Technicien de Laboratoire en Immunohistochimie - CDI H/F - Charles River Laboratories

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.

Qui sommes-nous ?

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

Le poste

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

Les missions

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

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

Qualifications souhaitées

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

Vous possédez idéalement une première expérience professionnelle dans le domaine.

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

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

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

Modalités

• Convention collective de l'industrie pharmaceutique, groupe : 3
• Contrat : Non-cadre (accord de modulation 35h)
• Salaire : A compter de 25 714 € 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

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 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..

Equal Employment Opportunity

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

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to ****@****.**. 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.

• Chimie