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.
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
Dans le cadre du développement de nos activités scientifiques, nous recherchons un(e) Associate Director Laboratory Operations pour piloter la performance opérationnelle de plusieurs laboratoires stratégiques et accompagner la transformation de nos plateformes analytiques.
Rattaché(e) au Sr Director Laboratory Sciences, vous jouez un rôle clé dans la mise en œuvre de la stratégie opérationnelle du site, en garantissant l’excellence scientifique, la qualité des opérations et le développement des équipes.
Vos missions
À la tête d’une organisation d’environ 120 collaborateurs, vous assurez la supervision opérationnelle de plusieurs laboratoires couvrant notamment les activités de Formulation, Formulation Analysis, Clinical Pathology, Immunochemistry, Cell-Based Assays, Flow Cytometry et Molecular Biology/Genomics.
À ce titre, vous :
- Pilotez la performance opérationnelle, la capacité des laboratoires, l’allocation des ressources et l’atteinte des objectifs de qualité, de délais et de productivité.
- Animez et développez une équipe de managers et responsables de laboratoire en favorisant l’engagement, la montée en compétences et la performance collective.
- Garantissez le respect des exigences réglementaires et des standards BPL au sein des différentes activités.
- Définissez, suivez et analysez les indicateurs de performance afin d’identifier les opportunités d’amélioration et de mettre en œuvre les plans d’action associés.
- Conduisez les initiatives d’excellence opérationnelle visant à optimiser les processus, améliorer l’efficacité des flux de travail et accroître la capacité des laboratoires.
- Portez les projets de modernisation technologique, notamment à travers le déploiement de nouvelles plateformes analytiques et le développement de l’automatisation des activités de laboratoire.
- Accompagnez les transformations organisationnelles dans un environnement en croissance tout en maintenant un haut niveau de qualité, de conformité et de satisfaction client.
- Collaborez étroitement avec des experts scientifiques, responsables opérationnels et partenaires internationaux afin d’aligner les priorités et soutenir les objectifs stratégiques de l’organisation.
- Contribuez activement à l’équipe de direction Laboratory Sciences et accompagnez le Sr Director Laboratory Sciences dans le déploiement de la stratégie du département.
Qualifications souhaitées
Titulaire d’un Doctorat (PhD), PharmD, DVM, MSc ou d’un diplôme équivalent en sciences de la vie, vous justifiez d’au moins 10 ans d’expérience dans l’industrie pharmaceutique, biotechnologique ou au sein d’une CRO, dont 5 années minimum dans des fonctions de management d’équipes scientifiques ou d’opérations de laboratoire.
Vous avez démontré votre capacité à piloter des organisations scientifiques complexes, à manager des managers et à faire évoluer les équipes dans des environnements exigeants et réglementés. Vous possédez une expérience solide des environnements BPL ainsi que de la gestion de plusieurs laboratoires ou départements techniques.
Votre parcours vous a permis de développer une compréhension des enjeux liés à plusieurs disciplines telles que la formulation, l’analyse de formulation, la pathologie clinique, l’immunochimie, la cytométrie en flux, les essais cellulaires ou encore la biologie moléculaire et la génomique.
Vous avez également conduit avec succès des projets d’amélioration continue, d’automatisation ou de modernisation d’équipements analytiques. Une expérience de l’automatisation des activités d’immunochimie et de l’optimisation des flux analytiques constitue un véritable atout. Une connaissance des méthodologies Lean, Operational Excellence ou Six Sigma sera particulièrement appréciée.
Évoluant dans un contexte international et matriciel, vous communiquez avec aisance en anglais, tant à l’écrit qu’à l’oral, et êtes capable d’animer des réunions, présenter des résultats et porter des initiatives stratégiques auprès d’interlocuteurs variés.
Modalités
- Convention collective de l’industrie pharmaceutique, groupe : 7
- Contrat : Cadre (RTT)
- Salaire : A compter de 70 000 € bruts / an sur 13 mois
- Prise en charge de la mutuelle à 100%, restaurant d’entreprise, CSE
- Primes de transport, d’intéressement/participation, accord de télétravail…
- Site non-accessible en transport en commun – Moyen de locomotion indispensable
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.
