28/hour and $30/hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations.

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.

Documentation Data Reviewer 1 1 1 (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay for this position is $23.50/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

SCHEDULE: Monday - Friday 8:00am - 4:30pm (must be onsite 5 days a week)

We are currently seeking a Data Analyst II for our Quality Control team located at our Mattawan, MI site.

Quality Control supports the review and archival of analysis performed and provides administrative support to the Project Scientists in Laboratory Science disciplines that may include dose formulations, large and small molecule analysis, molecular and cell-based assays, Biomarker, and flow cytometry-based lab work. Staff participate in the review of methods; equipment records and the creation of report tables. Staff participate in the tracking and managing study related materials, providing requested data/information to the Project Scientist or Sponsor as required. Staff are knowledgeable in the application of GxP’s and applicable SOPs, protocols and ensuring adherence to regulatory documents.

Essential Duties and Responsibilities

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Accurately identify and effectively communicates any issues with data
Effectively support administrative tasks including but not limited to, filing, ordering, distribution of documents and study related materials as needed
Independently compile and archive data books and departmental records
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational area
Review and issue data sets in adherence to established timelines
Accurately review departmental and study specific data to ensure adherence to SOPs, methods/protocols, industry standards, and regulatory requirements as applicable in timely manner
Oversee and maintain responsibility for one operational area with minimal oversight
Identify data discrepancies involving collection and analyses compared to study plan by working with appropriate personnel with oversight
Ensure sample analysis data collected is accurate against study plans, methods/type of analysis conducted and subjects' collection time points with oversight
Create and compile report tables with oversight
Review methods for accuracy, consistency and formatting with oversight
Review and monitor study schedules to ensure timelines are met with oversight
Ensure documents align with requirements indicated in Client Information Database (CID)
Attend study and/or department related meetings to assure understanding of assigned projects
Attain CRL personnel and Sponsor signature/approval for study documents and distribute documents when necessary
Assist in preparation, review and/or processing of specialty data shared with Sponsors
Independently generate and maintain standard and complex draft study plans/protocols/amendments and reporting templates in accordance with CRL or Sponsor specific requirements within one operational area
Review laboratory study data to provide financial information for Unit Based Invoicing
Perform all other related duties as assigned

Job Qualifications

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

Competencies

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

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.

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)

Resumen de trabajo

Acerca de Microbial Solutions

Acerca de Charles River

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

Para más información, visite www.criver.com.

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

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

• Jornada laboral de 40 h de lunes a viernes.

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

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

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

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

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

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

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

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

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

Requisitos

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

Acerca de Charles River

Para más información, visite www.criver.com.

Lead Cagewash Technician (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Lead Cagewash Technician to join our Insourcing Solutions team, located in Bethesda, MD.

As the Lead Cagewash Technician, you will provide quality assurance and control, in addition to coordinating preventative maintenance of equipment, as well as prioritizing workload on the assigned side to ensure daily goals are met and the integrity of the research is maintained.

Additional responsibilities include:

Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Responsible for conducting trouble shooting on the equipment and reporting any problems to the Cagewash Supervisor. If necessary, communicating directly with the manufacturers on problems with the equipment.
In the absence of the Cagewash Supervisor, is responsible for scheduling the staff, ensuring work and all related paperwork is completed.
Sanitize, maintain, and repair animal caging materials as needed and ensure cagewash facilities are kept clean and organized
Other tasks may include assisting with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories.
Assist with training and redirection of workload as necessary to ensure a cohesive team and that daily goals are met.

Qualifications

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

High school diploma or GED
Minimum six months of successful performance in cagewash facility operations

The pay range for this position is $19.00 - $19.50 per hour.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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 Associate - (EG) (Kingston, NY, US, 12401)

Job Summary

As an Animal Care Associate for our production site in Stone Ridge, NY, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world.

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

* Up to $500 sign on bonus (CRL employees not eligible)

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

No experience required. On the job training will be provided.

Role Specific Information:

Location: Stone Ridge, NY
This is a temporary opportunity with the potential to be hired as a full-time, employee*
Schedule: Monday - Friday - 1st shift, some rotating weekends required. Early morning hours.
Up to $500 sign on bonus (CRL employees not eligible)
Benefits: 401K participation/Paid Sick Time and Paid Volunteer Time Off

The hourly pay rate for this position is $17.75. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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 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。

Technicien.ne en Santé Animale (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Technicien.ne en santé animale pour notre équipe de Toxicologie située au site de Senneville, 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-cliniques.

Dans ce poste, les principales responsabilités incluront:

Administrer les éléments de test et/ou médicament (Gavage, injection intramusculaire, sous-cutanée et intraveineuse);
Effectuer les prélèvements d’échantillons (sang, urine, etc.);
Faire la prise de données (prise de poids, consommation de nourriture, signes cliniques, etc.);
Manipuler les animaux pour toutes activités qui le requiert;
Nettoyer tous les types d’habitacles d’animaux et leurs accessoires.

Éléments clés

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

Bon sens de l’observation;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
Bonne compréhension de l’anglais écrit;
Diplôme collégial en Santé animale ou en Bioécologie;
Baccalauréat en Biologie ou toutes autres disciplines en lien avec la Science animale.

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: 23.00$ de l’heure avec des primes de:
o Soirée: 2.50$;
o Fin de semaine: $2.75;
o Heure supplémentaire: Temps et demi;
o Fériés: Temps double;
Bonus annuel basé sur la performance;
Horaire: Poste à temps plein standard : 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 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.

InVivo Animal Health Technician (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As an Animal Health Technician for our Toxicology team at the Senneville location, 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:

Administer test items / medications to animals (Gavage, intramuscular, subcutaneous and intravenous injections);
Perform sample collection (blood, urine, etc.);
Collect data (body weight, food consumption, clinical signs, etc.);
Handle animals for any activities that requires it;
Clean all types of animal housing and accessories.

Key Elements

If you have the following qualifications, we'll train you for the rest:

Good observation skills;
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Understanding of written English;
College Diploma in Animal Health or in Environmental and Wildlife management;
Bachelor’s degree in Biology or any related Animal Science discipline.

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: $23.00 per hour with primes of:
o Evenings: $2.50;
o Weekend: $2.75;
o Overtime: Time and a half;
o Holidays: Double time;
Annual bonus based on performance;
Schedule: Full time regular schedules: Mostly during the day, rotating weekends, and holidays. Depending on needs, there may be extra time in the evening or at night;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

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

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly 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 (San Diego, CA, US, 92121)

Job Summary

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

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

Additional responsibilities include:

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

Job Qualifications

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

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

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

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

For more information, please visit 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.

Technician I, Necropsy (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our Necropsy team at our Safety Assessment site located in Ashland, Ohio. Candidate will be working 4/10's either Monday-Thursday or Tuesday-Friday 8a-630pm, weekend rotation, holiday rotation and overtime are required for this role.

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 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.

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, euthanasia, and 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.
Prosect and perform functions in a time frame set by training group for core skill completion.
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.

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

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.
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

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.

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.

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.

Prosector - Necropsy (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Prosector – Necropsy

As an Prosector for our Necropsy team in Sherbrooke (QC), you will be responsible for performing post-mortem examination of animals while following ethical regulations and study design guidelines.

In this role, key responsibilities include:

Euthanize animals prior to necropsy.
Perform animal tissue evaluation for pathologists.
Weigh and document all abnormalities of the organs.
Evaluate for abnormalities and follow tissue conversation methods.

Key Elements

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

College Diploma in Animal Health, inventory and research in biology or in Biotechnology or bachelor’s degree in Biology or any related to science discipline. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to work under time constraints and adapt to change.
Demonstrate flexibility and ability to work independently.
Understanding and writing English is required.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Role Specific Information:

Location: 1580 Ida-Métivier, Sherbrooke, Qc, J1E 0B5. Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Pay: Starting at 22.00$/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. Position mostly to work Monday to Friday – Week-end Rotation only.

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.

Immunology Analyst (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Analyst Immunology

As an Analyst for our Immunology team in Sherbrooke, you will perform analysis of samples. You will also record data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.

In this role, key responsibilities include:

Carry out sample analysis in a multidisciplinary laboratory, using a wide variety of techniques such as Flow Cytometry, ELISA, Luminex
Prepare technical worksheets and procedures;
Receive, store, verify and process biological samples for analysis;
Take part in the routine duties of the laboratory such as preparation of reagents, instrument calibration, product reception;

Key Elements

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

Collegial diploma in Science or B. Sc. degree in Biology or related field;
Knowledge of basic laboratory techniques and Immunology techniques such as ELISA;
Knowledge of flow cytometry, ECLIA and/or Luminex
Reading and writting English is required. Bilingualism is preferable;

Role Specific Information:

Location: 1580 rue Ida-Métivier, Sherbrooke. Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Pay: Starting at 23.00$/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. Mostly to work from Monday to Friday.

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
Access to a doctor and various health professionals (telemedicine).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. This is Your Moment!

Equal Employment Opportunity

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

Analyste en Immunologie (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Analyste en Immunologie

En tant qu’Analyste pour notre équipe d’immunologie notre site de Sherbrooke, vous aurez la charge d’effectuer l'analyse des échantillons. Vous allez également enregistrer les données conformément aux politiques et aux normes de l'entreprise pour répondre aux exigences de qualité et d'exactitude.

Dans ce rôle, les principales responsabilités incluront:

Effectuer des travaux d'analyse d'échantillons dans un laboratoire multidisciplinaire en utilisant une vaste gamme de techniques; tel que la cytométrie en flux, les ELISA, le luminex
Documenter, effectuer et analyser des essais;
Recevoir, entreposer, vérifier et préparer les échantillons biologiques à des fins d'analyse;
Participer aux tâches quotidiennes du laboratoire telles que la préparation de réactifs, calibration des instruments et réception des produits.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

DEC en Sciences ou B. Sc. en Biologie ou domaine connexe;
Connaissance des techniques de laboratoire de base et des techniques d'immunologie tel qu'ELISA;
Connaissance en cytométrie de flux, en ECLIA et/ou en luminex, un atout ;
Habileté à effectuer des essais de manière autonome;
La lecture et l'écriture de l'anglais sont requis. Le bilinguisme est préférable

Informations spécifiques au poste:

Localisation : 1580 Rue Ida-Métivier, Sherbrooke. Facilement accessible par le transport en commun (Rabais avec la STS). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 23.50$/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. Horaire du Lundi au Vendredi la plupart du temps.

