Addetto alla cura degli animali da laboratorio (TRIESTE) - Contratto a chiamata (Trieste, IT, 34127)

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.

Riepilogo del lavoro

Per nostro cliente sito in Milano ricerchiamo uno stabularista con contratto a chiamata.

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

Buona capacità comunicativa e di lavoro in team
Disponibilità a con contratto a chiamata

Disponibilità a lavoro nel week-end e festività

Buona conoscenza del pacchetto office

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 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.

Alternance : Chargé de mission HSE - F/H (Saint-Nazaire, FR, 44600)

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 ?

Vous êtes étudiant dans une formation QHSE ? Vous recherchez un contrat d'apprentissage avec des missions opérationnelles et polyvalentes ?

Nous recherchons pour la rentrée 2026, notre futur(e) alternant(e), Chargé(e) de mission HSE.

Missions et responsabilités :

- Participer à l'animation et au déploiement des politiques Hygiène, Sécurité et Environnement (HSE) ; communiquer, sensibiliser, former et faire appliquer.
- Contribuer à la mise en oeuvre des projets HSE, notamment ceux en lien avec la prévention des risques et des accidents.
- Participer à l'analyse des accidents et presqu'accidents (enquêtes, suivi des plans d'actions).
- Apporter un appui dans les volontés d'améliorations et d'évolutions en matière d'hygiène, de sécurité, d’environnement et de conditions de travail (études de postes, EPI, protections collectives, évolutions de process, etc.).
- Participer à la rédaction et la mise à jour de la documentation HSE en lien avec la réglementation et les pratiques de l’entreprise.
- Contribuer à l'identification des risques dans les différents secteurs de l'entreprise et la mise à jour des documents associés.
- Participer à la mise en place et au suivi des indicateurs HSE (reporting accidents/incidents).
- Participer aux inspections HSE dans les zones de travail.
- Suivre la conformité du matériel de sécurité et des EPI.

Votre profil :

- Etudiant(e) en recherche d'un apprentissage pour sa formation de niveau Bac+4/5
- Faire preuve de dynamisme, d'organisation et de rigueur
- Bonne maitrise de l'anglais (écrit et oral)

Modalités :

Convention collective de l'industire pharmaceutique
Contrat : apprentissage

À propos de l'évaluation de 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.

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.

Responsable d'Etudes Développement Chromatographie - CDI - F/H (Saint-Nazaire, FR, 44600)

Résumé du travail

Le poste

Notre Laboratoire Chromatographie recrute un Responsable d’Etudes Développement LC-MS/MS - H/F en CDI, basé sur le site de Saint-Nazaire (44). Le site est spécialisé dans la mise en place de méthodes de Bioanalyse pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération
(LC-MS/MS). Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Les missions

Vous ferez partie d’une équipe dans laquelle votre rôle sera de conduire des études de développements de méthode de bioanalyse sur de nouveaux médicaments.

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

Qualifications recherchées

De formation Bac + 5 minimum, vous disposez d'une expérience supérieure à 2 ans en technique de bioanalyse (préparation d’échantillons biologiques, LC-MS/MS).
Un minimum d’un an d’expérience en réalisation d’étude de bioanalyse est souhaité (LC-MS/MS).
Autonome, rigoureux(se), fiable, organisé(e), vous possédez un bon sens du relationnel.
Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l'Industrie Pharmaceutique : groupe 6
Contrat : CDI cadre (forfait jours, RTT)
Salaire : Environ 38 000€ brut/an, sur 12 mois, selon expérience
Mutuelle et Tickets Restaurant

À propos de l'évaluation de sécurité

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

Veterinary Technician 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.

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

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:

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:
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/hoof/teeth clipping/trimming.
Proficient animal restraint techniques.
Monitor critical care animals (e.g., place IVs, monitor fluids, etc.).
Daily walk through of animal rooms
Participate in colony management (biosurveillance, routine health monitoring, nail trims, etc.)
Animal observations, reporting abnormalities
Monitor animal health, visually, and by following detailed schedules.
Assist in maintaining accurate record keeping procedures for the veterinary department.
Assist in keeping inventory and stocking the vet rooms (e.g., drugs and supplies). Assist in organizing and maintaining the vet exam rooms.
May be responsible for tissue sampling, radiography, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
Assist in surgery and peri-surgery care, (e.g., prepare animals for surgery, prepare surgical packs, administer supportive therapy as directed).
Assistance in acclimation and behavior management of animals in our care.
Provide environmental enrichment for laboratory animals according to facility and Federal guidelines.
Participate in animal receipt as necessary.
Triage and recheck all animal species on site.
Participate in weekend assistant rotation.
Perform all other related duties as assigned.

Job Qualifications

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

Education: High school diploma or General Education Degree (G.E.D.) preferred. Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
Experience: 0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred
Certification/Licensure: Licensed as a veterinary technician (RVT, LVT, CVT) is required, and you must be able to obtain an OH license. AALAS (ALAT) certification desired.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Demonstrate understanding of Standard Operating Procedures. Excellent organizational, time management and recordkeeping skills. Basic word processing skills required. Excellent communication skills both written and verbal. Must be proficient in routine veterinary technical and husbandry techniques. Must work well with team members as well as function independently. Must be flexible with daily routine to meet demands of veterinary medical department.

Compensation Data

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

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

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 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 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.

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.

Trainer I (Ashland, OH, US, 44805)

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 Overview

BASIC SUMMARY:

A Trainer I - Necropsy has substantial knowledge in basic tasks and is able to perform the intermediate tasks and procedures of the department training plan. The trainer is performing tasks independently which may include delivering, documenting, and reporting technical skill training and programs involving their training focus for basic skills. Tasks may include documenting and reporting technical skill training and programs involving their training focus for both basic and some advanced skills. Conduct classroom and on-job training sessions. The trainer assists with more advanced tasks that may include working with additional species, and/or specialized procedures to support the study and training needs.

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.

Job Description

QUALIFICATIONS:

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

Experience: 1-2 years of relevant experience.

Certification/Licensure: None

Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data.

Ability to communicate verbally and in writing at all levels inside and outside the organization.

Excellent written and verbal communication skills. Knowledge of English.

Ability to manage multiple tasks and priorities to achieve goals.

Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.

Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notifications.

Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.

Ability to exercise independent decision-making and self-manage under the direction of a supervisor.

Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.

Ability to work under specific time constraints.

PHYSICAL REQUIREMENTS:

Employee 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, wearing safety equipment (PPE) according to OSHA regulations and company standards.

Must be able to frequently hold species firmly while utilizing fine motor skills.

Specific vision abilities required by the job include close vision, color vision, depth perception and the ability to adjust focus.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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.

Study Coordinator I (Ashland, OH, US, 44805)

Job Overview

BASIC SUMMARY:

Responsible for monitoring study progress (as applicable) and generation of end-of-study reports for assigned studies with a high level of supervision/instruction. Ensure that reports adhere to study protocols, standard templates and styles, Sponsor templates and styles, and applicable regulations. Provide protocol and report support to SD/PI and assist with providing information/data requested by Sponsors

The Salary range for this position is $49,000 - $57,000 annually. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Function as lead writer for standard study reports.
Attend study meetings as applicable to assure a full understanding of assigned projects and results, including objectives, timelines, and reporting requirements.
Participate in client interactions (if applicable).
Ensure that all protocol and amendment requirements are met.
Ensure reports meet regulatory and client requirements.
Generate, format, and/or review report components/text using pre-defined templates.
Generate, format, and/or review data tables from multiple data collection systems.
Generation of Common Technical Documents (CTD) and any other regulatory agency summary table requirement (as needed).
Ability to compile and/or interpret scientific data, meeting with Study Director/PI as needed.
Provide editorial/formatting review of final study protocols, amendments, and report text (as applicable). Provide comments and/or suggested changes to Study Director/PI.
Proficient in generating reports in one major area.
Other duties as assigned by departmental management.

QUALIFICATIONS:

Education: High School diploma or General Education Degree (G.E.D.), preferred. Associate’s degree (A.A./A.S.) or equivalent from a two-year college, recommended. Bachelor’s degree (BA/BS) or equivalent in science or related discipline, strongly recommended.
Experience: 1-2 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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.
Other: This position requires analytical thinking skills and a good understanding of scientific processes. Strong interpersonal/organizational skills and attention to detail are required, as well as strong written, verbal, and analytical skills. Must be proficient with spreadsheet, word processing, and publishing software. Familiarity with preclinical study protocols/reports, knowledge of GLP regulations/FDA electronic reporting compliance, and scientific/medical writing and terminology preferred. Ability to adjust priorities to adhere to stringent deadlines. Ability to work with all levels of staff. Ability to interact effectively with diverse personalities and ethnic backgrounds is essential.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear, and type at a computer.
Able to lift up to 50 Ibs.
Specific vision abilities required by this job include close vision and the ability to adjust focus.
Must be able to regularly sit approximately 6 to 8 hours a day.
Must be able to frequently type an average of 6 hours a day.
Must perform data entry to and make edits on information contained on a personal computer.
Must be able to regularly communicate with personnel inside/outside the company as appropriate.

WORK ENVIRONMENT:

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

COMMENTS:

This position may require overtime, weekend, and/or after hours shift coverage, as needed.

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Technician I - Inhalation (Ashland, OH, US, 44805)

Job Overview

BASIC SUMMARY:

A Technician I - Inhalation is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study, which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. The technician may occasionally perform basic skills independently but continues working under supervision to gain proficiency on skills still in development.

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

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human- animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Ensure high levels of study quality to meet study goals.
Follow all PPE, safety, cleaning, and cross-contamination elimination practices.
Maintain appropriate communication with other personnel.
Support team-mates, technicians, and members of other departments.
Follow direction from team leaders, trainers, research associates and supervisors.
Use and maintain instrumentation and equipment according to SOPs.
Perform all tasks per SOP, BOP, and/or protocols.
Perform all other related duties as assigned.

Job Description

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.
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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.
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 work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Ability to ensure the studies and fulfill the by performing the totheGood (GLP), integrity regulatory agencies requirements activities according Laboratory Practices Standard Operating(SOP),(BOP) and the Institutional Animal Care and Use rules.

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.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

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

Job Summary

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

A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study, which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. The technician may occasionally perform basic skills independently but continues working under supervision to gain proficiency on skills still in development.

Essential Duties and Responsibilities: (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 handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Ensure high levels of study quality to meet study goals.
Follow all PPE, safety, cleaning, and cross-contamination elimination practices.
Maintain appropriate communication with other personnel.
Support team-mates, technicians, and members of other departments.
Follow direction from team leaders, trainers, research associates and supervisors.
Use and maintain instrumentation and equipment according to SOPs.
Perform all tasks per SOP, BOP, and/or protocols.
Perform all other related duties as assigned

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.
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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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 Enviornment:

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.

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.

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.

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

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

Job Summary

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

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

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

The pay range for this position is $21.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

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

Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Must be authorized to work in United States without a sponsor visa now or in the future.
Other: Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experiences preferred.

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

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

Equal Employment Opportunity

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

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

Job Summary

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

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. 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.
Must be authorized to work in United States without a sponsor visa now or in the future.

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.

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

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

Equal Employment Opportunity

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

Animal Care Technician (Raleigh, NC, US, 27610)

Job Overview

As an Animal Care Technician 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. On the job training will be provided.

Essential Duties & 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 Requirements

Animal Care Technician I

No experience required

Animal Care Technician II

Candidates must possess one of the following:

1 year of related experience and/or training in animal husbandry
Associate's Degree or higher level education

The pay range for this position is $17.75 to $19.00 USD per hour.  Please note the range covers levels I - II, salary will depend on level, in addition to factors such as experience, skills, and certification.

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.

Equal Employment Opportunity

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

Production Supervisor (Small Animal) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Production Supervisor to support our Breed Operation in Raleigh, NC. As the Production Supervisor, you will provide daily supervision of personnel and operations to ensure achievement of departmental goals and levels. You will independently handle routine personnel-related issues; assist in the handling of complex personnel-related issues.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, SOPs, safety procedures and biosafety protocols. Schedule and prioritize workload of group members.
Assist in the coordination and scheduling of activities of the department through hands-on technical support, delegation of responsibility and/or authority to departmental subordinates.
Oversee production and shipping activities of assigned group, including SOPs and OORs. Ensure proper record-keeping and report preparation.
Review safety issues and Workers’ Compensation claims.
Actively interact with and provide technical assistance to customers as required to resolve customer requests, inquiries, and complaints.
Review customer complaints and participate in the development and implementation of any resulting procedural changes. Create and maintain complaint chart.
Audit production rooms and/or isolators.
Review and ensure appropriate inventory levels of departmental supplies.
Interview and select qualified non-exempt personnel. Recom¬mend personnel actions, including hiring, promotions and raises. Partner with Human Resources and departmental management to assist in the handling of disciplinary issues. Draft appropriate personnel action paperwork.
Identify training and development needs of direct reports. Assist in the development, implementa¬tion and delivery of depart¬mental training programs; ensure that direct reports receive departmental orien¬tation and necessary on-the-job training. Oversee main¬tenance of group training manual and training records.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
Schedule overtime as authorized. Review and approve timecards. Coordinate vacation/time off schedules.
Recommend short-range operating objectives, organizational structure of direct reports and staffing requirements. Assist in the development of a departmental plan for backup and succession of key technical personnel.
May assist in development of departmental budget.
Ensure optimum performance of group function. Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Assist in the development, maintenance and communication of departmental systems and SOPs. Assist in the development and communication of job descriptions for subordinate positions.
Ensure that departmental equipment is maintained in good working condition and that departmental area(s) are maintained in a clean and orderly condition. Ensure proper recycling and setup of cages in assigned area(s).
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s degree in life sciences or related discipline and 4 years of supervisory experience of a high-performing team to deliver complex initiatives and/or support operations, and assistance in cross-functional collaboration to drive successful business outcomes.
Associates degree in life sciences or related discipline and 6 years of supervisory experience
High school diploma or GED and 8 years of supervisory experience

ADDITIONAL QUALIFICATIONS:

Effective communication and interpersonal skills required.
Demonstrated computer skills (data input, word processing) required.

PREFERRED QUALIFICATIONS:

ALAT certification

SALARY

The pay range for this position is $70,000 - $80,000 / annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

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

Animal Packer (Raleigh, NC, US, 27610)

JOB SUMMARY

As an Animal Packer in Raleigh, NC, you will be responsible for packing and shipping containers and maintaining all documentation relating to shipment.

* This is a temporary opportunity with the potential to be hired as a full-time, employee. On the job training will be provided.

In this role, key responsibilities may include:

Packing and shipping containers according to appropriate packing/shipping documentation.
Completing paperwork related to packing and shipping.
Unloading delivery trucks and placing supplies in appropriate areas.
Operating forklift to transport supplies within the warehouse area.
Performing physical environment housekeeping and sanitizing of all support work areas.
Checking live traps each weekday morning and reporting all findings.
May provide other support services, including materials delivery and housekeeping, as assigned.

MINIMUM QUALIFICATIONS :

No experience required

PREFERRED QUALIFICATIONS:

One year related animal experience
One year of warehouse or stockroom experience
Forklift experience

Role Specific Information:
Location: Raleigh, NC
Schedule: Schedule may vary between the hours of 5:00 AM and 3:00 PM

The pay for this position is $17.75 / hour.

Equal Employment Opportunity

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

Addetto alla cura degli animali da laboratorio - ROVERETO (part-time) (Rovereto, IT, 36068)

Riepilogo del lavoro

Per nostro cliente sito in Rovereto ricerchiamo un Animal Caretaker con contratto a chiamata

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;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

Charles River Insourcing Solutions℠ è in grado di snellire la ricerca con efficienza operativa ed economica, grazie all’insourcing strategico di servizi di ricerca GMP, GLP e non-GLP che vanno dalla scoperta alla valutazione della sicurezza. Insourcing Solutions℠ offre al cliente la possibilità di mantenere il controllo della propria struttura e competenze, avvantaggiandosi nel contempo dello spazio a disposizione.

Di cosa si occupa la Charles River

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.

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.

QC Associate (Charleston, SC, US, 29407)

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 Overview

We are seeking a QC Associate for our Microbial Solutions site in Charleston, SC.

This role will, ensure the quality and integrity of product by testing incoming materials, excipients and final product. Perform environmental monitoring of LAL (Limulus Amebocyte Lysate) and Crude Lysate production areas to ensure appropriate conditions are maintained. Perform Crude Lysate recovery procedures during the Bleeding Season.

The QC Associate will be responsible for the following:

Ensuring the quality and integrity of product by testing PTS cartridges, Limulus Amebocyte Lysate (LAL), incoming materials, and excipients.
Perform Crude Lysate recovery procedures during the Horseshoe Crab Bleeding Season (Summer Months).
Long-Term Stability monitoring of samples.
Using technical writing to perform investigations and complete exception records.
Attention to detail in all aspects of work is essential.

Qualifications

The following are the Minimum Requirements for the QC Associate position:

Bachelor's degree (B.A./B.S.). An equivalent combination of education and experience may be accepted as a satisfactory substitue for the specific education and experience listed above. Computer literacy must include word processing, spreadsheet and Technical Writing.

The following are Preferred Qualifications related to the QC Associate position, but are not required to be considered for this position:

One year of experience with GMP products.
Prior experience with laboratory operations and auditing.

The pay for this position is $22/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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 worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

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

Lab Technician I (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie

als

Lab Technician (m/w/d)

Zu Deinen Aufgaben gehören:

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

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein erfolgreich abgeschlossenes Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
strukturiertes, zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien, Verantwortungsbewusstsein, Verlässlichkeit, hohes Sicherheitsempfinden und Teamfähigkeit
hohe Lernbereitschaft zur Weiterbildung
hohe Leistungsbereitschaft
fähig Entscheidungen zu treffen
fähig zur kritischen Selbstreflexion
ausgeprägtes Informations- und Kommunikationsverhalten (intern und extern)
fähig Konflikte zu lösen
Gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus

Wir bieten Dir:

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

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233452 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. 15 A-B
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Job Description

Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Executes scientific testing strategies and studies. May participate in development as part of team. May lead assay research, assay validation or study conduct, or is involved in preparation of material (e.g. protein, nucleic acid, cells, etc.). Reviews and interprets study data, communicates results to clients and writes final reports. Ensures compliance with protocols and all applicable SOPs. Troubleshoots and resolves assay or technical issues in the laboratory when scientific expertise is needed. Contributes to specific dataset interpretation, or when appropriate answering questions from regulatory authorities. For singular focus of Chemistry or Biology disciplines, refer to specified role on job architecture.

Education

No degree required

Physical Requirements

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein 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.

Equal Employment Opportunity

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

BTA / Biologielaborant (m/w/d) - Genotypisierung / PCR (Erkrath, NW, DE, 40699)

Wir bei Charles River setzen uns mit Leidenschaft dafür ein, die Lebensqualität der Menschen zu verbessern. Unser Auftrag, unsere wissenschaftliche Führungsrolle und unser starkes Zielbewusstsein leiten uns bei allem, was wir tun, und wir gehen jeden Tag mit dem Wissen an, dass unsere Arbeit dazu beiträgt, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt zu verbessern.

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie

als

Lab Technician (m/w/d)

Zu Deinen Aufgaben gehören:

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

Das bringst Du mit:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein erfolgreich abgeschlossenes Studium zum Bachelor of Science im Bereich Biologie / Biotechnologie / Biochemie etc.
strukturiertes, zielorientiertes Arbeiten unter Einhaltung enger Zeitlinien, Verantwortungsbewusstsein, Verlässlichkeit, hohes Sicherheitsempfinden und Teamfähigkeit
hohe Lernbereitschaft zur Weiterbildung
hohe Leistungsbereitschaft
fähig Entscheidungen zu treffen
fähig zur kritischen Selbstreflexion
ausgeprägtes Informations- und Kommunikationsverhalten (intern und extern)
fähig Konflikte zu lösen
Gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie gute deutsche und englische Sprach- und Schriftkenntnisse setzen wir voraus

Wir bieten Dir:

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

Wir alle bei Charles River Laboratories teilen eine große Leidenschaft, wenn wir unsere gemeinsame Mission verfolgen: Wir wollen ein gesünderes Leben schaffen. Die Möglichkeit, im Leben von Menschen auf der ganzen Welt etwas zu bewirken, ist das, was uns jeden Tag aus dem Bett treibt. Stell dir vor, du könntest deine Talente einsetzen, um neue Entdeckungen und klinische Durchbrüche voranzutreiben, die die Gesundheit der Menschen weltweit verbessern. Deshalb ist eine Karriere bei uns so viel mehr als nur ein Job. Es ist eine zielgerichtete Reise.

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 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.

Weitere Informationen finden Sie unter www.criver.com.

Wissenschaftler (m/w/d) - Molekulargenetik / Genotypisierung (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort für ein Jahr befristet

eine/n

Wissenschaftler (m/w/d)

Unterstütze uns bei:

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

Überzeuge uns durch:

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

Wir bieten Dir:

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

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233450 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. 15 A-B
40699 Erkrath

Über Research Models & Services

Über Biologics Testing Solutions

Weitere Informationen finden Sie unter www.criver.com.

Scientist I (Erkrath, NW, DE, 40699)

Für die Abteilung Genetic Testing Services am Standort Erkrath suchen wir ab sofort für ein Jahr befristet

eine/n

Wissenschaftler (m/w/d)

Unterstütze uns bei:

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

Überzeuge uns durch:

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

Wir bieten Dir:

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

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

Job Description

Education

Four-year degree required

Physical Requirements

Equal Employment Opportunity

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

Sen.Lab Technician I (Erkrath, NW, DE, 40699)

Du arbeitest gern präzise, verantwortungsvoll und mit modernen bioanalytischen Methoden? Du bringst Erfahrung in Zellkultur, Bioassays oder regulierten Laborprozessen mit und möchtest in einem GMP-Umfeld den nächsten Schritt machen? Dann werde Teil unseres Teams im Bereich Bioassays an unserem Standort in Erkrath - für die Dauer von 2 Jahren.

In dieser Position übernimmst Du eine wichtige Rolle in der Durchführung und Sicherstellung von zellbasierten Bioassays im GMP-Umfeld.

Zu Deinen Aufgaben zählen:

Durchführung von zellbasierten Bioassays im Rahmen von Routineprüfungen unter GMP-Bedingungen
Unterstützung von Scientists bei der Planung, Vorbereitung und dem Abschließen von Prüfungen
Mitwirkung bei der Bearbeitung interner GMP-Dokumente (z.B. SOPs und Abweichungen)
Eigenständige Prüfung der Labordokumentation
Auswertung, Zusammenfassung und Dokumentation von Analyseergebnissen
Fachliche Unterstützung des technischen Personals bei der Durchführung von GMP-Prüfungen
die Pflege und Aufrechterhaltung des GMP-Systems im Laboralltag
Verantwortung für Geräte und Infrastruktur im LAborbereich
Mitarbeit bei Gerätequalifikationen, Validierungen und weiteren qualitätssichernden Maßnahmen
Laborarbeiten mit Zellkulturen und Viren der Risikogruppe S1 und S2

Das bringst Du mit:

abgeschlossene Ausbildung als BTA / Biologielaborant (m/w/d) o.ä. oder
ein naturwissenschaftliches Studium (B.Sc. oder M.Sc) in Biologie, Biochemie ö.ä.
praktische Laborerfahrung in mindestens einem der folgenden Bereiche: Zellbiologie / Zellkultur, Bioassays, Immunologie, regulierte Laborprozesse
sorgfältige, strukturierte und zuverlässige Arbeitsweise
sehr gute Deutsch- und gute Englischkenntnisse
Erfahrung im GMP-regulierten Umfeld

Auch wenn du nicht alle Punkte erfüllst: Bewirb dich gerne, wenn du praktische Laborerfahrung in Zellkultur, Bioassays oder qualitätsgesicherten Prozessen mitbringst.

Das erwartet Dich

Befristete Festanstellung für 2 Jahre
Strukturierte Einarbeitung in ein spannendes Laborumfeld
Verantwortungsvolle Aufgaben im Bereich Bioassays & Zellkultur
Kollegiales Team mit enger Zusammenarbeit zwischen Labor und Wissenschaft
Möglichkeit zur fachlichen Weiterentwicklung im Bereich Bioassays, GMP und Qualitätsprozesse

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb dich bitte unter der Job-ID 233332 über unser Karriereportal https://jobs.criver.com/ mit deinem Lebenslauf und Motivationsschreiben.

Wir freuen uns auf deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

Job Description

Education

No degree required

Physical Requirements

Equal Employment Opportunity

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

Senior Laborant (m/w/d) - Zellkultur / GMP (Erkrath, NW, DE, 40699)

In dieser Position übernimmst Du eine wichtige Rolle in der Durchführung und Sicherstellung von zellbasierten Bioassays im GMP-Umfeld.

Zu Deinen Aufgaben zählen:

Durchführung von zellbasierten Bioassays im Rahmen von Routineprüfungen unter GMP-Bedingungen
Unterstützung von Scientists bei der Planung, Vorbereitung und dem Abschließen von Prüfungen
Mitwirkung bei der Bearbeitung interner GMP-Dokumente (z.B. SOPs und Abweichungen)
Eigenständige Prüfung der Labordokumentation
Auswertung, Zusammenfassung und Dokumentation von Analyseergebnissen
Fachliche Unterstützung des technischen Personals bei der Durchführung von GMP-Prüfungen
die Pflege und Aufrechterhaltung des GMP-Systems im Laboralltag
Verantwortung für Geräte und Infrastruktur im LAborbereich
Mitarbeit bei Gerätequalifikationen, Validierungen und weiteren qualitätssichernden Maßnahmen
Laborarbeiten mit Zellkulturen und Viren der Risikogruppe S1 und S2

Das bringst Du mit:

abgeschlossene Ausbildung als BTA / Biologielaborant (m/w/d) o.ä. oder
ein naturwissenschaftliches Studium (B.Sc. oder M.Sc) in Biologie, Biochemie ö.ä.
praktische Laborerfahrung in mindestens einem der folgenden Bereiche: Zellbiologie / Zellkultur, Bioassays, Immunologie, regulierte Laborprozesse
sorgfältige, strukturierte und zuverlässige Arbeitsweise
sehr gute Deutsch- und gute Englischkenntnisse
Erfahrung im GMP-regulierten Umfeld

Auch wenn du nicht alle Punkte erfüllst: Bewirb dich gerne, wenn du praktische Laborerfahrung in Zellkultur, Bioassays oder qualitätsgesicherten Prozessen mitbringst.

Das erwartet Dich

Befristete Festanstellung für 2 Jahre
Strukturierte Einarbeitung in ein spannendes Laborumfeld
Verantwortungsvolle Aufgaben im Bereich Bioassays & Zellkultur
Kollegiales Team mit enger Zusammenarbeit zwischen Labor und Wissenschaft
Möglichkeit zur fachlichen Weiterentwicklung im Bereich Bioassays, GMP und Qualitätsprozesse

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb dich bitte unter der Job-ID 233332 über unser Karriereportal https://jobs.criver.com/ mit deinem Lebenslauf und Motivationsschreiben.

Wir freuen uns auf deine Bewerbung!

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

Weitere Informationen finden Sie unter www.criver.com.

Shipping & Receiving Associate (Erkrath, NW, DE, 40699)

Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet

eine / einen

Mitarbeiter Logistik (m/w/d) - Wareneingang und Versand

Du behältst den Überblick, wenn Proben und Warensendungen bei Charles River in Erkrath eintreffen: Du nimmst sie an, prüfst sie und sorgst dafür, dass alles zur richtigen Zeit am richtigen Ort ist. So unterstützt du aktiv die Entwicklung und Prüfung neuer Medikamente in unseren Laboren.

Vorkenntnisse in der Logistik sind von Vorteil, aber kein Muss – wir freuen uns ausdrücklich auch über motivierte Quereinsteiger*innen.

Deine Aufgaben:

Annahme eingehender Kundenproben für unsere GMP-Analytik, inklusive der Registrierung in unseren Laborinformations-Management System (LIMS)
Bereitstellung von Proben für die analytischen Labore
Ordnungsgemäßen Lagerung und Entsorgung von Proben im zentralen Prüfsubstanzlager
Organisation und Verwaltung des zentralen Warenlagers (Bestellung, Annahme, Erfassung, Ausgabe)
Sicherstellung und Überwachung des Warenbestandes
Versand von Prüfsubstanzen, Waren und Dokumenten einschließlich der Sendungsanmeldung
der Vorbereitung und Abwicklung von Sendungen
der Zusammenarbeit mit den operativen Einheiten und dem Projektmanagement als zentrale Anlaufstelle für Prüfsubstanz-Management, Versand & Logistik

Du bist die richtige Person für uns, wenn:

Du Erfahrung im Wareneingang,Versand oder der Logistik
Du an einem biotechnologischen oder pharmazeutischen Arbeitsumfeld interessiert bist
Du zielorientiert und strukturiert arbeitest
Du ein ausgeprägtes Verantwortungsbewusstsein hast
Du dich gut organisieren kannst und kannst gleichzeitig flexibel Situationen reagieren
Du sehr gute Deutsch- und grundlegende Englischkenntnisse hast

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233438 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-b
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Job Description

Manages customer inventories through analysis and operations of the replenishment system. Ensures availability of product through the monitoring and oversight of inventory systems. Plans, implements and controls the efficient, effective flow and storage of goods, services and related information, for the purpose of compliance with customer expectations. Maximizes the efficiencies of shipments. Resolves unacceptable situations with customers, as well as problems between shipping locations, carriers, receiving departments, inventory analysts, and buyers to insure planned arrival of product. Acts as liaison between customer, sales, customer service and carriers. Advises on trends and/or shifts in demand that could impact company's service levels.

Education

No degree required

Physical Requirements

Equal Employment Opportunity

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

Mitarbeiter Logistik (m/w/d) - Wareneingang & Versand (Erkrath, NW, DE, 40699)

Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet

eine / einen

Mitarbeiter Logistik (m/w/d) - Wareneingang und Versand

Deine Aufgaben:

Annahme eingehender Kundenproben für unsere GMP-Analytik, inklusive der Registrierung in unseren Laborinformations-Management System (LIMS)
Bereitstellung von Proben für die analytischen Labore
Ordnungsgemäßen Lagerung und Entsorgung von Proben im zentralen Prüfsubstanzlager
Organisation und Verwaltung des zentralen Warenlagers (Bestellung, Annahme, Erfassung, Ausgabe)
Sicherstellung und Überwachung des Warenbestandes
Versand von Prüfsubstanzen, Waren und Dokumenten einschließlich der Sendungsanmeldung
der Vorbereitung und Abwicklung von Sendungen
der Zusammenarbeit mit den operativen Einheiten und dem Projektmanagement als zentrale Anlaufstelle für Prüfsubstanz-Management, Versand & Logistik

Du bist die richtige Person für uns, wenn:

Du Erfahrung im Wareneingang,Versand oder der Logistik
Du an einem biotechnologischen oder pharmazeutischen Arbeitsumfeld interessiert bist
Du zielorientiert und strukturiert arbeitest
Du ein ausgeprägtes Verantwortungsbewusstsein hast
Du dich gut organisieren kannst und kannst gleichzeitig flexibel Situationen reagieren
Du sehr gute Deutsch- und grundlegende Englischkenntnisse hast

Weitere Informationen finden Sie unter www.criver.com.