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.
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.
Helping you find your moment
You take great care and effort when you apply for a job with us. Rest assured that we’ll be just as diligent in finding the role that’s right for you. Here’s how our hiring process works:
Job Search
Learn about CRL, our culture, and why we do the work we do while also searching for roles that match your interests and expertise.
Application
Create a profile and apply to as many roles as you have an interest.
Note: Depending on the role, you may be required to include a resume in your application.
Assessment and application review
Complete assessments, if requested, to determine whether the role is likely to be a good fit for you – and vice versa. The recruiter will review your resume and qualifications against the requirements of the role and will determine next steps.
Note: At any point in the process, you can log into your profile to review the status of your application.
Interview
Engage in our interview process by meeting with a group of interviewers who will provide information on the company, culture, and your role while also asking you questions to assess your skills, interests, and expertise. This is also a great time for you to ask questions and better understand how we foster a sense of belonging at Charles River.
Note: Charles River leverages technical and behavioral-based interview questions based on our DNA (Care, Lead, Own, and Collaborate). Please familiarize yourself with the DNA and be prepared to relate your experiences to them.
Job offer and onboarding
Receive a competitive offer either by phone or email from a Charles River recruiter or hiring manager. The offer will include your title, salary, location, and other relevant information.
Note: Upon acceptance, you will work with your recruiter to confirm a start date and will receive paperwork to electronically complete prior to your start. For US-based roles, upon your acceptance, you will be required to take a pre-employment drug screen and pass a criminal background check.
Featured jobs
Important things are happening every moment at Charles River. This means exciting new career opportunities for you to explore. Take a look and apply today!
Looking for something else? Search all jobs.
Moment by moment
At Charles River, you’ll be able to contribute to incredible breakthroughs while experiencing exciting opportunities for growth and development.
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UX/UI Designer
Advocate for user-centered design solutions. Create distinctive, consistent, branded digital experiences across multiple platforms, devices, and channels.
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Sr. UX/UI Designer
Define and drive UX/UI strategies and interaction designs – from scratch and for scale – that solve business and user problems.
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Associate Director
Work with Sr. UX/IX Designers and developers to assess problems and develop solutions. Execute on plan by building coding standardisations and automating processes.
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Director, Digital Data Enablement
Lead UX management and operational teams across business units and technical teams. Identify and define fit-for-purpose strategies to integrate best practices.
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Sr. Director UX/UI Design
Mentor, coach, and guide designer teams on design strategy related to research insights, execution, continuous integration, and automated deployment.
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Animal Care Technician I-IV
Maintain the well-being of our animals by providing food, water, and a clean environment.
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Animal Care Technologist I-IV
Provide specialised care to maintain and monitor our animal's health and physical environment.
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Veterinary Technician
Help monitor, document, and triage all laboratory animal health cases.
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Team Leader / Supervisor
Supervise, train, mobilise, empower, and develop a high-performing team.
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Research Associate
Coordinate and plan activities according to study plan guidelines.
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Intern Level I
Support process/procedure improvement based on site and department needs. Gain knowledge of our corporate environment to navigate cross-functional department collaboration.
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Intern Level II
Complete comprehensive departmental projects incorporating mentorship of Level I interns as a professional development component.
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Biomanufacturing Technician I-III
Oversee the production, formulation, and banking of cellular products while maintaining compliance with GMP, GDP, and aseptic guidelines.
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Biomanufacturing Lead / Specialist
Maintain in-depth knowledge of specialised equipment to address questions as a Subject Matter Expert for the required equipment.
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Clinical Veterinarian I-III
Responsible for delivering professional veterinary services and helping to manage all phases of health care for the animal colony.
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Senior Clinical Veterinarian
Utlise knowledge of laboratory animal medicine to optimise the scientific objectives of animal research protocols.