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.

Field Customer Support Specialist I (US)

Job Summary

We are seeking an Instrument Field Support Specialist for our Nexus Robot and Endosafe range within our Microbial Solutions business covering North America.

The following are responsibilities related to the Instrument Field Support Specialist for our Nexus Robot and Endosafe range:

Provide customer-facing technical repair and maintenance services for endotoxin, and microbial detection laboratory instruments on site at customer locations.
•   Schedule and perform on-site service visits within an assigned region for product installations, annual qualification, routine preventive maintenance and analysis of product performance.
•   Provide technical assistance and problem resolution to customers via telephone, email, or on-site communication.
•   Complete all required field service activities and documentation as assigned based on specific product, customer and/or standard operating procedural requirements.
•   Assisting field sales personnel in product demonstrations, new customer training, and product validations.
•   Responsible for completing all service and compliance documentation as required by company policy, cGMP and FDA.
•   Responsible for resolving client testing laboratory instrument service issues.

Job Qualifications

The following are minimum qualifications related to the Instrument Field Support Specialist for our Nexus Robot and Endosafe range:

Qualification in Engineering, Chemistry, Microbiology, Biology or equivalent experience in the field
•   High level of Technical ability and able to work under pressure
•   3+ years of related experience
•   Ability to work from a home-based office
•   Frequent travel, sometimes with short notice

Compensation Data

The pay range for this position is $86,000 to $90,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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

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.

Prosecteur.trice - Nécropsie (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Prosecteur.trice - Nécropsie

En tant que prosecteur.trice pour notre équipe de Nécropsie à notre site de Sherbrooke, vous aurez la mission d'effectuer l'examen post-mortem des animaux tout en suivant les règlements éthiques et les directives des plans d'étude.

Dans ce rôle, les principales responsabilités incluront:

Euthanasier les animaux avant de faire la nécropsie.
Faire l'évaluation des tissus animaux pour les pathologistes.
Peser et documenter toutes les anomalies des organes.
Faire l'évaluation des anomalies et respecter les méthodes de conversation des tissus.

Éléments Clés

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

DEC en santé animale, inventaire et recherche en biologie, biotechnologie ou autre DEC en sciences ou un BAC en biologie. 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.
Comprendre et écrire l'anglais est requis.
Habileté à travailler en équipe et à faire face aux changements.
Capable de faire preuve d’une grande minutie et de façon autonome.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Informations spécifiques au poste:

Localisation : 1580 rue Ida-Métivier, Sherbrooke, Qc, J1E 0B5. Facilement accessible par le transport en commun (Rabais avec la STS). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 22.00$/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. Horaire régulier du Lundi au Vendredi et Travail de fin de semaine occasionnel par rotation.

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.

Assistant Administratif - F/H - CDD 12 mois (Saint-Nazaire, FR, 44600)

Le poste

Notre site de St Nazaire (44) est spécialisé dans la mise en place de tests de bioanalyses pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération. 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.

System Engineering (Charleston, SC, US, 29407)

Job Summary

We are seeking a highly motivated and detail-oriented Systems Engineer to support our Research & Development (R&D) team throughout the product development lifecycle. This role will focus on facilitating cross-functional collaboration, documenting system requirements and workflows, and ensuring serviceability and risk mitigation are addressed from concept to launch.

Key Responsibilities:

· Lead Product Requirements Document (PRD) review sessions with R&D subject matter experts (SMEs) and managers.

· Collaborate with Product Management (PM) to clarify product requirements and expectations.

· Document System Requirements and Technical Specifications (SRTS) by translating PRD items into actionable technical tasks (“how” responses).

· Provide ongoing technical and documentation support to R&D throughout development.

· Ensure cross-functional team members (R&D SMEs, PMs, Technical Services) have the information they need.

· Lead cross-functional technical discussions as needed.

· Gather and integrate input from internal stakeholders (Field Service, Production, Service Depots, etc.) to ensure products are designed with serviceability in mind.

· Capture and document user workflows with input from SMEs to ensure user needs are clearly understood and incorporated into design.

· Lead Failure Modes, Effects, and Criticality Analysis (FMECA) work sessions to ensure risks are documented, mitigated, and validated through testing.

Job Qualifications

· Bachelor’s degree in engineering, or related technical field.

· 3–5 years of experience in systems engineering, product development, or technical project coordination.

· Proven ability to translate business and user needs into detailed technical requirements.

· Experience working with cross-functional teams in an R&D environment.

· Familiarity with FMECA, risk analysis methodologies, and serviceability planning.

· Excellent communication, facilitation, and documentation skills.

· Detail-oriented, proactive, and comfortable managing multiple tasks in a fast-paced environment.

Preferred Skills:

· Experience in laboratory analytical devices.

· Understanding of product lifecycle processes, from concept through manufacturing.

· Azure DevOps.

· Strong analytical thinking and systems-level problem-solving skills.

Compensation Data

The pay range for this position is $85,000 to $95,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Equal Employment Opportunity

Associate Director, Laboratory Support & Logistics, Lab Sciences (Reno, NV, US, 89511)

Job Summary

The Associate Director of Laboratory and Logistics position at Charles River Laboratories in Reno, NV is responsible for overseeing the laboratory logistics and support functions (e.g., Sample Management, Data Management, Scientific Coordination, and Scientific Writing teams) in the Laboratory Sciences department. This leadership role drives operational excellence by ensuring clinical and non-clinical study samples, data, and reports are managed in a compliant, secure, efficient, and timely manner, in accordance with sponsor and regulatory specifications.

· Sample Management Oversight: Oversee the Sample Management team to ensure biological specimens (e.g., plasma, whole blood, tissues, etc.) are properly received, labeled, stored, tracked, and dispositioned for clinical and non-clinical studies.

· Data Management Leadership: Oversee the Data Management team to ensure efficient review of laboratory data and study reports according to CRL Standard Operating Procedures (SOPs), Business Operating Procedures (BOPs), study documentation (e.g., Plans, Protocols, and Methods), relevant regulations, and sponsor specifications.

· Scientific Coordination and Scientific Writing Oversight: Oversee Scientific Coordinators and Scientific Writers to ensure study data and reports progress through the process and are delivered to the sponsor within the agreed timelines, according to their specifications. Ensure adequate support of scientific staff is maintained. Ensure study progress is appropriately tracked and communicated to all stakeholders.

· Stakeholder Collaboration: Liaise with sponsors, clinical project managers, scientific and operational staff, and other internal teams to align on deliverables, timelines, and quality expectations.

· Staff Management: Lead, train, and mentor a multidisciplinary team, fostering a culture of accountability and continuous improvement. Develop and oversee study macro scheduling at time of study award and liaise with Operations and Scientific management to adjust the schedule as necessary on an ongoing basis. Ensure appropriate systems are kept up to date with accurate delivery dates.

· Regulatory Compliance: Ensure all processes adhere to the relevant regulatory guidelines, maintaining audit-ready documentation and addressing discrepancies promptly.

· Ensure appropriate resources are provided for the conduct of non-clinical and clinical studies by monitoring the daily macro level scheduling through supervisors and making recommendations to management for expected additional staffing needs based on review of projected workload.

· Resolve technical and operational issues inter- and intra-departmentally (e.g., troubleshooting procedural and technique issues).

· Continuously review and improve departmental processes and procedures to uphold the highest industry standards and sponsor requirements while also implementing efficiencies.

Job Qualifications

· Education: Bachelor’s degree (B.A./B.S.) or equivalent in a biological science or related field

· Experience: Minimum 10 years’ experience working in a hospital, contract research/manufacturing, or biotech/pharmaceutical industry conducting scientific research. Experience working in a regulated (GMP, CAP, CLIA, GLP, etc.) laboratory environment required. Management experience required. At least 3 years’ experience in a supervisory/management role.

· 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: Excellent verbal and written communication, and organizational skills. Demonstrated independent analytical and problem-solving abilities. Demonstrated proficiency in managing a team supporting or working in a laboratory environment

Note: The pay range for this position is $105,000 - $115,000 anually. 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.

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)

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.

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.

Quality Operations Specialist (Dublin, IE, D09)

Job Summary

Our fabulous Charles River Microbial Solutions International Ltd colleagues in Dublin are currently looking for a Quality Operations Specialist. This is a new role primarily based within the Accugenix Laboratory and is a fantastic opportunity for anyone looking to gain invaluable experience at the beginning of their QA career.

• Perform release activities to support Laboratory, Warehouse and Instrument Services.
• Approve customer test reports and participate in reagent release activities to support laboratory operations.
• Review SOPs, protocols/batch records, reports, quality and regulated QMS records.
(e.g. deviations, change controls, or CAPA) involving technically complex issues and processes for accuracy and compliance with all applicable regulations and internal policies.
• Participate in the support of client site visits.
• Participate in the performance of internal facility inspections.
• Perform facility and equipment records and logbook reviews.
• Participate in execution of Quality Assurance projects.
• Assist with providing basic regulatory training to operations personnel.
• Participate in the preparation of support during regulatory / customer, as required.
• Assist in correction of any regulatory risk areas as identified by Senior Quality Systems team members.
• Assist with analysis and collection of site Quality Metrics via QMS.
• Provide timely responses to Customer inquiries to support their qualification / regulatory requests.
• Assist in the development of recommendations for corrective and preventative actions to respond to client visit and regulatory inspection findings.

Charles River Laboratories offer a competitive remuneration and benefits package for this role together with on-going learning and development opportunities and structured career progression schemes.

Job Qualifications

• Education: Bachelor’s degree (B.S. / BA.A.) or equivalent, preferably in a life science.

• Experience: This is an entry level role. Whilst some experience within a laboratory based QA role would be advantageous full training will be provided. An aptitude for life sciences and an ethusiasm for learning are essential.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

• Other: Some experience with Microsoft Office® applications. This position requires the ability to communicate clearly, effectively and professionally; easily grasp instructions without follow-up; attention to detail and strong writing skills are essential.

• Attributes: This role is suited to someone who is highly self motivated, well organised and can maintain excellent focus when dealing with large volumes of work of a repetitive nature.

Additional Information:

This role is based onsite.

37.5 hours standard week Monday - Friday inclusive.

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.

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.

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 228532 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.

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.