Scientist I (Erkrath, NW, DE, 40699)

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

eine/n

Wissenschaftler (m/w/d)

Unterstütze uns bei:

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

Überzeuge uns durch:

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

Wir bieten Dir:

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

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233344 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. 15 A-B
40699 Erkrath

Job Description

Education

Four-year degree required

Physical Requirements

Equal Employment Opportunity

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

Wissenschaftler (m/w/d) - Molekulargenetik / Genotypisierung (Erkrath, NW, DE, 40699)

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

eine/n

Wissenschaftler (m/w/d)

Unterstütze uns bei:

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

Überzeuge uns durch:

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

Wir bieten Dir:

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

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

Über Research Models & Services

Weitere Informationen finden Sie unter www.criver.com.

Lab Technician I (Erkrath, NW, DE, 40699)

Für die Abteilung Bioassays am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie

als

Lab Technician (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 abgeschlossene Ausbildung als BTA / Biologielaborant (m/w/d), einen Bachelorabschluss mit Schwerpunkt Biologie oder eine vergleichbare Ausbildung im Labor
praktische Erfahrung 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
sehr gute Deutsch- und gute Englischkenntnisse

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 233330 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. 15 a-b
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Job Description

Education

No degree required

Physical Requirements

Equal Employment Opportunity

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

BTA / Biologielaborant (m/w/d) - Zellkultur (GMP) (Erkrath, NW, DE, 40699)

Für die Abteilung Bioassays am Standort Erkrath suchen wir ab sofort und unbefristet

eine/n

BTA / Biologielaboranten / B.Sc. Biologie

als

Lab Technician (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 abgeschlossene Ausbildung als BTA / Biologielaborant (m/w/d), einen Bachelorabschluss mit Schwerpunkt Biologie oder eine vergleichbare Ausbildung im Labor
praktische Erfahrung 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
sehr gute Deutsch- und gute Englischkenntnisse

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

Weitere Informationen finden Sie unter www.criver.com.

Shipping and Receiving Associate (Erkrath, NW, DE, 40699)

Job Overview

Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet

eine / einen

Mitarbeiter Logistik (m/w/d) - Wareneingang und Versand

Deine Aufgaben:

Annahme eingehender Kundenproben für unsere GMP-Analytik, inklusive der Registrierung in unseren Laborinformations-Management System (LIMS)
Bereitstellung von Proben für die analytischen Labore
Ordnungsgemäßen Lagerung und Entsorgung von Proben im zentralen Prüfsubstanzlager
Organisation und Verwaltung des zentralen Warenlagers (Bestellung, Annahme, Erfassung, Ausgabe)
Sicherstellung und Überwachung des Warenbestandes
Versand von Prüfsubstanzen, Waren und Dokumenten einschließlich der Sendungsanmeldung
der Vorbereitung und Abwicklung von Sendungen
der Zusammenarbeit mit den operativen Einheiten und dem Projektmanagement als zentrale Anlaufstelle für Prüfsubstanz-Management, Versand & Logistik

Du bist die richtige Person für uns, wenn:

Du Erfahrung im Wareneingang,Versand oder der Logistik
Du an einem biotechnologischen oder pharmazeutischen Arbeitsumfeld interessiert bist
Du zielorientiert und strukturiert arbeitest
Du ein ausgeprägtes Verantwortungsbewusstsein hast
Du dich gut organisieren kannst und kannst gleichzeitig flexibel Situationen reagieren
Du sehr gute Deutsch- und grundlegende Englischkenntnisse hast

Haben wir Dein Interesse geweckt?
Wenn ja, bewirb Dich bitte unter der Job-ID 233439 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-b
40699 Erkrath
Bei Fragen bitte an RecruitBPS@crl.com wenden

Job Description

Education

No degree required

Physical Requirements

Equal Employment Opportunity

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

Inventar/Lager - Mitarbeiter (Erkrath, NW, DE, 40699)

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.

Für die Abteilung Operations Support am Standort Erkrath suchen wir ab sofort unbefristet

eine / einen

Mitarbeiter Logistik (m/w/d) - Wareneingang und Versand

Deine Aufgaben:

Annahme eingehender Kundenproben für unsere GMP-Analytik, inklusive der Registrierung in unseren Laborinformations-Management System (LIMS)
Bereitstellung von Proben für die analytischen Labore
Ordnungsgemäßen Lagerung und Entsorgung von Proben im zentralen Prüfsubstanzlager
Organisation und Verwaltung des zentralen Warenlagers (Bestellung, Annahme, Erfassung, Ausgabe)
Sicherstellung und Überwachung des Warenbestandes
Versand von Prüfsubstanzen, Waren und Dokumenten einschließlich der Sendungsanmeldung
der Vorbereitung und Abwicklung von Sendungen
der Zusammenarbeit mit den operativen Einheiten und dem Projektmanagement als zentrale Anlaufstelle für Prüfsubstanz-Management, Versand & Logistik

Du bist die richtige Person für uns, wenn:

Du Erfahrung im Wareneingang,Versand oder der Logistik
Du an einem biotechnologischen oder pharmazeutischen Arbeitsumfeld interessiert bist
Du zielorientiert und strukturiert arbeitest
Du ein ausgeprägtes Verantwortungsbewusstsein hast
Du dich gut organisieren kannst und kannst gleichzeitig flexibel Situationen reagieren
Du sehr gute Deutsch- und grundlegende Englischkenntnisse hast

Jobübersicht

Biologics Testing Solutions

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.

Addetto alla cura degli animali da laboratorio - BOLOGNA e FORLI' (solo Weekend) (BOLOGNA, IT, 40126)

Riepilogo del lavoro

Per nostro cliente sito in Bologna e Forlì ricerchiamo un Animal Caretaker con contratto part-time per supporto nei weekend

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;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

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 orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

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

Job Summary

We are seeking a Technician I for our Animal Care Services 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 support a study may include performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. The technician is working under close supervision to gain proficiency.

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

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, restraint on multiple species as well as feeding, watering, and husbandry of multiple species.
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 $17/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

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

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: 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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

Physical Demands:

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

Work Environment:

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

Comments:

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

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.

Equal Employment Opportunity

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

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

In Vivo Technician I- EG (Spencerville, OH, US, 45887)

Job Summary

We are seeking an In Vivo Technician I for our In Vivo Team at our Safety Assessment site located in Spencerville, OH.

A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency

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

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, and restraint on multiple species as well as feeding, watering, husbandry of multiple species. Clinical observations, acclimation observations, and body weight determination on multiple species as well as qualitative and quantitative food consumption. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay range for this position is $19-20/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

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

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

Physical Demands:

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

WORK ENVIRONMENT:

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

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.

Equal Employment Opportunity

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

Seasonal Help - EG (Spencerville, OH, US, 45887)

Job Summary

BASIC SUMMARY:

Responsible for routine laboratory procedures (e.g., animal care, facility cleaning, labeling, lab support basic procedures, etc.), facility/groundskeeping, and/or other administrative/IT functions, as assigned.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

May perform area support cleaning, study set up, laboratory administrative functions, and/or basic animal husbandry.
May clean rooms and/or facility to include possible handling of biohazard materials.
May assist with use of balances and other laboratory equipment.
May perform basic facility/groundskeeping functions.
May perform administrative functions in various departments, including IT.
Use Good Laboratory Practice Regulations (GLP), SOP’s and company policies when performing all job functions.
Perform all other related duties as assigned.

The starting pay for this position is $15.00 per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: H.S. diploma preferred.
Experience: None
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Ability to handle common laboratory species in selected departments.
Must be authorized to work in the United States without a sponsorship visa, now or in the future.

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 for the departments requiring such functions.
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.
May be required to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities may be required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
While performing the duties of any administrative-type functions, the employee may be assigned to regularly talk, hear and work/type at a computer.

WORK ENVIRONMENT:

If assigned to works in a research environment, it may require 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 may be required to work 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 and department assigned, if applies.

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.

Equal Employment Opportunity

For more information, please visit 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 te unas 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 sentir 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 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.

Veterinario (CALCO, IT, 23885)

Selezioniamo un medico veterinario da inserire nell’ambito delle attività di ricerca e laboratorio presso la nostra sede di Calco.

La risorsa contribuirà al mantenimento degli standard di benessere animale e alla corretta applicazione delle normative vigenti, collaborando strettamente con il Veterinario Designato e con il personale tecnico-scientifico.

Requisiti:

Laurea in Medicina Veterinaria e iscrizione/disponibilità di iscrizione all'albo professionale;
Conoscenza della normativa relativa alla protezione degli animali utilizzati a fini scientifici;
Capacità organizzative, attitudine alla collaborazione in contesti multidisciplinari e predisposizione alla formazione continua.

Riepilogo del lavoro

Insourcing Solutions

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 orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

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.

Addetto alla cura degli animali da laboratorio - MILANO (CALCO, IT, 23885)

Riepilogo del lavoro

For an important customer IS belonging to the world of research we are looking for an Animal Technician. The resource will be included in the team operating in the structure.

Animal Care and Colony Management: Provides feeding, watering, health checks, observes behavior, performs veterinary procedures and manages colonies.
Technical Support and Training: Trains users and new employees, assists research staff with animal procedures, and ensures compliance with SOPs and guidelines.
Operational Management and Documentation: Maintains animal records, collects data for management software, monitors environmental conditions, manages consumables and equipment, and supports budget preparation.
Cleaning and Safety: Performs cleaning and decontamination procedures, operates autoclaves, disposes of carcasses according to protocols, uses PPE, and prevents cross-contamination.
Compliance and Inspections: Ensures readiness for regulatory inspections, follows health, safety, and environmental rules, and collaborates with the manager to improve efficiency and quality of services.

Di cosa si occupa la Charles River

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.

Technicien de Toxicologie - F/H- CDD (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 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

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)
Salaire : A compter de 25 715 € 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 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.

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

Responsable d'Équipe de Zootechnie Rongeurs - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ? 

 Le poste 

Sous la responsabilité du Responsable du service de Toxicologie Rongeurs, vous aurez pour mission d’assurer la gestion de l’équipe de zootechniciens au quotidien.

 Les missions 

Animer une équipe de zootechniciens au quotidien,
Planifier l’activité hebdomadaire en assurant la présence des ressources nécessaires,
Contrôler le respect des suivis de procédures dans le cadre des Bonnes Pratiques de Laboratoires (BPL),
Fixer les objectifs et plan d’actions de son équipe,
Suivre les formations dans les outils dédiés,
Participer et animer des réunions liées à l’activité,
Faire remonter les issues ou améliorations possibles auprès du Responsable de Service.

Conditions spécifiques du poste 

Amplitude horaire : retours possibles
Permanences de WE
Contact avec les animaux

Qualifications souhaitées 

De niveau bac+3 minimum, vous possédez une expérience significative réussie en tant que manager ou responsable d’équipe.

Vous êtes reconnu pour vos capacités de communication, votre organisation et votre diplomatie.

 Modalités 

Convention collective de l’industrie pharmaceutique, groupe : 5  
Non-cadre (accord de modulation 35h)
Salaire : A compter de 32 292 € bruts / an sur 13 mois  
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE  
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail,... 
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment 

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

À propos de Charles River 

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. 

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

Technicien de Laboratoire en Histologiee - F/H - CDD (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

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

Les missions 

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

Réaliser les techniques de laboratoire en Histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…).
Assurer la réalisation des autopsies pour toutes les espèces utilisées dans le cadre de nos études.

Dans le cadre de ces missions, vous devrez :

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
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 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.

Lab Technician II (Cologne, NW, DE, 51105)

Für die Abteilung Virus Clearance am Standort Köln suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet

eine/n

BTA / Biologielaborant / B.Sc. Biologie

als

Lab Technician II (m/w/d)

Unterstütze uns bei:

der äußerst sorgfältigen, zuverlässigen und selbständigen Durchführung und Dokumentation von Virussicherheitsstudien (Viral clearance studies) nach GLP
der Organisation und Ausführung vielfältiger Methoden (z.B. Virusfiltrationen, Inaktivierungen und Chromatographien) zur Validierung von Herstellungsprozessen biologischer Arzneimittel im Rahmen dieser Studien
dem Umgang mit Chemikalien und Laborgeräten
der Durchführung von zellkulturbasierten Assays und deren Auswertung mittels Lichtmikroskopie
den Prozessdurchführungen mit Viren der Gefahrstufen BSL-2 und BSL-3**
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GLP-Systems u.a. Pflege und Wartung von Laborgeräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen
der Betreuung von nationalen und internationalen Kunden während ihres Aufenthaltes in unseren Laboren, z.B. bei der Benutzung von Geräten und bei sicherheitsrelevanten Fragen
https://www.criver.com/products-services/biologics-testing-solutions/viral-clearance-and-tse-clearance-studies?region=3696

Überzeuge uns durch:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant oder ein erfolgreich abgeschlossenes Bachelorstudium in Biologie / Biotechnologie / verwandten Naturwissenschaften
Mindestens drei Jahre Berufserfahrung als BTA / Biologielaborant / B.Sc. Biologie-Biotechnologie
Freude am Umgang mit Laborgeräten und experimentellen Aufbauten
Erfahrungen im Umgang mit Zellkulturen inkl. sterilem Arbeiten (wünschenswert)
Erste theoretische und praktische Kenntnisse im Bereich Chromatographie mit ÄKTA und der Bedienung von ÄKTA-Systemen (wünschenswert)
die Fähigkeit zu sehr strukturierten, zielorientierten und konzentrierten Arbeiten unter Einhaltung enger Zeitlinien
ausgeprägtes Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel) 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
eine intensive Einarbeitung
ein Gleitzeitsystem
diverse Benefits
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 233548 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. 15 A-B
40699 Erkrath

Job Description

Education

No degree required

Physical Requirements

Equal Employment Opportunity

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

BTA / Biologielaborant (m/w/d) - Viral Clearance (Cologne, NW, DE, 51105)

Für die Abteilung Virus Clearance am Standort Köln suchen wir zur Erweiterung des Labor-Teams ab sofort unbefristet

eine/n

BTA / Biologielaborant / B.Sc. Biologie

als

Lab Technician II (m/w/d)

Unterstütze uns bei:

der äußerst sorgfältigen, zuverlässigen und selbständigen Durchführung und Dokumentation von Virussicherheitsstudien (Viral clearance studies) nach GLP
der Organisation und Ausführung vielfältiger Methoden (z.B. Virusfiltrationen, Inaktivierungen und Chromatographien) zur Validierung von Herstellungsprozessen biologischer Arzneimittel im Rahmen dieser Studien
dem Umgang mit Chemikalien und Laborgeräten
der Durchführung von zellkulturbasierten Assays und deren Auswertung mittels Lichtmikroskopie
den Prozessdurchführungen mit Viren der Gefahrstufen BSL-2 und BSL-3**
der Betreuung und Sicherstellung der Pflege und Aufrechterhaltung des GLP-Systems u.a. Pflege und Wartung von Laborgeräten, sowie deren Qualifikation und dem Erstellen von Standardarbeitsanweisungen
der Betreuung von nationalen und internationalen Kunden während ihres Aufenthaltes in unseren Laboren, z.B. bei der Benutzung von Geräten und bei sicherheitsrelevanten Fragen
https://www.criver.com/products-services/biologics-testing-solutions/viral-clearance-and-tse-clearance-studies?region=3696

Überzeuge uns durch:

eine erfolgreich abgeschlossene Ausbildung als Biologisch-technischer Assistent / Biologielaborant oder ein erfolgreich abgeschlossenes Bachelorstudium in Biologie / Biotechnologie / verwandten Naturwissenschaften
Mindestens drei Jahre Berufserfahrung als BTA / Biologielaborant / B.Sc. Biologie-Biotechnologie
Freude am Umgang mit Laborgeräten und experimentellen Aufbauten
Erfahrungen im Umgang mit Zellkulturen inkl. sterilem Arbeiten (wünschenswert)
Erste theoretische und praktische Kenntnisse im Bereich Chromatographie mit ÄKTA und der Bedienung von ÄKTA-Systemen (wünschenswert)
die Fähigkeit zu sehr strukturierten, zielorientierten und konzentrierten Arbeiten unter Einhaltung enger Zeitlinien
ausgeprägtes Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
Team- und Kommunikationsfähigkeit
Dienstleitungsorientierung
Gute Kenntnisse von Microsoft Office (Word, Excel) 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
eine intensive Einarbeitung
ein Gleitzeitsystem
diverse Benefits
eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
eine angemessene Vergütung

Wir alle bei Charles River Laboratories teilen eine große Leidenschaft, wenn wir unsere gemeinsame Mission verfolgen: Wir wollen ein gesünderes Leben schaffen. Die Möglichkeit, im Leben von Menschen auf der ganzen Welt etwas zu bewirken, ist das, was uns jeden Tag aus dem Bett treibt. Stell dir vor, du könntest deine Talente einsetzen, um neue Entdeckungen und klinische Durchbrüche voranzutreiben, die die Gesundheit der Menschen weltweit verbessern. Deshalb ist eine Karriere bei uns so viel mehr als nur ein Job. Es ist eine zielgerichtete Reise.

Biologics Testing Solutions

Weitere Informationen finden Sie unter www.criver.com.

Preclinical Autopsy Technician - 2nd Shift (Mattawan, MI, US, 49071)

Job Overview

We are seeking an experienced Technician I – Necropsy for our 2nd Shift Pathology Services Team in Mattawan MI.

A Technician I – 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 12:00PM to 8:30PM with overtime, as necessary.

Job Description

Performs euthanasia and post-mortem examination of animals, including the removal, processing, and preserving of organs for microscopic evaluation by a veterinary pathologist.

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.

Physical Requirements

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.

Minimum Requirements

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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

Technician I (Mattawan, MI, US, 49071)

Job Overview

We are seeking a Technician I for our Clinical Pathology Team in Mattawan MI.

A Technician I – Clinical Pathology 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 biological sample management including labeling, delivery, aliquoting, processing, and verification; cleaning of lab and equipment; preparation, staining, and consolidation of slides. The technician is working under close supervision to gain proficiency.

The pay for this position is $20/hr annually USD. 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 9:00AM to 5:30PM with a weekend/holiday rotation and overtime, as necessary.

Job Description

Performs technical tasks in the conduct of in vivo research studies or support services in accordance with good animal welfare practices. Prepares, collects and records research data and specimens in compliance with applicable regulations and SOPs. For singular focus of Necropsy or Histology or Aquatics, refer to specified role on job architecture.

Minimum 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. 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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

Manager-LBA Project Scientist (Mattawan, MI, US, 49071)

Job Overview

The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies.

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

Efficiently perform supervisory responsibilities in accordance with organizational policies and applicable laws to include interviewing, hiring, training and developing employees
Develop organizational strength by hiring, identifying and developing personnel who are scientifically and/or technically strong
Establish culture and atmosphere to maintain good retention and low turnover using available tools and metrics
Assist with providing costing estimates for components of applicable studies
Provide short- and long-term solutions that support continuous improvement
Develop and maintain 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
Ensure laboratory tasks and operations are executed in compliance with SOPs, protocols, regulatory requirements
Establish and review Standard Operating Procedures (SOPs), protocols, policies, best practices and study procedures
Develop and maintain contemporaneous knowledge of regulatory requirements
Effectively plan, assign and direct work within one operational area with expanded scope and/or complexity
Monitor performance metrics for operational area
Function as a Principal Investigator, Individual Scientist, and/or Project Scientist as required by operational area or resourcing need
Skillfully oversee the design, conduct, interpretation and reporting of studies
Effectively utilize project management systems
Lead implementation of new procedures and refinement of existing procedures to meet current and future business needs
Performs all other related duties as assigned

Job Description

Bachelor’s degree or equivalent with 8-10 years of relevant experience. Between 3-4 years of management experience required
Bioanalysis experience required
Experience in a regulated environment required
Experience in a Contract Resource Organization 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
Must be authorized to work in the United States without a sponsor visa, now or in the future.

The pay for this position is $115/year.

Physical Demands:
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.

Work Environment:
General office working conditions, the noise level in the work environment is usually quiet.
While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Preclinical Autopsy Technician (Mattawan, MI, US, 49071)

Job Overview

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

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.

Job Description

Performs euthanasia and post-mortem examination of animals, including the removal, processing, and preserving of organs for microscopic evaluation by a veterinary pathologist.

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.

Physical Requirements

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.

Minimum Requirements

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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

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

Job Summary

OURLY 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: Zero - 6 months
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
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

Animal Research Technician (Temporary- Potential Permanent) (Mattawan, MI, US, 49071)

Job Summary

We are seeking Temporary to Potential Permanent Animal Research Technician at our Safety Assessment site located in Mattawan, MI. The pay for this position is $19/hour plus benefits.

A Technician is responsible for assisting management, scientists, veterinarians and study related items. The technician performs basic skills independently and continues to work under supervision to gain proficiency on skills still in development. They administer substances to animals, perform husbandry duties including cleaning/transporting caging and providing food and water; perform observations of animals to determine morbidity/mortality; collect and handle data and specimens.

Training Schedule:

Week 1: Tuesday-Friday 8:00AM – 4:30PM

Week 2+: Monday-Friday 7:00AM* – 3:30PM* All roles and shifts require flexibility to work extended hours outside of scheduled shift based on business need, sometimes with short notice.

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*
Sunday – Thursday with holiday rotations 07:00AM* – 3:30PM*
Tuesday – 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.

Successful Candidates will possess the 6 Cs of Success:

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

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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

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

Equal Employment Opportunity

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

Animal Research Technician - 2nd Shift (Mattawan, MI, US, 49071)

Job Summary

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

A Technician I – Technical Operations is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. The technician is working under close supervision to gain proficiency.

Successful Candidates will possess the 6 Cs of Success:

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

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Must be authorized to work in the United States without a sponsor visa, now or in the future

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.

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.

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

About 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.

Equal Employment Opportunity

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

Animalier Contrôle de Production - F/H - CDI Week-end étudiant (L'Arbresle, FR, 69592)

Nous recherchons un Animalier Contrôle de production F/H - en CDI week-end et jours fériés pour 6 heures d'intervention par semaine : 3h les samedis matins, 3h les dimanches matins.

Vous serez intégré au sein d'une équipe et travaillerez en autonomie sur différentes espèces de rongeurs (rats, souris, cobayes) sur notre site des Oncins basé à l'Arbresle (69).

Missions principales

Observer les animaux (rongeurs) selon les consignes préalablement transmises adaptées à chaque projet
S’assurer du bien-être des animaux et alerter en cas de nécessité
Distribuer l’aliment et vérifier l’abreuvement
Nettoyer les lieux d’hébergement et les locaux en respectant les règles d'hygiène et de biosécurité
Garantir la mise à jour des registres de suivi.

Profil

Idéalement étudiant en filière scientifique
Vous êtes rigoureux, de confiance et aimez travailler au contact des animaux
Vous êtes à l'aise avec les outils informatiques
Vous avez à cœur l'éthique animale, êtes autonome, proactif et avez le sens du travail en équipe.

Informations contractuelles

Formation au poste inclue.
Nous vous proposons un CDI avec le Rythme de travail suivant : 6h/ semaine les samedis, dimanches matin (3h/jour) et éventuellement les jours fériés.
Prime de transport, 13e et 14e mois, Intéressement, participation, mutuelle et prévoyance, CE,
Localisation : Saint Germain Nuelles (69)

Site non accessible en transport en commun - Moyen de locomotion indispensable.

Equal Employment Opportunity

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

Animal Care Technician (Hollister, CA, US, 95023)

Job Overview

As an Animal Care Technician for our production site in Hollister, CA, 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. On the job training will be provided.

Essential Duties & 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 Requirements

Animal Care Technician I

No experience required

Animal Care Technician II

Candidates must possess one of the following:

1 year of related experience and/or training in animal husbandry
Associate's Degree or higher level education

The pay range for this position is $18.00 to $19.50 USD per hour.  Please note the range covers levels I - II, salary will depend on level, in addition to factors such as experience, skills, and certification.

Equal Employment Opportunity

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

Primate Technician I 1 (Houston, TX, US, 77047)

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

This is an entry-level position where you can gain experience and begin your career in life sciences. Training provided!

As a Primate Technician I, you will be responsible for the daily care of research animals. Your contribution will ensure the health and well-being of our animals, as well as impact the lives of patients across the world.

Training schedule: Monday - Friday, 6:15am - 2:45pm

Permanent schedule: Sunday - Thursday or Tuesday - Saturday, 5:45am - 2:15pm

Responsibilities:

Providing food and water
Inspect feeding and watering devices for proper function
Cleaning and sanitizing cages and enclosures
Observe animals for overall health and wellbeing
Assisting with the movement of animals
Log animal care data and maintain accurate records
Other assigned duties, including restocking supplies

Work Environment & Physical Demands:

Work is performed in an warm, climate controlled environment.
PPE (protective equipment) includes regular use of surgical mask, cap, goggles, face shield, scrubs, and boots.
The warm setting, physicality of the job duties, and use of personal protective equipment (PPE), when combined, frequently cause employees to become hot and sweaty.
Job duties require employee to regularly stoop, crouch, kneel, and reach up with hands and arms to perform repetitive tasks, and walk and stand for extended periods of time.
Employee must be able to regularly lift, hold and/or move up to 50 pounds.

Job Qualifications

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

High School Diploma or GED preferred, but not required
Animal care experience preferred
Previous experience in a physically demanding role
Previous experience maintaining records and complying with regulations and Standard Operating Procedures (SOPs)
Strong attention to detail
Enjoys being part of a team
Flexible and available to work holidays (on rotational basis) and overtime as needed

The starting pay for this position is $17.75 per hour.

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

With over 20,000 employees within 110 facilities in 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.

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.

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

Clinical Veterinarian I (Houston, TX, US, 77047)

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. Oversee and perform veterinary procedures that support the colony. Oversee all aspects of the animal care and use program as needed. May supervise or oversee veterinary technicians and manage the activities of assigned section to ensure effective performance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provides professional veterinary services to support or manage oversight of all animal care and use functions involving laboratory animals.
Develops, implements and controls procedures related to the acquisition, maintenance, quarantine, and disposition of all research animals including provision of appropriate clinical, preventive and emergency veterinary care for various species.
Provides support in protocol design, facility design, biosecurity practices, occupational health program, equipment procurement, animal model selection and development, surgical services and animal and colony health monitoring programs.
Ensures compliance with established company, regulatory and industry standards.
Maintains broad knowledge of state-of-the-art principles and theories as pertains to the veterinary and comparative medicine field.
Maintains knowledge of regulatory compliance requirements.
Ensure facility is in compliance with all applicable regulations, guidelines and standards that relate to animal care and use (e.g. USDA, FDA, AAALAC).
May advise senior management in animal welfare, care and use matters as they relate to application of new technology, the use of alternatives, support of the 3Rs and new animal models.
Assist in the development and deliver training for staff. Training may include veterinary diagnostics, techniques and minor surgical procedures.
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.
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.

Job Qualifications

Education: Veterinary degree (D.V.M./V.M.D.) or international equivalent.
Experience: Zero to two years related experience with animal care and surgical techniques. Experience in a research/lab animal/GLP environment preferred, but not 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: Must be licensed in country, province or state of employment to fulfill requirements to practice veterinary medicine, and sign health certificates. Must be able to maintain current licensure/certification. USDA accreditation or application submitted within 1 month of hire.
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.
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.

WORK ENVIRONMENT:

General office and research laboratory working conditions, the noise level in the work environment is usually quiet, although hearing protection may be required for short periods when working with certain species.
While performing the duties of this job the employee will be required to wear protective clothing (safety glasses, face shield, N-95, cap, gloves, scrubs), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases. The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

Comments:

This position requires weekend/holiday coverage, on-call rotation, and the necessity to return to the facility outside of normal business hours.
This position may require domestic and international travel to provide support other sites within our portfolio.

Compensation Data

The pay range for this position is $145.000 - $165,000. 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 (if necessary), sign-on bonus and a retention bonus will be part of the overall compensation package as well.

Equal Employment Opportunity

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

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

Job Overview

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 Description

Performs technical laboratory activities in support of client studies or procedures.
Performs analysis of data for quality and completeness and determines if results are as expected.
Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.
Executes scientific testing strategies and studies.
May participate in development as part of team.
May lead assay research, assay validation or study conduct, or is involved in preparation of material (e.g. protein, nucleic acid, cells, etc.).
Reviews and interprets study data, communicates results to clients and writes final reports.
Ensures compliance with protocols and all applicable SOPs.
Troubleshoots and resolves assay or technical issues in the laboratory when scientific expertise is needed.
Contributes to specific dataset interpretation, or when appropriate answering questions from regulatory authorities.

The following are Minimum Requirements related to the Research Analyst I 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.

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.

The schedule is Sunday-Thursday, 7:30 am-4:30 pm.

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Cagewash Technician I (Reno, NV, US, 89511)

Job Overview

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

The Cagewash Technician will assist in cleaning and disinfecting animal housing, feed and water containers using the automated cage washer, and cleaning of laboratory areas. This individual will also be responsible for recording all required tasks on relevant logbook records accurately and completely. The Cagewash Technician will also assist with animal care technical duties such as changing liners and sanitizing animal room walls and floors.

Job Description

Performs duties related to the maintenance of experimental animals such as cleaning cages, holding animals for treatment by laboratory technician or maintaining inventory and animal identification records. Performs cleaning/sanitation of animal facility and equipment.

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

•   High School diploma or General Education Degree (G.E.D) preferred.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   While performing the duties of this job, the employee is regularly required to talk, hear, and lift.
•   Specific vision abilities required by this job regularly requires close vision and the ability to adjust focus.
•   Must be able to regularly lift and manipulate up to 50 pounds on a repetitive basis each day.

Salary: The pay range for this position is $20.00 USD per hour with room for advancement. 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, 7 am - 4 pm daily or 6 am - 3 pm may be also be available.

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.

Equal Employment Opportunity

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

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

Job Overview

JOB SUMMARY:

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

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

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

Job Description

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

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Animal Care Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking an Animal Care Technician I for our Safety Assessment site located in Reno, NV.

The Animal Care Technician I will be trained in basic skills required to support our research studies onsite. Duties may include cleaning, sanitizing, animal handling, animal husbandry, changing out animal cages, observing, monitoring, and recording basic information about animal health.

RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Perform duties such as animal husbandry, animal handling, cage manipulation, and movement, equipment storage/tracking, wash systems, and water delivery system maintenance for various animal species throughout the site.
Collect, document, review, and verify data on forms, or in electronic data systems.
Review documentation for quality control purposes.
Stocking supplies and facility cleaning duties.
Use and perform maintenance on instruments and equipment.
Progress through training for skills required in this position.

The starting pay for this position is $19.00 USD per hour with room for avancement through Animal Care Technician V.