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Principal Veterinarian / Associate Director
Conduct veterinary consultations, make treatment recommendations, communicate with study directors, and follow cases through to resolution.
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Director, Laboratory Animal Medicine
Provide technical and professional oversight of all animal care and use functions involving site laboratory animals.
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Technician I-III
Follow SOP and protocols in the areas of animal handling, husbandry, and blood/urine collection.
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Technician IV-V
Handle advanced technician duties, including anesthesia, leadership and specialised sample collections.
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Project Leader (Scientific)
Serve as a scientific expert for the Lab with responsibility for staff-conducted studies.
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Team Leader (People Leader)
Oversee team activities and gain leadership skills on the path to becoming a Team Supervisor.
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Team Supervisor (People Leader)
Responsible for overall employee supervision, staff development, and team success.
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Financial Analyst
Help analyse financial data, extract/define relevant information, and interpret data.
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Financial Analyst II
Responsible for analysis, forecasting, budgeting, accounting administration, and reporting of projects.
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Senior Financial Analyst
Handle weekly and monthly forecasting and annual budget preparation. Prepare financials and key indicators for business reviews.
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Manager, Business Finance
Partner with operating businesses to raise standards in key decision areas. Present a dynamic industry, competitor, and economic context.
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Finance Director, Operation
Support all business aspects, working with site teams to direct weekly/monthly forecasting and annual budget preparation.
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Biomanufacturing Technician I
Support the production, formulation, and banking of novel cellular products (including cGMP, GDP, and aseptic processing).
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Biomanufacturing Technician II
Perform specialised activities in the production, formulation, and banking of novel cellular products (including cGMP, GDP, and aseptic processing). Train Biomanufacturing Technician 1.
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Biomanufacturing Technician III
Help advance the production, formulation, and banking of novel cellular products (including cGMP, GDP, and aseptic processing) while interacting with clients.
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Biomanufacturing Lead / Specialist
Maintain in-depth knowledge of specialised equipment to address questions as a Subject Matter Expert for the required equipment.
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Biomanufacturing Supervisor
Oversee biomanufacturing personnel, ensuring compliance with cGMP’s, CRL quality systems, and process documents in biomanufacturing.
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Biomanufacturing Manager
Lead biomanufacturing activities in the start-up and cGMP production of novel cellular products. Schedule and manage staff, ensuring a safe and compliant working environment.
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Client Manager
Ensures high-quality customer service through multi-site coordination. Deliver timely, accurate, and comprehensive responses to sponsor requests.
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Business Development Director
Deliver profitable sales growth by targeting and visiting clients to build strong relationships and customer loyalty.
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Senior Business Development Director
Plan and execute a territory-based field sales strategy. Drive growth through targeted long- and short-term account plans.
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Regional Sales Manager
Manage sales team within North America's Safety Assessment sales region to achieve sales and profit goals.
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Director
Partner with site leadership to achieve performance goals, develop staff, and deliver succession planning.
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Senior Director / General Manager
Lead a multi-functional team to ensure integrated operations. Collaborate with senior leadership to form plans, objectives, and policies.
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Executive Director
Lead a global, mutidisciplinary team. Develop short and long-term strategic plans tp maximise growth and profitability.
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Corporate Vice President
Provide leadership, direction, and advice to leadership and finance teams. Accountable for financial planning, directing, and controlling.
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About Charles River
Charles River is an early-stage Contract Research Organisation (CRO). Here, we are passionate about our role in improving the quality of people’s lives. With 100 sites around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients’ unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies, hospitals, and academic institutions around the world.
Supporting your well-being
Your dedication and passion make a life-saving difference in lives around the world. We’re committed to providing you with benefits that elevate your quality of life.
About Charles River
Charles River is an early-stage Contract Research Organisation (CRO). Here, we are passionate about our role in improving the quality of people’s lives. With 100 sites around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients’ unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies, hospitals, and academic institutions around the world.