Technicien de Laboratoire en Pathologie Technique - F/H - CDD 6 mois (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 900 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Dans le cadre d'un projet important et pour renforcer notre équipe, nous recherchons un Technicien de Laboratoire (F/H) en CDD pour une durée de 6 mois au sein de notre département de Pathologie Technique.
Sous la responsabilité de votre manager d'équipe (10-15 personnes), vous pratiquerez les autopsies et préparerez les lames histologiques pour interprétation par nos vétérinaires pathologistes.
Vous participerez également à la vie du laboratoire, en apportant un regard critique sur votre travail.
Vous savez identifier les anomalies, problèmes ou difficultés rencontrés dans votre quotidien.

Les missions

1. Histologie

Assurer la préparation des échantillons pour toutes les espèces
Réaliser l'inclusion des organes en blocs de paraffine
Réaliser la coupe des lames histologiques au microtome
Effectuer la coloration standard des lames et le montage
Utiliser en routine les automates à déshydrater, de coloration et les colleuses de lamelles

2. Autopsie

Assurer la réalisation des autopsies de toutes les espèces utilisées en toxicologie
Réaliser la saisie des données manuscrites ou à l'aide de système informatique
Contribuer à la qualité des études en assurant sans erreur les techniques de prélèvement et de fixation des organes

Conditions spécifiques du poste

Amplitude horaire : 7h/19h avec planning à la semaine
Astreintes (week-ends, jours féries)

Qualifications souhaitées

Vous êtes titulaire d'un diplôme de niveau Bac+2 dans le domaine de la biologie, et avez un attrait pour le domaine de la physiologie et l'anatomie.
Vous êtes à l'aise avec le travail en équipe mais également capable d'évoluer en autonomie. Vous êtes observateur, minutieux et rigoureux.
Vous avez des bases en anglais écrit et lu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25500 € bruts / an, sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement, de participation, accord d’ancienneté,...
Site non accessible en transport en commun : moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

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

Executive Director DSA Commercial Finance (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

ROLE SUMMARY:

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.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

Education: Bachelor’s degree (B.A./B.S.) or equivalent required.
Experience: 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.
Other: Comprehensive understanding of operational, sales and financial issues for business unit required

COMMENTS:

This position may require domestic and international travel.

Compensation Data

The pay range for this position is $230,000/yr - $260,000/yr. 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.

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.

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

Résumé du travail

Qui sommes-nous ?

Le poste

Au sein du département Pharmacie et dans une équipe composée de 22 collaborateurs, vous aurez pour objectif de vous assurer de la préparation des produits pour nos études.

Les missions

Etudes :

Réaliser tous les types de préparations galéniques (solutions, suspensions, remplissage de gélules, etc…) suivant les spécifications des dossiers d’études, des procédures et des BPL pour tous types d’études,
Réaliser les prélèvements d’échantillons de préparations galéniques et leur stockage, pour la réalisation d’analyses,
Mesurer les densités des substances d’essai, véhicule et formulation,
Livrer les substances d’essai ou les préparations galéniques aux services demandeurs sur notre site, selon le planning de livraison,
Assurer l’enregistrement des nouveaux lots de véhicules dans le système informatique,
Maintenir le matériel et les locaux propres à son poste de travail.

Documentation/Données :

Assurer l’acquisition des données d’études dans un environnement BPL,
Créer et /ou contrôler les conditions de préparations des études en cours dans le système informatique.

Conditions spécifiques du poste 

Prise de poste le matin (aux environ de 7h30)

Travail le week-end et jours fériés

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 idéalement spécialisé dans la formulation scientifique.

Vous maitrisez l’anglais, à l’écrit comme à l’oral.

Vous êtes rigoureux, ponctuel et assidu.

Vous possédez un bon 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.

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.

Technician - Molecular Imaging (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay range for this position is $20.00 - $21.50. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

SCHEDULE: Monday - Friday, 8:00am - 4:30pm

We are seeking a Research Technician for our Molecular Imaging Team located in Mattawan, MI.

A Research Technician 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.

Job Qualifications

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

Minimum: High School Diploma or GED
Experience: minimum of 1 year of work exerience preferred
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints

The pay range for this position is $20-21.50/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.

Befristeter Vertrag: 18 Monate -Human Resources Business Partner (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

Job Summary

An unserem Standort in Sulzfeld bieten wir eine Stelle als Human Resources Business Partner (HRBP) an. Sie verstärken unser HR-Team und unterstützen und beraten bei HR-relevanten Themen und Prozessen.

Zu den Hauptaufgaben dieser Position gehören:
- Enge Zusammenarbeit mit dem line-Management, um die korrekte Anwendung von HR-Richtlinien und -Praktiken sicherzustellen. Bei Bedarf sollen Änderungsvorschläge für Richtlinien und Praktiken unterbreitet werden.
- Coaching und Zusammenarbeit mit Führungskräften bei der Lösung komplexer Probleme im Bereich der Mitarbeiterbeziehungen; bei Bedarf soll rechtliche Beratung eingeholt werden.
- Vorbereitung von Betriebsratsinformationen und der erforderlichen Dokumente.
- Sicherstellung der zeitnahen Bearbeitung von Dokumenten und Transaktionen, Übermittlung relevanter Vertragsinformationen, zeitnahe Eingabe von Änderungen in das HR-System, Digitalisierung und Aktualisierung der Personalakten. Aktualisierung und Aufrechterhaltung der SOX-Kontrollen und Gewährleistung der vollständigen Compliance/Prüfung von HR-Daten.
- Sicherstellung der Einhaltung lokaler, staatlicher und bundesstaatlicher Vorschriften und Pflege der erforderlichen Dokumentation zu Compliance-Zwecken; Überwachung und Prüfungen der HR-Dokumentation nach Bedarf.
Unterstützung der Führungskräfte bei der Analyse ihrer Profilanforderungen zur Personalbeschaffung, Erstellung und Veröffentlichung von Stellenanzeigen; Auswahl und Durchführung von Vorstellungsgesprächen, Bewertung von Kandidaten, Beratung der Führungskräfte und Unterbreitung von Stellenangeboten.
- Analysieren und Bearbeiten von Änderungen der Vergütung und der Zusatzleistungen, Durchführung des jährlichen Lohnerhöhungsprozesses und der Bonusauszahlungen und Erstellen der entsprechenden Dokumentation.
- Unterstützen bei den Onboarding- und Offboarding-Prozessen und Sicherstellen, dass alle erforderlichen Dokumentationen und Systemaktualisierungen vollständig sind. Führen von Onboarding-Meetings und Kündigungsgesprächen.
-Sie kommunizieren aktiv vor Ort, um Führungskräfte und Mitarbeiter über HR-relevante Themen zu informieren.

Für diese Position erwarten wir folgende Mindestqualifikationen:
-Bachelor-Abschluss im Bereich Personalmanagement (People & Culture Studies);
-3 Jahre einschlägige Berufserfahrung als HR-Generalist/HRBP oder in einer ähnlichen Funktion.
-Gute Englischkenntnisse sind für die Position erforderlich.
-Proaktiver Teamplayer, sowohl abteilungsintern als auch unternehmensweit.

Rollenspezifische Informationen:
• Befristeter Vertrag: 18 Monate
• Standort: 97633 Sulzfeld; Kostenlose Parkplätze.
Arbeitszeit: Montag bis Freitagmittag, Vollzeitbeschäftigung bevorzugt, Teilzeit ist jedoch möglich.
Ein Arbeitstag zu Hause nach 6 Monaten in der Position ist möglich.

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

Senior 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.

DIRECT LABOR - Research Services Manager (Chaoyang District, BJ, CN, 100012)

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.

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.

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.

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)

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

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

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

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

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.

Clerk (Malvern, PA, US, 19355)

Job Summary

Perform routine clerical duties in support of a manager, director and/or department.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide routine clerical support, such as preparing routine departmental and corporate forms, collating and distributing information, and receiving and distributing mail.
May be responsible for records entries in files, charts, or computer spreadsheet.
Retrieve and deliver requested departmental files and/or documents both intra-departmentally and between other buildings or departments on site.
Establish and maintain files.
May provide telephone coverage, as needed.
Relay information and requests to department personnel.
May maintain inventory of office supplies and other non-technical supplies as assigned.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.) and one year of college or equivalent college-level coursework.
Experience: 1-2 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: None.
Other: Experience utilizing computers for data entry, spreadsheets and document preparation. Ability to read, speak and understand English required. Experience in laboratory animal setting and/or knowledge of related technical terminology strongly preferred.

The pay range for this position is $20.00 to $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.

Equal Employment Opportunity

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

Automation Equipment Technician I (Charleston, SC, US, 29407)

Job Summary

Charles River Labs located in Charleston, SC is looking for a Automated Equipment Technician for our Microbial Solutions business.

The Automated Equipment Technician is responsible for the maintenance, upkeep, and proper functioning of all Production automation and associated equipment. This role ensures that production goals can be met by maintaining the automated production line in proper working condition through both preventative maintenance and repair / replacement of components.

Job Duties

Full knowledge of production lines as well as other production equipment.
Perform and document scheduled, routine maintenance on all production equipment.
Support Class 100 fill operations using automated and manual equipment.
Coordinate professionally with outside vendors that calibration/maintenance of equipment is performed on time and the impact to Production is minimal.
Troubleshoot, maintain and repair mechanical and electrical controls as well as pneumatic and hydraulic systems.
Responsible for proficiency with all SOP’s in areas of the department and documentation as required by FDA, company policy and cGMP.
Perform all other related duties as assigned.
After hours and weekend work may be required.

Job Qualifications

Education: Associate's degree in sciences or electronics or closely related technical field preferred. High school diploma or General Education Degree (G.E.D.) or trade school graduate or equivalent.
Experience: 3-5 years experience working on Production automation and related systems, preferably in a pharmaceutical- type environment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other:

Laboratory experience, operation of production equipment, proficient with Microsoft Office products, and familiar with CAD tools a plus.
Must be capable of working from and understand equipment manuals, specifications, mechanical drawings, electrical schematic and ladder logic displays.
Advanced ability to troubleshoot equipment with but not limited to: Direct Logic PLC, Rockwell Automation, AC/DC Drive Systems, robotic programming and diagnostics (Robotic Systems).

Compensation Data

The pay range for this position is $28/hr - $29.25/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

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

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2019.

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.