Schedule is M-F, 7 am - 4 pm while in training for roughly 6 monts. After training, work week is either Tues-Sat or Sun-Thurs, 7 am - 4 pm daily.

Job Qualifications

Education: High School Diploma, General Education Degree (G.E.D) preferred, but not required.
Experience: No previous experience required.
Strong communication skills and attention to detail.

Preferred Qualifications:

Previous experience in a physically demanding work environment.
Previous personal or professional experience in animal care.
Ability to manage multiple tasks and priorities.
Computer skills
Ability to maintain a safe work environment by observing all safety procedures and making use of protective clothing.
Ability to follow all Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule, which may include evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under time constraints.

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

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

Equal Employment Opportunity

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

饲养员-DIRECT LABOR (Chengdu City, SC, CN, 610213)

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

工作总结

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。

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。

Addetto alla cura degli animali da laboratorio - ANCONA (part-time) (ANCONA, IT, 60015)

Riepilogo del lavoro

Per nostro cliente sito in Ancona ricerchiamo un Animal Caretaker con contratto part-time

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;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

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 orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

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.

Addetto alla cura degli animali da laboratorio - ANCONA (part-time) (ANCONA, IT, 60015)

Riepilogo del lavoro

Per nostro cliente sito in Ancona ricerchiamo un Animal Caretaker con contratto part-time

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;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

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 orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

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.

Business development and operational manager Germany/North Europe (Munchen, DE, 80333)

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.

Riepilogo del lavoro

Reporting to the Associate Director & Business Development Manager Europe, you will help in identifying new potential customers and/or unexplored markets and lead operational activities including team management at client site. Working closely with Associate Director and client service team to create new pipeline to drive increases in business and lead the operational tasks coming from contracts in place.

Supporting in building new business pipeline for the countries he/she is responsible, as well as upselling and cross-selling to existing clients.
Work as part of a deal team to ensure the best customer experience and response.
Involvement in the development of pricing, preparing models for the calculation of ad hoc pricing for new business opportunities and Bids.
Preparation of customers presentation or new opportunities info packages to support Management decision making
Manage the operational team in the assigned territory, select appropriate managers and support the staff engagement and company culture
Ensure contractual compliance within operations and resource support for the Insourcing Solution teams.
Liaise with support functions to identify relevant information for Company presentation and tender preparation.
Monitor KPIs and performance of contracts and business development activities.
Analyzing data to identify operational trends and opportunities for improvement
Leading projects aimed at improving operational efficiency and reducing costs
Reviewing all operational processes for efficiency, scale and quality improvements

Language: Mandatory German and English, preferred Italian
Master’s Degree: business or biology or management
Project Management knowledge;
MS Office package and Presentation skills;
Gross Annual Salary: 55.000€

Business development and operational manager Germany/North Europe (Munchen, DE, 80333)

Jobübersicht

In dieser Funktion berichten Sie an den Associate Director & Business Development Manager Europe und unterstützen bei der Identifizierung neuer potenzieller Kunden und/oder bislang nicht erschlossener Märkte innerhalb eines definierten Portfolios. Zudem übernehmen Sie die Leitung operativer Aktivitäten einschließlich des Teammanagements direkt beim Kunden.

In enger Zusammenarbeit mit dem Associate Director und dem Client Service Team tragen Sie zur Entwicklung neuer Vertriebspipelines zur Steigerung des Geschäftsvolumens bei und verantworten die operativen Aufgaben aus bestehenden Verträgen.

Unterstützung beim Aufbau neuer Business-Pipelines in den verantworteten Ländern sowie Upselling- und Cross-Selling-Aktivitäten bei bestehenden Kunden
Mitarbeit in Deal-Teams zur Sicherstellung einer optimalen Customer Experience und einer schnellen, qualitativ hochwertigen Kundenreaktion
Beobachtung von Branchentrends, Wettbewerbsentwicklungen und neuen Marktchancen
Repräsentation des Unternehmens mit Professionalität, Engagement und einem klaren Fokus auf den Aufbau strategischer Partnerschaften
Mitwirkung bei der Preisgestaltung, einschließlich der Erstellung von Kalkulationsmodellen für ad-hoc-Preise bei neuen Geschäftsmöglichkeiten und Ausschreibungen
Erstellung von Kundenpräsentationen und Informationsunterlagen zu neuen Geschäftschancen zur Unterstützung von Managemententscheidungen
Führung und Steuerung der operativen Teams im zugewiesenen Gebiet, Auswahl geeigneter Führungskräfte sowie Förderung von Mitarbeiterengagement und Unternehmenskultur
Sicherstellung effizienter und qualitativ hochwertiger Abläufe beim Kunden, inklusive Mitarbeiterkompetenzen, Zertifizierungen und lösungsorientiertem Problemlösungsansatz
Gewährleistung der vertraglichen Compliance innerhalb der operativen Abläufe sowie Sicherstellung der Ressourcenunterstützung für Insourcing-Teams
Unterstützung beim Aufbau neuer Business-Pipelines in den verantworteten Ländern sowie Upselling- und Cross-Selling-Aktivitäten bei bestehenden Kunden
Mitarbeit in Deal-Teams zur Sicherstellung einer optimalen Customer Experience und einer schnellen, qualitativ hochwertigen Kundenreaktion
Beobachtung von Branchentrends, Wettbewerbsentwicklungen und neuen Marktchancen
Repräsentation des Unternehmens mit Professionalität, Engagement und einem klaren Fokus auf den Aufbau strategischer Partnerschaften
Mitwirkung bei der Preisgestaltung, einschließlich der Erstellung von Kalkulationsmodellen für ad-hoc-Preise bei neuen Geschäftsmöglichkeiten und Ausschreibungen
Erstellung von Kundenpräsentationen und Informationsunterlagen zu neuen Geschäftschancen zur Unterstützung von Managemententscheidungen
Führung und Steuerung der operativen Teams im zugewiesenen Gebiet, Auswahl geeigneter Führungskräfte sowie Förderung von Mitarbeiterengagement und Unternehmenskultur
Sicherstellung effizienter und qualitativ hochwertiger Abläufe beim Kunden, inklusive Mitarbeiterkompetenzen, Zertifizierungen und lösungsorientiertem Problemlösungsansatz
Gewährleistung der vertraglichen Compliance innerhalb der operativen Abläufe sowie Sicherstellung der Ressourcenunterstützung für Insourcing-Teams

Masterabschluss in Betriebswirtschaft, Biologie, Management oder einem vergleichbaren Studiengang
Kenntnisse im Projektmanagement
Sehr gute Kenntnisse im MS-Office-Paket sowie ausgeprägte Präsentationsfähigkeiten
Sprachen: Deutsch und Englisch zwingend erforderlich, Italienisch von Vorteil

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

Technicien de Laboratoire en Pathologie Clinique - 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 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 renforecer notre équipe Pathologie Clinique au sein du Laboratoire d'Evaluation Biologique (LEB), nous recherchons un Technicien de laboratoire en Pathologie Clinique (F/H) en CDI.

Les missions

Réaliser les dosages et expérimentations dans les activités suivantes : Hématologie, Coagulation, Biochimie, Examens urinaires.
Être capable d'accepter ou non des résultats biologiques en respectant des critères d'acceptation.
Réaliser des immunoessais en plaque de type ELISA/ECLIA/Multiplexin dans les activités suivantes : Dosages de Biomarqueurs, Immunogénicité des vaccins, Dosages pharmacocinétiques, Dosages ADA (Anti-Drug-Antibodies)
Etre capable de comprendre et d'accepter des résultats obtenus selon une courbe de calibration en respectant des critères d'acceptation
Réaliser la compilation informatique des résultats obtenus pour les différentes études.
Réaliser la maintenance sur les appareils/automates utilisés dans les différentes activités.
Réaliser les traitements et reprises des échantillons avant stockage au laboratoire.
Superviser, contrôler et réaliser les envois d'échantillons vers d'autres sites

Conditions spécifiques du poste

Amplitude horaire : 7h/18h avec planning à la semaine
Permanences matin, soir et week-ends sur la base du volontariat

Qualifications souhaitées

Issu(e) d'une formation de niveau bac+2 minimum dans le domaine de la biologie, vous connaissez tout ou partie des techniques utilisées dans notre laboratoire : ELISA ; ECLIA ; Multiplexin ; ELISPOT ; Cytométrie en flux.

Vous aimez le travail en équipe mais êtes également capable d'évoluer en autonomie.

Vous savez vous organiser et réaliser vos missions avec rigueur.

La connaissance des BPL ou autres référentiels qualité est un atout.

Le groupe étant international, des bases en anglais sont indispensables. Un bon niveau serait un plus.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDD Non-cadre (accord de modulation 35h)
Salaire : A compter 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, etc.
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

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

Technicien Animalier Etudiant - F/H - CDI Week-end Intermittent (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste

Pour travailler au sein de nos animaleries (rongeurs ou non-rongeurs) pendant les week-ends et vacances scolaires, nous recherchons plusieurs étudiants.

En contrat CDI Intermittent, vous interviendrez en tant que Technicien Animalier (F/H) après une formation initiale de 6 semaines, à temps complet, dispensée sur l'été 2025.

Les missions

Assurer le bien-être et les soins aux animaux dans les conditions optimales d’hébergement en étude : alimentation, abreuvement, change des animaux
Participer à l’entretien des installations : nettoyage et rangement du matériel
Observer l’état physiologique et sanitaire des animaux
Assurer les soins et traitements prescrits par les vétérinaires, les techniques de contention
Effectuer le relevé des observations cliniques et l’acquisition des données selon le plan d’étude et les protocoles

Qualifications souhaitées

Vous êtes reconnu(e) pour votre rigueur et votre adaptabilité. Vous savez travailler seul(e) comme en équipe.
A l'aise avec les outils informatiques, vous maitrisez les logiciels bureautiques (Word, Excel).
Notre environnement est propice aux étudiants de formations en biologie ou sciences.

Modalités contractuelles

Convention collective de l'industrie pharmaceutique, groupe : 2
Salaire de base : 12,25€ bruts/heure + majoration forfaitaire de 45%
Contrat : CDI Intermittent (environ 200h par an, hors formation initiale)
Formation rémunérée à temps plein de 6 semaines minimum sur les mois de juin à août 2026 selon disponibilités
Planning annuel donné en août
Lieu de travail : St Germain Nuelles (69) - Permis B et véhicule obligatoire.

À propos de Safety Assessment

À propos de Charles River

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

Technicien Animalier - Contrat VSDL - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste

Afin de renforcer nos animaleries en charge de la bonne conduite de nos études de toxicologie, nous recherchons un Technicien animalier F/H en CDI.

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

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

Il s'agit d'un contrat "fin de semaine", du vendredi au lundi.

Missions

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

Conditions spécifiques du poste

Amplitude horaire hebdomadaire du service 6h/18h

Contrat Cyclique de 4 jours travaillés consécutifs – découpés en 6 périodes hebdomadaires :

Période 1 : vendredi, samedi, dimanche, lundi
Période 2 : vendredi, samedi, dimanche, lundi
Période 3 : vendredi, samedi, dimanche, lundi
Période 4 : vendredi, samedi, dimanche, lundi
Période 5 : mardi, mercredi, jeudi, vendredi
Période 6 : vendredi, samedi et dimanche

Qualifications souhaitées

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

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

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

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

Modalités contractuelles

Convention collective de l'industrie pharmaceutique, groupe : 3
Contrat : CDI non cadre à temps partiel (28h, accord de modulation)
Rémunération sur 13 mois + majoration forfaitaire
Prise en charge de la mutuelle à 60%, restaurant d'entreprise, CSE
Primes de transport, d'intéressement/participation, accord d'ancienneté, etc.
Site non accessible en transport en commun, moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

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

Technicien de Laboratoire en Immunologie - F/H - CDD 9 mois (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. En rejoignant 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 passionnante à nos côtés.

Qui sommes-nous ?

Le poste

Dans le cadre d'un remplacement au sein de notre Laboratoire d'Evaluation Biologique (LEB), nous recherchons un Technicien de Laboratoire en Immunologie (F/H) en CDD pour une durée de 9 mois. Vous intégrerez un département scientifique dynamique et en constante évolution, composé de techniciens, opérateurs et directeurs d'études. Sous la responsabilité de votre manager, vous travaillerez plus spécifiquement dans une équipe de 9 personnes dédiées à l'analyse technique des biomarqueurs.

Les missions

Réaliser des Immunoessais en plaque de type ELISA/ECLIA/Multiplexin dans les activités suivantes : Dosages de Biomarqueurs, Immunogénicité des vaccins, Dosages pharmacocinétiques, Dosages ADA (Anti-Drug-Antibodies)
Réaliser les lyses, marquages cellulaires et titrations d'Anticorps pour l'activité Immunophénotypage
Réaliser le traitement et analyse informatique des échantillons sur la plateforme : Cytométrie en flux
Être capable d'accepter ou non des résultats biologiques en respectant des critères d'acceptation
Être capable de comprendre et d'accepter des résultats obtenus selon une courbe de calibration en respectant des critères d'acceptation
Réaliser la compilation informatique des résultats obtenus pour les différentes études
Réaliser la maintenance sur les appareils/automates utilisés dans les différentes activités
Réaliser les traitements et reprises des échantillons provenant des animaleries avant stockage au laboratoire

Conditions spécifiques du poste

Amplitude horaire : 7h/18h avec planning à la semaine
Permanences matin, soir et week-ends sur la base du volontariat

Qualifications souhaitées

Vous aimez le travail en équipe mais êtes également capable d'évoluer en autonomie.

Vous savez vous organiser et réaliser vos missions avec rigueur.

La connaissance des BPL ou autres référentiels qualité est un atout.

Le groupe étant international, des bases en anglais sont indispensables. Un bon niveau serait un plus.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDD Non-cadre (accord de modulation 35h)
Salaire : A compter 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, etc.
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

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

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

Job Summary

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

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

Additional responsibilities include:

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

Job Qualfications

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

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

Experience and/or training working with mechanical equipment preferred

The pay for this position is $18.34 per hour.

Equal Employment Opportunity

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.
Must be authorized to work in the United States without a sponsor visa, now or in the future

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.

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

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

Equal Employment Opportunity

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

Animal Packer (Kingston, NY, US, 12401)

Job Overview

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

*This is a temporary opportunity with potential to become a full-time CRL employee*

Salary: $17.75/hour

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.

Some benefits included: Paid Sick time/Volunteer Time off/401K Participation

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

MINIMUM QUALIFICATIONS:

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

PREFERRED QUALIFICATIONS:

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

The hourly pay rate for this position is $17.75.

Equal Employment Opportunity

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.

Equal Employment Opportunity

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

Animal Care Technician I (Cambridge, MA, US, 02141)

Job Description

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

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

Key Responsibilities

Handle, transfer, and deliver animals, supplies (including caging, gases, dry ice, and liquid nitrogen), and waste to and from work areas as needed.
Perform daily cage duties, including recycling and scheduled sanitation procedures.
Monitor daily animal health and welfare while conducting routine health observations.
Operate cage washers and autoclaves to sterilize caging equipment and instruments.
Maintain quality assurance documentation, including temperature strips, room environmental reports and logs, and washer or autoclave logs.
Perform animal husbandry duties to maintain the quality and health of research animals, including daily water bottle and cage checks, providing appropriate food and water, performing cage changes and cleaning, and recording animal health concerns in accordance with SOPs and specified protocols.
Communicate procedural questions or training needs to the Team Lead or Facility Supervisor.
Perform humane euthanasia in accordance with the Guide for the Care and Use of Laboratory Animals.
Monitor client rack and row assignments in shared animal holding rooms to ensure proper labeling and assignment based on facility needs.
Maintain a clean and organized work environment, including animal rooms, corridors, cage wash areas, procedure rooms, anterooms, storage areas, and grounds, following established cleaning procedures and schedules.

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-$23 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.

Laboratory Operations Technician I (Wilmington, MA, US, 01887)

Job Overview

Responsible for performing a wide variety of tasks related to laboratory operations and animal husbandry in a Good Manufacturing Practice (GMP) compliant laboratory setting. Tasks may include but are not limited to management of laboratory materials, operation of autoclave and cagewash, maintaining proper disposition of biohazard materials and chemicals, assist in safety and compliance activities in laboratory facilities, assist in equipment programs, coordinate with laboratory personnel and external vendors to support laboratory activities, and perform routine and moderately complex animal husbandry duties.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform autoclave and cagewash runs in support of laboratory operations including but not limited to cage parts, animal enrichment devices, and reagents
• Collaborate with laboratory personnel and external vendors to ensure proper disposition of biohazard materials and chemicals; sterilize and discard used lab materials as required; assist with packing and transfer of biohazard materials
o Clidox deactivation
o Prepare dirty bedding and decontaminate dirty cages in a biological safety cabinet (BSC) for disposal
• Perform physical environment cleanliness and upkeep and maintain recordkeeping to GMP standards and/or Standard Operating Procedures (SOPs)
• Collaborate with different function groups to coordinate activities related to laboratory supplies, inventory management, and orders of critical materials
o Regularly take inventory of and restock laboratory supplies, reagents, and critical components to support laboratory testing
o Interact and coordinate with IVB personnel to assure that lab supplies are received in timely manner and alternative options provided as needed
 Manage deliveries
 Perform goods receipts in SAP for animal and supply orders
o Work with management to create, implement and maintain disposable cage inventory system
o Interact with management to ensure appropriate level of cage supplies are available for laboratory use
o Identify and implement improvement opportunities pertaining to supplies inventory management
• Assist and participate in laboratory equipment preventative maintenance programs
• Assist and participate in safety and lab compliance initiatives and implement at the site
• Train on all basic procedures, processes, and documentation pertaining to Laboratory Operations and the site as assigned
• Provide a support function to address unexpected problems at short notice
• Maintain exact and detailed documentation appropriate to the function, including training records
• Conduct clinical observations to ensure health of animals and perform animal husbandry duties
• Operate equipment and use supplies according to safety guidelines
• Perform all other related duties as assigned

Qualifications

• Education: High school diploma or General Education Degree (GED).
• Experience: 1 to 3 years related experience in a laboratory 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: Able to work independently under minimal supervision. Excellent verbal, written communication, and organizational skills. Demonstrated independent problem-solving abilities. Proficient with computers. Ability to interact appropriately with all levels of employees. Ability to work effectively as a member of a team. Ability to handle stress effectively and adapt to change.

The pay for this position is $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.

Equal Employment Opportunity

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

Embryology Laboratory Technologist (Wilmington, MA, US, 01887)

Job Description

We are seeking an Embryology Lab Technologist in our Embryology Department at our Wilmington, MA location.

Work Schedule: Monday-Thursday - 6:00 am - 3:30 pm & Friday 6:00 am - 10:00 am

This individual will assist in production of embryos via in vitro fertilization (IVF), collection of embryos from naturally mated animals, cryopreservation of embryos and sperm, quality control (QC) of the produced material, and keeping track of Key Performance Indicators (KPI) to gauge production success rates. Training in skills to promote further career advancement is part of this position and may include learning basic rodent survival surgery and embryo microinjection.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Use IVF to generate rodent embryos.
Collect embryos from oviduct and uterine tissue from naturally mated rodents.
Assess embryo quality.
Embryo cryopreservation.
Collect and cryopreserve sperm.
QC cryopreserved material.
Assist in maintenance of cryopreserved material.
Conduct Mouse Embryo Assays and Sperm Motility Assays to QC media and plasticware used in the lab.
Occasionally assist with dissection of rodent reproductive tracts.
Occasionally assist with animal husbandry in both Individually Ventilated Cage (IVC) Racks and in rodent Isolator Units.
Assist supervisors with mentoring and training of new personnel.
May act as team leader in specific departmental projects.
Understand and comply with all Standard Operating Procedures (SOPs) and biosecurity procedures.
Ensure proper record-keeping using the Internet Colony Management (ICM) software.
Use simple computer programs, databases, and applications
Comply with all local, state, and federal laws governing the use of research animals.
Work under deadlines with general guidance.
Weekends and holidays may be required
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

Candidates must possess one of the following:

Bachelor's degree (B.A./B.S.) in Biological Science, Lab Animal Science, or related discipline.
Associate degree plus 1 year husbandry or lab experience in a laboratory/animal facility.
High school diploma/General education development plus 2-3 years husbandry or lab experience in a laboratory/animal facility.

In addition:

Must be comfortable handling rodents, primarily mice and rats.
Proficient in computers (ie: MS Office Suite).
Ability to accurately complete detailed work.
Ability to lift 35 lbs. in weight.

PREFERRED QUALIFICATIONS:

Broad knowledge of biology lab practices.
Prior experience working with rodents.
General familiarity working with computer databases.

The hourly pay rate for this position is $24.00.

Equal Employment Opportunity

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

Laboratory Technician I (2nd shift) (Wilmington, MA, US, 01887)

Job Summary

We are seeking a Laboratory Technician I to work in our MDX Department located in Wilmington, MA.

• Shift is: 1pm - 9pm or 2pm - 10pm (Monday through Friday)
• Great pay with a shift differential & benefits.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Performs technical laboratory activities in support of client studies or procedures.
Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.
Reconciles customer paperwork with submission documentation to ensure accuracy.
Makes detailed observations and maintains documentation of all laboratory work.

MINIMUM QUALIFICATIONS:

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

High School diploma or General Education Development (GED).
1 year experience in a laboratory or animal science environment.
Experience working in a fast paced environment.
Must be detail oriented and a multitasker.
Works independently, but also a team player.
Computer skills (Microsoft Office).

PREFERRED QUALIFICATIONS:

Bachelor’s degree (B.S.) or equivalent in biological sciences or related discipline.
1 years of previous related experience in a Pharmaceutical, Biotech, or Contract Research Organization laboratory environment.
Experience with Aseptic techniques.

The pay range for this position is $22.00-23.50 / 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.

Serology Technologist (Wilmington, MA, US, 01887)

Job Overview

Under direct supervision, perform specimen receipt, preparation and testing as specified In IVB SOP and Protocols in compliance with GMP regulations as they apply to the conduct of nonclinical research.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform laboratory activities Including but not limited to reagent preparation, laboratory maintenance I monitoring, and routine testing of client samples.
• Specific primary areas of testing responsibility include
• Immunoassay methods
o ELISA
o IFA
• Hemagglutination
• Assist In the receipt of samples to be tested
• Prepare data forms for routine serology testing. Record assay parameters as required by protocol.
• Ensure proper sample dilution is performed.
• Operate and maintain pipettes.
• May assist in the preparation of departmental media and diluents, including knowledge of proper labeling technique and storage conditions.
• Assist in ensuring adequate supply of materials required for assays.
• Ensure raw data records are accurate, complete, and In appropriate order, and meet protocol specifications and/or GMP requirements.
• Assist in Interaction with project managers and technical staff In planning and conduct of serology assays.
• May support core IVB activities such as clinical observations, animal husbandry, share responsibility for general housekeeping and maintaining appropriate inventory levels of departmental supplies.
• Responsible for proficiency In all departmental SOPs with general knowledge of the lab/production processes.
• Perform all other related duties as assigned.

Qualifications

Education: Assoclate's degree (A.A. /A.S.) or equivalent In Biological Sciences or related discipline. Bachelor's degree preferred.
Experience: One to two years related technlcal experience In a laboratory environment.
Other: Strong organizational and prioritization skills required. Attention to detail and accuracy a must. Effective verbal and written communication skills required. Able to communicate effectively In a small group or one on one setting.

Equal Employment Opportunity

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

Research Technician I (Worcester, MA, US, 01608)

Job Overview

This is a Full Time position Working Tues-Saturday (40 Hours/Week)

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.

Job Description

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.
Under supervision, perform basic formulation procedures (i.e. simple dilutions, label and dispense).

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 $24.50/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Animal Care Technician I (Boston, MA, US, 02210)

Job Summary

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

Key Responsibilities

Handle, transfer, and deliver animals, supplies (including caging, gases, dry ice, and liquid nitrogen), and waste to and from work areas as needed.
Perform daily cage duties, including recycling and scheduled sanitation procedures.
Monitor daily animal health and welfare while conducting routine health observations.
Operate cage washers and autoclaves to sterilize caging equipment and instruments.
Maintain quality assurance documentation, including temperature strips, room environmental reports and logs, and washer or autoclave logs.
Perform animal husbandry duties to maintain the quality and health of research animals, including daily water bottle and cage checks, providing appropriate food and water, performing cage changes and cleaning, and recording animal health concerns in accordance with SOPs and specified protocols.
Communicate procedural questions or training needs to the Team Lead or Facility Supervisor.
Perform humane euthanasia in accordance with the Guide for the Care and Use of Laboratory Animals.
Monitor client rack and row assignments in shared animal holding rooms to ensure proper labeling and assignment based on facility needs.
Maintain a clean and organized work environment, including animal rooms, corridors, cage wash areas, procedure rooms, anterooms, storage areas, and grounds, following established cleaning procedures and schedules.

Job Qualifications

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

The pay range for this position is $20-$23 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.

Research Technician I - 2nd Shift (Shrewsbury, MA, US, 01545)

Job Overview

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

Job Description

Full Time Position - Monday- Friday 2:30 - 11:00pm.

The Research Technician 1 will collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.

The following are minimum qualifications:

Education: High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline.
Experience: 6 months to 1 year related experience in animal research and/or husbandry or must have fully satisfied technical and experience requirements for the previous level.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred.
Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay range for this position is $24.50 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Research Scientist 1 - Immunochemistry (Shrewsbury, MA, US, 01545)

Job Overview

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:

•   Function independently as a Project Scientist, Principal Investigator, Contributing Scientist in the direction and execution of assigned studies in compliance with regulations as they apply to the conduct of preclinical and clinical research. Provide scientific expertise in study conduct, design, and interpretation.
•   Participate in and coordinate all phases of the study planning process with appropriate departments.
•   Develop assays, generate high-quality laboratory method, protocols, amendments, reports, and facilitate appropriate changes to study design for assigned projects and programs.
•   Review, interpret, integrate, and present data on assigned studies.
•   Writes and edits draft or final reports that document all study related procedures and results.
•   Analyze scientific problems, troubleshoot analytical methods and technical issues.
•   Function independently as the point of contact for the planning and execution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
•   Provide prompt verbal or written communication with Sponsors on study related business.
•   Mentor technical staff in areas such as protocol interpretation, method development and refinement, study-related problem resolution, and execution of validation studies.
•   Provide technical and scientific guidance to the research staff.
•   Contribute to testing of new biomarker technologies or introduce improvements in existing technologies.

The pay range for this position is between $100,000 to $108,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

QUALIFICATIONS:
• Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or PhD/DVM preferred.

• Experience: Minimum of 6 years related experience in the development and/or validation of biomarker, PK and ADA assays is preferred (eg: ligand binding assays, enzymatic assays, Luminex, Bioplex, MSD, Quanterix Simoa, ProteinSimple Ella). Experience in a contract research organization is preferred.

• Other: Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Experience with Watson LIMS (preferred).

Education

Four-year degree required

Advanced degree or certification required

Physical Requirements

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.

Equal Employment Opportunity

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

Account Manager - Sydney, Remote (US)

SUMMARY

Responsible for selling and promoting Charles River Microbial Solutions products/services to assigned customers in New South Wales, ACT and South Australia - this is a remote position. Maintain and increase sales at new and existing accounts through proactive and outbound field account management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Sell the company’s Endosafe, Accugenix and Celsis products/services to accounts by contacting both established customers and developing new prospects.
• Diligently maintain SFDC or any other Charles River CRM system, incl. adding customers and customer information, logging customer calls and meetings, creating and updating sales opportunities, and capturing marketing event leads.
• Maintain a working knowledge of all Endosafe, Accugenix and Celsis products, services and policies.
• Participate in all required specialized training for specific product/ service line(s)
• Develop an effective Territory Plan to ensure that all customers in the given territory are proactively engaged with on a regular basis.
• Manage a quarterly Territory Management Plan including opportunities and sales strategies.
• Attend customer conferences, networking events and other industry events to build contact lists, showcase our products and promote Charles River’s products and services.
• Maintain customer appointments and perform "cold" calls requiring professional business acumen.
• Conduct product demonstrations to potential customers as well as provide product training and support when needed.
• Research business and trade media to identify new potential customers in our industry
• Establish customer needs and requirements for Company products and services.
• Initiate all administrative details to execute the sales process flow.
• Share customer problems/concerns with your supervisor for quality resolution.
• Proactively and collaboratively engage with other internal departments
• From time to time, attend regional or international sales meetings.
• Perform all other related duties as assigned.

The following are minimum qualifications related to this position:

• Education: Bachelor’s degree (B.A. /B.S.) or equivalent in life sciences, sales or related field required. Master’s degree preferred.
• Experience: Minimum 5 years relevant industry experience, with at least 2 of those years having direct client interface.
• 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 interpersonal, customer relationship and leadership skill

Equal Employment Opportunity

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

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

Job Overview

Responsible for handling and restraining animals, clinical observations, monitoring food consumption and body weights, animal husbandry, and performing accurate data collection and reporting.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•    Observe animals for general health and overall well being.
•    Collect and record research data in compliance with Good Laboratory Practice Regulations (GLPs), study protocols and Standard Operating Procedures (SOPs).
•    Perform basic in-life technical procedures upon completion and sign-off of specific skill training. (e.g., clipping, handling, chipping, binding, removals, body weight,).
•    Assist in cohabitation smears of all species.
•    Perform computer input under supervision.
•    Read basic study protocols and extract pertinent information.
•    Review documentation of functions performed as part of quality control requirements.
•    Retrieve and view Standard Operating Procedures using appropriate database.
•    Use GLPs, SOPs, processes and company policies when performing all job functions.
•    Handle, restrain, and provide care for all 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. Perform all other related duties as assigned.

The pay range for this position is $21.70/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

QUALIFICATIONS:
•    Education: High school diploma or General Equivalent Degree (G.E.D.).
•    Experience: 0-6 months related experience in animal research and/or husbandry 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: Ability to handle common laboratory animal species. Basic knowledge of GLP regulations preferred.

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Laboratory Assistant - Lab Support (Temp) (Horsham, PA, US, 19044)

Job Overview

Perform basic laboratory and record-keeping tasks to support site operations.

Job Description

This is a Full Time (40 hours/week) Temp Position (6 months to 1 year)

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Clean and sanitize hallways, labs, and test article preparation rooms.
⦁ May be responsible for preparing simple lab solutions (ex. Bleach)
⦁ Monitor and maintain inventory of assigned areas (ex. PPE Stations, Hazard waste boxes, glassware, etc).
⦁ Order supplies for the lab and departments (ex. cleaning supplies, glassware, etc)
⦁ Pickup and deliver packages from receiving in a timely manner.
⦁ Assist with melting wax, printing labels for specimen collection.
⦁ Operate basic lab equipment and perform routine maintenance, as needed.
⦁ Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
⦁ Submit Work Orders for equipment or facility issues.
⦁ Prep cages, glassware and supplies for autoclaving.
⦁ Perform Pest Control checks of areas and document as per SOP.
⦁ Perform test article and control article discards under a fume hood.
⦁ Assist with the receipt and documentation of feed and bedding.
⦁ Perform and document weekly eye wash checks.
⦁ Assist in the breakdown and setup of study rooms.
⦁ Perform weekly census of animals.
⦁ Collaborate with technical staff in Operations, Pathology and Lab Sciences.
⦁ Assist in the archiving of non-study/study/ facility data (ex. cage wash forms).
⦁ Assist with clerical duties (ex. filing, making copies, etc.).
⦁ Perform all other related duties as assigned.

