Responsable QA Validation Syst. Informatisés H/F
GSKPays de la Loire, France
Posted April 10, 2026
Contract / Temporary
About the Company
GSK is a leading biopharmaceutical company in France with over 3,300 employees across three production sites and the company's headquarters.
Job Description
GSK Laboratory is seeking a Quality Assurance Validation Systems Specialist to join their site in Mayenne, France. The successful candidate will be responsible for directing the activities of validation of computerized systems for a production site based in France.
Requirements
- Engineering degree, life sciences, pharmacy, computer science, or a similar technical discipline
- Minimum 5 years of experience in validating computerized systems in a pharmaceutical or highly controlled environment
- Practical knowledge of the validation life cycle (planning, IQ/OQ/PQ, testing, and reporting), GAMP 5, and Annex 11 of the BPF
- Experience in preparing or revising validation documentation and test evidence
- Data Integrity requirements knowledge/experience
Benefits
- Paid employment contract for an indefinite term
- Annual salary
- Employee benefits (not specified)