Archives - Associate (Mattawan, MI, US, 49071)

Job Summary

An Archivist II supports the receipt, login, distribution, disposal, and general oversight of materials submitted for archival purposes. The individual in this role: manages study-related records, biological specimens, and study samples, and supports the archival process by storing, distributing, and maintaining materials within the archive management system

Job Qualifications

Essential Duties and Responsibilities

Perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Identify and communicate any issues with data to management.
Uphold archive security procedures and maintain the integrity of archived materials
Independently perform tasks including but not limited to, organizing, filing, retrieving facility and study related records, biological specimens, and samples
Independently assist internal customers with requests for current and finalized study materials under the control of the Archives discipline
Utilize the archival management system for indexing and maintaining materials in the archives or records management area, with minimal oversight
Review departmental and study specific data to ensure adherence to SOPs, methods/protocols, industry standards, and regulatory requirements, as applicable, in timely manner, with minimal oversight
Actively participate in process improvement initiatives with oversight
Perform all other related duties as assigned.

Minimum Qualifications

Education and Experience: HS/GED/Associate’s degree with 1-2 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: None.

Other:

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 Duties and Responsibilities, 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.

Workplace Requirements

While performing the duties of this job, the employee must be able to perform general office and/or laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, typing/entering data into a computer, using appropriate instruments, reaching with hands and arms, 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.
General office working conditions, the noise level in the work environment is usually quiet.
While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions

All employees are required to satisfactorily perform the essential duties and responsibilities of their position. · The essential duties and responsibilities listed above are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required. Duties and responsibilities may change without notice. · Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job or as otherwise required to comply with applicable law. .

Equal Employment Opportunity

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

Clinical Pathology Technician 1 (Reno, NV, US, 89511)

Job Summary

***Hours are from 7:30 a.m. To 4:00 p.m.***

BASIC SUMMARY:
Perform a wide variety of basic laboratory tasks. Maintain and perform record keeping. Review data recorded for others for quality control.

Receive, process, track and store samples received into the laboratory. Prepare and process biological samples prior to analysis.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform a wide variety of basic laboratory tasks.
•   Under supervision may act as lead/primary technician on routine studies.
•   Operate general laboratory equipment (i.e.: centrifuge, pipettes, water baths) used in the processing of b biological samples.
•   Perform all specialized processing under supervision
•   Read study protocols and extract pertinent information with guidance.
•   Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
•   Monitor, and perform tasks, related to individual study assignments.
•   Receive, process, track and store all samples received into the laboratory.
•   Observe and assist with technical/study related duties with guidance.
•   File and maintain data for department activities.
•   Maintain and perform record keeping.
•   Review data recorded by others for quality control.
•   Assist with training for less experienced staff.
•   May perform phlebotomy when appropriately certified.
•   Perform all other related duties as assigned.

QUALIFICATIONS:
•   Education: High school diploma or General Education Degree (G.E.D.).
•   Experience: Experience in a laboratory setting 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: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database).

***The pay range for this position starts at $19.00. 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

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.

Client Manager (High Peak, GB, SK23 6FJ)

Job Summary

Could you be our next Client Manager, based at our site in High Peak, Derbyshire?

Have you got the ability to upsell and expand on existing relationships?

Do you have a Biological Science focus degree?

You will represent the company to external and internal customers, answer service and technology-related questions, interpret and clarify customer study designs to place into proposals/contracts, develop pricing strategies for customer contracts and negotiate for maximum company revenue. You will also assist in developing strategies to grow current business as well as win new business. The role will also require you to provide valuable insight into forecasting services by business line, customer and facility as well as ensuring maximum capacity utilisation by working with operations to identify studies and clients to prioritise.

Main Tasks

Assist operation in drafting proposals and schedules of work (SOWs).

Qualify bids and scopes of work with client to ensure appropriate service is provided.

Work with the Legal team to ensure all required legal documents are in place.

Work closely and effectively with the High Peak Client Service team, and the wider CRL Sales / Business Development team to progress opportunities optimally.

Follow up with clients in conjunction with Business Development to ensure that proposals/study plans are complete and answer their needs.

Creatively identify ways to secure open opportunities by working with scientific staff, finance, management and others.

Identify new business opportunities with clients and liaise with appropriate internal staff for follow-up.

Develop and / or review proposals and SOWs for accuracy.

When appropriate, prepare sale price estimates for protocols, bid requests, study revisions and additions using site’s suggested selling price.

Review and approve bid and proposal packages within authorised limits.

Assist management in monitoring sale pricing practices to determine accuracy and relevance to study type, service and operation processes.

Assist management in making recommendations on desirable proposals based on established financial and operational criteria, as required.

Ensure that scientific staff visiting clients are fully informed about clients needs.

Daily management of pipeline data in SalesForce (CRM).

Work with Project Management Office / Finance and Operations to ensure accurate pipeline data are available.

Job Qualifications

Bachelor’s degree (B.A. / B.S.) or equivalent in biological science related subject.
Proven experience of working within the pharma/bioscience industry or equivalent.
Excellent communication skills, both written and verbal English.
High levels of self-motivation and proactivity under minimal supervision.
Ability to work in a dynamic working environment
Ability to deal with priorities and tight deadlines.
Track record of consistently achieving or over-achieving targets.
Proficient in Microsoft Office and other IT platforms.
Good numeracy and literacy skills.
Strong attention to detail.

Specific Skills

A sufficient understanding of the drug discovery process (especially biologics) and biological/medical science to be able to hold appropriate credible scientific and business discussions with drug discovery and academic clients.
Experience of presenting scientific data to a variety of stakeholders.

Advantageous Skills

Second language (particularly Mandarin, Japanese, Korean).
Experience using a Customer Relationship Management tool, particularly Salesforce.
Experience of working with clients based in Asia.
Experience in a contract research and / or pharmaceutical setting preferred.
Experience in client-facing roles with project management skills.

What We Offer You

A very comprehensive benefits package from day one, including a large pension contribution, private medical, and more!
The opportunity to get industry standard training and experience.
Global opportunities and strong career progression.
Personal development and skills enrichment as one of our key focuses.
To be able make a difference to health and well being of people.
Flexible working opportunities.

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.

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.

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.

Equal Employment Opportunity

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

Supervisor, InVivo Operations (Stilwell, KS, US, 66085)

Job Summary

We are seeking an supervisor to join our Integrated Toxicology (ITox) team at the Kansas 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 our team, you will have a significant impact on the health and well-being of people across the globe. This role will be responsible for the oversight of in-vivo operations staff and all daily functions to support animal care and study execution. They will provide, coordinate, document, and schedule routine and highly complex training activities for In-Life, Animal Care, and Cage Wash personnel. This individual will also be responsible for defining a new technical training plan, in alignment with the global program, that includes developing, revising, and implementing the use of training documents and processes. They will also provide leadership and/or support of new hire orientation.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide guidance in the day-to-day activities of assigned departmental employees to ensure accurate, high-quality work, and adherence to pertinent departmental policies, practices, and procedures (SOPs, safety procedures and biosafety protocols). Ensure schedule is prepared daily, accurately reflecting required tasks and workload. Serve as a model as it relates to effective time management, communication, and utilization of resources.
Perform technical tasks to support completion of study tasks (as needed).
Lead and mentor less experienced training personnel.
Work with department management to coordinate and facilitate multi-species technical training at all levels of complexity for department personnel.
Maintain and update all documents and databases used for the support and conduct of training tasks, including but not limited to training standards, training records, training timelines, and proficiency standards.
Provide oversight, scheduling, and coordination of training animal use to enable optimal learning while prioritizing animal care and welfare.
Practice/maintain advanced technical skills and procedures, work independently, and follow operating procedures and processes.
May conduct sponsor/visitor tours and interact with clients.
Provide input/review of new, and/or revised processes, operating procedures, training standards, quizzes, proficiency standards, and other training documents.
Assist in facilitating, coordinating, and scheduling new hire orientation and on-the-job training for personnel.
Participate in recruiting efforts by assisting in interviews and selecting qualified non-exempt level departmental personnel.
Assist in the scheduling, coordination, and execution of study procedures.
24/7 emergency duty coverage as assigned.
Perform all other related duties as assigned.

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.
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 ALAT/LAT level strongly preferred; or other applicable certification/licensure.
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 GLPs 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.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 25 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, 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.

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

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.

Laboratory Clerk - Sample Management (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Laboratory Clerk for our Sample Management team at the Laval location, you will assist the Technicians and provide general technical support.

In this role, primary responsibilities include:

Receive or pick up samples from the facility;
Prepare the required materials for the study conduct;
Keep the samples well organized within the freezers and ensure proper documentation;
Perform maintenance/cleaning of the fridges and freezers;
Keep the working area clean and organized.

Key Elements

If you have the following qualifications, we'll train you for the rest:

At least secondary 3 completed;
Good organizational, interpersonal and communication skills;
Detail oriented and meticulous;
Ability to work under time constraints and to adapt to change;
Ability to work in a team environment.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $17/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm. 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);
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.

Commis de laboratoire - Gestion des échantillons (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Commis de laboratoire pour notre équipe de Gestion des échantillons située au site de Laval, vous assisterez les Techniciens.nes et fournirez un soutien technique général.

Dans ce poste, les principales responsabilités incluront:

Recevoir ou ramasser les échantillons de l'installation;
Préparer le matériel nécessaire à la conduite de l'étude;
Vous êtes responsable de l'organisation des échantillons dans les congélateurs et veillez à ce qu'ils soient correctement documentés;
Effectuer l'entretien et le nettoyage des réfrigérateurs et des congélateurs;
Veiller à la propreté et à l'organisation de l'espace de travail.

Éléments clés

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

Au minimum, 3ème secondaire complété;
Bonnes compétences en matière d'organisation, de relations interpersonnelles et de communication;
Souci du détail et méticulosité;
Capacité à travailler dans des délais serrés et à s'adapter au changement;
Capacité à travailler en équipe.

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;
Salaire: 17$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire 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);
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.

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.

Equal Employment Opportunity

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

Director, Digital & Growth Marketing Strategy (Wilmington, MA, US, 01887)

Job Summary

Charles River Laboratories is seeking a seasoned Director of Digital Marketing Strategy & Growth Marketing to lead the strategy and development of digital marketing programs across the global organization. This senior leadership role will drive enterprise-wide digital transformation in marketing, with a strong focus on customer acquisition, engagement, digital demand generation, and marketing technology innovation in alignment with our business strategies.