The pay range for this position is between $17.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.).
⦁ Experience: None
⦁ Certification/Licensure: None
⦁ Other: Must be detail-oriented and have general familiarity with lab procedures. Good verbal communication skills required. Basic computer skills; familiarity with Microsoft Office software.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Cage Wash Technician I (Horsham, PA, US, 19044)

Job Overview

Clean and disinfect animal housing, feed and water containers using the automated cage washer.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Assist with Animal Care technical duties such as changing liners and sanitizing animal room walls and floors.
Based on laboratory schedule, prioritize the sanitization of animal cages, racks, feeders, bottles and sippers, according to S.O.P.’s, using the automated cage wash machines.
Clean and maintain a clean cage wash area.
Ensure preparation of feed jars for washing, including discarding of old feed.
Ensure that storage areas are maintained in an organized fashion.
Lubricate rack wheels after being washed.
Perform daily routine maintenance checks on the automated cage wash machines.
Receive, store, and distribute animal husbandry supplies. Report low inventory to supervisor.
Record all required tasks on relevant logbook records accurately and completely.
Report the need for equipment repair (cages, racks, cage wash machines, etc.) to the appropriate personnel.
Sanitize floors, walls, and other surfaces in the automatic cage wash area.
Secure cage wash area and compressor room at the end of the day.
Perform all other related duties as assigned.

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

QUALIFICATIONS:
Education: High School Diploma or General Education Degree (G.E.D.).
Experience: NA
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: Strong organizational skills necessary.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

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

Job Overview

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

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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

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

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

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

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

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

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

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

· Perform other related duties as assigned

QUALIFICATIONS:

· Education: Bachelor’ degree (B.S.) preferred

· Experience: Minimum of 0 to 1 years laboratory experience

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

· Certification/Licensure: Must have valid, state-issued, driver’s license.

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

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Sample Processing Material Technician (Wayne, PA, US, 19087)

Job Overview

Responsible for performing a wide variety of tasks involved in sample reception and other related sample processing activities, inventory management of client-supplied sample and other materials, and internal and external cell banks. Specific activities include, but are not limited to: sample receipt, inspection, distribution, storage, shipping, disposal and inventory of client sample materials. Additionally, completes follow-up and coordination activities with Project Management, Operational Labs and clients in support of the sample testing and storage materials.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform daily tasks including sample receipt, storage, distribution and shipment of materials.
Support other laboratory technicians by receiving and distributing internal samples and seed banks, receiving and quarantining materials.
Manage inventory of client-supplied sample materials, client cell banks and internal cell banks.
Create, update, and monitor client storage files and internal seed bank files.
Perform periodic inventory reconciliation activities as directed by Sample Processing Management team.
Perform data entry into the Laboratory Information Management System (LIMS) to record all sample material transactions in accordance with Sample Processing Standard Operating Procedures (SOPs).
Complete follow-up correspondence with Project Management and Operational Labs to ensure the sample reception process can be completed in a timely and accurate manner.
Must regularly communicate with associates / technicians / clients to ensure timely and accurate information flow related to all sample processing activities.
Maintain proper documentation including training records, room monitoring, cleaning and equipment logbooks in accordance with SOPs.
Maintain current knowledge of relevant Federal and State regulations.
Perform all other related duties as assigned.

Qualifications

Education: Bachelor's degree (B.A./B.S.) or equivalent in scientific discipline preferred.
Experience: 0 to 2 years related experience in a laboratory environment.
Other: Able to work independently under minimal supervision. Knowledge of GMPs/GLPs required. Ability to communicate verbally and through written correspondence. Work is highly computer system oriented.

The pay for this position is $23.51 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.

Glassware Technician (Wayne, PA, US, 19087)

Job Overview

Perform daily activities as they relate to glassware processing and autoclave sterilization activities. Always ensuring the associated laboratory spaces are well
organized, and in compliance with site procedures, site proper health and safety requirements and cGMP regulatory expectations. Follow cGMP documentation and processing of operational materials for cleaning of glassware and sterilization of dry goods and liquids to constantly meet the operational demand of the laboratories and ensure business continuity.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage autoclave room activities including autoclaving, documentation, and disposal of laboratory trash.
• Perform proper washing and sterilization of laboratory glassware.
• Perform general cleaning and maintenance of autoclave and glassware lab spaces.
• Provide operational support duties such as delivery of clean and/or sterilized glassware to operational owners, media preparation, equipment monitoring, and administrative duties.
• Position may include parameter monitoring duties and general microbiology assay support during requalification events for equipment.
• Perform all other related duties as assigned.

Qualifications

• Education: High school diploma or General Education Degree (G.E.D)
• Experience: One to two years related experience. Experience in a laboratory support environment preferred.
• Certification/Licensure: None
• Other: Excellent communication skills both written and verbal are required. Use of a computer and Microsoft Word and Excel preferred.

The pay for this position is $19.32 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.

Project Manager (Wayne, PA, US, 19087)

Job Overview

Manage communication for client projects, including workflow, technical details, and deliverables necessary to meet project timelines and budgets. Collaborate cross-functionally with sales, client services, scientists, operational managers, finance, and quality assurance colleagues to ensure accurate tracking and reporting of project timelines, scope, and budget; oversee and implement change controls, when needed. Deliver exceptional product quality and customer service through frequent and open communications with internal and external stakeholders.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Act as a central conduit for project communications between clients and Charles River staff for biologics testing projects. Coordinate project update meetings, calls, and status reports and create detailed meeting minutes; publish, and track, deliverables, and action items.
Coordinate project start-up and key tasks such as kick-off meetings, project scheduling, and document and material transfers.
Develop and maintain project timelines through collaboration with technical leads and site schedulers.
Partner with operations/technical management to prioritize ongoing work to manage and meet competing project deadlines.
Ensure accurate and efficient in-take and log-in of client samples and material; ensure compliance with internal SOPs and timelines to enable timely initiation of client testing.
Collaborate with cross-functional representatives to track and disseminate ongoing project status, including additions and changes to the scope of work, for cost and billing purposes.
Manage and control project scope, timelines, and budget, and when appropriate, submit scope changes and SOW revisions/amendments to client services team.
Collaborate with sales colleagues to submit new SOW requests to client services team; may assist with scope and pricing reviews.
Utilize project management software that allows timely and open communication of project status to all stakeholders.
Update various information systems related to project and customer data such as project trackers, timelines, and LIMS.
Oversee delivery of final reports and project documents to clients; monitor and track these tasks when completed by non-PM teams or staff.
Collaborate with laboratory, finance, and accounts payable departments to ensure accurate and timely client invoicing and verify project pricing and completion in LIMS/SAP.
Follow-up on discrepancies in client billing/invoicing and when needed request credit/debit memos to address billing errors.
Field and respond to customer requests, inquiries, and complaints; able to identify when escalation or help is needed and can engage the appropriate colleagues.
Participate in local/departmental committees and initiatives (i.e. process improvements, harmonization).
Ensure adherence to pertinent regulatory requirements and to departmental policies, GMP practices, and procedures [SOPs, safety procedures and biosafety protocols].
Perform all other related duties as assigned.

QUALIFICATIONS:

Education: Bachelor's degree (B.A./B.S.) or equivalent in project management, business, biological sciences, or related discipline.
Experience: minimum 4 years related experience in project management in a laboratory or research environment. Experience in a CRO/CMO preferred
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Ability to multi-task, excellent written and verbal communication skills, organizational skills, and attention to detail. Possess analytical thinking and problem-solving skills. Ability to prioritize and re-evaluate priorities as situations change. Working knowledge of computer software (MS Office, MS Teams, Excel, Smartsheet) and database experience preferred)

Compensation Data

The pay rate for this role is $65,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Physical Requirements

Equal Employment Opportunity

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

DNA Sequencing Analyst (Newark, DE, US, 19711)

Job Overview

Charles River Labs is seeking an experienced professional for a Data Sequencing Analyst, focused on Next Gen and Sanger Sequencing, position located in Newark, Delaware.

The Data Sequencing Analyst will be responsible for the analytical process work for the DNA sequence laboratory. Assemble all sequence data and generate identification reports. Ensure that all regulatory requirements and GMP compliance are adhered to.

The hours for this position are 10:00am-6:30pm.

Essential Duties and Responsibilities

Analyze, generate and evaluate identification reports with accuracy and precision meeting the standards of all accrediting and regulatory agencies.
Provide support for trouble shooting problems in the MALDI & sequencing laboratory.
Maintain and enhance sample tracking databases in accordance with SOPs.
Apply attention to detail in identification, record keeping and result verification.
Provide support for laboratory as needed.
Provide support for regulatory agencies as required.
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.

Qualifications

Education: Bachelor’s Degree (B.A. /B.S.) in Biological Science or related discipline required.
Experience: Three years of experience in Biology or related field. Laboratory, sequencing and data assembly experience is preferred. Experience in using sequencing software and/or NCBI a preferred.

The pay range for this position is $50k-60k. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

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

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.

Behavior Research Specialist (Poolesville, MD, US, 20837)

Job Overview

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

As the Behavior Research Specialist (Levels I, II) you will maintain, monitor and provide the necessary care to meet the needs of lab animal psychological well-being and behavioral health under the guidance of the DVR program. You will also maintain and monitor the health and physical environment of animals involving complex instructions and requiring technical expertise. May also support IACUC/Ethics Committee including animal welfare regulatory compliance and related government/external funding agency requirements.

Job Description

Additional responsibilities include:

Reviews, comprehends and complies with all SOP's and quality assurance standards pertaining to specific area.
Conduct behavioral assessments on NHPs as requested.
Establish pairs/social groups and monitor for compatibility. Maintaining the required goal of the QASP.
Use positive reinforcement to train animals for various husbandry and veterinary procedures.
Participate in discussions pertaining to enrichment.
Evaluate and implement novel behavioral data collection methodologies.
Prepare for incoming shipments of NHPs and work with animal care managers/staff on adjustments to husbandry.
Organize and maintain related data and demonstrate proficiency using computer programs; able to enter and/or interpret data in spreadsheets for data analyses.
Perform all other duties as assigned by management.
Occasional work with other species (such as but not limited to various ungulates and mice)

Job Qualifications

The following are minimum requirements related to the Behavior Research Specialist (Levels I, II) position:

Level I

Education: Bachelor's degree (BS) in a scientific discipline or an Associate's degree (AS/AA) and related practical experience.

Experience: A minimum of three (3) years of experience in a laboratory animal setting of which at least one (1) year preferred NHP (non-human primates) experience. Experience performing animal observations and behavioral assessments, as well as an understanding of the applications of positive reinforcement training, highly desired.

Level II

Education: BS or MS (preferred) degree in a scientific discipline or have an Associate's (AS/AA) degree and related practical experience.

Experience: Five years’ experience in a laboratory animal facility of which at least two (2) years preferred with NHP (non-human primates). Performing animal observations and behavior assessments highly desired; and an understanding of the applications of positive reinforcement training.

The pay range for this position is $33.00 to $35.00 USD per hour.  Please note the range covers levels I - II, salary will depend on level, in addition to factors such as experience, skills, and certification.

Equal Employment Opportunity

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

Veterinary Technician (Poolesville, MD, US, 20837)

Job Overview

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

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

Additional responsibilities include:

Reviews, comprehends, and participates in the development of all SOP's and quality assurance standards pertaining to specific area. Cares for and maintains laboratory animals in accordance with Animal Welfare Act and the “Guide for the Care and Use of Laboratory Animals, as well as, NIH policies and Guidelines and other pertinent regulations and policies.
Communicate with animal care staff, co-workers, veterinary staff, supervisors, PI, and collaborators.
Provides veterinary technical and surgical support for NHPs (e.g. animal handling and restraint, collect blood and other tissues samples, perform injections, treatments, surgical preparation, pre-, peri-, and post-operative observations, anesthesia, intubations, placement of indwelling catheters, femoral, and necropsy).
Provides research support to investigators via Technical Request forms.
Operates and maintains a variety of medical equipment (e.g. blood gas analyzer, CBC machine, x-ray, anesthetic machines, EKG monitors, blood pressure recorders, IV pumps, surgical and dentistry instruments, irradiator and sterilizers).
Arranges, cleans and maintains procedure, treatment, and necropsy/procedure rooms.
Quality Control of treatment and procedure rooms including cleaning, supplies, and monitoring expirations dates.

Responsibilities continued

Calculate drug dosages and administration frequencies.
Provides research support to investigators via Technical Request forms.
Accurately maintain electronic medical records and update treatment plans.
Monitors the environment and provides animal health surveillance as directed by facility veterinarian.
Assists in the maintenance and detailed documentation of accurate surgical, anesthetic and treatment procedures in the animal medical records and files. Assists in keeping medical records and files current through timely placement of information and supporting documents.
Quality Control of treatment and procedure rooms including cleaning, supplies, and monitoring expirations dates.
Provides limited support to the nonhuman primate environmental enrichment and psychological well-being plan, as needed in the absence of Behavioral staff.
Maintains and operates equipment and uses supplies according to SOPs and safety guidelines; performs general housekeeping and adheres to safety procedures. Complies with safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances.
Actively interacts with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance.
Maintains required attendance levels and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
Performs other duties as assigned.

Job Qualifications

Level I

Education: All candidates must possess a high school diploma or GED.

In addition, to qualify you must meet at least ONE of the following requirements:

AA in Veterinary Technology.
2-3 years' experience working with animals in biomedical research or companion veterinary medicine.
AALAS certification at the Laboratory Animal Technician (LAT) level.

Level II

Education: HS diploma or general education degree (GED) required. BS degree in Animal Science, Biology or similar, discipline or AA in Veterinary Technology preferred.
Experience: 3-5 years' experience working with animals (in biomedical research preferred), of which 1 year must be with non-human primates
Certification/Licensure: Eligible to take the AALAS Laboratory Animal Technician (LATG) certification.

The pay range for this position is $28.00 to $33.00 USD per hour.  Please note the range covers levels I - II, salary will depend on level, in addition to factors such as experience, skills, and certification.

Physical Demands & Work Environment

While performing the duties of this job, the employee is regularly required to walk, stand; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee frequently is required to stoop, kneel, crouch, or crawl. The employee is occasionally required to sit.
The employee must regularly lift and/or move up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus.
While performing the duties of this job, the employee is exposed to laboratory animal caging (non-human primates) and is regularly exposed to warm and/or humid conditions and chemicals.
The noise level in the work environment is usually moderate.
The employee works in various weather conditions.

Equal Employment Opportunity

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

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

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

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

• Jornada laboral de 40h 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.

Zootecnia de vivarios de investigación - Colaborador 1 1 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.

Primate Technician I (Frederick, MD, US, 21701)

Job Summary

This is an entry-level position where you can gain experience and begin your career in life sciences. Training provided!

Work schedule: Sunday - Thursday, 6:00am - 2:30pm or Tuesday - Saturday, 6:00am - 2:30pm

Responsibilities:

Providing food and water
Inspect feeding and watering devices for proper function
Cleaning and sanitizing cages and enclosures
Observe animals for overall health and wellbeing
Assisting with the movement of animals
Log animal care data and maintain accurate records
Other assigned duties, including restocking supplies

Work Environment & Physical Demands:

Work is performed in an warm, climate controlled environment.
PPE (protective equipment) includes regular use of surgical mask, cap, goggles, face shield, scrubs, and boots.
The warm setting, physicality of the job duties, and use of personal protective equipment (PPE), when combined, frequently cause employees to become hot and sweaty.
Job duties require employee to regularly stoop, crouch, kneel, and reach up with hands and arms to perform repetitive tasks, and walk and stand for extended periods of time.
Employee must be able to regularly lift, hold and/or move up to 50 pounds.

Job Qualifications

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

High School Diploma or GED preferred, but not required
Animal care experience preferred
Previous experience in a physically demanding role
Previous experience maintaining records and complying with regulations and Standard Operating Procedures (SOPs)
Strong attention to detail
Enjoys being part of a team
Flexible and available to work holidays (on rotational basis) and overtime as needed

The starting pay for this position is $19.75 per hour.

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

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.

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

Job Summary

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

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

Additional responsibilities include:

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

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

The pay for this position is $20.32 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 (B35) (Bethesda, MD, US, 20892)

Job Summary

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

The responsibilities of the Animal Care Technician I are to perform daily animal health observations, animal husbandry duties, to maintain the quality and health of research animals, to include performing daily water bottle and cage checks, cage changing and/or cage cleaning as required; providing food and water; and recording health concerns.

In addition:

Maintain accurate records of animal breeding, housing, or support areas.
Receive, inspect, and house incoming animals.
Assist with restraint, handling, and manipulation of various animal species.
May become involved in breeding and weaning procedures.
Monitor personnel and equipment entry into various rooms.
Operate required equipment and performs general housekeeping.

Job Qualifications

A candidate that possesses a high school diploma or general education degree is preferred; experience performing basic animal care desired. Interest in achieving ALAT certification upon eligibility.

The pay for this position is $22.50 USD per hour.

Equal Employment Opportunity

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

Cagewash Technician I (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.

Job Qualifications

A candidate that possesses a high school diploma or general education degree preferred. Experience and/or training working with mechanical equipment preferred.

The pay for this position is $20.50 USD per hour.

Equal Employment Opportunity

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

Animal Support Technician I (Bethesda, MD, US, 20892)

Job Summary

The Animal Support Technician I will maintain and monitor the health, production and physical environment within multiple client’s lab animal facilities. Perform animal care and husbandry, to include daily equipment checks; providing appropriate food and water; performing cage changing and/or cage cleaning; cage wash duties and sanitation. Provide environmental enrichment appropriate to species.

Additional responsibilities include:

Maintain accurate records of animal breeding, health, and housing/isolator or support areas.
Record animal health concerns and administer treatment as prescribed.
Animal care may include a variety of species.
Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility/attending veterinarian.
Follow all procedures necessary to properly maintain animal housing areas, including room or facility personnel entry; personnel protective equipment use, and sanitation/decontamination of equipment and materials.
Receive, inspect and house incoming animals.
Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adhere to safety procedures.
Sanitize, maintain, and repair caging materials as directed. Maintain cage wash facilities in a clean and organized manner.
This is a floater role that provides support to IS clients in Bethesda on the NIH campus. It may also be tasked with supporting sites in Poolesville, Gaithersburg, Baltimore, or DC. Most of the support will be in Bethesda.

Job Qualifications

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

Associate’s degree (A.A/A.S) in biology, animal science or related with a minimum of 6 months’ animal handling experience required.
Bachelor’s degree (B.A./B.S.) in biology, animal science or related field no experience required.
AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) preferred.
Must have valid driver’s license and reliable transportation.

The pay range for this position is $20.32 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.

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

Job Qualification

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.

Job Description

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 $20.25 USD per hour.

Equal Employment Opportunity

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

Animal Support Technician I (Bethesda, MD, US, 20892)

Job Summary

Additional responsibilities include:

Maintain accurate records of animal breeding, health, and housing/isolator or support areas.
Record animal health concerns and administer treatment as prescribed.
Animal care may include a variety of species.
Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility/attending veterinarian.
Follow all procedures necessary to properly maintain animal housing areas, including room or facility personnel entry; personnel protective equipment use, and sanitation/decontamination of equipment and materials.
Receive, inspect and house incoming animals.
Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adhere to safety procedures.
Sanitize, maintain, and repair caging materials as directed. Maintain cage wash facilities in a clean and organized manner.
This is a floater role that provides support to IS clients in Bethesda on the NIH campus. It may also be tasked with supporting sites in Poolesville, Gaithersburg, Baltimore, or DC. Most of the support will be in Bethesda.

Job Qualifications

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

Associate’s degree (A.A/A.S) in biology, animal science or related with a minimum of 6 months’ animal handling experience required.
Bachelor’s degree (B.A./B.S.) in biology, animal science or related field no experience required.
AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) preferred.
Must have valid driver’s license and reliable transportation.

The pay range for this position is $20.32 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.

Animal Support Technician I (Bethesda, MD, US, 20892)

Job Description

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

Additional responsibilities include:

Maintain accurate records of animal breeding, health, and housing/isolator or support areas.
Record animal health concerns and administer treatment as prescribed.
Animal care may include a variety of species.
Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility/attending veterinarian.
Follow all procedures necessary to properly maintain animal housing areas, including room or facility personnel entry; personnel protective equipment use, and sanitation/decontamination of equipment and materials.
Receive, inspect and house incoming animals.
Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adhere to safety procedures.
Sanitize, maintain, and repair caging materials as directed. Maintain cage wash facilities in a clean and organized manner.
This is a floater role that provides support to IS clients in Bethesda on the NIH campus. It may also be tasked with supporting sites in Poolesville, Gaithersburg, Baltimore, or DC. Most of the support will be in Bethesda.

Job Qualifications

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

Associate’s degree (A.A/A.S) in biology, animal science or related with a minimum of 6 months’ animal handling experience required.

Bachelor’s degree (B.A./B.S.) in biology, animal science or related field no experience required.

AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) preferred.

Must have valid driver’s license and reliable transportation.

The pay range for this position is $20.32 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.

Breeder Technician (Bethesda, MD, US, 20892)

Job Description

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

As a Breeder Technician, you will monitor daily animal health and welfare while performing duties to maintain the quality and health of research animals, to include but not limited to water bottle, cage, food, and water checks; cage changes; utilizing microisolator techniques, as required; and recording animal health concerns while reporting to veterinary staff.

Additional responsibilities include:

Maintain accurate records of animal breeding, health, and housing/isolator or support areas. Follow breeding and weaning procedures to ensure required production levels.
Perform technical support to include, but not limited to animal handling and restraint, weaning, tail snips, ear tagging, blood collection, tissue collection, time-mating, rodent breeding colony management as needed, as well as assist with research procedures.
Provide rodent identification using various techniques. Assist veterinary staff with providing blood collection, clinical and post-operative care, and observations. Ability to use an anesthesia machine and monitor anesthetized rodents.
Receive, inspect, and house incoming animals, and complete related receiving duties.
Perform cleaning and sanitation of work areas and facility equipment.
Provide customer service to research staff and complete submitted service requests.
General housekeeping.
Assist with receipt, stocking, and maintenance of supply inventories.

Job Qualifications

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

High school diploma or GED plus 3 years lab animal (rodent) experience or AA/AS degree plus 2 years lab animal (rodent) experience or BA/BS degree or higher and 1 year lab animal (rodent) experience.
AALAS certification eligibility at the LAT level required, existing LAT certification preferred. (HS Diploma + 3 years lab animal experience, AS + 2 years lab animal experience, BS +1 year lab animal experience, or ALAT certification + 6 month lab animal experience)
Proficient in computer (MS Office Suite)

The pay range for this position is $25.00 USD per hour.

Equal Employment Opportunity

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

Animal Care Technician I (Bethesda, MD, US, 20892)

Job Description

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

The responsibilities of the Animal Care Technician I are to perform daily animal health observations, animal husbandry duties, to maintain the quality and health of research animals, to include performing daily water bottle and cage checks, cage changing and/or cage cleaning as required; providing food and water; and recording health concerns.

In addition:

Maintain accurate records of animal breeding, housing, or support areas.
Receive, inspect, and house incoming animals.
Assist with restraint, handling, and manipulation of various animal species.
May become involved in breeding and weaning procedures.
Monitor personnel and equipment entry into various rooms.
Operate required equipment and performs general housekeeping.

Job Qualifications

A candidate that possesses a high school diploma or general education degree is preferred; experience performing basic animal care desired. Interest in achieving ALAT certification upon eligibility.

The pay for this position is $22.50 USD per hour.

Equal Employment Opportunity

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

Animal Caretaker (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker to join our Insourcing Solutions team located in Baltimore, MD.

As the Animal Caretaker, you will provide basic husbandry to rodents and lagomorphs, monitor environmental parameters for abnormalities and provide customer assistance to the investigative staff.

Additional responsibilities include:

- Perform daily animal husbandry duties to maintain quality and health of research animals, including: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning.

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $21.00 USD per hour.

The schedule is Monday through Friday 7AM-3:30PM, must be available to work some weekends and holidays when necessary.

Equal Employment Opportunity

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

Addetto alla cura degli animali da laboratorio - VERONA (part-time) (Verona, IT, 37135)

Riepilogo del lavoro

Per nostro cliente sito in Verona ricerchiamo un Animal Caretaker con contratto part-time

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;

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro con contratto a chiamata
Buona conoscenza del pacchetto office

Insourcing Solutions

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 orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

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.

Technicien·ne, Nécropsie - Senneville (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

Prosecteur·trice - Nécropsie

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) ou 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.).
La lecture et l'écriture de l'anglais sont requis. Le bilinguisme français et anglais est préférable.

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?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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 5 jours de congé personnel;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Formations de développement payées;
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.

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

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

Animal Care Attendant - Senneville Location (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: $19 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Start time mostly around 9-10AM. Weekend rotations and holidays with overtime on evenings or nights when needed;
Permanent position, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Animalier·ère - Site de Senneville (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Animalier·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.

Élémens 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: 19 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire: Heure de début majoritairement vers 9h-10h. Fin de semaine en rotation et 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?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Laboratory Clerck - Sample Processing - Student position (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Overview

As a Student Laboratory Clerk for our Sample Processing team located in Senneville, you will mainly be responsible for sample preparation, retrieving all specimens and transport them in a timely manner to the laboratory. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Prepares the required material for the study conduct according to information received and keep a functional inventory of the required material
Conduct the preparation and the distribution of biological samples
Perform the filing, archiving, transfer, or disposal of material
Printing and labelling of samples (blood, urine, etc.)
Retrieving and transportation of collected samples to the appropriate laboratory

Key Elements

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

High School diploma or equivalent
Passion for science
Good attention to details
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.)
Understanding of written English is mandatory. Bilingualism French and English is preferable

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: $17.50 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Weekdays, between Monday to Friday. Depending on the needs, you may have to do overtime on weekends
Temporary position for the summer period, full-time at 37.5hrs per week, possibility to stay part time after summer to be discussed (minimum 1 day/weekend + holiday).

Why Charles River ?

Free gym on site
Cafeteria 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.

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.

Equal Employment Opportunity

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

Commis de laboratoire - Traitement des échantillons - poste étudiant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Commis de laboratoire étudiant pour notre équipe de Traitement des échantillons situé à notre site de Senneville, vous serez principalement responsable de la préparation des échantillons, de la récupération de tous les échantillons et de leur transport en temps voulu vers le laboratoire. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Prépare le matériel nécessaire pour le déroulement des études selon les informations reçues et veillez à l’approvisionnement nécessaire du matériel
Faire la préparation et la distribution des échantillons biologiques
Effectue le classement, l’archivage, le transfert ou la disposition de matériel
Impression et étiquetage des échantillons (sang, urine, etc.)
Récupération et transport des échantillons collectés vers le laboratoire approprié

Éléments Clés

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

Diplôme d’études secondaires ou l’équivalent
Passion pour les sciences
Bonne attention aux détails
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.)
La compréhension de la lecture en anglais est obligatoire. Le bilinguisme français et anglais est préférable

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: 17.50 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire : Horaire de jour en semaine du lundi au vendredi. En fonction des besoins, vous pourriez avoir à effectuer du temps supplémentaire les fins de semaine
Poste temporaire pour la période estivale, temps plein à 37.5hrs par semaine. Possibilité de rester à temps partiel à l’automne à discuter.

Pourquoi Charles River?

Gym gratuit sur place
Cafétéria 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.

In Vivo 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: $23.50 per hour with primes of;
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- 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.

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.

Equal Employment Opportunity

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

Technicien.ne In Vivo (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire du poste

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.);
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: 23.50$ de l’heure avec des primes de:
- Soirée: 2.50$;
- Fin de semaine: $2.75;
- Heure supplémentaire: Temps et demi;
- 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.

Commis de laboratoire - Traitement des échantillons (Montreal (Senneville), Quebec, CA, H9X 3R3)

Aperçu du poste

En tant qu’Assistant·e de laboratoire pour notre équipe de Traitement des échantillons situé à notre site de Senneville, vous serez principalement responsable de la préparation des échantillons, de la récupération de tous les échantillons et de leur transport en temps voulu vers le laboratoire. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Prépare le matériel nécessaire pour le déroulement des études selon les informations reçues et veillez à l’approvisionnement nécessaire du matériel;
Faire la préparation et la distribution des échantillons biologiques;
Effectue le classement, l’archivage, le transfert ou la disposition de matériel;
Impression et étiquetage des échantillons (sang, urine, etc.);
Récupération et transport des échantillons collectés vers le laboratoire approprié.

Éléments Clés

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

Diplôme d’études secondaires ou l’équivalent;
Passion pour les sciences;
Bonne attention aux détails;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

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 : 17.50$/hrs;
Bonus annuel basé sur la performance;
Primes : Fin de semaine (2.75$/hrs), temps supplémentaires (temps et demi);
Horaire : Horaire de jour en semaine du lundi au vendredi. En fonction des besoins, vous pourriez avoir à effectuer du temps supplémentaire les fins de semaine;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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 5 jours de congé personnel;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Formations de développement payées;
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.

Laboratory Clerk - Sample processing (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Laboratory Assistant for our Sample Processing team located in Senneville, you will mainly be responsible for sample preparation, retrieving all specimens and transport them in a timely manner to the laboratory. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Prepares the required material for the study conduct according to information received and keep a functional inventory of the required material;
Conduct the preparation and the distribution of biological samples;
Perform the filing, archiving, transfer, or disposal of material;
Printing and labelling of samples (blood, urine, etc.);
Retrieving and transportation of collected samples to the appropriate laboratory.

Key Elements

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

High School diploma or equivalent;
Passion for science;
Good attention to details;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: 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: $17.50/hrs;
Annual bonus based on performance;
Premiums: Weekends: ($2.75/hrs), Overtime (Time and a half);
Schedule: Weekdays, between Monday to Friday. Depending on the needs, you may have to do overtime and work on weekends;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
3 weeks’ Vacation & 5 Personal day policy;
Access to a doctor and various health professionals (telemedicine);
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Paid development training;
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.

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.

Equal Employment Opportunity

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

Technician, Necropsy - Senneville Location (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Prosector - Necropsy

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 (any other Biology related field) or 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.).
Reading and writing English is required. Bilingualism French and English is preferable.

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 ?

We offer competitive benefits and advantages from day one to support your well-being;
Employee and family assistance program;
3 weeks’ Vacation & 5 Personal day policy;
Access to a doctor and various health professionals (telemedicine);
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Paid development training;
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.

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.

