Quality Assurance Auditor

il y a 4 jours

SaintGermainNuelles, France Charles River Laboratories Temps plein

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.

We are seeking a **Quality Assurance Auditor** for our **Safety Assessment **site located **in Saint-Germain Nuelles.**

An Auditor ensures that the test site is compliant with GLP regulations and can conduct preclinical studies.

**Main tasks are the following**:

- Carry out inspections to support all regulated work intended to support the company's business segments (processes, equipment, material, installation, etc.).
- Guarantee compliance of research activities with international regulation (GxP)
- Monitor study plans and final reports to ensure clarity, precision, and accuracy
- Conduct audits for suppliers, subcontractors, and vendors
- Participate in regulatory trainings for all employees
- Support the team in planning and organizing the department activities (audits, inspections,, KPI, etc.)
- Advice scientific teams and management on QA related matters

**Requirements**:

- Scientific background and education
- Previous experience as an auditor or inspector in a GLP environment
- IT skills
- English proficiency

**what we offer**:

- 13 months-based salary around 28k+ transportation costs compensation + Insurance + cafeteria + profit sharing & participation + seniority plan
- 35h work basis with adjustment agreement

**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.

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