As a strategic partner to the global Marketing organization, the Director will play a pivotal role in positioning Charles River as a digital-first, customer-centric leader in the life sciences sector. The ideal candidate is a visionary marketer with strong analytical skills, technical fluency, and proven success scaling digital initiatives in complex, matrixed organizations.

Position will work remotely from home office.

Essential Duties and Responsibilities

Digital Demand Generation & Growth Marketing
• Lead the design and execution of omnichannel demand generation programs to drive qualified leads, pipeline acceleration, and customer retention across diverse business units.
• Implement and refine account-based marketing (ABM), personalization strategies, and marketing automation workflows to improve conversion and ROI.
• Define performance metrics and KPIs to evaluate campaign effectiveness, leveraging A/B testing, marketing analytics, and CRM integration.

Digital Experience & Content Strategy
• Oversee the strategy for Charles River’s digital platforms (e.g., website, landing pages, email, social, paid media) to deliver seamless, engaging experiences across the buyer journey.
• Collaborate with internal stakeholders and external agencies to optimize content strategy and ensure alignment with SEO, thought leadership, and scientific storytelling goals.

Marketing Strategy, Leadership & Planning
• Lead the development and ongoing refinement of a global marketing roadmap that aligns digital and growth marketing initiatives with corporate strategic goals, business unit priorities, and revenue targets.
• Oversee annual and quarterly marketing planning cycles, coordinating with operational and strategic marketing teams to ensure cross-functional alignment, budget discipline, and resource allocation across campaigns, content, media, and technology.
• Translate corporate objectives into actionable, measurable marketing plans that balance brand-building, demand generation, and customer experience goals.
• Serve as a key liaison between Global Strategic Marketing, Commercial Operations, and Marketing Operations to ensure campaign integration and alignment with product launches, key initiatives, and customer milestones.
• Establish consistent marketing planning processes, templates, and governance frameworks to ensure agility, scalability, and visibility across all functions.
• Drive accountability through clear performance metrics, reporting cadences, and dashboards, enabling real-time insights and adjustments to optimize marketing ROI.
• Partner with Market Intelligence team on scenario planning, market analysis, and competitive intelligence efforts to inform prioritization of initiatives, new opportunity development, and audience targeting strategies.
• Partner with IT, data science, and commercial operations to refine data pipelines, segmentation models, lead scoring, and attribution frameworks. Champion a culture of innovation, continuous improvement, and data-driven decision-making within the marketing function.

Team Leadership & Collaboration
• Build and lead a high-performing, globally distributed team of digital and growth marketing professionals.
• Partner cross-functionally with commercial, strategic, scientific, and operational marketing teams to drive campaign adoption and ensure alignment with customer insights.
• Coach, mentor, and develop talent to support organizational growth and succession planning.

Job Qualifications

• Bachelor’s degree in Marketing, Business, Communications, or related field; MBA or relevant Master’s degree strongly preferred.
• 12+ years of experience in B2B digital marketing, including at least 5 years in a senior leadership role.
• Proven success leading digital transformation and growth marketing in life sciences, or related technical industries.
• Expertise in marketing technology platforms including CRM, Marketing Automation, analytics, and content management systems.
• Strong understanding of demand generation, funnel metrics, buyer journey mapping, and performance marketing best practices.
• Excellent leadership, communication, and stakeholder management skills; experience working in a global matrixed environment is essential.
• Demonstrated ability to drive change, innovate, and deliver measurable business impact through marketing strategy.

Compensation Data

The pay range for this position is $135,000K - $185,000K USD annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

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

Technicien de Laboratoire en Pathologie Technique - 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 900 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 répondre à notre charge importante, nous recrutons un Technicien de Laboratoire (F/H) en CDI pour rejoindre notre département de Pathologie Technique.
Sous la responsabilité de votre manager d'équipe (10-15 personnes), vous pratiquerez les autopsies et préparerez les lames histologiques pour interprétation par nos vétérinaires pathologistes.
Vous participerez également à la vie du laboratoire, en apportant un regard critique sur votre travail.
Vous savez identifier les anomalies, problèmes ou difficultés rencontrés dans votre quotidien.

Les missions

1. Histologie

Assurer la préparation des échantillons pour toutes les espèces
Réaliser l'inclusion des organes en blocs de paraffine
Réaliser la coupe des lames histologiques au microtome
Effectuer la coloration standard des lames et le montage
Utiliser en routine les automates à déshydrater, de coloration et les colleuses de lamelles

2. Autopsie

Assurer la réalisation des autopsies de toutes les espèces utilisées en toxicologie
Réaliser la saisie des données manuscrites ou à l'aide de système informatique
Contribuer à la qualité des études en assurant sans erreur les techniques de prélèvement et de fixation des organes

Conditions spécifiques du poste

Amplitude horaire : 7h/19h avec planning à la semaine
Astreintes (week-ends, jours féries)

Qualifications souhaitées

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25500 € bruts / an, sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement, de participation, accord d’ancienneté,...
Site non-accessible en transport en commun : moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

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

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.

Senior Full Stack Drupal/React Developer (MADRID, M, ES, 28029)

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

Drive the build and maintenance of high-performance, decoupled web applications that pair Drupal back-ends with React front-ends. You’ll collaborate closely with different teams to deliver secure, scalable solutions and ensure continuous delivery of quality code that meets regulatory standards.

Essential duties and responsibilities

Analyse, design, develop, integrate, and document Drupal & React based websites
Create reusable React components that consume Drupal JSON:API endpoints
Write and maintain unit, integration, and end-to-end tests
Configure / tune Apache Solr (Search API Solr) for fast, faceted search
Optimize caching layers, harden security, and monitor Web Vitals
Configure and maintain GitHub Actions pipelines and broader CI/CD automation
Work in containerised, high-scale environments (Docker / Kubernetes)
Participate in backlog grooming, sprint planning, and other ceremonies
Conduct peer code reviews and provide constructive feedback
Follow SOX, SOP, GLP, GMP and related standards
Produce clean, well-documented, efficient code
Leverage approved AI tools to streamline daily development tasks
Perform related duties as assigned

Competitive salary and benefits package reflective of location and scope of experience.

Job Qualifications

Bachelor's degree (B.A./B.S.) or equivalent in Computer Science, Engineering, Information Systems, or a related discipline
Strong track record of development experience in Drupal & React with demonstrable outcomes
Drupal Expertise
Deep knowledge of Drupal 10+ core APIs and Composer workflows
Proficient with decoupled architectures (JSON:API)
Strong PHP (modern OOP, Dependency Injection, SOLID principles)
React Expertise
Familiar with React, NextJS and Jest best practices

Preferred but not Essential

Chakra UI experience
Understanding of React components lifecycle: mounting, evolving,unmounting

Soft Skills

Clear written & verbal communication. Fluency in English essential.
Exemplary attention to detail
Effective planning and organisation skills with the ability to effectively prioritise in the face of multiple requirements
Able to explain technical decisions and trade-off's succinctly
Strong collaboration and influencing skills
Ability to work calmly and efficiently under pressure in order to meet stringent deadlines and maintain continuity
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above

Equal Employment Opportunity

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

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。

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 8:00am - 6:30pm

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.

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.

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

Job Summary

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

NOTE: The shift for this position is rotating schedule 12:00pm - 8:00pm 2-2-3-3

The following are responsibilities related to the Biomanufacturing Supervisor.

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

Job Qualifications

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

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

Compensation Data

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

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.

Facility Manager II (33) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Facility Manager II to join our Insourcing Solutions team, located in Bethesda, MD.

As the Facility Manager II, you will be the primary point of contact for the facility, utilizing existing SOPs and quality assurance standards to oversee and coordinate the daily activities of the facility within varied animal care environments, including scheduling of staff.

Additional responsibilities include:

Oversee the animal surveillance program and all aspects of husbandry, including technical and cage wash support.
Provide quality assurance to include animal health surveillance; monitoring of the effectiveness of facility sanitation, cage washing and autoclaving procedures; monitoring of incoming animal shipments for container integrity and animal health; monitor the heating, ventilation, and air conditioning (HVAC); internal facility reports for monitoring deviations from pre-established parameters; and other quality assurance services as deemed necessary (e.g., water cultures).
Participate in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations.
Assist in assessing, developing, and presenting training for staff and investigators.
Participate in QC/QA, and ensure CAPA development, implementation, and adherence.
Occasionally provide technical support (e.g., restraining animals, collecting blood, collecting tissues, performing injections, treatments, surgical preparation, assisting with research procedures).
Occasionally provide animal husbandry and environmental enrichment.
Provide data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements.
Prepare and submit written records, charts, logs, and inventories.
Actively interact with Project Officers, facility veterinarian(s) and investigators to solve customer requests, inquiries, and complaints.

Job Qualifications

The following are minimum requirements related to the Facility Manager II position:

High school diploma or GED required.
Bachelor’s degree in animal science or related preferred
Minimum of 6 years’ experience in a research vivarium facility, with at least 2 years’ experience in an ABSL3 environment, and 3 years of supervisory experience
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

The pay range for this position is $45.00 to $50.00 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.

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

Security Officer - Wilmington/Shrewsbury, MA (Sat & Sun, 6p-6a) (Wilmington, MA, US, 01887)

Job Summary

Charles River Laboratories is seeking a PART TIME (24 hrs. per week, benefit eligible) Security Officer for their Wilmington and Shrewsbury, MA sites.

Shift is overnights, Saturday & Sunday, 6pm-6am (12hrs) + 15% Differential

Following established procedures and guidelines, monitor and ensure compliance with company security and safety policies. Monitor all access activities to the facility by checking and issuing security badges. Monitor security, safety and integrity of buildings and environs and respond to any unusual circumstances. Protect facility from unwanted actions or espionage. Provide a safe and secure environment for employees, clients, visitors and animals.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
Monitor security systems and/or environmental systems and investigate and/or report any incidents.
Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physcial security measures; and monitors the critical building systems.
Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
Document all security department activity and generates incident reports as necessary.
Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
Contact emergency personnel as required and in accordance with adherence to pertinent departmental policies, practices, and procedures.
Assist in directing appropriate emergency response efforts when required.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Must be willing to work on a Part time schedule – 24hrs per week (position will be Benefits Eligible)
Shift: Sat & Sun 6pm-6am (12hrs) + 15% Differential.

Compensation Data

The base pay for this position is $22/hr. + 15% shift differential. Please note that salaries vary within the range (if applicable) based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

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

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.