Equal Employment Opportunity

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

Senior Equipment & Validation Engineer / Team Lead (Singapore, SG)

Job Overview

This role’s focus is on the provision of technical guidance, planning, coordinating and resourcing validation projects on-site. He/She ensures the qualification and validation of equipment, facilities, utilities, and processes are carried out in accordance with cGMP and ISO 17025 guidelines. This role is also expected to lead projects with various stakeholders and will be responsible for a small team to deliver results and projects for the site.

Job Description

DUTIES AND RESPONSIBILITIES

Manage and lead parts, if not all of the lifecycle for validation projects, including but not limited to; delivering on time, to specification and ensuring the delivery of a quality validation project.
Responsible for leading, guiding and preparing the installation of and revising test validation procedures/protocols in accordance with appropriate regulatory agency validation requirements, corporate, internal company standards and current industry standards
Lead, plan, communicate, coordinate and execute simple and complex projects within Charles River Singapore and other sites by using planning tools like Gantt chart and other Project Management Tools.
Write or assist in writing of SOPs for Equipment and Facility related Validation Projects.
Participate in validation project meetings, workshops, training of staff and production of related documentation.
Lead evaluation of Systems from different vendors for submission of Capital budgetary papers, and to recommend the most appropriate systems, based on User Requirement Specification, and/or other specifications as required from site management and project.
Provide progress reports on Projects and communicate with relevant stakeholders.
Manage direct relationships with key project stakeholders.
Lead and self-initiate projects to improve efficiency and productivity of the processes.
Represent the Department in client audits as required as a SME.
Independently perform investigations as required and effective apply 6M or Ishikawa fishbone diagram, or any other applicable tools for Root Cause Analysis and evaluate practicality of actions to be applied.
Able to communicate investigations succinctly and accurately.
Monitor and trend cost expenditure over a defined period for monitoring of cost effectiveness for the department.
Maintains proper records and documentation of activities that are compliant with good documentation practices, continuous compliance ISO/IEC 17025, cGMP, PIC/S, ISPE Guidelines, WHO Technical Reports, Company global SOPs and other data integrity principles for all activities.
To work closely with all departments to ensure the operation of a validated environment according to existing QMS and/or other regulatory requirements.
Performs all functions as tasked with high degree of accuracy and strict adherence to company’s quality requirements.
Reviews aspects/areas for improvement within your own duties/responsibilities and make recommendations to your line manager for your own or team improvements.
Adheres to Company Policies and Procedures.
Undertakes any other duty or responsibility, at the request of your manager that may be required within reason within the remit of your role.

General requirements

Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements.
Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements.
Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements.
Performs all other related duties as assigned.

Qualification

Education: Possesses at minimum, a degree in Engineering, Biomedical Sciences or any related field.
Experience:
1. Minimum ≥ 5 years of relevant experience working in an ISO17025 / GMP environment is preferred.
2. Understanding of IT is expected, related to installation of software, interface of hardware and software and basic administrative controls of Windows (Such as adding user groups) is preferred.
3. Understand concepts and rationale, and execute System Commissioning, Qualification and Validation for systems as per requirements stated in ISPE GAMP 5 and USP <1058> document is required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Others:
1. Effective communication and supervisory skills
2. Ability to organize and prioritize work to meet deadlines
3. Ability to read, write, speak and understand English

Equal Employment Opportunity

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

Clinical Veterinary Surgeon 2 (Tranent, GB, EH33 2NE)

Job Summary

An exciting opportunity has arisen for a veterinarian to join our dedicated team passionate about animal welfare. We are a growing group of 5 vets plus dedicated support staff.

At Charles River, we take a passionate approach to improving human and animal health. Our motivating force is the knowledge that our high quality of work provides people with the potential to live healthier and better lives. Scientific excellence and outstanding customer service are the hallmarks of Charles River.

As one of the world’s largest Contract Research Organisations with more than 7000 employees and a market leader in the development of novel human and veterinary medicines, Charles River can offer you the chance to build on your skills and knowledge and work with world-class experts. With more than 60 facilities in 16 countries, we have built a company uniquely designed to meet the needs of our clients in the Pharmaceutical, Biotechnology, Veterinary Medicine, and Agrochemical sectors.

At our world class preclinical facility in Elphinstone, Tranent (close to Edinburgh), our Department of Veterinary Services provides expert advice on animal health and welfare in a diverse mix of laboratory and farm animal species.

Acting as a deputy Named Veterinary Surgeon in accordance with the Animals (Scientific Procedures) Act, you will provide clinical care services to the broad range species at our site in Tranent. As a laboratory animal veterinarian, you are the advocate for the animals, you will use your clinical and interpersonal skills to ensure delivery of the highest standards of welfare, ethical consideration, and compliance in association with the Animal Welfare and Ethical Review Body.

You will assist in the conduct of clinical work across site, including medical and surgical case management, as well as supporting our studies by provision of specialist veterinary services in fields such as anaesthesia, surgery, and ophthalmology.

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.

Job Qualifications

Eligibility for membership of the Royal College of Veterinary Surgeons and a relevant clinical work experience is essential.

You will have graduated with a Veterinary degree and have good observational and fine motor skills. You will have established skills in medicine and surgery translatable to the species you will be working with and the drive to expand your skillset. You will have the confidence and ability to communicate effectively with internal and external clients, as well as regulatory bodies. Previous experience in the laboratory animal field would be advantageous, although full training will be provided.

Participation in an out of hours on-call rota will be required although this is not onerous.

In return we offer a competitive salary and benefits package and a real commitment to your training and development needs. This includes the opportunity for undertaking, publishing and presenting relevant personal research, as we support and encourage you to develop your veterinary career.

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.

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

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

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

Assistant Animal Technician 1 (Tranent, GB, EH33 2NE)

Job Summary

We are looking to expand our team of Animal Technicians at our world class facility here at Tranent.

We are a progressive and close-knit team, working hard to ensure the safety of new medicines which target life threating and debilitating diseases and especially proud of our contribution in developing the Covid-19 vaccines. We are passionate about our animals, striving to provide the best possible care with a culture of continuous improvement.

Candidates must have a passion for working with animals and share our commitment to their welfare. In this role you will perform routine and moderately complex animal husbandry and clinical observations in a regulatory compliant laboratory setting. You should have a minimum of 4 Nat 5 or equivalent qualifications.

In return we provide all the training and support you need. A positive attitude with a good work ethic is essential, as we need reliable individuals with a good attendance record.

This is a physically demanding role so you need to know you will be active and on your feet for most of the working day. Here are some of things you will be involved with as an Animal Technician:

Husbandry duties / delivering essential care and well-being services to the animals
Positive interaction with animals, including providing treats, fruits and vegetables
Participating in animal training programmes
Handling animals for procedures
Performing physical environment cleanliness and upkeep and maintaining accurate records
Documenting animal behaviours and activities

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 all across the globe.

In return, we’ll help you build a career with a progressive and dynamic global company by providing full on-site training, a structured career path and starting pay of £12.60 per hour (annual salary of £23,842), and a generous benefits package including an 8% employer contribution pension scheme, volunteering and bonus opportunities.

Profile and Requirements

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

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

Assistant Study Coordinator (Tranent, GB, EH33 2NE)

Job Overview

We have an exciting opportunity for an Assistant Study Coordinator to join our friendly Toxicology Administration & Reporting department. This role is full time, on site (with hybrid options after a period of training), and is located in our world class facility in Tranent (EH33 2NE).

The role is well suited to an individual who enjoys collaborating with others, organisation, working to tight timescales, and who would like to build a career supporting scientific studies. You will work closely with Study Directors and cross functional teams, and have the chance to grow and progress through a clear departmental development career pathway.

This role is offered Full time, the Salary of £25,352.56 per annum as well as 29 days paid Holidays, Pension, Private Healthcare, Health Insurance, Employee discount scheme, Free Gym on site, Cafeteria with great food, Free onsite parking and more.

Key Responsibilities and Experience

Key Responsibilities

Work collaboratively with Study Directors to develop study protocol and other relevant study documentation
Set up, schedule and assist in the running of a variety of Toxicology studies.
Liaise with various contributing areas to the study to schedule in all key activities required.
Serves as a contact, along with the Study Director, in communication and interactions with other departments, with assistance as applicable

Experience and requirements

Experience in a busy office environment.
Strong technical experience in Microsoft Office.
Proven organisational skills with the ability to work within tight timeframes.
Good, confident communication and people skills which enable you to effectively collaborate with internal/external employees of all levels.
A proactive working style with the ability to plan ahead.

Equal Employment Opportunity

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

Sample Shipping Coordinator (Tranent, GB, EH33 2NE)

Job Overview

We have an exciting career opportunity for a Sample Shipping Co-Ordinator. This role is full time, on site and is located in our world class facility in Tranent (EH33 2NE).

Are you highly organised, detail‑driven, and experienced in shipping scientific materials?
In this hands‑on role, as a Sample Shipping Coordinator for the Sample Shipping Logistics team located at the Edinburgh site, you will play a critical part in the coordination and shipment of biological samples and test/control materials that support vital scientific studies.

You will work closely with Internal team, couriers, and global consignees, you’ll ensure shipments are prepared accurately, compliant with regulations, and delivered on time.
This is an excellent opportunity for someone who thrives in a fast‑paced, regulated environment, enjoys working with precision, and takes pride in delivering high‑quality work that directly supports research and compliance.

This role is offered initially on a 9 month Fixed term basis with a possibility of the role being extended, The Salary of £25,352.5622 per annum as well as Paid Holidays (pro-rata based on contract duration), Pension, Private Healthcare, Health Insurance, Employee Discount Scheme, Free Gym on site, Cafeteria with great food, Free onsite parking and more

Key Responsibilities and Experience

Key Responsibilities

Verify and organize Samples and Test Materials for Shipment
Shipment Packing/Labeling/Marking and tracking
Deal with Study directors to plan shipment of their study materials
Verify and organize shipment through border via company courier
Fill in appropriate documentation for shipment purposes
Liaise with consignees to ensure they have their import requirements in place
Understanding and assigning relevant HTS codes to materials
Understanding and assigning cost to shipments
Ensure that work is performed in accordance with the requirements of a study plan and in full compliance with GLP, where these conditions apply

Experience and requirements

Experience in shipping biological samples or test materials
IATA certification is an asset
Knowledge and application of GLP
Ability to work in a fast-paced environment with time constraints and requirements to adapt to change.
Work with precision, pay attention to detail, and strive for quality work.
Detail oriented and meticulous
Manual handling – this role is focused on moving and handling of items and will require moving and handling of equipment and shipping items

Equal Employment Opportunity

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

Cleaner (Tranent, GB, EH33 2NE)

Job Description

We are looking to recruit a Cleaner for our site in Tranent facility EH33 2NE, Edinburgh.

The shift pattern is Monday to Friday 07:30 – 15:30 and will require the successful candidate to be on site.
Own transport would be beneficial to be able to get to site due to the location.

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

This is a full-time position (36.25 hours per week) however, part-time hours will be considered.
The salary for the role is £24,050.50 per annum, Paid monthly as well as employee benefits like private healthcare, Pension, Free Gym on site, Subsidised Cafeteria and others.

Equal Employment Opportunity

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

Cleaner (Edinburgh, GB, EH14 4AP)

Job Description

We are looking to recruit a Cleaner for our site in Riccarton site, EH14 4AP, Edinburgh.

The shift pattern is Monday to Friday 07:30 – 15:30 and will require the successful candidate to be on site
Own transport would be beneficial to be able to get to site due to the location.

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

Equal Employment Opportunity

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

Animalier·ière - Poste étudiant (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire du poste

Étudiant·e d’été en Soins aux Animaux –Aucune Expérience requise.

En tant qu’Étudiant·e d’été en Soins aux Animaux pour notre équipe de Toxicologie à notre site de Sherbrooke, vous aurez la charge de veiller au bien-être de tous nos animaux ainsi qu’à intégrité de nos études pré-cliniques.

Dans ce rôle, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie
Assister les techniciens dans leurs tâches quotidiennes
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux

Éléments Clés

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

Capable de suivre des instructions précises.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.
Être étudiant·e en Santé Animale, Bioécologie ou autre domaine relié aux Sciences est un atout. Stage Alternance Travail Étude possible.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation : 1580 Rue Ida-Métivier, Sherbrooke (Qc), J1E 0B5.
Transport: Facilement accessible par le transport en commun (Rabais avec la Société des Transport de Sherbrooke). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire: 19.00 $ de l’heure
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire : Poste d’été (30 à 37.5HR/semaine). Possibilité de rester à l’automne à discuter. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire.

Pourquoi Charles River?

Congés Personnels
Gym sur place et gratuit
Plusieurs activités sociales

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

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

Animal Care Technician -Student (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Student - Animal Care - No experience necessary

As a Student in Animal Care for our Toxicology team in Sherbrooke, you will be responsible of ensuring the welfare of the animals and the integrity of our pre-clinical studies.

In this role, key responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry.
Assist the technicians in their daily tasks .
Handle animals.
Participate in the physical/social activities of the animals.

Key Elements

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

Able to follow precises instructions.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.
Passionate about animals.
Be a student in Animal Health, Bioecology or in sciences related is an asset. ATE internship possible.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Job specific information:

Location: 1580 Ida Métivier, Sherbrooke (Qc), J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Pay: $19.00 per hour.
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: During summer (30 to 37.5 hours/week), possibility to stay after school to be discuss. Depending on the needs, you may have to do overtime.

Why Charles River?

Personal Days
Free gym on site;
Many social activities!

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!

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

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

Equal Employment Opportunity

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

Sample Management - Technician (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Technician – Sample Management

As a Technician for our Sample Management team at the Sherbrooke location, you will be performing sample management activities and follow directives from the study plans.

In this role, primary responsibilities include:

Perform reception, verification, storage, data review and sample inventories using the Watson LIMS® computer system;
Generate study data base in the Watson LIMS® computer system;
Communicate with clients and testing facilities to inform them of the planned sample shipment schedule as well as all outgoing shipments, to send them the confirmation of receipt of external samples and to provide any other information as needed;
Perform the preparation of the sample shipments to other locations, the archival preparation or disposition of the samples, as well as all follow-ups attached to these tasks.
Perform the sample preparation centrifugation and decantation.

Key Elements

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

College or Bachelor diploma in a relevant field;
Being able to perform repetitive motions such as handling frozen samples several times during the day;
Being able to move around in the freezer room, the office area and in the shipping area;
Good working knowledge of computers;
Ability to quickly adapt to changes based on priorities;
Flexibility and ability to work independently or in collaboration.
Understanding written English is required.

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: 21.50$/hrs
Schedule: Mostly Monday to Friday, depending on the needs, you may have to do overtime and work on Ween-ends (prime 2.75$/h).
Permanent position, 37.5hrs per week

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Free gym on site;
Cafeteria on site;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ vacation & 5 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.

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.

Equal Employment Opportunity

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

Technicien·ne en Gestion des échantillons (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Technicien·ne - Gestion des échantillons

En tant que Technicien·ne pour notre équipe de Gestion des échantillons située au site de Sherbrooke, vous serez responsable d’accomplir les tâches de gestion des échantillons et suivre les directives des plans d’étude.

Dans ce poste, les principales responsabilités incluront:

Effectuer la réception, la vérification, l’entreposage, la révision des données et les inventaires des échantillons reçus en utilisant le système informatique Watson LIMS®;
Créer les bases de données des profils d’étude dans notre système informatique Watson LIMS®;
Communiquer avec les clients et les sites de tests afin de les informer de la planification d’envoi des
échantillons en début d’étude et avant chaque envoie, afin de confirmer la réception des échantillons externes et pour fournir toutes autres informations selon les besoins;
Effectuer la préparation de la livraison des échantillons vers d’autres emplacements, la préparation d’archivage ou la disposition d’échantillons, ainsi que les suivis qui s’y rattachent.
Effectue la préparation, la centrifugation et la décantation des échantillons.

Éléments Clés

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

Diplôme d’étude collégiale, Attestation d’étude collégiale ou Baccalauréat dans un domaine pertinent au poste;
Connaissance pratique en informatique;
Être en mesure d’effectuer des mouvements répétitifs tels que la manipulation d’échantillons congelés de façon répétitive à plusieurs moments au cours de la journée;
Être en mesure de se déplacer dans la salle des congélateurs, dans les bureaux et dans le local d’expédition;
Capacité de s'adapter rapidement aux changements en fonction des priorités;
Faire preuve de flexibilité et être capable de travailler de manière autonome et en équipe
La compréhension de l’anglais écrit est requis.

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: 21.50$/hrs
Horaire: Horaire du Lundi au Vendredi la plupart du temps, selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire et travailler les fins de semaine (prime de 2.75$/h).
Poste permanent, 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payée;
Gym gratuit sur place;
Cafétéria sur place;
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 & 5 journées personnelles 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.

Animal Care Technician - Sherbrooke (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Animal Care Technician – On site training

As an Animal Care Technician for our Toxicology team for our site located in the city of Sherbrooke (QC), you will be responsible of ensuring the welfare of the animals and the integrity of our pre-clinical studies.

In this role, key responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry.
Assist the technicians in their daily tasks .
Handle animals.
Participate in the physical/social activities of the animals.

Key Elements

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

Able to follow precises instructions.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.
Passionate about animals.
High School Diploma (DES) required - Having an AEP in Animal Care is an asset.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Job specific information:

Location: 1580 Ida Métivier, Sherbrooke (Qc), J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Salary: Starting at 19.00$/hrs. Opportunity to start at higher level and higher salary with specific research experience.
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

We offer competitive benefits and advantages from day one to support your well-being;
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 want to contribute to the wellbeing of our communities across the country and around the world, join our team. 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.

Equal Employment Opportunity

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

Animalier·ère - Sherbrooke (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Technicien·ne en Soins aux Animaux – Formation sur place

En tant que Technicien·ne en Soins aux Animaux pour notre équipe de Toxicologie à notre site situé dans la ville de Sherbrooke, vous aurez la charge de veiller au bien-être de tous nos animaux ainsi qu’à intégrité de nos études pré-cliniques.

Dans ce rôle, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie
Assister les techniciens dans leurs tâches quotidiennes
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux

Éléments Clés

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

Capable de suivre des instructions précises.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.
Diplôme d'étude Secondaire (DES) requis - Diplôme AEP en soins animaliers est un atout.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation : 1580 Rue Ida-Métivier, Sherbrooke (Qc), J1E 0B5.
Transport: Facilement accessible par le transport en commun (Rabais avec la Société des Transport de Sherbrooke). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 19.00$/HR.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/HR).

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Superviseur.e, Services techniques InVivo (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Superviseur.e pour notre équipe de Services techniques InVivo à notre site de Laval, vous devrez encadrer, former et soutenir le personnel technique. Votre contribution assurera une efficacité maximale de l’équipe et aidera à résoudre les problèmes les plus difficiles.

Dans ce rôle, les principales responsabilités incluront:

Assurer le travail du personnel du département pour maximiser l’efficacité et la productivité;
Superviser le processus de formation et les opportunités de développement pour tout le personnel technique;
S’assurer que toutes les ressources sont disponibles et que l’environnement de travail est sécuritaire;
S’assurer que les procédures et les équipements sont conformes aux exigences des Bonnes Pratiques de Laboratoire (BPL).

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme d’études collégiales en Biologie, Science animales, en administration ou toutes autres disciplines connexes;
Au minimum de 3 à 5 ans d’expérience dans un ORC (Organisme de recherche sous contrat) ou bien en gestion de personnel avec une expérience de travail avec les animaux;
Bonnes aptitudes interpersonnelles et de communication;
Bonnes compétences en résolution de problème;
Bon sens de l’écoute et vision stratégique;
Le bilinguisme français et anglais est obligatoire.

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;
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 faire du temps supplémentaires et des fins de semaine;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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);
4 semaines de vacances & 10 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.

Supervisor, Technical Services InVivo (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Supervisor for our Technical Services InVivo group in Laval, you will have to coach, train, and support the technical staff. Your contribution will ensure maximum efficiency of the team and help resolve more challenging issues.

In this role, primary responsibilities include:

Ensure work of departmental staff to maximize efficiency and productivity;
Oversee the training process and developpment opportunities for all technical staff;
Ensure that all the resources are available, and that the working environment is safe;
Ensure that the procedures and equipment comply with Good Laboratory Practices (GLP).

Key Elements

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

Collegial diploma in Biology, Animal Health, Administration or any related discipline;
Minimum of 3 to 5 years’ experience in a CRO (Contract Research Organisation) or in management with experience working with animals;
Good interpersonal and communication skills;
Strong problem-solving skills;
Good listener and strategic vision;
Bilingualism French and English is required.

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. Depending on the business needs, you may have to do overtime and weekends;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ vacations & 10 sick/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.

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.

Equal Employment Opportunity

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

Animal Health Technician (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Animal Health Technician for our Toxicology team in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Collection of biological samples (blood, urine, etc.);
Data collection (body weight, food consumption, clinical signs, etc.);
Injections (subcutaneous, intramuscular, etc.);
Animal contention;
Animal room cleaning.

Key Elements

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

College Diploma in Animal Health - New graduates are welcome, no working experience required!;
College Diploma in Bioecology, Biology, Biotechnology, or any other related disciplines with experience in injections and/or blood collection on animals;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Good observation skills;
Problem solving skills.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: Starting at 23.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience;
Premiums: Weekends ($2.75), Overtime (time and a half), Holidays (double time);
Annual bonus based on performance;
Schedule: Flexible schedule, the candidate must be available during the day, evenings and weekends. Depending on the needs of the company, you may be required to work overtime, holidays and night shifts;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Technicien.ne en santé animale (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Technicien.ne en santé animale pour notre équipe de Toxicologie à notre site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Collecte d’échantillons biologiques (sang, urine, etc.);
Prise de données (prise de poids, consommation de nourriture, signes cliniques, etc.);
Injections (sous-cutanée, intramusculaire, etc.);
Manipulation des animaux;
Nettoyage des salles d’animaux.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en santé animale - Les nouveaux diplômés sont les bienvenus, aucune expérience de travail requise !;
Diplôme collégial en Bioécologie, Biologie, Biotechnologie ou toute autre discipline connexe avec expérience en injections et/ou prélèvements sanguins sur les animaux ;
Capacité à travailler physiquement (soulèvement jusqu'à 20 kg, marcher, rester debout, se pencher, etc.);
Bonnes capacités d'observation;
Compétences en résolution de problèmes.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 ;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: à partir de 23,50$/hrs. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Primes: Fin de semaine ($2.75), temps supplémentaires (temps et demi), jours fériés (temps double);
Bonus annuel basé sur la performance;
Horaire: Horaire flexible, le candidat doit être disponible de jour, de soir et de fin de semaine. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire, des jours fériés et des horaires de nuit;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Summer Student - Animal Food Room Clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

Summer Student position – Animal Food Room Clerk - No Experience required

As an Animal Food Room Clerk for our Toxicology team at the Laval location, you will perform food management and prepare daily enrichment given to animals in a way that respects established processes.

In this role, primary responsibilities include:

Perform the preparation of food, fruits and enrichment for animals to meet quality standards, while providing service to vivarium staff;
Maintain a clean and orderly work environment;
Report any problem or potential problem in the conduct of daily activities to the Supervisor or delegate;
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) and the Institutional Animal Care and Use Committee (IACUC) rules.

Key Elements

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

High School diploma or equivalence;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Able to follow precises instructions and procedures;
Ability to manage time effectively;
Ability to work autonomously.

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;
Temporary position, student job;
Schedule:
- Summer period: 37.5 hours/week. Monday to Friday daytime, but you may have to do some weekends on rotation depending on the needs.
- School period: 15 hours/week. Mostly on weekends, but you can provide more availabilities during the week depending on your schedule.

Why Charles River ?

Employee and family assistance program;
Excellent welcome program for new employees;
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.

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.

Equal Employment Opportunity

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

Étudiant.e d'été - Commis à la salle de nourriture pour animaux (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

Poste d’étudiant.e d’été – Commis à la salle de nourriture pour animaux – Aucune expérience requise.

En tant que Commis à la salle de nourriture pour animaux pour notre équipe de Toxicologie située au site de Laval, vous effectuerez la gestion de la nourriture et préparerez l’enrichissement quotidien donné aux animaux d’une manière qui respecte les processus établis.

Dans ce poste, les principales responsabilités incluront:

Effectuer la préparation des aliments, des fruits et des enrichissements pour les animaux afin de répondre aux normes de qualité, tout en offrant un service au personnel du vivarium;
Maintenir un environnement de travail propre et ordonné;
Signaler tout problème ou problème potentiel dans la conduite des activités quotidiennes au superviseur ou à son délégué;
Assurer l'intégrité des études et satisfaire aux exigences des organismes de réglementation en effectuant les activités conformément aux Bonnes Pratiques de Laboratoire (BPL), aux Procédures Opérationnelles Normalisées (PON) et aux règles du Comité institutionnel de soins et d'utilisation des animaux (CISUA).

Éléments clés

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

Diplôme d'études secondaires ou équivalent;
Capable de travailler physiquement (soulever jusqu'à 20 kg, marcher, se tenir debout, se pencher, etc.);
Capable de suivre des instructions et des procédures précises;
Capacité à gérer son temps efficacement;
Capacité à travailler de manière autonome.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: 18.25$/hrs;
Poste temporaire, emploi étudiant;
Horaire:
- Période estivale : 37.5 heures/semaine. Du lundi au vendredi de jour, mais vous pourriez devoir travailler certaines fins de semaine selon les besoins.
- Période scolaire : 15 heures/semaine. Principalement les fins de semaine, mais vous pouvez offrir plus de disponibilités pendant la semaine selon votre horaire.

Pourquoi Charles River?

Programme d'aide aux employé·es et à leur famille;
Excellent programme d’intégration à nos nouveaux employé·es;
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 (San Diego, CA, US, 92121)

JOB SUMMARY

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

As the Animal Care Technician II, you will observe, monitor, and document the health and physical environment within the CRADL animal facility, maintaining both routine and specialized aspects of husbandry. Perform daily animal care, while also providing study-specific services such as enrichment, breeding support, and technical husbandry needs. Maintain facility standards through proactive attention to biosecurity and compliance and collaborate with veterinary staff to ensure animal health and research protocols are supported in alignment with regulatory requirements.

Work schedule: Sunday-Thursday, 7:00 am – 3:30 pm

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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.

Cage Wash:
- Operate a washer for cleaning and sanitizing animal cage supplies through automatic processes.
- Operate autoclave machine 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, 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.
Animal Care:
- Apply SOPs, BOPs, and quality standards with increased independence, ensuring compliance during both routine and study-specific husbandry activities. Support training of ACT 1 staff by reinforcing proper use and interpretation of procedures.
- Monitor daily animal health and welfare while performing daily animal health observations with greater independence.
- 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.
- Dispose of biological, hazardous, and animal facility waste following established procedures.
- Dispose of biological, hazardous, and animal facility waste following established procedures.

Essential Duties and Responsibilities (Continued)

- Perform humane 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.
- Operate equipment and use supplies according to safety guidelines; perform general housekeeping (i.e. check pest traps, common area cleaning, testing eye wash stations and emergency showers) and adhere to safety procedures.
- Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility veterinarian.
- Independently receive, inspect, and house incoming animals based on site needs.
- May be involved in strictly maintaining and following breeding and weaning procedures to ensure appropriate production levels.
  - Cage card distribution including but not limited to printing cage cards for incoming shipments and requests from clients.
- Collect census data from animal cages, including but not limited to upload of manual census data, or upload data from handheld scanners into approved software and verify data prior to posting and reconciliation.
- Independently monitor client row assignments in shared animal holding rooms to ensure racks/rows are labeled and assigned correctly per facility needs.
Report non-compliance or animal welfare concerns to the appropriate Animal Welfare Team member or IACUC office.
Maintain an organized and clean work environment, including animal rooms, common areas, cage washrooms, procedure rooms, anterooms, storage areas, and grounds by cleaning at prescribed intervals based on site needs, and complete sanitation ATP monitoring based on SOPs.
Training and Development
- 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.
- Communicate procedural questions and self-identified training deficiencies to team lead or Facility Supervisor.
- Act as subject matter expert in animal husbandry and operations signed off as competent and instructed by Facility Supervisor.
Technical Services:
- - - Ability to perform or obtain competency in non-invasive technical procedures as required, such as body weights, food and water intact measurements, animal identification (e.g., ear tagging), tissue collection, dosing administration (SC, IP, PO) based on site needs.
    - Perform health surveillance sample collections based on site needs.
    - Perform post-surgical observations and associated record keeping.
- Maintain required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.
- Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

High school diploma or General Education Degree (G.E.D.).
A minimum of twelve (12) months directly related laboratory animal experience in a laboratory animal facility or basic technical skills (dosing, tissue collection).

PREFERRED QUALIFICATIONS:

Bachelor’s degree (B.A./B.S.) in animal or life sciences field.
Assistant Laboratory Animal Technician (ALAT) or Laboratory Animal Technician (LAT) certification.

The pay range for this position is $23.50-25.50 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.

Associate Director, Learning and Process Enablement (Wilmington, MA, US, 01887)

Job Overview

The Learning and Process Enablement Lead plays a critical operational role in ensuring CRL’s talent and learning processes run efficiently, consistently, and at scale. This role leads the execution engine that enables enterprise programs, including leadership development offerings, talent processes (performance, succession, engagement, careers/skills), assessment programs, learning delivery, digital roadmap and operational coordination.

This position manages a team of mid-career professionals (A2–A3) who coordinate and deliver enterprise programs, administer tools and assessments, support learning logistics, track completions, maintain reporting, and ensure communications and materials flow appropriately across GTM&D. The role partners closely with Talent Partners (strategic process owners), Talent Technology and Digital solutions leaders, Learning & Development program designers and owners and Well-being/Belonging leads to operationalize program and process strategy with speed, accuracy, and quality.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES

Translate talent and learning process strategy into clear, repeatable operational workflows across the enterprise.
Lead learning delivery execution, including session setup, facilitator coordination, registration management, roster tracking, and course maintenance.
Manage assessment program operations (e.g., 360 assessments, team diagnostics). Support CVP in creating alignment with multiple stakeholders across many levels including HR executives, business executives, TM team, HRT teams, IT teams and others
Ensure quality, consistency, and timely delivery of all GTM&D processes and programs and coordinate enterprise talent processes such as performance cycles, OTR preparation, engagement administration, and career framework rollout.
Supervise A2–A3 staff providing learning operations, talent coordination, reporting, and administrative support.
Oversee communications, templates, calendars, and readiness materials.
Support Talent Partners by providing operational backbone for process execution.
Collaborate with Digital Solutions to ensure system configuration and workflows meet operational needs.
Partner with People Analytics on dashboards, metrics, and outcome reporting.
Identify opportunities to simplify, standardize, automate, and scale operational processes.

QUALIFICATIONS

7+ years experience in L&D operations, HR program management, or talent operations.
Experience coordinating learning and talent management programs at scale.
Strong project management and organizational skills.
Demonstrated ability to lead mid-level professionals.
Experience collaborating across HR functions and COEs.
Strong communication and stakeholder management skills.
Ability to work in a fast paced environment.
Experience with SuccessFactors, Eightfold, and LMS administration preferred.
HR or project management certifications preferred.