Data Review Analyst I (Reno, NV, US, 89511)

Job Summary

This is not a Remote role. Candidate must reside in Reno, NV

We are seeking a Data Analyst I for our site located in Reno, NV.

The Data Analyst I is responsible for QC reviewing all tabulated study data to ensure it is accurate and complete. Ensure that all data received for review follows SOP guidelines that apply to the recording of study data.

•   Complete QC for tabulated study data produced in operational departments.
•   Ensure all report table corrections are completed by the appropriate staff members and that they are completed correctly.
•   Demonstrate comprehension of applicable regulatory driving documents, including protocols/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc. as they relate to reported study data.
•   Ensure sample analysis data collected is appropriate and in scope with driving documents (protocol/phase plans, Analytical Procedures, Data Transfer Agreements, SOPs/BOPs, etc.) for what is intended to be reported.
•   Develop effective communication skills through informal discussions with peers, supervisor, and team.
•   Develop critical thinking, troubleshooting, and time management skills to ensure data quality and study timelines are maintained.
•   Identify process improvement initiatives based on observed trends and errors.
•   Support data review assistants with data review on all paper and electronic data produced in operational departments as needed.
•   Support with archiving, collating, and organizing all completed and reviewed data and/or file as needed.
•   Perform all other related duties as assigned.

Job Qualifications

The following are minimum qualifications related to the Data Analyst 1 position:

•   Education: High school diploma or General Education Degree (G.E.D.) required.
•   Experience: Minimum of 2-4 years related experience, including GLP and/or GCP 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: Strong organizational skills and acute attention to detail. Proficient in utilizing personal computer, e-mail, and standard office software packages (word processing, spreadsheet, presentation, database). Basic understanding of processes used for study data collection. Basic understanding of SOPs, GLPs, and other applicable regulatory guidelines governing the recording and review of study data.

The pay range for this position is $22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

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

Scientific Coordinator-Lab Sciences (Reno, NV, US, 89511)

Job Summary

Responsible for providing protocol and report support to Study Directors, and scientists, and assist with providing information/data requested by sponsors. Publish data tables and develop Material and Methods. Assist with management of QA audits and assure necessary corrections and follow-up take place.

•   Attend post-award and/or pre-study meetings and monitor events during the in-life phase to assure a full understanding of assigned projects and results, including objectives, timelines and reporting requirements.
•   Create/customize planning tools to facilitate prioritization of daily activities.
•   Interact regularly with sponsors: send amendments and regulatory forms for signature, respond to sponsor-requests for information and tables, and assist with sponsor on-site visits. Serve as primary point of contact to the sponsor when study director is not available.
•   Write initial protocol drafts. Upon study director approval, distribute draft protocols for internal and/or sponsor review, and coordinate amendment/revision process.
•   Facilitate signature/approval process for protocol, amendments and other required forms.
•   Tabulate study data and schedule data review meetings.
•   Extract information from protocol and study data to generate the materials and methods sections of preclinical study reports and/or clinical subreports including text tables.
•   Create data tables for report from automated data collection systems or manual data if applicable.
•   Create/generate special tables for sponsors as needed.
•   Generate and format data tables for reports.
•   Create interpretive tables as directed by the study director.
•   Maintain reporting timelines.
•   Assemble report (text and data tables) for senior scientific review, QA audits, and final report compilation.
•   Assist with management of QA audits and assure necessary corrections and follow-up take place.
•   Answer QA audit findings as directed by the study director.
•   Ensure that all study books are corrected appropriately, and that documentation is GLP compliant prior to submission to QA.
•   Assist in IACUC form preparation and perform IACUC literature searches.
•   Assist in documentation of deviations from the protocol or Standard Operating Procedures (SOP).
•   Work closely within a small team environment.
•   Perform all other related duties as assigned.
•   Under direction of the study director, receive, review and accept proof corrections from report coordination staff and make recommended corrections as appropriate.
•   Provide editorial/formatting review of final study protocols, amendments and report text. Provide comments and/or suggested changes to study director.
•   Upload data/reports to CR Sponsor portal and/or Sponsor portal.

Job Qualifications

•   Education: Bachelor’s degree (B.A./B.S.) or equivalent in science or related discipline.
•   Experience: 1-3 years related experience in a laboratory or scientific research 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: None.
•   Other: This position requires analytical thinking skills and a good understanding of scientific processes. Strong organizational skills and attention to detail required, as are computer skills including MS Office software and database management. Must be familiar with medical terminology and have a thorough understanding of technical aspects of research studies (e.g. observing dosing, treatments, surgical procedures, and necropsy evaluations).

The pay range for this position is $25.00 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.

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.

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

Job Summary

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

Essential Duties & Responsibilities:

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

Job Qualifications

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

Compensation Data

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

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.

Central Services Technician I (South San Francisco, CA, US, 94080)

Job Summary

We are looking for a Central Services Technician I (Cage Processing) to join our Insourcing Solutions team located in South San Francisco, CA.

As the Central Services Technician I (cage processing), 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.

Additional responsibilities include:

Operate commercial tunnel and rack washers for cleaning and sanitizing animal cage supplies through automatic processes.
Operate commercial autoclave machinery 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.
Handle and transfer supplies (caging, gases, dry ice, liquid nitrogen), and waste as needed to and from work area(s).
Perform daily cage wash area duties including recycling and scheduled sanitation procedures with documentation.
Provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas with supporting documentation under supervision.
Provide quality assurance to the cagewash area.
Ability to work in a repetitive high throughput environment.

Job Qualifications

The following are the minimum requirements related to the Central Services Technician position:

High School diploma, General Education Degree (G.E.D.) or equivalent required.
Ability to read, write, understand, and follow directions.
Ability to recognize and communicate verbally and/or in writing, problems requiring the attention of high-level personnel in a timely and appropriate manner.
Rodent husbandry experience preferred.
ALAT certification preferred.

The pay range for this position is $21.04 - $25.20 USD per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

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

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.

Veterinary Technician Assistant I (Worcester, MA, US, 01608)

Job Summary

We are seeking a Veterinary Technician Assistant for our Discovery site located in Worcester.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases. Also responsible for daily health observations, preventative health care, environment enrichment and handling and restrain of laboratory animals. In addition, this individual will may also perform technical in-life procedures.

ESSENTIAL DUTIES:

Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Veterinarians.
Perform routine veterinary technical and husbandry skills including the following:
- Generate animal treatment records and perform treatment distribution
- Administration of various therapeutic measures by IM, SQ, topical, oral routes, etc. o Proficient animal restraint techniques.
- Observe basic care animals o Daily walk through of animal rooms
- Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
- Animal observations, reporting abnormalities
- Perform animal follow-ups as needed
Monitor animal heath, visually and by following detailed schedules.
Maintain accurate record keeping procedures for the veterinary department May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
May assist in surgical pack preparation and cleaning of surgical instruments. Assistance in acclimation and behavior management of animals in our care.
Provide environmental enrichment for laboratory animals according to facility and Federal guidelines.
Assist in keeping inventory and stocking the vet rooms (i.e. drugs and supplies).
Assist in organizing and maintaining the vet exam rooms.
Record keeping of required logs.
Triage and recheck non-USDA covered species.

The pay range for this position starts at $22 to $24 per 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

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.

Equal Employment Opportunity

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

Cleaner (Tranent, GB, EH33 2NE)

Job Summary

We are looking to recruit a Cleaner for our Safety Assessment site located at Tranent, East Lothian. We are flexible in start and finishing times.

As a Cleaner you will have responsibility of cleaning services for office, laboratory and general areas within the Company including cleaning of surfaces, floors, benches and corridors as required.

The following is required for this role:

Previous cleaning experience would be a distinct advantage
Ability to work within a team
Good attention to detail
Flexible and hard-working attitude

The salary for the role is £23,842.35 per annum, which equates to £12.60 per hour.

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.

Technician 1 - Histology, 2nd Shift (Mattawan, MI, US, 49071)

Job Summary

We are seeking an experienced Technician 1 - Histology for our 2nd Shift Pathology Services Team in Mattawan MI.

A Technician 1 – Histology 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 handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. 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 handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. 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.
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.

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.

Technician I, Animal Care Services (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Animal Care Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $19/hour plus benefits.

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 husbandry needs, animal handling, cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. The technician is working under close supervision to gain proficiency.

Potential Permanent Schedules: May vary based on business need and available roles to include:

Monday – Friday with weekend and holiday rotations 07:00AM* – 3:30PM*
Saturday - Wednesday with holiday rotations 07:00AM* – 3:30PM*
Wednesday - Saturday with holiday rotations 07:00AM* – 3:30PM*

All roles and shifts require flexibility to work extended hours outside of scheduled shift based on business need, sometimes with short notice.

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 husbandry needs, animal handling, cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: None.
Other:

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.

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.

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.

Technical Trainer (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Technical Trainer to join our Insourcing Solutions team supporting our client site in Bethesda, MD.

As the Technical Trainer you will develop, deliver, document, and report technical skills training programs involving both small and large laboratory animal species in accordance with client’s facility SOPs, Charles River policy and applicable Federal regulations. You will float from building to building to provide training to all staff.

Responsible for the delivery of technical, husbandry and cagewash training for staff in multiple buildings (floating trainer), to include initial, ongoing and refresher.
Perform continuing education and training to maintain and enhance employee skills and capabilities, including SOP or ASP revisions, animal welfare topics, operations and maintenance, and technical advancements.
Coordinate training schedules with the hiring and training demands of the sites.
Provide didactic and hands-on technical training on SOPs. Monitor technical methods used by employees and make on the spot corrections.
Ensure completion of training documentation/summaries. Route where needed. Maintain up to date electronic and paper records.
Report on progress of employees under guidance during training periods.
Work with management to develop adjunct training team members to be qualified trainers in specific job functions and or topics.
Identify and make recommendations on improving procedures in the animal facilities, to include identifying SOPs for revision.
Perform quality assurance responsibilities for the facilities to include the continual monitoring of staff past the proficiency point to verify continual compliance to SOPs and to monitor for drift, and to monitor on trends identified through the QA/QC audits/reviews.
Assist in developing/maintaining/updating training matrices and syllabus. Formulate teaching outline and determine instructional methods such as individual training, group instruction, demonstrations, meetings, and workshops.
Provide technical support, animal husbandry, and assist with research procedures as needed.

Job Qualifications

The following are minimum requirements related to the Technical Trainer position:

Education: HS diploma. Bachelor of Science degree or Associate of Arts degree in Veterinary Technology or equivalent college level program desired.
Experience: Minimum of five (5) years related predominately to lab animal husbandry and technical experience. Minimum of five (5) years in a training role with a focus on training with various lab animal species on husbandry and technical procedures.
Certification/Licensure: Not required. AALAS Laboratory Animal Technician (LAT) certification preferred.

The hourly range for this position is $40-45 USD per hour. Please note that salaries vary within the range based on factors including, skills, certifications, and location.  

Equal Employment Opportunity

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

Associé.e Scientifique - Toxicologie (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Associé.e Scientifique – Toxicologie

En tant qu’Associé.e Scientifique pour notre équipe de Toxicologie située au site de Sherbrooke, vous serez responsable des études non-cliniques.

Dans ce poste, les principales responsabilités incluront:

Conçoit, écrit, révise et édite les plans d'étude, les amendements et les calendriers d'étude qui définissent et programment toutes les activités d'étude.
Travaille de façon autonome et efficace sur des études/programmes complexes.
Supervise et coordonne tous les aspects des procédures d'étude, qu'elles soient réalisées au sein du département ou par les départements de service.
Communique de façon efficace avec le Client et à l’interne de manière à établir un lien de confiance
Guide les équipes techniques lors du déroulement de l’étude et participe à la mise en place de nouvelles procédures.
En consultation avec le Client, s’implique dans le design de l’étude/programme et anticipe de façon proactive les limitations techniques/scientifiques.
S'assure que les projets sont réalisés conformément aux procédures opérationnelles standard et aux règles de bonnes pratiques de laboratoire et connaît les règlements, directives et lignes directrices appropriés.
Rédiger, examiner et réviser, si nécessaire, les projets de rapports ou les rapports finaux qui documentent toutes les procédures et les résultats liés à l'étude.
Communiquer rapidement, oralement ou par écrit, avec les clients sur les affaires liées à l'étude
Être le seul point de contrôle pour les décisions reliées aux études attribuées, et en ce sens, être très disponible.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Education: Minimum d'un baccalauréat (BSc) en sciences de la santé, sciences biomédicales, pharmacologie, ou d’un programme équivalent.
Expérience : minimum de 2 ans en recherche préclinique ou une expérience connexe.
Une combinaison équivalente d'études et d'expérience peut être acceptée comme substitut satisfaisant à l'éducation et à l'expérience spécifiques énumérées ci-dessus.
Habileté à travailler de manière autonome et organisée.
Capacité à travailler sous des contraintes de temps et de faire face à une variété de problèmes urgents sur une base régulière dans un environnement qui évolue rapidement.
Le bilinguisme est requis.

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: 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: Selon échelle salariale et équité interne.
Bonus annuel basé sur la performance.
Horaire: De jour du lundi au vendredi. Selon les besoins de l’entreprise et les délais à respecter, vous pourriez avoir à effectuer du temps supplémentaires.
Poste permanent dès l’embauche, temps plein à 37.5hrs minimum 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.

Scientific Associate - Toxicology (Fleurimont, Quebec, CA, J1E 0B5)

Job summary

Scientific Associate – Toxicology

As a Scientific Associate for our Toxicology team at the Sherbrooke location, you will be supporting non-clinical studies.

In this role, primary responsibilities include:

Designs, writes, reviews and edits study plans, amendments and study schedules that define all study activities.
Works autonomously and efficiently on complex studies/programs.
Supervises and coordinates all aspects of study procedures, whether performed within the department or by other departments.
Communicate effectively with Sponsors and internally to build trust
Guides the technical teams during the course of the study and participates in the implementation of new procedures.
In consultation with Sponsor, engages in study/program design and proactively anticipates technical/scientific limitations.
Ensures that projects are carried out in accordance with standard operating procedures and rules of good laboratory practice and knows the appropriate regulations, directives and guidelines.
Writes, reviews and revises, if necessary, draft reports or final reports that document all procedures and results related to the study.
Communicates promptly, orally or in writing, with sponsors on study-related matters.
Be the sole point of control for decisions related to the studies assigned, and in this sense, be very available.

Key Elements

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

Education: Minimum of a Bachelor's degree (BSc) in Health Sciences, Biomedical Sciences, Pharmacology, or equivalent program.
Experience: minimum of 2 years of experience in preclinical research or related experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to work autonomously and be very organized.
Able to work under time constraints and possess the ability to deal with a variety of pressing issues on a regular basis in a rapidly changing environment.
Bilingualism 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: 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: As per internal equity and salary scale
Annual bonus based on performance.
Schedule: Daytime between Monday to Friday. Depending on the needs and deadlines to be respected, you may have to do overtime.
Permanent position as of the hiring, full-time minimum 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.

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.

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.

QA System Specialist (m/w/d) (Erkrath, NW, DE, 40699)

Für die Abteilung Quality Assurance am Standort Erkrath suchen wir ab sofort und unbefristet eine/n

QA Specialist (m/w/d) Schwerpunkt computergestützte Systeme & GxP

Ihre Aufgaben:

Sicherstellung der Compliance computergestützter Systeme (lokal, bereichs- und funktionsübergreifend) mit globalen regulatorischen Anforderungen sowie den internen CRL-Standards
Freigabe und Überwachung der Implementierung und Instandhaltung dieser Systeme gemäß aktueller regulatorischer Vorgaben
Unterstützung bei der Validierung von Computersystemen (CSV) sowie bei Qualifizierungsprojekten für technisches Equipment
Mitwirkung bei der Einführung elektronischer Dokumentations- und Managementtools für Gerätequalifizierungen
Organisation und Durchführung risikobasierter Inspektionen von Laboren, Anlagen und Systemen; Erstellung von Auditberichten und Verfolgung von CAPAs
Analyse und Berichterstattung qualitätsrelevanter KPIs sowie Unterstützung der vierteljährlichen Management Reviews (QMR)
Kontinuierliche Optimierung bestehender Systeme und Prozesse im Hinblick auf regulatorische Anforderungen, Effizienz und Best Practices
Eskalation identifizierter Compliance-Lücken und aktive Mitwirkung bei der Entwicklung bzw. Überarbeitung von Richtlinien und SOPs
Unterstützung des QA-Teams bei regulatorischen und qualitätsbezogenen Fragestellungen
Review und Freigabe studienbezogener Dokumentation mit Fokus auf Prozessoptimierung

Ihr Profil:

Abgeschlossenes naturwissenschaftliches, technisches oder vergleichbares Studium
1–5 Jahre Berufserfahrung im Qualitätsmanagement innerhalb eines GxP-regulierten Umfelds (z. B. Pharma, Biotech, Auftragsforschung)
Erfahrung im Umgang mit computergestützten Qualitätssystemen (z. B. TrackWise, Veeva oder vergleichbar) und Kenntnisse in der Computer System Validation (CSV)
Vertraut mit regulatorischen Anforderungen (FDA, EMA, GxP) und Qualitätssystemen
Strukturierte, proaktive Arbeitsweise sowie ausgeprägte Team- und Kommunikationsfähigkeiten
Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift

Wir bieten Ihnen:

Eine verantwortungsvolle Position in einem weltweit agierenden Life-Science-Unternehmen
Kollegiales Arbeitsumfeld mit flachen Hierarchien und kurzen Entscheidungswegen
Individuelle Weiterbildungs- und Entwicklungsmöglichkeiten
Flexible Arbeitszeiten und attraktive Sozialleistungen

Haben wir Ihr Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 228245 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath
Email: RecruitBPS@crl.com

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.

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.

Gestionnaire Senior, Import/Export (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.

Associate Director - Laboratory Animal Medicine & Surgery (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As an Associate Director for our Laboratory Animal Medicine & Surgery team at the Senneville location, you will be responsible for providing professional veterinary services and overseeing the department. You will also act as a resource for all procedures involving animals and their environment, identifying deficiencies and recommending improvements, providing guidance to assure regulatory compliance and adherence to ethical standards, and coordinating responses to regulatory bodies and client audits.

In this role, primary responsibilities include:

Provide professional expertise for guidance on procedures and techniques involving live animals ensuring quality of veterinary care as well as animal care procedures, animals’ environment, housing, husbandry and social needs are met and comply with internal policies and procedures, and meet requirements as demanded by regulatory agencies;
Ensure that all animal care and use procedures performed at the site are maintained at levels necessary to perform high quality studies that are in compliance with internal policies and external standards such as AAALAC International and the Canadian Council on animal Care (CCAC);
Interact with clients;
May be responsible for the day to day management of staff within the department including timesheet review, workload management, absences, vacations, disciplinary actions, and for the salary administration of staff;
Support the adoption of efficient and innovative technologies and methodologies for animal care and use and site operations;
Provide optimal medical care as per accepted veterinary practices, and to remain current with diagnostic procedures/tests and medical treatments, as applicable to laboratory animal medicine.

Key Elements

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

Doctor of Veterinary Medicine (DVM) degree or equivalent;
Must have a valid and up-to-date OMVQ licence;
At least 5 years’ experience as a Clinical Veterinarian, with a focus on laboratory animal medicine and animal care;
At least 2 years’ experience managing direct reports;
Bilingualism English & French is mandatory;
Working experience with Good Laboratory Practices (GLP) is an asset;
Excellent organizational and communication skills;
Strong problem-solving and analytical skills;
Ability to coach personnel.

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. You will have to do a weekend rotation (on-call) once every 6 weeks;
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);
Annual OMVQ membership refunded;
Paid development training & annual conferences;
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.

Directeur.trice Associé.e - Médecine & Chirurgie des animaux de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Directeur.trice Associé.e pour notre équipe de Médecine & Chirurgie des animaux de laboratoire située au site de Senneville, vous serez responsable de fournir des services vétérinaires professionnels et de superviser le département. Vous agirez également en tant que ressource pour toutes les procédures impliquant des animaux et leur environnement, identifiant les lacunes et recommandant des améliorations, fournissant des conseils pour assurer le respect des réglementations et le respect des normes éthiques, et coordonnant les réponses aux organismes de réglementation et aux audits des clients.