Compensation Data

The pay rate for this role is $139,018 - $185,357 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Physical Requirements

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.

Equal Employment Opportunity

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

Cloud Engineer (Tranent, GB, EH33 2NE)

Job Overview

Are you passionate about Cloud Engineering?

Charles River Laboratories is seeking an enthusiastic and growth‑oriented individual to join the Global Infrastructure Services team as a Junior Cloud Engineer.

In this role, you will work as part of a collaborative, cross‑functional engineering team to support the delivery of secure, reliable, and effective cloud infrastructure solutions across Azure and AWS.

As a Junior Cloud Engineer, you will assist with day‑to‑day cloud operations, basic troubleshooting, and the deployment of cloud resources using Infrastructure‑as‑Code (IaC) and automation tools. You will develop hands‑on experience with cloud platforms, server technologies, networking fundamentals, and monitoring systems while contributing to ongoing cloud initiatives and supporting the organization’s multi‑cloud strategy.

Through consistent, high‑quality execution and a willingness to learn, you will help strengthen team productivity, enhance customer satisfaction, and support the continued modernization of CRL’s cloud environment

This is a remote role, with the ideal candidate based in UK/IRL or EU.

Job Description

Role Accountabilities:

• Support the organization’s digital transformation and cloud strategy by assisting with cloud migrations, basic configuration tasks, and operational activities under the guidance of senior engineers.

• Contribute to a high‑performing engineering team by helping deliver standardized, reliable, and well‑documented hybrid cloud services and infrastructure components.

• Collaborate with other IT teams to support the development, deployment, and troubleshooting of technical solutions, escalating issues when necessary.

• Assist senior engineers and external partners by gathering information, performing defined tasks, and supporting the delivery of cloud‑based solutions.

Essential Duties and Responsibilities:

• Assist with application migrations to Azure and AWS under the guidance of senior engineers, including basic configuration tasks and use of standard cloud migration tools.

• Support the deployment of IaaS and PaaS resources by following established designs, templates, and best practices created by senior staff.

• Contribute to day‑to‑day cloud operations, including monitoring, basic troubleshooting, and routine maintenance tasks across hybrid and multi-cloud environments.

• Participate in project work by completing clearly defined tasks, escalating issues appropriately, and collaborating with project leads.

• Help automate and standardize operational processes by writing simple scripts (e.g., PowerShell, Bash, Python) and using automation tools under supervision.

• Assist with deploying application artifacts to development, testing, and production environments using supported CI/CD and cloud deployment tools.

• Create and update documentation for cloud configurations, deployment steps, troubleshooting procedures, and operational workflows.

• Develop working knowledge of configuration management tools (such as Terraform, CloudFormation, ARM) and participate in routine configuration updates.

• Collaborate with team members to learn cloud engineering best practices and actively participate in knowledge-sharing sessions and cross-training.

• Perform other related duties as assigned to support IT operations and cloud initiatives.

Requirements and Profile

Required Qualifications:

Education: Bachelor’s degree (B.A./B.S.) or equivalent in computer science, engineering, or related discipline.

Experience:

• Some related IT experience, or equivalent hands‑on training, internships, or coursework in cloud technologies.

• Foundational understanding of cloud computing concepts and basic hands‑on experience with Azure or AWS (lab work, certification labs, or entry‑level projects).

• Exposure to containerization technologies such as Docker or Kubernetes, with the ability to perform basic container management tasks.

• Familiarity with infrastructure‑as‑code tools (e.g., Terraform, Bicep, CloudFormation) and CI/CD pipelines, with willingness to learn and expand skills.

• Basic knowledge of Kubernetes or other orchestration platforms, with interest in developing deeper capabilities.

• Understanding of DevOps principles such as automation, version control, and repeatable deployments.

• Experience working in collaborative environments, including exposure to Agile or Scrum methodologies (academic, internship, or professional).

Other:

• Effective communication skills for large, multi-national audiences.

• Effective cross-functional leadership and collaboration skills.

• Utility player – broad understanding of tools and technologies

• Flexibility and willingness to learn new toolsets and solutions

• Some awareness of business acumen –understanding of customer value

Certification/Licensure: Azure and/or AWS certification a plus.

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 fostering a sense of belonging and work daily in this direction.

Senior Cloud Engineer (Tranent, GB, EH33 2NE)

Job Overview

Do you have expertise in Cloud Engineering?

Are you a Subject Matter Expert in Azure?

Charles River Laboratories is looking for an energetic professional to provide engineering and architecture expertise within the Global Infrastructure Services team as an individual contributor and part of a cross functional team of engineers.

The Senior Cloud Engineer will be an integral component in delivering effective and secure end-to-end cloud infrastructure technology solutions.

This role will require a mix of subject matter expertise in cloud computing technologies along with legacy data center environments. You will be challenged to find approaches that enable rapid adoption of new cloud services and drive transformation for our business and IT processes. The cloud engineer will take part in infrastructure as code deployment tooling and supporting services.

Through excellence in delivery, they will help to achieve and maintain a high level of employee engagement, customer satisfaction and team productivity.

This is a remote position, with the ideal candidate based in the UK/IRL or EU.

Job Description

Role Accountabilities:

• Supporting the digital transformation initiative and cloud strategy by designing and implementing cloud migrations and services as part of a dedicated team of engineers.

• Contributing to a high performing team that delivers consumable, standardized hybrid cloud infrastructure services and solutions (resilient, high quality, secure, highly automated and up to date)

• Collaborating and consulting with other IT practices to support technical solution development and deployment

• Working with external strategic partners to develop and deliver technical solutions

Essential Duties and Responsibilities:

• Design, build and deploy IaaS and PaaS infrastructure solutions in AWS

• Lift and Shift application migrations to AWS using cloud migration technologies

• Participate in multiple highly complex projects/tasks simultaneously and prioritize as required

• Develop and document technical designs and requirements for integration and implementation of new and existing cloud applications and systems

• Document cloud infrastructure engineering procedures and collaborate on various information technology projects.

• Maintains and grows knowledge of platform configuration management and troubleshooting

• Embrace a team mentality by mentoring more junior engineers and cross-training with other engineers

• Perform all other related duties as assigned

Requirements and Profile

Required Qualifications and General Skills:

• Bachelor’s degree (B.A./B.S.) or equivalent in computer science, engineering, or related discipline.

• Effective communication skills for large, multi-national audiences.

• Able to work collaboratively across geographical regions

• Utility player – broad understanding of tools and technologies

• Flexibility and willingness to learn new toolsets and solutions

• Business acumen – understanding of customer value

Technical Experience:

• Significant IT industry experience with a strong track record of hands-on experience using Azure and AWS Cloud, including Transit Gateway and Hub/Spoke micro-segmented or zero trust designs

• Demonstrable experience with designing cloud implementation architectures and solutions using DevOps mindset, automation, and PaaS & IaaS resources.

• Experience migrating Windows and Linux workloads to public cloud infrastructure

• In-depth knowledge of networking, firewalls, load balancers

• Experience using infrastructure as code and tooling (Azure DevOps Pipelines, GitHub Actions, Terraform, Ansible, CI/CD)

• Experience with Cloud Security standards and frameworks including NIST, CIS , etc

• Experience working on or with teams using Agile methodologies such as Scrum.

Other:

• Experience with containers such as Docker, OpenShift a plus

• Ability and willingness to cross train, document and operationalize new technologies

• In depth knowledge of hybrid cloud infrastructure design and implementation

• Experience with building and maintaining systems for regulated workloads

Certification/Licensure: AWS certification a plus.

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 fostering a sense of belonging and work daily in this direction.

Research Associate I (Ashland, OH, US, 44805)

Job Overview

Research Associate: 2nd Shift 2:00 p.m. - 12:30 a.m. Monday - Thursday (10% Shift Differential)

Supervises and coordinates all study-related activities of research technical staff to ensure compliance with the protocol and applicable SOP's and maintains the raw data for nonclinical studies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Coordinates assignments to facilitate scheduling of study-related events on assigned studies (in conjunction with other departments) to ensure protocol requirements are met.
Scope of work includes studies of all duration, size, and complexity generally with some supervision.
Review study protocols and provide recommendations to study director/supervisor on technical and logistical aspects of protocol design.
Assist in preparing responses to both internal and external quality assurance audits.
Responsible for the accurate preparation and review of study calendars from draft and final protocols and ensuring all protocol-driven activities are accurately scheduled.
Monitors scientific projects, and the conduct of procedures in accordance with the study protocol, and applicable SOP's.
Acts as liaison between technical staff, internal departments, and Study Director on assigned studies.
Responsible for the preparation of study notebooks, organization of study data, timely (including daily) review of all study-related data generated by Technical Operations (according to established metrics) and submission of study notebook to Quality Assurance.
May perform limited technical activities as needed.
Participate in the team meetings.
Coordinate ordering of study equipment and supplies.
Perform all other related duties as assigned.

QUALIFICATIONS:

Education: High School diploma or General Education Degree (G.E.D.) preferred.
Experience: 2 years of related experience in a GLP environment. Experience with research and investigative procedures, techniques, and literature.
Ability to organize, prioritize work and meet deadlines.
Computer literacy with word processing, spreadsheet, and data base programs.

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear, and type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.
Employees working with animals must be able to lift, move and/or hold up to 40 pounds; this includes equipment and large and small animals.

WORK ENVIRONMENT:

While performing the duties of this job, the employee occasionally wears protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots).
Occasionally works with biohazards and sharps.
Occasionally works with live animals (small, medium and/or large) with risk of exposure to allergens and/or zoonotic diseases.
While performing the duties of this job the employee is occasionally exposed to fumes or airborne particles, unpleasant odors, and wet, humid and/or extreme temperature conditions.
The noise level in the work environment is usually low and occasionally moderate.

The pay rate for this position is $25/hour.

Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

Analytics Associate (Mattawan, MI, US, 49071)

Job Overview

An Analytics Associate is responsible for producing custom tables with statistical analyses using established systems and / or standardized code, to be completed in an accurate and timely manner consistent with the direction provided by the study director.

Job Description

Produce data listings, summaries, graphs, and statistical analysis results for report writing using established systems and/or standardized code. Minor, study-specific changes may be made to standardized code files as required by the study design and will be reviewed during the output verification process.
Review data to verify integrity and consistency for completeness, accuracy, and suitability, including data adherence to protocol, data coding integrity, reliability of collection, and interpretation.
Maintain organized, complete, and up-to-date study documentation, testing, and validation/quality control documents and programs in compliance with company standards and GLP guidelines.

Minimum Qualifications:

Education and Experience: Bachelor’s degree (mathematics, statistics, or computer science preferred); contract research organization experience preferred.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Experience with Excel is required.
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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

The pay for this role is $27/hour.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Research Analyst I - Formulations (Stilwell, KS, US, 66085)

Job Summary

Charles River Laboratories (CRL) is seeking a research analyst to join our integrated toxicology (ITox) team at the Kansas City 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. As a Research Analyst, 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.

From test article receipt to disposition, the Formulations team works with internal customers and clients providing logistical resources to produce reproducible formulations, investigating/troubleshooting where necessary to achieve a time-oriented, quality formulation bound by protocol and standard operating procedure requirements. The research analyst is proficient in the setup and execution of formulations, under supervision and learning to perform skills independently. Additionally, the research analyst will work towards supporting the site through cross training and working cross functionally as workload allows outside of the lab.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Calculate required vehicle and test article amounts based on study criteria for preparations.
Work towards independently generating, verifying, and/or reviewing instructions, and other study data as needed, based on body weights, days of dosing, etc.
Ability to follow detailed protocols and other reference materials to generate instructions for preparation and sampling of formulated test materials.
Apply laboratory experience to participate in troubleshooting.
Demonstrates effective communication skills through formal discussions.
Actively participate in laboratory development and process improvement initiatives.
Recognize Formulation and/or data issues and communicate those issues to the Study Director and Management.
Verify and/or review shipments and formulation procedures to ensure quality and completeness.
Identify potential scientific issues and develop solutions.
Execution of formulation instructions and preparation procedures.
Effectively direct junior technical staff in the execution of formulation instructions and preparation procedures.
Assist to sterilize laboratory equipment using autoclave or other methods
Assist in washing and maintenance of glassware and lab cleanliness
Consult with Sponsor representatives and Principal Investigators/Study Directors on appropriate formulation methods for assigned compounds.
Participate in scientific discussions with internal and external customers.
Participate in laboratory investigations, providing scientific input and direction, as needed.
Participate in the development of procedures for formulation of test articles and compounds in vehicle components for dosing.
Be responsible for the disposal and transport of residual dosing material, non-regulated pharmaceutical solids, accumulated single-use containers to designated waste receiving areas
Demonstrate effective communication skills through informal discussions with peers, management, and team
Cross functionally train and execute on learned/honed skills outside of the Formulations Lab to support the overall pulse of the workload as we embrace a one team culture.
Performs all other related duties as assigned.

Job Qualifications

Education:

Bachelor’s degree (B.A./B.S.), or equivalent, in a scientific related discipline.

Experience:

One year in a relevant field, preferably a pharmaceutical, chemistry, or contract research laboratory.
Certification/Licensure: None.
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 requirements by performing the activities according to the 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.
Must be authorized to work in the United States without a sponsor visa, now or in the future

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.

The pay rate for this role is $23.50/hour.

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.

Equal Employment Opportunity

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

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

Job Summary

As a Research Scientist for the Immunochemistry department located in Ville Saint-Laurent, you will be supporting non-clinical and clinical studies requiring measurement of large molecules (biologics, ADC, peptides, oligonucleotide-therapeutics) in biological matrix using ligand binding assay techniques.

In this role, primary responsibilities include:

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

Key Elements

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

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

Role Specific Information:

Location: 7170 rue Frederick-Banting, Ville St-Laurent / Free Parking
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River?

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

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

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.

Equal Employment Opportunity

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

Chercheur.se scientifique - Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que chercheur.se scientifique en Immunochimie notre équipe située au site de Ville Saint-Laurent, vous participerez à des études non cliniques et cliniques nécessitant la mesure de grosses molécules (produits biologiques, ADC, peptides, oligonucléotides thérapeutiques) dans une matrice biologique à l'aide de techniques d'analyse de liaison de ligands.

Dans ce poste, les principales responsabilités incluront:

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

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

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

Informations spécifiques au poste:

Localisation : 7170 rue Frederick-Banting, Ville St-Laurent / Stationnement gratuit
Bonus annuel basé sur la performance
Horaire : Du lundi au vendredi, de 8h à 16h15.
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine

Pourquoi Charles River?

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

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

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

Associate Quality Systems Specialist (Newark, DE, US, 19711)

Job Overview

Responsible for assisting / performing facility, process, vendor and local validation activities to assure compliance with applicable federal, state, and local regulations as well as corporate policies, Good Manufacturing Practice (GMP), applicable ISO requirements and Standard Operating Procedures (SOP). Responsible for supporting preliminary reviews of local quality requirements from the Quality Management System (QMS). Assist in executing continuous improvement initiatives as supported by QMS metrics and/or site management.

ESSENITAL DUTIES AND RESPONSIBILITIES:
• Assure Charles River’s compliance with applicable federal, state, and local regulations as well as corporate policies to avoid any business interruptions. Communicate all identified compliance and quality risks to supervisor.
• Review SOPs, protocols/batch records, reports, quality and regulated 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.
• Prepare written and signed records of all audits and inspections as required and may sign records as a trainee, countersigned by supervisor/trainer, documenting the performance of audits and inspections and reporting to management.
• Participate in the process the execution of improvements that have been agreed upon with Operations and Quality Management.
• Participate in the preparation of study and QA files in preparation for sponsor site visits and regulatory inspections; assure QA audit files are retained.
• Participate in the preparation of support during regulatory inspections, as required.
• Communicate all identified compliance and quality risks to senior team members and quality management.
• Perform facility and equipment records and logbook reviews.
• Where appropriate, approve customer test reports and participate in reagent release activities to support laboratory operations.
• Assist with analysis and collection of site Quality Metrics via QMS.
• Assist with preparations for Quality Management Review (QMR).
• Participate in the execution of identified process-improvement for dashboard analysis and analyze metric data for QMS.
• Participate in execution of Quality Assurance projects.
• Perform all other related duties as assigned.

Qualifications

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

• Experience: Minimum of 6 months in a Quality Assurance or regulated industry role.

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

The pay for this position is $22.50 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.

Technician I Methods Qualification and Validation (Wayne, PA, US, 19087)

Job Overview

Under direct supervision, responsible for performing daily laboratory activities necessary for analytical and/or bioanalytical method testing but not limited to, reagent preparation, laboratory maintenance/monitoring and method performance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform laboratory activities necessary for molecular biology testing including but not limited to;
Reagent preparation including buffers, chemicals solutions, complex mixtures and media preparations according to standard test methods.
Perform tasks using aseptic techniques including work within a biological safety cabinet.
Participate in the general maintenance of all equipment related to the preparation of assay materials and the analysis of samples, and schedule repairs as required. Perform any maintenance and/or monitoring as necessary.
Conduct aseptic growth and manipulation of bacteria, yeast, virus, and mammalian cells;
Make detailed observations and accurately and precisely record data, summarize data for reports and document all activities performed in accordance with current Good Manufacturing Practice (cGMP).
Perform a variety of molecular biology laboratory experiments, test and procedures including isolation and analysis of DNA and RNA, PCR, QF-PCR, RT-QF-PCR, restriction endonuclease digestion agarose gel electrophoresis, various blotting techniques, ELISA, and/or sequencing;
Report results of experiments, test, and procedures and analyze data.
Efficiently organize and plan daily activities
Maintain a safe working environment by adhering to company policies and procedures.
Follow all SOPs, STMs, and cGMP/cGLP guidelines as they relate to specific tasks.
Perform all other related duties as assigned.

Qualifications

Education: Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline.
Experience: 0-1 years related experience in biological lab.
Certification/Licensure: None.
Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred. Must possess excellent interpersonal skills to maintain communication across biological functional groups. Able to communicate effectively in a group or one on one setting. Basic Microsoft Office skills are a plus.

The pay for this position is $24.70 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.

Technicien·ne - 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 ou Membre de l’OPTMQ sont des atouts.
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: 23.50$/hrs
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Bonus annuel basé sur la performance;
Horaire: Dimanche au Jeudi de 8h am à 4h15 pm
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payée;
Gym gratuit sur place;
Cafétéria sur place;
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 & 5 journées personnelles 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.

Technician - 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

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

College diploma in science;
Relevant experience ore OPTMQ Member are assets
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: 23.50 $/per hour
Schedule: Sunday to Thursday (8h am to 4h15 pm)
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Annual bonus based on performance;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
Free gym on site;
Cafeteria on site;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ vacation & 5 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.

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.

Equal Employment Opportunity

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

饲养员（离职替换）-DIRECT LABOR (Pinghu, ZJ, 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

欲了解更多信息，请访问www.criver.com。

研究模型饲养- 支持类 1 1 1 1 1 1 1 (Foshan City, GD, 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。

重要信息：应聘此职位，必须在申请过程中上传并提交简历，请确保正确添加工作履历和教育背景。

工作总结

重要信息：此职位需要上传简历，如您尚未在候选人简介中上传简历，请返回至上传字段并附上简历。

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。

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18个国家和地区拥有70家设施及11000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。2016年，公司收入增长23.3％，达到16.8亿美元，而2015年收入是13.6亿美元。

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。我们支持了2016年FDA批准的所有药物中约70％的药物的开发工作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com

Szövettani technikus (Veszprem, HU)

A Charles River munkatársai 75 éve dolgoznak együtt az új gyógyszeres terápiák felfedezésén, fejlesztésén és biztonságos előállításán. Ha csatlakozik családunkhoz, jelentős hatást gyakorolhat az emberek egészségére és jólétére világszerte. Akár az élettudományok, a pénzügyek, az informatika, az értékesítés vagy más területről van szó, képességei fontos szerepet játszanak majd a munkánkban. Cserébe mi segítünk neked olyan karriert építeni, amiért szenvedélyesen rajonghatsz.

Szövettani technikus

Cégünk Szövettani technikus munkakörbe új munkavállalót keres.

Főbb feladatok, munkák:

Szövettani munkavégzésre keresünk technikust (asszisztenst), minimum középfokú végzettséggel. Szakirányú végzettség hiánya nem kizáró ok.

A munkakörbe tartozó feladatok:

• Szövettani vizsgálati anyagok előkészítése, rögzítése, indítása, víztelenítése, beágyazása, metszése, festése
• Fixáló és egyéb oldatok elkészítése
• Kenet készítése, festése
• Festőautomata, beágyazó és egyéb szövettani automata berendezések működtetése
• Szövettani minták archiválása, tárolása

Az álláshoz tartozó elvárások:

• Középfokú végzettség (érettségi)

Egyéb juttatások:

Éves bónusz, Cafeteria, Nyelvtanulás támogatása, 13. havi fizetés

Munkavégzés helye:

Veszprém Szabadságpuszta

A biztonsági értékelésről

A Charles River elkötelezett amellett, hogy partnereinket kivételes biztonságossági értékelési szolgáltatásokkal, korszerű létesítményekkel és szakértői szabályozási tanácsadással segítse felgyorsítani gyógyszereik preklinikai fejlesztését. Tapasztalt csapatunk az egyedi, speciális toxikológiai és vizsgálati új gyógyszeralkalmazási vizsgálatoktól kezdve a testre szabott formulákon át a teljes laboratóriumi támogatásig képes olyan programokat tervezni és végrehajtani, amelyek előre látják a kihívásokat és elkerülik a szűk keresztmetszeteket a zökkenőmentes és hatékony piacra jutás érdekében. Évente körülbelül 300 új vizsgálati készítményt (IDN) vizsgálnak a biztonságossági értékelő központjainkban.

A Charles Riverről

A Charles River egy nemzetközi szerződéses kutatási szervezet (CRO). A laboratóriumi orvostudomány és az állatorvosi tudományok területén szerzett erős alapokra építve létrehoztuk a felfedezési és biztonságossági értékelési szolgáltatások változatos portfólióját, mind a helyes laboratóriumi gyakorlat, mind egyéb módon, hogy ügyfeleinknek átfogó támogatást nyújtsunk a célpontok azonosításától a preklinikai fejlesztésig. A Charles River számos olyan terméket és szolgáltatást is kínál, amelyek támogatják ügyfelei klinikai laboratóriumi vizsgálati igényeit és gyártási műveleteit. A termékek és szolgáltatások e széles körű portfóliója lehetővé teszi ügyfeleink számára, hogy rugalmasabb gyógyszerfejlesztési modellt hozzanak létre, amely csökkenti a költségeket, növeli a termelékenységet és javítja a hatékonyságot, ami gyorsabb piacra jutást eredményez.

20 ország 110 telephelyén több mint 20.000 alkalmazottal stratégiai pozícióban vagyunk, hogy összehangoljuk a globális erőforrásokat és multidiszciplináris szemléletet alkalmazzunk, hogy megoldásokat dolgozzunk ki ügyfeleink egyedi kihívásaira. Ügyfélkörünkbe nemzetközi biotechnológiai és gyógyszeripari vállalatok, kormányzati szervek, valamint kórházak, oktatási és kutatási intézmények tartoznak világszerte.

A Charles River nagyon komolyan veszi a minél több ember életminőségének javítására irányuló erőfeszítésekhez való hozzájárulását. Küldetéstudatunk, tudományos kiválóságunk és eltökéltségünk mindig is vezérelt bennünket. Minden nap azzal a tudattal állunk hozzá, hogy munkánkkal világszerte számtalan férfi, nő és gyermek egészségének és jólétének javításához járulunk hozzá. Büszkék vagyunk arra, hogy az elmúlt öt évben az FDA által jóváhagyott gyógyszerek mintegy 80%-át mi fejlesztettük ki.

A Charles River Laboratoriesnál minden tehetséget elismerünk és felveszünk. Olyan vállalat vagyunk, amely elkötelezett a sokszínűség és befogadás elve mellett, és nap mint nap ebben az irányban dolgozunk.
További információkért látogasson el a www.criver.com weboldalra.

További információkért látogasson el a www.criver.com weboldalra.

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

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

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

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

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

Missions principales

Réception des animaux (rongeurs)

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

Entretien et soins des animaux

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

Entretien du matériel et des locaux

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

Votre profil

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

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.

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.

Senior Event Specialist, APAC (Singapore, SG)

Job Summary

Charles River is seeking a Snr Events Specialist to support our portfolio in the APAC region. This remote-based role will work closely with both the corporate and regional commercial teams to deliver impactful, revenue-focused, and brand-aligned events. The Snr Events Specialist will own the regional tradeshow calendar, lead preshow planning to establish clear objectives, ensure flawless onsite execution, and evaluate performance to maximize return on investment.

Job Responsibilities

Research, plan, and execute a program of APAC focused tradeshows, and hosted events across the Charles River portfolio.
Serve as the primary liaison between internal stakeholders, external vendors, and event attendees to ensure successful delivery, whilst supporting revenue growth, and strengthening market presence.
Act as the subject matter expert and sole point of contact for APAC tradeshows and events.
Drive improvements in event lead quality and velocity, ensuring compliance with corporate standards for lead capture, processing, and best practices.
Partner with regional marketing and CRL creative to ensure all messaging and design are on-brand, strategically aligned, and tailored to the target audience.
Track, analyze, and report ROI metrics for each event; provide recommendations for continuous improvement to maximize impact and revenue outcomes.
Oversee all aspects of event planning and logistics, including vendor contracts, purchasing, shipping, and onsite coordination.
Collaborate with other CRL departments on projects that generate revenue and strengthen client relationships.
Perform other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent or related discipline.
Experience: Four to six years related experience and/or training, including experience managing large tradeshows.
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: Proficiency in English is essential; multiple languages are advantageous. Knowledge of CRM systems, Smartsheet and Cvent or similar software/tools preferred

PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

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 fostering a sense of belonging and work daily in this direction.

Senior Scientist - AI/ML (Saffron Walden, GB, CB10 1XL)

Job Overview

At Charles River, we help our clients discover, develop, and manufacture new therapies that make a meaningful difference to patients’ lives. Our success is built on deep scientific expertise, collaboration across disciplines, and innovative thinking.

We are now seeking a Senior Scientist – AI / Machine Learning to strengthen and expand our AI enabled drug discovery capability at our Chesterford Research Park site. This role is central to operationalising our AI/ML strategy and delivering high quality, data driven insights across integrated drug discovery programmes.

Apply today and help us advance the future of AI enabled drug discovery.

Candidates must have full and permanent Right to Work in the UK as we are unable to offer sponsorship for this role.

The Role

As a Senior Scientist in AI/ML, you will work with scientific independence under strategic direction, applying advanced machine learning and informatics approaches to real drug discovery challenges.

You will:

• Develop, deploy, and apply AI/ML models for molecular design, prediction, and decision making.

• Apply AI/ML and (chemo)informatics to support high quality scientific decisions across client programmes.

• Drive innovation in AI, automation, and in silico strategies, accelerating progression from hit to candidate.

• Collaborate closely with medicinal chemists, biologists, computational scientists, project leaders, and clients.

• Present scientific results, challenges, and recommendations clearly to internal and external stakeholders

• Maintain awareness of emerging AI/ML technologies and scientific literature, sharing knowledge across teams.

• Contribute to scientific proposals, client presentations, and business development activities.

• Mentor and support colleagues, helping to build informatics and AI capability across the organisation.

• Function as an ambassador for Charles River at conferences and external scientific events when required.

Skills, Qualifications & Experience

Essential:

• PhD in Computational Chemistry, AI/ML, Chemoinformatics, or a related discipline

or BSc/MSc in chemistry or computer science with significant industry experience applying AI/ML in drug discovery.

• Demonstrable experience developing and deploying AI/ML methods in a drug discovery environment.

• Strong Python programming skills, including experience with Jupyter notebooks and modern IDEs.

• Experience working with structured and unstructured data.

• Proven ability to work effectively in multi disciplinary, project based teams.

• Strong problem solving skills with the ability to communicate complex ideas clearly and pragmatically.

Desirable:

• Industry experience within a CRO or pharmaceutical drug discovery organisation.

• Sound understanding of the mathematics and statistics underpinning AI/ML.

• Experience using commercial and open source molecular modelling software.

• Exposure to bioinformatics or biologics focused data.

Additional Information

• This role is hybrid/onsite, with regular attendance required at our Chesterford Research Park (Saffron Walden) site.

• Travel may be required for client meetings and scientific conferences.

What We offer You

At Charles River Discovery UK, we offer a competitive and comprehensive benefits package designed to support our employees’ health, wellbeing, and professional growth. A generous Bonus and non-contributory pension, health, dental and much more.

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.

Steam Mechanical Engineer (Margate, GB, CT9 4LT)

Job Overview

Rota - 35 Hrs per week

Monday - Thursday 8.00 am - 4.30 pm

Friday 8.00 am - 1.00 pm

Out of hours callouts - rostered - 1 in 4 weeks (Paid at additional rate)

* Please not due to nature of role flexibilty surrounding core hours is essential.

Overall responsibility:

Steam Mechanical Engineer to operate, maintain, and repair site steam-based systems,. To ensure high-pressure systems meet safety, efficiency, and regulatory standards (e.g., pressure vessel compliance).

Core Responsibilities

System Maintenance: Performing planned and reactive maintenance on industrial boilers, steam pipework, and condensate systems.
Safety Compliance: Ensuring all steam systems adhere to health, safety, and statutory requirements.
Troubleshooting: Diagnosing and fixing mechanical, electrical, and control issues within steam plants. E.G Steam traps PRVs etc
System Optimisation: Improving efficiency and reliability of heating, cooling, and steam generation processes

Plus other related or nonrelated maintenance works required to maintain critical plant onsite.

Mechanical repairs and improvements to Company properties, both on a responsive basis and strategic basis.
Mechanical tests and reports on company property and carry out the necessary repairs.
Preventative planned maintenance and complete relevant job documentation.
Respond to reactive work orders and complete, as necessary.
Installation, repair, and modification of pipe work throughout site, both copper and iron.
Responsible for the operation and daily testing of steam controls of site boilers. (BOAS training can be provided).
Responsible for the operation and upkeep of this site biomass boiler.
Carry out feed water and boiler water analysis.

Qualifications and Experience

At a minimum, City& Guilds Mechanical installation
Steam qualification / or equivalent time served
Some IT literacy
Experience of working in a busy environment to tight deadlines.
Maintaining Steam Boilers
Planned preventive maintenance
HVAC
LTHW Boilers
Some controls experience
Good understanding of pressure system regulation.
Installation experience
Fault finding

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Team Leader (Margate, GB, CT9 4LT)

Job Overview

Team Leader – Barrier Production

Location: On Site - Margate, Kent | Full time (35 Hrs) Mon-Thurs 7.5hrs, Friday 5hrs

Lead people. Shape culture. Support world‑class research.

This is a leadership role first and foremost. You don’t need to walk in as a technical expert — we can teach the technical skills. What matters most is your ability to lead, coach, motivate and develop people.

We're looking for a confident, resilient and positive people leader to guide a team working within a high‑standard barrier rodent model production environment. You will be required to be hands on for this position.

Job Description

What you’ll do

As our Team Leader, you will:

Lead & Develop People.
Inspire, support and develop a team of animal technicians and working with rodents.
Set clear expectations around behaviour, performance and accountability.
Build a positive, inclusive and psychologically safe team culture.
Address challenges early, fairly and constructively.
Drive Operational Excellence.
Coordinate daily and weekly work to meet production and welfare standards.
Monitor workloads, staffing and training needs, adapting plans as required.
Maintain high standards of barrier practice, routines and cleanliness.
Ensure all work meets training documentation, regulatory requirements and internal quality standards.
Be a Visible, Hands‑On Leader.
Spend the majority of your time in the barrier facility—engaged, accessible and working alongside the team.
Act as the first point of escalation for operational, welfare or people issues.
Collaborate & Improve.
Work closely with peer leaders and managers to ensure smooth operations (some weekend/bank holiday working on a rota basis).
Support audits, inspections and continuous improvement initiatives.

What we’re looking for

Experience leading or influencing people in an operational, regulated or production environment.
Confidence to hold honest conversations and make fair, balanced decisions.
Calm, steady and consistent leadership — especially under pressure.
A genuine passion for helping others grow, not just managing tasks.
Strong communication skills, integrity, and self‑awareness.

(Experience in laboratory, animal care or technical production environments is helpful but not essential — we’ll teach you what you need to know.)

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Facility Supervisor (Seattle, WA, US, 98102)

Job Summary

We are seeking a Facility Supervisor to join our Insourcing Solutions team, located in Seattle, Washington.

The Facility Supervisor provides direct supervision of daily activities of Charles River Accelerator & Development Labs (CRADL) animal facilities. They will be responsible for the supervision and training for employees in the Animal Care & support series. They maintain performance levels consistent with and according to company standards, the CRADL organization and client requirements. They prioritize and complete on-going tasks independently following established policies and guidelines. They will liaise with clients to ensure satisfaction with technician performance.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

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.

• Supervise, directly and through others, the daily activities of employee conducting husbandry and support services in the facility. Responsible for personnel management activities such as: mentorship,
personnel actions (hiring, promotions, terminations, etc.), training & development, providing regular direction and feedback on performance, disciplinary actions, delivering annual performance and
salary reviews.
• Plan, create, assign and monitor work schedules for employee including weekend, holiday and on-call coverage to ensure optimal team performance. Ensure of team to match needs of organization as
priorities change.
• Monitor and analyze the performance of employees to ensure highest level of animal care and support, timely reporting of health concerns, and client needs.
• In coordination with Human Resources representative, conduct interviews, assist in recruitment efforts, investigate personnel problems, and respond to employees in accordance with company
policies and procedures.
• Communicate with clients, listen to feedback/concerns and respond promptly and professionally, demonstrating strong organizational skills to manage multiple tasks, prioritize effectively, and ensure
that client service operations run smoothly.
• Serve key clients and assist in driving sales by presenting site capabilities through providing tours and competency assessments.
• Serve as a model to CRADL employees as it relates to CRL Core Values (CARE, LEAD, OWN, COLLABORATE). Provide mentorship, leadership and motivation to all CRADL personnel.
• Monitor and document task completion and deviations from defined KPI’s and submit monthly to CRADL management in a timely fashion to support contract deliverables.
• Participate in periodic meetings with CRL Operations employees to keep them informed of current and future projects, policies and procedures.Investigate animal welfare concerns as directed by the Animal Welfare Team or Attending Veterinarian. Propose and deliver appropriate mitigations to active concerns while preventing future recurrences, solicit relevant information from employee and researchers to accurately assess and Effectively promote animal welfare.
• Provide animal husbandry backup on animal welfare checks/receiving, cage changing, and facility support as required.
• Ability to provide technical backup on dosing, injections, collections as needed.
• Monitor acquisition, receipt, storage and issue of supplies and animals.
• Generate work orders and ensure documentation of all corrective maintenance and preventative maintenance procedures. Follow up to ensure timely resolution to issues and provide update to management when resolved.
• Provide timely, concise and effective communication regarding all facility utilities, infrastructure, process equipment, and supply chain and housing system issues to management.
• Inspect animal housing systems to ensure proper setup and function.
• Coordinate the movement of animals throughout the facility and assign housing locations for receipt of new animals.
• Participate in the development of projections for equipment, supplies and personnel needed to effectively operate the research facilities.
• Participate in the development and implementation of CRADL organization and site-specific policies and SOPs.
• Supervise the use of all space throughout the facility (animal housing, procedural, service, and storage areas) and works with the Manager in assigning the space to clients.

.

• Perform CRADL equipment asset management and tracking inventory for reporting purposes.
• Place & receive orders to maintain appropriate levels of inventory of supplies including bedding, feed, cleaning materials and husbandry supplies.
• Conduct frequent quality assurance inspections of all 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.
• Conduct frequent quality assurance inspections to verify that employees are adhering to established room/cage/rack sanitation schedules.
• Oversee adherence to all CRADL organizational and site operational procedures and all required documentation related to the department.
• Supervise record maintenance. Generate and submit internal and external reports in the required formats and timeframes, and report to management on operations related issues.
• Participate in all IACUC semi-annual activities including follow-up on any findings for the site and the organization.
• Act as subject matter expert in all animal husbandry and services.
• Conduct and participate in Train the trainer sessions.
• Identify employee training needs and ensure necessary training is conducted and competence for duties is achieved.
• 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.
• Deliver consistent practice of site and personnel safety policies, procedures and oversee hazardous work in partnership with EH&S Specialists.
• Maintain required attendance level and adherence to work schedule in accordance with required employee levels to ensure that assigned duties are completed.
• Perform all other related duties as assigned.

PHYSICAL REQUIREMENTS:

While performing the duties of this job, the employee is frequently required move about inside the facility, communicate, and operate a computer. The employee is frequently required to stand; walk;
use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee frequently is required to stoop, kneel, crouch, or crawl. The employee is occasionally
required to sit. The employee must regularly lift and/or move items weighing up to 50 pounds independently and occasionally lift and/or move items weighing up 100 pounds with assistance.

MINIMUM QUALIFICATIONS:

High School Diploma or General Education Degree (GED).
Minimum of four (4) years experience in a laboratory animal facility of which two (2) years is supervisory or lead technician experience.

PREFERRED QUALIFICATIONS:

Bachelor's degree (B.A./B.S.) in animal science or life sciences fields.
Laboratory Animal Technologist (LATG) certification from AALAS or Certified Supervisor (CS) certification from ICPM.

The pay range for this position is $85,000K - $95,000K USD annually. 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.

Mitarbeiter für Technische Instandhaltung (Sulzfeld, Bavaria (Bayern), DE, 97633)

Wir suchen ab sofort

eine/n Mitarbeiter/in (m/w/d)

für Außenbereichstätigkeiten

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

Technisches Gebäudemanagement:

Arbeit mit der Software MAXIMO
Reparatur und Unterhalt für den gesamten Standort, Planung, Durchführung, Dokumentation
Nachhaltigkeitsplanung und -strategie
Betreiben, Instandhalten und Optimieren der technischen Anlagen
Bestandsmanagement

Infrastrukturelles Gebäudemanagement:

Schädlingsbekämpfung
Abfallmanagement
Nachhaltigkeitsplanung und -strategie
Lagerhaltungsmanagement
Grünanlagenpflege

Fachliche und persönliche Anforderungen:

Fachlich:

Ausbildung im technischen Bereich, vorzugsweise HKLS oder Elektro
Erfahrung im Handling und der Wartung von technischen Anlagen und Geräten
Erfahrung im Projektmanagement
Sehr gute Deutschkenntnisse

Persönlich:

Zuverlässigkeit
Belastbarkeit
Durchsetzungsfähigkeit
Teamfähigkeit
Kommunikationsfähigkeit
Rufbereitschaft
Selbständigkeit

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, Sachbezug, VWL-Förderung, Gesundheitstage, Betriebliche Altersvorsorge, Dienstrad, Förderung von sozialem Engagement in der Region 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

Über Research Models & Services

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

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

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierpfleger / Mitarbeiter in der Tierbetreuung (m/w/d) in Vollzeitfür unsere Niederlassung in 97633 Sulzfeld

Ihre Aufgaben:

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

Die Anforderungen:

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

Unser Angebot:

eine ausführliche und betreute Einarbeitung im Rahmen unseres Trainingskonzepts
ein leistungsgerechtes Einkommen
eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team
Teilnahme an diversen Unternehmensveranstaltungen
zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, givve-Card, VWL-Förderung u.v.m.)

Auch Bewerber ohne spezifische Vorkenntnisse/ Quereinsteiger sind uns willkommen!Sie sind interessiert?

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

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 SulzfeldEmail: BewerbungenRMS@crl.com, www.criver.com

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

Über Research Models & Services

Über Charles River

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

Weitere Informationen finden Sie unter www.criver.com.

Mitarbeiter/in in der Tierpflege (m/w/d) 1 (Sulzfeld, Bavaria (Bayern), DE, 97633)

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierpfleger / Mitarbeiter in der Tierbetreuung (m/w/d) in Vollzeitfür unsere Niederlassung in 97633 Sulzfeld

Ihre Aufgaben:

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

Die Anforderungen:

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

Unser Angebot:

eine ausführliche und betreute Einarbeitung im Rahmen unseres Trainingskonzepts
ein leistungsgerechtes Einkommen
eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team
Teilnahme an diversen Unternehmensveranstaltungen
zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, givve-Card, VWL-Förderung u.v.m.)

Auch Bewerber ohne spezifische Vorkenntnisse/ Quereinsteiger sind uns willkommen!Sie sind interessiert?

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

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 SulzfeldEmail: BewerbungenRMS@crl.com, www.criver.com

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

Über Research Models & Services

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

Scientifique en Immunologie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique pour notre équipe d’Immunologie situé au site de Senneville, vous serez responsable de la conception, de la réalisation et du compte rendu des études de science de laboratoire de manière efficace, rentable et avec une qualité scientifique maximale.

Dans ce poste, les principales responsabilités incluront:

Concevoir, rédiger, réviser et éditer des plans d'étude, des amendements et des calendriers d'étude qui définissent et planifient toutes les activités de l'étude;
Superviser et coordonner tous les aspects des procédures de sciences de laboratoire liées à l'étude, qu'elles soient effectuées au sein du département ou par des départements de service;
Analyser les problèmes scientifiques, résoudre les méthodes d'analyse et les problèmes techniques ;
Rédiger des documents scientifiques, examiner et interpréter les données brutes ;
Rédiger, réviser et éditer des rapports scientifiques autonomes, provisoires et/ou finaux, qui documentent toutes les procédures et tous les résultats liés à l'étude;
Communiquer rapidement, oralement ou par écrit, avec les directeurs d'étude et/ou le promoteur sur les questions liées à l'étude en temps voulu;
Veiller à l'exactitude et à l'exhaustivité des estimations de coûts des projets;
Informer le Scientifique principal et/ou le Directeur scientifique des problèmes scientifiques ou techniques dès qu'ils se manifestent.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un Baccalauréat en Immunologie ou dans toute autre discipline connexe;
Minimum de 2 ans d’expérience dans l’utilisation de la Cytométrie en flux multi-paramètres;
Expérience avec les techniques d’Immunodosage (ELISA, ECL, Luminex) et les essais sur cellules (ELISpot, bioessais) est un atout;
Excellentes compétences organisationnelles;
Bonnes compétences interpersonnelles et en communication;
Solides compétences en résolution de problèmes;
Travailler avec précision, être attentif aux détails et viser un travail de qualité.

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 9h00 à 17h15;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Immunology Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Scientist for our Immunology team at the Senneville location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In this role, primary responsibilities include:

Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
Analyze scientific problems, troubleshoot analytical methods and technical issues;
Write scientific documents, review and interpret the raw data;
Write, review, and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
Ensure the accuracy and completeness of project cost estimates;
Notify the Principal Scientist and/or the Scientific Director of scientist or technical problems as soon as they become apparent.

Key Elements

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

Holder of a Bachelors in Immunology or any other related discipline;
Minimum of 2 years’ experience in the use of multi-parameter flow cytometry;
Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and cell-based assays (ELISpot, bioassays) is an asset;
Outstanding organizational skills;
Good interpersonal and communication skills;
Strong problem-solving skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

Location: 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, 9:00am to 5:15pm;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Report Compiler 1 (Tranent, GB, EH33 2NE)

Job Overview

We are seeking a Report Compiler for our Administration & Reporting department located in Elphinstone, Tranent, EH22 2NE.

This role is full time, on site (with hybrid options after a period of training).

The Administration and Reporting department is responsible for collating, tabulating and reporting scientific data from safety assessment studies and using reporting software to compile the study report to the standards required by the Company, its clients and international regulatory authorities.

Key Responsibilities and Experience

Key responsibilities

Timely collation and tabulation of data from safety assessment studies to meet tight deadlines.
Preparation and formatting of the draft material and methods of scientific studies in accordance to the study design and Sponsor requirements.
Development of reports to the standards required by the Company, its clients and international regulatory authorities.
Quality control of own work and the work of others
Work closely with study management and Quality Assurance.
Use appropriate publishing software for compilation of reports and reporting components before issuing reports to the Sponsor.

Experience

University entrance standard educational qualifications. A degree is welcome, but not essential.
Strong proficiency in IT literacy i.e. extensive experience in use of word-processing, electronic text production and report writing is essential
Proven experience of working within given timescales with excellent attention to detail
Effective written and verbal communication skills
Experience of managing own workloads and prioritising conflicting responsibilities

This role is offered Full time, the Salary of £27,951 per annum as well as 29 days paid Holidays, Pension, Private Healthcare, Health Insurance, Employee discount scheme, Free Gym on site, Cafeteria with great food, Free onsite parking and more.

Equal Employment Opportunity

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

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

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Baltimore, MD.

As the Animal Care Technician I, 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 I position:

High school diploma or GED
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 $20.32 USD per hour. The schedule is Monday through Friday 7AM-3:30PM, must be available to work some weekends and holidays when necessary.

Equal Employment Opportunity

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

Preclinical Autopsy Technician I (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.
Must be authorized to work in United States without a sponsor visa now or in the future.

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.

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

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

Equal Employment Opportunity

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

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

Job Summary

As a Research Scientist for our Immunotoxicology team at the Senneville location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In this role, primary responsibilities include:

Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
Analyze scientific problems, troubleshoot analytical methods and technical issues;
Write scientific documents, review and interpret the raw data;
Write, review, and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
Ensure the accuracy and completeness of project cost estimates;
Notify the Principal Scientist and/or the Scientific Director of scientist or technical problems as soon as they become apparent.

Key Elements

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

Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years’ experience working in a Scientific position;
PhD in Immunology or any biological related discipline;
Experience in the development, optimization and use of multi-parameter flow cytometry;
Experience with the BD flow cytometer platforms; spectral flow cytometry experience is an asset;
Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and cell-based assays (ELISpot, bioassays) is an asset;
Outstanding organizational skills;
Good interpersonal and communication skills;
Strong problem-solving skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

Location: 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, 9am to 5:15pm;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
Paid development training;
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.

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.

Equal Employment Opportunity

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

Scientifique de recherche en Immunologie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique de recherche pour notre équipe d’Immunotoxicologie situé au site de Senneville, vous serez responsable de la conception, de la réalisation et du compte rendu des études de science de laboratoire de manière efficace, rentable et avec une qualité scientifique maximale.

Dans ce poste, les principales responsabilités incluront:

Concevoir, rédiger, réviser et éditer des plans d'étude, des amendements et des calendriers d'étude qui définissent et planifient toutes les activités de l'étude;
Superviser et coordonner tous les aspects des procédures de sciences de laboratoire liées à l'étude, qu'elles soient effectuées au sein du département ou par des départements de service;
Analyser les problèmes scientifiques, résoudre les méthodes d'analyse et les problèmes techniques ;
Rédiger des documents scientifiques, examiner et interpréter les données brutes ;
Rédiger, réviser et éditer des rapports scientifiques autonomes, provisoires et/ou finaux, qui documentent toutes les procédures et tous les résultats liés à l'étude;
Communiquer rapidement, oralement ou par écrit, avec les directeurs d'étude et/ou le promoteur sur les questions liées à l'étude en temps voulu;
Veiller à l'exactitude et à l'exhaustivité des estimations de coûts des projets;
Informer le Scientifique principal et/ou le Directeur scientifique des problèmes scientifiques ou techniques dès qu'ils se manifestent.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d'une Maîtrise en Immunologie ou dans toute autre discipline connexe avec un minimum de 3 à 5 ans d'expérience dans un poste scientifique;
Doctorat en immunologie ou dans toute discipline biologique connexe;
Expérience dans le développement, l'optimisation et l'utilisation de la Cytométrie en flux multiparamétrique;
Expérience avec les plateformes de Cytomètre en flux BD. L'expérience en cytométrie en flux spectrale est un atout;
Expérience avec les techniques d'immunoessai (ELISA, ECL, Luminex) et les essais cellulaires (ELISpot, bioessais) est un atout;
Excellentes compétences organisationnelles;
Bonnes compétences interpersonnelles et en communication;
Solides compétences en résolution de problèmes;
Travailler avec précision, porter attention aux détails et viser un travail de qualité.

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 9h à 17h15;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Formations de développement payées;
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.

Cagewash Attendant I (50) (Bethesda, MD, US, 20892)

Job Summary

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

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

Additional responsibilities include:

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

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

The pay for this position is $20.32 USD per hour. Schedule: Monday through Friday 7AM-3:30PM.

Equal Employment Opportunity

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

Technicien.ne de laboratoire en formulation (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Technicien.ne de laboratoire pour notre équipe de Formulation située au site de Senneville, serez responsable de préparer les différentes formulations requises pour le dosage, en solution, suspension ou mélange de poudre, pour nos équipes de recherche.

Dans ce poste, les principales responsabilités incluront:

Préparer des formulations pour le dosage, en solution, suspension ou mélange de poudre en utilisant différentes techniques tout en respectant les règles des BPL;
Utiliser différents programmes informatiques et équipements tels que PH mètre, appareil d’homogénéisation, balance, osmomètre, densimètre et boîte à gants;
Manipuler des échantillons sous la hotte en utilisant une méthode aseptique;
Préparer le matériel de l’étude selon le protocole.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

AEC/DEC en sciences de laboratoire ;
À l’aise de suivre des procédures strictes ;
Personne motivée, autonome et minutieuse ;
Attitude positive et un bon esprit d’équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 23,50$ de l’heure;
Bonus annuel basé sur la performance;
Horaire:
- Horaire du lundi au vendredi, de 8 h à 16h15, avec disponibilité requise une fin de semaine sur deux;
- ou 4 jours/37.5h du vendredi au lundi, heure de début entre 6 et 9 heures du matin; inclus la fin de semaine,
- une formation de 3 semaines sera donnée du lundi au vendredi, de 8h à 16h15,
- Journées fériées;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

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

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

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

Laboratory Technician in formulation (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a laboratory Technician for our formulation team located at the Senneville site, you will be responsible of preparing different formulations required for dosing, in solution, suspension or powder mix , for our research teams.

In this role, primary responsibilities include:

Prepare formulations for dosing, in solution, suspension or powder mix using various techniques while adhering to GLP regulations;
Operate various computer programs and equipment such as PH meter, homogenizer, balance, osmometer, densimeter and glove box;
Handle samples in a fume hood using aseptic method;
Prepare study materials according to protocol.

Key Elements

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

AEC/DEC in laboratory sciences ;
Comfortable following strict procedures;
Motivated, autonomous, and meticulous person;
Positive attitude and good team spirit.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 23,50$/hour;
Annual bonus based on performance;
Schedule:
- Schedule from Monday to Friday, from 8:00 a.m. to 4:15 p.m., with availability required every other weekend.
- or 4 days/37.5 hours from Friday to Monday inclusive, including the weekend, with a start time between 6:00 a.m and 9:00 a.m.
- A three-week training period will be provided, Monday to Friday, from 8:00 a.m. to 4:15 p.m.
- Holidays;
- Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

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

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

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.

Equal Employment Opportunity

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

Animal Care Technician I (EG) (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 22/hour USD per hour. 

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.

EG - Formateur.trice, Soins aux animaux (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Formateur.trice en soins aux animaux pour notre équipe de Toxicologie située au site de Laval, vous formerez le personnel technique et vous assurerez que les dossiers de formation sont à jour et que les techniques enseignées sont réalisées d'une manière qui respecte les processus établis.

Dans ce poste, les principales responsabilités incluront:

Former sur les méthodes de nettoyage et de contention des animaux;
Former à l’enregistrement des données telles que le poids corporel, la consommation alimentaire et les signes cliniques afin de répondre aux normes de qualité et de compétence;
Évaluer le niveau de compréhension de l’employé par rapport à la formation reçue;
Assurer l’intégrité des études et répondre aux exigences des organismes réglementaires en réalisant les activités conformément aux Bonnes Pratiques de Laboratoire (BPL), aux Procédures Opératoires Standard (POS) et aux règles du Comité institutionnel de soins et d’utilisation des animaux (CICUA) ;
Assurer le suivi des différentes modifications apportées aux procédures et aux méthodes de travail et participer aux efforts d’amélioration des processus;
Assurer une bonne communication avec les superviseurs des différents départements pendant et après la formation des employés.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d'études secondaires;
Au moins 2 à 3 ans d'expérience dans un centre de recherche en tant que Commis en soins aux animaux / Préposé.e à l’entretien des animaux;
Être une référence, un exemple et un leader en matière de bien-être animal, santé et sécurité, qualité et assiduité;
Bonnes compétences d’observation;
Capacité à inspirer confiance et assurance grâce à de solides compétences interpersonnelles et une collaboration efficace;
Capacité à travailler physiquement (soulever jusqu’à 20 kg, marcher, rester debout, se pencher, 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 poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: À partir de 22$/hrs;
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?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Trainer, Animal Care (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Animal Care Trainer for our Toxicology team at the Laval location, you will train technical staff and ensure that the training records are up to date and that the techniques taught are done in a way that respects established processes.

In this role, primary responsibilities include:

Train animal room cleaning and restraint methods;
Train on the data recording such as body weight, food consumption and clinical signs in order to meet quality and competence standards;
Evaluate the employee's level of understanding in relation to the training received;
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) and the Institutional Animal Care and Use Committee (IACUC) rules;
Ensure the follow-up of the various changes brought to the procedures and the methods of work and participate in process improvement efforts;
Ensure good communication with the supervisors of the different departments during and after completion of the employees’ training.

Key Elements

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

High School diploma;
At least 2 to 3 years’ experience in a research center as an Animal Care Clerk/Animal Care Attendant;
Be a reference, an example and a leader for Animal Welfare, Health and Safety, Quality and attendance;
Good observation skills;
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
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: Starting at 22$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Technical Specialist II (High Peak, GB, SK23 6FJ)

Job Overview

Do you have expertise in working with robotics and liquid handling platforms?

Have you got the desire to improve health and lives?

Charles River Discovery are excited to be recruiting for a Technical Specialist II to join our High Peak, UK site. This is an onsite role, with expectation of being able to travel to High Peak daily.

The Technical Specialist II role is a laboratory based, hands-on position with responsibilities in applying technical expertise to support the delivery of a broad portfolio of client projects.

What you’ll be doing:

• Execute complex protocols independently, troubleshoot technical issues and train junior staff on standard techniques.

• Perform specialist functions within a defined area – Robotics, liquid handling and routine automation.

• Perform specialist functions relating to client project work as required.

• Lead implementation of process improvements, coordinate technical activities and mentor junior colleagues.

• Provide timely communication with technical and scientific staff liaising across departments at High Peak.

• Execution of routine technical and non-technical tasks with high level of competency and minimal supervision.

• Owns workload to meet agreed deliverables with awareness of how this impacts the immediate and wider team.

• Adherence to safe lab working policies, with some ability to suggest new ideas and provide solutions for immediate workspace.

• Demonstrate ability to identify range of technical issues, and report to relevant managerial delegate in a timely manner.

Requirements and Profile

Skills and Experience:

• BSc/MSc (preferred) within a relevant scientific discipline

• Track record of technical expertise in using robotics and liquid handling platforms in a laboratory-based environment, industry preferred.

• Experience of working at other CROs/Biotech/Pharma companies is highly advantageous.

• Excellent attention to detail, time management and communication skills also a must. Able to present scientific data to stakeholders competently.

• Able to effectively solve problems and collaborate with project teams to resolve any issues and support implementation as needed.

What We Offer You:

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

• Global opportunities and strong career progression.

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

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

• To continue your own career growth.

• Flexible and hybrid working.

• Parental leave.

• Group Life Assurance and Group Income Protection.

• Remote GP access 24/7.

• Well-being support and initiatives.

• Cycle to work scheme.

Applicants must have existing Right to Work in the UK as we are not able to provide sponsorship.

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.

Animal Care assistant (Laval, Quebec, CA, H7V 4B3)

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

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

Job Summary

As an Animal Care Clerk for our Toxicology team located in Laval, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry (clean the animal rooms and the cages);
Assist the Animal Health Technicians in their daily tasks;
Handle animals;
Participate in the physical/social activities of the animals.

Key Elements

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

Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
You are able to follow precises instructions (procedures);
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: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $19/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, evening, and weekends (1/2). Depending on the needs, you may have to do overtime night, and holidays;
Permanent position as of the hiring, 37.5hrs per week;
Career progression: If you are interested in progressing and learning more, we can train you to become an Animal Health Technician! Of course, that comes with a pay rise.

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);
Guaranteed hours because the research field is in high demand;
3 weeks’ Vacation & 5 Personal days;
Many social activities!

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

Equal Employment Opportunity

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

Assistant.e aux soins des animaux (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Commis aux soins des animaux pour notre équipe de Toxicologie situé au site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie (nettoyer les salles d’animaux ainsi que les cages);
Assister les Techniciens.nes en Santé animale dans leurs tâches quotidiennes;
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux.

Éléments clés

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

Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
Capable de suivre des instructions précises (procédures);
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 : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport : Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : 19$/hrs;
Primes : Soirée (2.50$), 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, de soir, et les fins de semaine (1/2). Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaires;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine;
Progression de carrière : Si tu es intéressé à progresser et à en apprendre plus, nous pouvons te former jusqu’à devenir Technicien(ne) en santé animale! Bien entendu cela vient avec une augmentation de salaire.

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);
Des heures garanties, car le milieu de la recherche est très en demande;
3 semaines de vacances ainsi que 5 journées personnelles;
De nombreuses activités sociales !

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

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

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

Job Overview

Job Summary:

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.

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.

Essential Duties and Responsibilities:

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.

Job Description

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.

Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Physical Demands:

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.

Regularly operates a wide variety of tools and controls for equipment in the laboratory.

Frequently moves formulations equipment (25-40 pounds) in the laboratory.

Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Medical Technologist I (Shrewsbury, MA, US, 01545)

Job Overview

Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain, and perform basic troubleshooting procedures on analyzers. Biological sample processing. Perform and review study ordered parameters and computer input of raw data.

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Perform all tasks in compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations.
Read study protocols and extract pertinent information with guidance.
Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and fecal analysis.
Operate, maintain, and troubleshoot clinical pathology analyzers with guidance.
Perform basic medical technology procedures such as blood slide differentials, reticulocyte counts and urinalysis with guidance.
Perform all specialized processing under supervision.
Prepare materials needed: labeling tubes, study books and appropriate paperwork prior to bleeding days.
Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
Manual entry of raw data into the computerized systems and review of data as needed.
Perform all other related duties as assigned.

The pay range for this position is between $30.00 and $33.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

QUALIFICATIONS:
Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) preferred.
Experience: 0-2 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is required. GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.

Education

Advanced degree or certification required

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Scientific Research In Vitro - Technical/Scientific (Saffron Walden, GB, CB10 1XL)

Job Summary

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Technical Specialist II - Stem Cells (Saffron Walden, GB, CB10 1XL)

Job Overview

Charles River Discovery are excited to be recruiting for a Technical Specialist II, Stem Cells to join our Chesterford Park site, set in Saffron Walden.

This is a permanent, onsite role with expectation to be based in the laboratory.

The Technical Specialist II will be applying lab-based technical expertise in Stem Cell culture in contribution to agreed specifications in delivering client projects to agreed deadlines. You’ll be an expert in stem cell culture as this is not an entry level role and candidates must have a track record of culturing and differentiation hES and iPS cells within industry.

Candidates must have full and permanent Right to Work in the UK to be considered as we are unable to offer sponsorship for this position.

What you’ll be doing:

• Culture and differentiation of hES and iPS cells in line with client and project needs.

• Isolating and culturing primary cells, recombinant cell line generation and preparation of cell lines for high throughput screening projects.

• An awareness of relevant scientific and contemporary cellular assay practices, with the ability to use this knowledge to troubleshoot assays

• Demonstrate deep understanding of a wide variety of stem cell culture methods, and able to apply learnings from one method to other areas.

• Independently perform and optimize stem cell differentiation in 2D and/or 3D culture systems.

• Execution of routine technical and non-technical tasks with high level of competency and minimal supervision.

• Owns workload to meet agreed deliverables with awareness of how this impacts the immediate and wider team.

• Adherence to safe lab working policies, with some ability to suggest new ideas and provide solutions for immediate workspace.

• Accountable for accurate reporting of billable time, aware of financial impact across projects portfolio and division.

• Stay up to date with sector insights relevant to the scientific field, sharing knowledge within the group.

• Recognise and identify solutions for technical problems of varying complexity, escalate to appropriate manager/project leader to agree and implement appropriate solution/s.

Skills & Qualifications

• Educated to MSc level at a minimum in a Biological Sciences discipline, any degree with stem cell/cell culture focus is highly desirable.

• Demonstrable experience in isolation and culturing of primary cells, recombinant cell lines for high throughput screening in industry ideally from another CRO or Biotech company.

• Significant hands-on experience in culturing and differentiation of hES and iPS cells, able to execute outstanding aseptic technique.

• Additional experience of working on drug discovery focused projects is highly advantageous.

• Excellent communication skills, able to liaise with internal and external stakeholders as needed and able to collate and present complex scientific datasets.

• Candidates must be able to travel to our Chesterford Park site on a daily basis.

What We Offer You:

• Global opportunities and strong career progression.

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

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

• To continue your own career growth.

• Flexible and hybrid working.

• Parental leave.

• Group Life Assurance and Group Income Protection.

• Remote GP access 24/7.

• Well-being support and initiatives.

• Cycle to work scheme.

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 (50) (Bethesda, MD, US, 20892)

Job Summary

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

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

Additional responsibilities include:

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

Job Qualifications

The following are minimum requirements related to the Cagewash Attendant I position:

High school diploma or GED preferred
Knowledge of detergent/disinfectant and operating knowledge of sanitization and sterilization equipment
Cagewash experience preferred
Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1 year of eligibility.

The pay for this position is $20.32 USD per hour. Schedule: Monday through Friday 7AM-3:30PM.