Dans ce poste, les principales responsabilités incluront:

Fournir une expertise professionnelle pour guider sur les procédures et techniques impliquant des animaux vivants, en veillant à ce que la qualité des soins vétérinaires ainsi que les procédures de soins aux animaux, l'environnement des animaux, le logement, l'élevage et les besoins sociaux soient respectés et conformes aux politiques et procédures internes, et répondent aux exigences demandées par les agences de réglementation;
S'assurer que toutes les procédures de soin et d'utilisation des animaux effectuées sur le site sont maintenues à des niveaux nécessaires pour réaliser des études de haute qualité conformes aux politiques internes et aux normes externes telles que AAALAC International et le Conseil canadien de soin des animaux (CCAC);
Interagir avec les clients;
Peut être responsable de la gestion quotidienne du personnel au sein du département, y compris la révision des feuilles de temps, la gestion de la charge de travail, les absences, les vacances, les actions disciplinaires, ainsi que de l'administration des salaires du personnel;
Soutenir l'adoption de technologies et de méthodologies efficaces et innovantes pour les soins et l'utilisation des animaux ainsi que les opérations sur le site;
Fournir des soins médicaux optimaux selon les pratiques vétérinaires acceptées, et demeurer à jour avec les procédures/tests diagnostiques et les traitements médicaux, tel que applicable à la médecine des animaux de laboratoire.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Docteur en médecine vétérinaire (DVM) ou équivalent;
Doit avoir un permis de l'OMVQ valide et à jour;
Au minimum 5 ans d'expérience en tant que vétérinaire clinicien.ne, avec un accent sur la médecine des animaux de laboratoire et le soin des animaux;
Au minimum 2 ans d'expérience en gestion de subordonnés directs;
Le bilinguisme français et anglais est obligatoire;
Une expérience de travail avec les Bonnes Pratiques de Laboratoire (BPL) est un atout;
Excellentes compétences organisationnelles et en communication;
Solides compétences en résolution de problèmes et en analyse;
Capacité à encadrer le personnel.

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. Vous devrez faire une rotation de fin de semaine (sur appel) une fois toutes les 6 semaines;
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);
Remboursement de l'adhésion annuelle à l'OMVQ;
Formation au développement rémunérée et conférences annuelles;
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.

Animal Care Technician II (Cambridge, MA, US, 02139)

Job Summary

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

As the Animal Care Technician II, Observe, monitor, and document the health and physical environment within the client’s animal facility. Perform animal care and husbandry.

Additional responsibilities include:
• Review, comprehend and comply with all SOPs and quality assurance standards pertaining to laboratory animals for research.
• Monitor daily animal health and welfare while performing daily animal health observations. Perform animal husbandry duties to maintain quality and health of research animals, to include: perform daily water bottle /automatic water line 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.
• Perform daily cage wash duties and sanitation.
• Maintain accurate records of animal breeding, health, and housing/isolator or support areas as required by Institute and facility.
• Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility veterinarian.
• Dispose of animal carcasses following established procedures.
• Receive, inspect and put away incoming animals; ensure and provide for sentinel animals in each rodent housing area.
• May be involved in strictly maintaining and following breeding and weaning procedures to ensure appropriate production levels.
• Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adheres to safety procedures.
• Maintain required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician II position:

• High school diploma or GED and 2 years related research husbandry experience, or Associates degree in Life Sciences or related field and 1.5 years related research husbandry experience, or Bachelor's degree in Life Sciences or related field and 1 year related research husbandry experience.
• AALAS certified as ALAT within 18 months of hire

The pay range for this position is $22-24 USD an hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

Equal Employment Opportunity

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

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

Für die Abteilung Bioassays am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie-Biotechnologie

als Technical Officer (m/w/d)

Zu Deinen Aufgaben gehören:

die Entwicklung und Durchführung zellbasierter Bioassays unter einem GMP-System
Laborarbeiten mit Zellkulturen und Viren bis hin zur Risikogruppe S2
die Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GMP-Systems u.a. Pflege und Wartung von Labor-Geräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen.
die permanenten Verbesserung unserer Prozesse und Techniken

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-Technischer Assistent / Biologielaborant (m/w/d), ein B.Sc. im Bereich Biologie / Biotechnologie oder eine vergleichbare Qualifikation
vorzugsweise Berufserfahrung in einem Arbeitsumfeld, das dem unseres Unternehmens ähnelt (Biotechnologie, Pharmazie, etc.)
nach Möglichkeit praktische Fähigkeiten in den gängigen zellkulturtechnischen Verfahren und in der Durchführung zellbasierter Bioassays
sehr strukturiertes, zielorientiertes und sorgfältiges Arbeiten unter Einhaltung enger Zeitlinien
Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Kundenorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel, Powerpoint) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus

Wir bieten Dir:

eine unbefristete Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten internationalen Unternehmen
flexible Arbeitszeiten
eine aktive Mitgestaltung des Tätigkeitsfeldes in einem motivierten Team
eine angemessene Vergütung
eine intensive Einarbeitung mit Onboarding Programm
kostenfreie Parkplätze / Fahrkostenzuschuss
Fortbildungsmöglichkeiten
Engagement Programm

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 227478 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen.
Wir freuen uns auf Deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Vorangehen - Wir gehen voran, wenn wir unsere Absichten und Werte entwickeln und unsere Kompetenz teilen, wenn wir für die Zukunft planen und Wandlungsfähigkeit und Flexibilität zeigen, wenn wir Innovation ermöglichen und die großartige Arbeit anderer schätzen.

Sorgfalt - Wir beweisen Sorgfalt, wenn wir einander, unsere Tiere und das gesellschaftliche Umfeld, in dem wir arbeiten und leben, respektieren, wenn wir einen positiven, gesunden Arbeitsplatz schaffen, wenn wir unsere Compliance-Standards einhalten, und wenn wir stets das Richtige tun.

Zusammenarbeit - Wir arbeiten zusammen, wenn wir klar und effizient in unserem direkten Umfeld ebenso wie weltweit kommunizieren, andere einbeziehen und unterschiedliche Ideen schätzen, wenn wir unseren Kunden zum Erfolg verhelfen und das Teamwork fördern und wenn wir allumfassend und ganzheitlich denken und handeln.

Verantwortung - Wir handeln wie Eigentümer, wenn wir Verantwortung für unsere Handlungen übernehmen, wenn wir auf interne und externe Kunden mit Geschwindigkeit und Genauigkeit reagieren, wenn wir sinnvolle Ziele setzen und erreichen und wenn wir nach kontinuierlicher Verbesserung streben.

Biologics Testing Solutions

Mit über 50 Jahren Erfahrung und bewährter regulatorischer Kompetenz kann die Charles River Biologics-Gruppe sich den Herausforderungen von Biotech- und Pharma-Unternehmen weltweit stellen. Wir unterstützen mit Dienstleistungen wie Kontaminations- und Verunreinigungstests, Proteincharakterisierung, Bioassays, virale Clearance-Studien sowie Stabilitäts- und Chargenfreigabeprogrammen Kunden während des gesamten biologischen Entwicklungszyklus, von der Einrichtung und Charakterisierung von Zellbanken bis hin zu präklinischen und klinischen Studien und der Markteinführung von Produkten. Ganz gleich, ob Kunden eigenständige Dienstleistungen, ein maßgeschneidertes Testpaket oder In-house-Support benötigen, unsere Biologics-Gruppe kann für jeden Bedarf eine maßgeschneiderte Lösung entwickeln. Jedes Jahr werden mehr als 20.000 biologische Testberichte und über 200 lizenzierte Produkte von unserem Biologics-Team ausgesendet.

Über Charles River

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.

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.

CSV Specialist I (Memphis, TN, US, 38118)

Job Summary

BASIC SUMMARY:
Responsible for computerized system validation activities within CRL Manufacturing Operations, including, but not limited to, equipment and software. Responsible for maintaining all documentation pertaining to validation activities. Serve as an information resource for validation team members, contractors, and vendors.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage the full lifecycle of validation projects, ensuring timely delivery, meeting specifications, and maintaining quality throughout.
• Prepare clear and concise validation deliverables for computerized systems, including Validation Plans, Requirement Specifications, Configuration Specifications, Risk Assessments, Test Scripts, Traceability Matrices, and Summary Reports.
• Assist system SMEs in the preparation of test scripts comprising formal testing of functional, system and regulatory requirements in conjunction with computerized system validation. Oversee test script execution.
• Manage validation project, ensuring timely completion and effective communication of project timelines and milestones.
• Adhere to pertinent regulatory requirements and departmental policies and procedures [SOPs, safety procedures and biosafety protocols].
• Write or assist in the writing of SOPs as they pertain to computer system validation and data integrity.
• Collaborate with cross functional teams involved in the validation and maintenance of computerized system (e.g. System Owner, IT, QA, Departmental Managers, vendors, etc).
• Provide guidance and support on Computer System Validation (CSV) practices, helping others develop skills and knowledge in regulatory compliance, validation processes, and industry best practices.
• Identify, schedule and track validation project tasks and timelines using appropriate tools.
• Effectively communicate project expectations to team members and stakeholders in a timely and clear manner.
• Schedule validation project team meetings to ensure project milestone schedules are maintained and deliverables satisfy requirements.
• Contribute to the development of corrective actions, as needed, for deficiencies that may be uncovered/observed during validation efforts to ensure compliance with applicable regulatory requirements, guidelines, procedures, and policies.
• Proactively identify opportunities for process enhancements and implement innovative solutions to drive efficiency, quality, and effectiveness, fostering a culture of continuous improvement.
• Serve as the primary point of contact for client and regulatory audits related to computer system validation, resolving or mitigating audit findings related to system validation.
• Assist, as needed, during client and regulatory audits and help to resolve or mitigate audit findings related to system qualification/validation.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s degree (B.A./B.S.) or equivalent in Computer Science, Information Technology, Engineering, Life Sciences, or related field.
• Experience: 2-5 years of experience in computer system validation within a regulated industry (pharmaceutical, medical device, biotechnology).
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: Certifications like Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or specialized CSV training can be advantageous.
• Other: Comprehensive knowledge of regulatory requirements, including GxPs, 21 CFR Part 11, and Annex 11 as they pertain to computerized systems, is preferred.
• Excellent organizational and analytical skills and demonstrated ability to shift priorities to meet a constantly changing environment.
• Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.
• Working knowledge and experience in Microsoft Office products (Outlook, Word, Excel, Power Point, Teams, SharePoint).
• Understanding of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Data Integrity, ALCOA++.

The pay range for this position is $ 75K-85K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Equal Employment Opportunity

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

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

Job Summary

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

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

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

Job Qualifications

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

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

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

Comments:
⦁ This position requires occasional domestic travel.

Compensation Data

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

Competencies

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

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.

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.