Equal Employment Opportunity

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

Molecular Technologist I (Newark, DE, US, 19711)

Job Overview

Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE.
This position is Monday - Friday 8:30 am to 5:00pm.

The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance.

Roles and Responsibilities:

•    Conduct accurate processing of customer samples in accordance with current SOPs.
•    Receive, unpack, log, and subculture customer samples according to current SOPs.
•    Aliquot and prepare reagents.
•    Perform test streaks for isolation, PCR, sequencing of customer samples and other laboratory processes including but not limited to mass spectrometry and ribotyping.
•    Perform continual maintenance, repair and cleaning of all laboratory equipment.
•    Perform pipette verification.
•    Operate and maintain laser cutter.
•    Provide backup for all laboratory functions when needed.
•    Dispose of microbe cultures, chemicals and glass in proper waste containers.
•    Collaborate with technical support to resolve discrepancies with customer samples.
•    Comply with all aspects of laboratory safety, safety stations, safety manuals, safety SOP, and MSDS sheets.
•    Suggest process improvements.
•    Perform or support special projects in the lab when needed.
•    Perform all other related duties as assigned.

Qualifications

•    Education: Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred.
•    Experience:  0-2 years related experience in a laboratory setting or academic setting.
•    Other: Must have working knowledge of the Quality System and Laboratory Information System. Must have ability to work in a fast paced and team oriented work environment. Strong attention to detail and accuracy required.

The compensation range for this position is $21- $22 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.

Opérateur·trice de lave-cage (poste de jour) (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Opérateur·trice de Lave-Cage – Horaire de jour – Aucune Expérience nécessaire

En tant qu’Opérateur·trice de Lave-Cage pour notre équipe de Toxicologie à notre site de Sherbrooke, vous aurez la charge d’assurer la propreté des équipements utilisés pour maintenir les conditions de vie des animaux selon les plus hauts standards de bien-être de l'industrie.

Dans ce rôle, les principales responsabilités incluront:

Faire fonctionner et effectuer les vérifications quotidiennes des laves-cages.
Surveiller l’utilisation des savons et les besoins divers des lave-cages.
Nettoyer tous types d’habitation d’animaux ainsi que leurs accessoires (jouet, bouteille, bols, etc…).
Effectuer l’entretien de base sur toutes les cages et accessoires afin de s’assurer que tout est sécuritaire pour les animaux.

Éléments Clés:

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

Organisé et Autonome.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit est un atout.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Informations spécifiques au poste :

Localisation: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transport: Facilement accessible avec le transport en commun. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire : 18.25$/HR.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/hr).

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
Gym gratuit sur place;
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 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.

Cage Wash Operator (Day Shift) - (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Cage Washer Operator – Day shift – No experience necessary.

As a Cage Washer Operator for our Toxicology team in Sherbrooke, you will be responsible for ensuring the equipment used to maintain the animal’s living conditions is cleaned according to the highest wellbeing standards in the industry.

In this role, key responsibilities include:

Operating and performing daily checks on cage washer machines.
Monitor the use of soaps and various needs of the cage washers.
Clean all types of animal housing and accessories (cage, toys, bowl, waterbottle, etc…)
Perform basic maintenance on all cages and accessories to ensure that everything is safe for the animals.

Key Elements:

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

Organized and self-driven.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role specific information:

Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station;
Salary: 18.25$/hrs
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

We offer competitive benefits and advantages from day one to support your well-being;
Free gym on site;
Employee and family assistance program;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

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!

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.

Equal Employment Opportunity

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

Chemical Formulation Technician (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Technician for our Formulation team at the Laval location, you prepare drug formulation that will be administered to animals under study.

In this role, primary responsibilities include:

Prepare drug formulation in suspension, capsule, solution, dermal cream, etc.;
Perform reception, verification and storage of Test items, chemicals, and products;
Use, calibrate and maintain various laboratory equipment.

Key Elements

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

No experience in Science and/or Laboratory is required;
High School diploma;
AEC or DEC in Biotechnology is an asset;
Team player with a collaborative and positive approach;
Strong observation & organizational skills;
Open-minded and willing to learn in a laboratory 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: $23.50/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime. You will also have to do weekend rotation (1/4). 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 ?

We offer competitive benefits and advantages from day one to support your well-being;
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;
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.

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.

Equal Employment Opportunity

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

Technicien.ne en formulation chimique (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Technicien.ne pour notre équipe de Formulation situé au site de Laval, vous serez responsable de préparer la formulation du médicament qui sera administré aux animaux sur étude.

Dans ce poste, les principales responsabilités incluront:

Préparer la formulation de médicaments en suspension, capsule, solution, crème corporelle, etc.;
Effectuer la réception, la vérification et le stockage des éléments de test, des produits chimiques et des produits;
Utiliser, calibrer et entretenir divers équipements de laboratoire.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Aucune expérience en science et/ou en laboratoire n'est requise;
Diplôme d'études secondaires;
Un AEC ou DEC en biotechnologie est un atout;
Esprit d'équipe avec une approche collaborative et positive;
Bonnes compétences en observation et en organisation;
Ouvert d'esprit et désireux d'apprendre dans un environnement de laboratoire.

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: 23.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour. Vous devrez également effectuer des rotations de fin de semaine (1/4). Selon les besoins de l’entreprise, vous pourrez être appeler à effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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;
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.

Analyste en Immunologie (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant qu’Analyste pour notre équipe d’Immunologie situé au site de Laval, vous serez responsable d’effectuer l'analyse des données pour déterminer si les résultats sont conformes aux attentes. 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 poste, les principales responsabilités incluront:

Effectuer des travaux d'analyse d'échantillons dans un laboratoire multidisciplinaire en utilisant une vaste gamme de techniques;
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

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

Aucune expérience en science et/ou en laboratoire n'est requise;
Diplôme d'études secondaires;
Un AEC ou DEC en biotechnologie est un atout;
Esprit d'équipe avec une approche collaborative et positive;
Bonnes compétences en observation et en organisation;
Ouvert d'esprit et désireux d'apprendre dans un environnement de laboratoire.

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: 23.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour. Selon les besoins de l’entreprise vous pourriez avoir à faire du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Immunology Analyst (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Analyst for our Immunology team at the Laval location, you will perform analysis of data for quality and completeness and determines if results are as expected. You will also record data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.

In this role, primary responsibilities include:

Carry out sample analysis in a multidisciplinary laboratory, using a wide variety of techniques;
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

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

No experience in Science and/or Laboratory is required;
High School diploma;
AEC or DEC in Biotechnology is an asset;
Team player with a collaborative and positive approach;
Strong observation & organizational skills;
Open-minded and willing to learn in a laboratory 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: $23.50/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday daytime. Depending on the business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Technicien·ne - Pathologie Clinique - Poste étudiant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Technicien·ne - Pathologie Clinique - poste étudiant

En tant que Technicien·ne pour notre équipe de Pathologie Clinique situé à notre site de Senneville, vous serez principalement responsable d’accomplir les tâches techniques et suivre les directives des plans d’étude/phase et les procédures. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Effectuer les préparations ainsi que les analyses des échantillons
Effectue le contrôle de qualité ainsi que les maintenances sur les différents instruments

Éléments Clés

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

Étudiant·e actuellement dans un programme en Science
Bonne attention aux détails
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.)
La compréhension de la lecture en anglais est obligatoire. Le bilinguisme français et anglais est préférable.

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: 23.50 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire : Horaire du lundi au vendredi de 8h00 à 16h15. En fonction des besoins, vous pourriez avoir à effectuer du temps supplémentaire les fins de semaine
Poste temporaire pour la période estivale, temps plein à 37.5hrs par semaine. Possibilité de rester à temps partiel à l’automne à discuter (tous les dimanches et les fériés).

Pourquoi Charles River?

Gym gratuit sur place
Cafétéria sur place
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine)
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.

Technician - Clinical Pathology - student position (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Technician, Clinical Pathology – Student position

As a Technician for our Clinical Pathology team located in Senneville, you will perform technical activities and follow directives from the study/phase plan and the procedures. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform the preparation and the analysis of samples
Perform the quality control procedure and maintenances on different instruments.

Key Elements

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

Student currently in a Science program
Good attention to details
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.)
Understanding of written English is mandatory. Bilingualism French and English is preferable

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: $23.50 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Weekdays, between Monday to Friday 8am to 4:15pm. Depending on the needs, you may have to do overtime on weekends
Temporary position for the summer period, full-time at 37.5hrs per week. possibility to stay part time after summer to be discussed (every Sunday + holiday).

Why Charles River ?

Free gym on site
Cafeteria on site
Access to a doctor and various health professionals (telemedicine)
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.

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.

Equal Employment Opportunity

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

Project Manager - Biologics (12-Months - Fixed Term Contract) (Erkrath, NW, DE, 40699)

Job Description

Location: Remote support for our US operations

Work Schedule: This role may be based in Germany, Ireland, or the UK and requires primary availability aligned with U.S. Eastern Standard Time (EST) hours. The position supports both APAC-based clients and U.S. sites, so flexibility is essential. Candidates must be comfortable accommodating occasional evening or after-hours client calls as business needs require.

Overview

We are seeking an experienced, client‑facing Project Manager to support biologics testing programs within our GMP Contract Testing Organization. This role reports to the Manager/Senior Manager of Project Management (U.S.-based) and partners closely with laboratory, quality, logistics, sales, and client services teams to ensure timely, compliant delivery of GMP testing projects.

The Project Manager will manage our key client accounts and other client programs that require complex planning and in-depth analysis to ensure that projects meet client expectations and deadlines. Functions as the primary client contact, with guidance from senior scientific staff, for activities related to the planning and execution of client programs. Interacts with clients in order to understand their requirements to disseminate and partner with Business Development, Client Services, Operational Staff, and Quality Assurance Staff. Organizes, collects, prepares, and distributes information necessary to ensure operational milestones are met from the development of contracts to final reporting. Recommends and implements study management improvements.

Key Responsibilities:

• Manage project scope, timelines, and budgets, including submission of scope changes and contract revisions
• Lead client and internal project meetings; prepare agendas, minutes, and follow up on action items
• Develop and maintain project timelines using project scheduling tools (e.g. Smartsheet)
• Support accurate intake, log‑in, and tracking of client samples
• Coordinate shipping and logistics for samples sent to subcontract laboratories
• Manage and approve project costs and invoicing
• Ensure compliance with GMP, SOPs, biosafety practices, and relevant regulatory requirements

Minimum Qualifications
• Fluent in English (written and spoken)
• Bachelor’s degree in biological or physical sciences (or related field)
• 4+ years of project management experience in a laboratory or research environment
• Strong organizational, communication, and problem‑solving skills
• Ability to manage multiple priorities in a fast‑paced, client‑facing role
• Proficiency with MS Office, Excel, MS Teams, Smartsheet, and project scheduling tools.

Preferred Qualifications
• CRO/CMO/CTO experience
• Experience working under a regulated system (cGMP, GLP)
• Current PMP certification

Physical Requirements

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

At Charles River, 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.

Assistant Technician 1 (Tranent, GB, EH33 2NE)

Job Overview

We are seeking an Assistant Technician for our Clinical Pathology Laboratory department site located in Elphinstone, Tranent.

Clinical Pathology is responsible for analysing biological samples, mostly fluids, taken from subjects which are part of toxicology and other regulatory studies. Training will be provided for use of our Laboratory Information Management System and working in a GLP environment.

Key responsibilities include the following:

•   Tube preparation and delivery
•   Preparation of study files
•   Monitoring and maintaining levels of consumable products
•   Data transfer and archiving procedures
•   Filing
•   Sample processing

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

•   A NAT5/Higher or equivalent qualification in two of Maths, Chemistry and Biology
•   Strong organisational skills with the ability to pay attention to detail
•   Good communication skills
•   IT literate with experience of Microsoft packages.

The salary for this role is £24,050.50 per annum.

Closing date for applications is 26 May 2026.

Job Description

Education

No degree required

Physical Requirements

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 Laboratories, we recognize and recruit all talent. We are a company committed to fostering a sense of belonging and work daily in this direction.

Strategic Business Specialist (Ballina, IE, F26D786)

Job Overview

The Strategic Business Specialist is a key contributor responsible for researching, designing, and evaluating advanced system and data-driven solutions to support organizational strategy as well as daily operations.

This role requires a highly analytical, detail-oriented professional with strong project management, communication, and collaboration skills, as well as a deep commitment to innovation within a rapidly evolving digital and scientific environment.

The position focuses on developing solutions to moderately complex business and technical challenges through rigorous data analysis, business intelligence, and systems integration. The Specialist identifies strategic opportunities and performance gaps, translates complex data into actionable insights, and ensures accurate interpretation of metrics across stakeholders. Responsibilities include defining assignment objectives, supporting long-range organizational goals, and delivering meaningful performance indicators to drive informed decision-making.

Operating under general supervision, the role exercises sound judgment and accountability, with work reviewed for quality, accuracy, and strategic alignment. The Specialist collaborates cross-functionally and engages periodically with senior internal and external stakeholders on matters requiring coordination and alignment. The role also supports business optimization, change management initiatives, and the continuous improvement of systems and processes, while mentoring associate-level team members.

The ideal candidate brings substantial experience in research or regulated environments, strong expertise in data analysis, visualization, and business intelligence tools, and working knowledge of programming and database management. A background in biotechnology, biological sciences, computer science, or related disciplines supported by equivalent professional experience—is required. Fluency in English is essential, with German proficiency and experience in GMP-regulated environments considered strong advantages.

Essential Duties and Responsibilities

Develop and execute comprehensive project management plans, ensuring clear, transparent communication across all organizational levels.
Design, build, and refine data queries by consolidating multiple data sources within business intelligence platforms; develop complex logic to support dashboards, workflows, and analytics across systems.
Coordinate the development of visual workflows, rigorously validate metric definitions, and enable stakeholders to accurately interpret data, minimizing misinterpretation and reducing time to insight.
Identify key collaborators and facilitate cross-functional coordination to ensure alignment with strategic objectives and business goals.
Establish and maintain strong, long-term partnerships to support optimized systems integration; respond to management and executive inquiries with thorough analysis, research, and actionable recommendations.
Perform routine systems analysis and data compliance reviews to enhance performance, ensure data integrity, and proactively diagnose and resolve issues.
Lead the delivery of key performance indicators and operational metrics to stakeholders, identifying opportunities for optimization and driving continuous improvement initiatives.
Promote awareness of business and system requirements across organizational units, identifying and addressing process inefficiencies and underperforming systems.
Monitor global performance metrics to detect outliers or adverse trends, proactively escalating risks to internal stakeholders and evaluating process constraints and bottlenecks.
Train, mentor, and support associate-level team members to strengthen analytical and technical capabilities.
Perform additional duties as assigned to support organizational objectives.

Qualifications and Experience

Qualifications - Education (either):

A Master’s degree (M.A. or M.S.) or equivalent in biotechnology or the biological sciences, with demonstrated experience in data analysis and a strong affinity for information and computer technology. An equivalent combination of education and relevant professional experience may be considered in lieu of a formal degree.
A Bachelor’s degree or equivalent in computer science or software engineering, with prior experience in data analysis within a GMP environment, or a computer science degree complemented by professional experience in the biological sciences, preferably within a GMP-regulated setting. An equivalent combination of education and experience may be accepted in place of a degree.
Language proficiency: Fluency in English is required; proficiency in German is considered an asset, as is knowledge of additional languages.

Experience

An excellent communicator with the ability to translate complex data into clear, actionable insights.
Demonstrated experience in developing and executing business strategies.
Proven capability in managing complex projects from initial conception through implementation.
Documented success in business optimization initiatives and change management efforts.
Comprehensive knowledge and practical experience with optimization and efficiency methodologies, such as Dynamic Work Design, Six Sigma, Agile, or similar frameworks.
Strong proficiency in Excel and Power BI is required; experience with other business intelligence tools, such as Tableau, is also acceptable.
Proven experience with, and foundational knowledge of, at least one programming language such as C++, Python, DAX, VBA, or equivalent.
Strong working knowledge of Microsoft Office applications.
Demonstrated analytical strength, including hands-on experience with data analysis and advanced data visualization techniques.
Proven ability to manage and analyze large datasets; experience with SQL and database management is strongly preferred.
Experience with software implementation and system rollouts is preferred.
Prior experience working in a GMP-regulated environment is desirable.

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.

Warehouse Operator (Dublin, IE, D09)

Job Overview

We are seeking a Warehouse Operator to join our team at our Rathcoole site in D24 NF21 Co.Dublin.

This role is Full time, Monday to Friday 08:30 to 16:30 (with occasional early finsh on Friday) Structured working week full time 37.5 hours.

It is an On Site role and the ideal candidate will have a vehicle and Full Licence or live in a commutable location close to D24 Eirecode.

This role comes with Salary, Paid Holidays, Pension Plan, Medical Insurance and other great employee benefits.

Ideally suited to someone who enjoys active, physical work and has some demonstrable track record of performance within a similar environment.

What you'll be doing

• Receive and distribute shipments according to established SOP & procedures.
• Package materials according to standard operation procedure.
• Maintain dock and warehouse area in an orderly fashion as per SOP.
• Prepare, maintain and distribute appropriate documentation for all materials shipped. GDP compliant.
• Coordinate and perform courier pick-ups/deliveries as necessary.
• Perform all other related duties as assigned by Manager or Supervisor.

Candidate Requirements

• Education: Leaving Certificate or higher.

• Experience: Some related 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: Valid driver’s license preferred.

• Fork Lift Truck Operator desirable, but not essential.

• Must have excellent organisational skills and the ability to manage multiple priorities; attention to detail, computer literacy; and the ability to interact appropriately at all levels.

• Ideally knowledge of electronic equipment, instrumentation and spare parts including experience of moving and handing in a safe manner.

• Ideally Awareness of supply chain processes and best practices.

• Ideally project experience or knowledge.

• SAP experience.

Benefits Summary

Annual Leave
All full-time employees receive 172.5 hours holiday per year (plus 10 bank holidays}. In addition, a further 7.5hrs wellbeing time is also applicable.
Group Personal Pension Plan– Irish Life
Personal enrolment into the Pension Scheme is mandatory from day 1 of employment whereby the company will match employee contributions of 5% of base salary. Contributions are paid monthly and will be allocated to individual employee fund.

Laya Healthcare Medical Insurance
Effective from your first day, colleagues can choose to have Private Medical Insurance with Laya.

Charles River Employee Discount Scheme (CREDS)
CREDS is a discount shopping website featuring over 3000 big-name retailers, set up specifically to benefit our colleagues. From mobile phones to groceries, clothes to electricals, and even holidays, with the option to accumulate cashback online, get instant discount codes or order top-up cards and vouchers to use in-stores.

Equal Employment Opportunity

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

Senior Data Scientist (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 Overview

At Charles River Laboratories, we’re transforming how we work by harnessing the power of AI, data, and digital innovation to accelerate the discovery and development of life-saving therapies. Our vision is to embed AI and advanced analytics across every stage of our scientific and operational workflows, empowering our teams with smarter tools, seamless data, and actionable insights to deliver client-centric services and solutions that better serve our customers and, ultimately, improve patients’ lives.

As a Senior Data Scientist and a member of our Enterprise Data & Analytics engineering team, you will play a pivotal role in this transformation. You’ll lead the design, development, and deployment of data-driven and AI-powered solutions that enhance customer value, streamline operations, and create meaningful, data-informed experiences for our employees. Through advanced analytics and generative AI, you’ll help Charles River unlock new possibilities in how we deliver science, innovation, and impact to our clients and the patients they serve.

In this role, primary responsibilities include:

Lead end-to-end data science initiatives, including data exploration, model development, validation, implementation, and support for mission-critical applications;
Collaborate closely with cross-functional data teams to automate data science pipelines and integrate models into business workflows and digital platforms;
Partner with business units in a consultative and collaborative manner, advising on the most effective approaches to leverage data science and Generative AI technologies to deliver innovative, high-impact solutions.

Job Description

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;
Experience in or strong understanding of the life science industry, particularly in leveraging data science to support operational excellence, is preferred.

Technical Expertise required:

5+ years’ hands-on experience processing, analyzing and modeling large and complex data sets;
3+ years’ experience with the full Machine Learning product lifecycle, with a demonstrated ability to take initiative and ensure proactive delivery of project milestones;
5+ years’ experience working with development toolsets such as SQL, PySpark, Python, Pandas or Scala;
Experience with Generative AI technologies for scientific document reading, summarization, and generation, including prompt engineering, retrieval pipelines, and LLM fine-tuning for domain-specific applications.

Equal Employment Opportunity

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

Animal Research Technician - 2nd Shift (Mattawan, MI, US, 49071)

Job Overview

We are seeking a Technician I for our 2nd Shift Toxicology Team in 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, conducting euthanasia, 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 hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

The working schedule for the role is Monday - Friday 2:00pm - 10:30pm.

Job Description

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, 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.

Minimum Requirements

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. 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.
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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.

Equal Employment Opportunity

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

Archive Associate I (Ashland, OH, US, 44805)

Job Overview

An Archive Associate I is learning and performing basic skills, procedures, and cooperating in a team environment. The archivist is learning daily tasks, performing, and becoming more efficient in skills required of the department training plan which may include organizing, filing, and retrieving facility and study-related records, biological specimens, and samples, assisting internal customers by checking study materials in and out, use of the archive management system, and upholding all archive security procedures to maintain integrity, confidentiality, and excellent customer service. The archivist is usually working closely with a trainer or buddy but becoming more independent.

Essential Duties and Responsibilities:

Ensure care and respect for all CRL resources including people, equipment, and facilities.
Perform basic skills of the department which may include organizing, filing, and retrieving facility and study-related records, biological specimens, and samples, assisting internal customers by checking study materials in and out, use of the archive management system, and upholding all archive security procedures to maintain integrity, confidentiality, and excellent customer service. 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.
Perform all other related duties as assigned.

Qualifications:

Education: High school diploma or General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
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.
Ability to push, pull, lift 30 lbs consistently throughout the day

Must be authorized to work in the United States without a sponsor visa, now or in the future.

The pay range for this position is $18-20/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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

Equal Employment Opportunity

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

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

Job Overview

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.

Job Description

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.

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.

Equal Employment Opportunity

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

Manager, Bioanalytical Chemistry (Mattawan, MI, US, 49071)

Job Overview

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

Essential Functions:

Efficiently perform supervisory responsibilities in accordance with organizational policies and applicable laws to include interviewing, hiring, training and developing employees
Develop organizational strength by hiring, identifying and developing personnel who are scientifically and/or technically strong
Establish culture and atmosphere to maintain good retention and low turnover using available tools and metrics
Assist with providing costing estimates for components of applicable studies
Provide short- and long-term solutions that support continuous improvement
Develop and maintain 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
Ensure laboratory tasks and operations are executed in compliance with SOPs, protocols, regulatory requirements
Establish and review Standard Operating Procedures (SOPs), protocols, policies, best practices and study procedures
Develop and maintain contemporaneous knowledge of regulatory requirements
Effectively plan, assign and direct work within one operational area with expanded scope and/or complexity
Monitor performance metrics for operational area
Function as a Principal Investigator, Individual Scientist, and/or Project Scientist as required by operational area or resourcing need
Skillfully oversee the design, conduct, interpretation and reporting of studies
Effectively utilize project management systems
Lead implementation of new procedures and refinement of existing procedures to meet current and future business needs
Performs all other related duties as assigned

Job Description

Bachelor’s degree or equivalent with 8-10 years of relevant experience. Between 3-4 years of management experience required
LCMS Experience Required
CRO Experience Preferred
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints
Must be authorized to work in the United States without a sponsor visa, now or in the future.

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

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

Education

Four-year degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Archive Customer Service Associate I (Horsham, PA, US, 19044)

Job Overview

Responsible for client communication, billing, and marketing of Charles River Archiving services. Responsible for the placement and retrieval of archived material in a secure and controlled access archive. Maintain accurate summary of records. Update inventories for access and retrieval of archive materials. Interact with clients.

Job Description

Required to live near the Horsham location.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
⦁ Performs and documents all procedures, materials, and results in compliance with regulatory standards as applicable to protocols, reports and standard operating procedures.
⦁ Upholds archive security procedures and maintains the integrity of archived materials and client confidentiality.
⦁ Performs tasks including but not limited to, client contract generation, organizing, filing, and retrieving records.
⦁ Utilize the archival management system for client contract generation.
⦁ Communicate with internal and external clients as it relates to contracting and archiving.
⦁ Develops skills aligned with the needs of one operational area (transfer of ownership, local or global account manager, contract development, marketing).
⦁ Prepare archiving contracts and relevant documents to notify clients of archived study materials.
⦁ Assist clients with regulatory retention periods in collaboration with the archivist.
⦁ Oversee client communication and requests regarding archived material.
⦁ Monitor and track archiving business activities.
⦁ Perform all other related duties as assigned.

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

QUALIFICATIONS:
⦁ Education: High school diploma or General Education Degree (G.E.D.)/ Associate’s degree (A.A./A.S.) / or equivalent desired in business or administrative assistant discipline.
⦁ Experience: 0.5-2 year of customer service experience required. 1-2 year of office experience or administrative/inventory management training preferred. Marketing experience preferred.
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None.
⦁ Other: Proficient computer skills with departmental databases, word processing (Word), and spreadsheet programs (Excel). Must be organized, have attention to detail and possess good problem-solving and communication skills.

PHYSICAL DEMANDS:
⦁ Regularly communicate with employees/customers through various technologies, media, sources and contacts. Must be able to exchange accurate information.
⦁ Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁ Occasionally move about inside the office to access file cabinets, office machinery, etc.
⦁ Occasionally lift and carry up to 40 pounds (archived material) up and down stairs, laterally from shelf to shelf and from and to shelves of varying height; up to 5 feet high.

WORK ENVIRONMENT:
⦁ General office working conditions; the noise level is usually quiet.
⦁ May work from home with reliable internet and communication access.

Comments:
⦁ May occasionally be required to work overtime or come into the office for meetings or trainings.

Education

No degree required

Physical Requirements

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.

Equal Employment Opportunity

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

Supervisor, Toxicology (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Supervisor – Toxicology

As a Supervisor for our Toxicology group at the Sherbrooke location, you will be supervising a team in order to mobilize, empower and develop employees.

In this role, primary responsibilities include:

Ensure employee and department performance management.
Give employees feedback in a timely manner.
Collaborate with the various company divisions to optimize operations.
Guide, train, coach, support and maintain a collaborative team and a continuous improvement approach.
Ensure and promote positive and effective working relationships with the management team, human resources and key collaborators.
Regularly communicate expectations regarding quality, performance, goals, animal welfare, and health and safety.
Review and respect budgets for assigned sectors.
Manage various operational challenges.
Apply the principles of Good Laboratory Practices (GLP) and Standard Operating Procedures (SOP).

Key Elements

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

Good interpersonal and communication skills
Strong problem-solving skills
Good listener and strategic vision
Bilingualism French and English is required.
Collegial diploma is science or any related field in management.

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
Pay: Salary based on experience and internal equity
Schedule: Full time, permanent position (37.5 hours/week).

Why Charles River?

We offer competitive benefits and advantages from day one to support your well-being;
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.

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.

Equal Employment Opportunity

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

Superviseur·e - Toxicologie (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Superviseur·e - Toxicologie

En tant que Superviseur·e pour notre équipe de Toxicologie situé au site de Sherbrooke, vous superviserez une équipe de façon à mobiliser, encadrer, responsabiliser et développer les employés.

Dans ce rôle, les principales responsabilités incluront:

Effectuer la gestion de la performance des employés et du département.
Donner de la rétroaction aux employés en temps opportun.
Collaborer avec les différents secteurs de l’entreprise afin d’optimiser les opérations.
Guider, former, encadrer, soutenir et maintenir une équipe collaborative dans l’amélioration continue.
Assurer et promouvoir des relations de travail positives et efficaces en partenariat avec l’équipe de gestion, des ressources humaines et des collaborateurs clés.
Communiquer régulièrement les attentes en matière de qualité, de performance, d’objectifs, de bien-être animal et de santé et sécurité.
Examiner et respecter les budgets pour les secteurs assignés.
Gérer les différents défis opérationnels.
Appliquer les principes de bonnes pratiques de laboratoire (BPL) et des procédures normalisées d'opération (PNO).

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Bonnes aptitudes interpersonnelles et de communication
Bonnes compétences en résolution de problème
Le bilinguisme français et anglais est obligatoire
Diplôme collégial en science ou tout autres domaines reliés à la gestion.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Informations spécifiques au poste:

Localisation: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5
Transport: Facilement accessible avec le transport en commun. Stationnement gratuit. Borne de recharge pour voiture électrique
Salaire selon expérience et équité interne
Horaire : Poste temps plein et permanent (37.5HR/semaine).

Pourquoi Charles River?

Nous offrons des avantages et bénéfices concurrentiels dès votre embauche pour soutenir votre bien-être;
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.

Tierarzt/Tierärztin (Sulzfeld, Bavaria (Bayern), DE, 97633)

Sie wollen etwas bewegen?

Wir sind das mittelständische Tochterunternehmen eines weltweit agierenden US-Konzerns und als Zulieferer für die biomedizinische Forschung tätig.

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierärztin / Tierarzt für unsere Niederlassung in 97633 Sulzfeld (m/w/d)

Job Summary

Unser Angebot:

Sie arbeiten in einem Team und erhalten eine ausführliche und betreute Einarbeitung
Ein leistungsgerechtes Einkommen,
Eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten und wachsenden Unternehmen
Zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, VWL-Förderung u.v.m.)

Profile and Requirements

Ihre Aufgaben:

Sie arbeiten im Team der Standorttierärzte/ärztinnen
Sie übernehmen die Verantwortung als einer/s der Tierschutzbeauftragten gemäß § 10 TierSchG und überwachen die Einhaltung der gesetzlichen Regelungen bezüglich Tierversuche und Haltungsbedingungen.
Sie sind unmittelbar in die intensive Kundenberatung bei tierschutz- und gesundheitsrelevanten Angelegenheiten eingebunden
Sie sind aktives Mitglied im konzernweiten Netzwerk der Veterinäre.

Sie wirken unterstützend mit bei der Implementierung bzw. Verbesserung unserer Biosicherheitsrichtlinien.
Sie planen und überwachen die Hygiene- und Genetikuntersuchungen unserer Zuchtbestände.
Sie führen interne Schulungen zu den Themen Tierschutz und Tiergesundheit durch.

Die Anforderungen:

Sie absolvierten ein Studium der Veterinärmedizin und haben eine abgeschlossene Promotion, idealerweise im versuchstierkundlichen Bereich
Sie verfügen über Berufserfahrung im Bereich Versuchstierkunde inklusive behördlich akzeptierter Qualifikationen wie FELASA B und ggf. FELASA C
Einsatzbereitschaft überwiegend vor OrtSie können selbständig, zuverlässig, flexibel und erfolgsorientiert arbeiten.
Sie beherrschen die deutsche und englische Sprache fließend in Wort und Schrift.

Sie sind interessiert?

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

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

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

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