Associate Director PV Compliance | Life Scientist (m/w/d)
BioNTech SE
Job Summary
This Associate Director of PV Compliance role, based in Mainz, London, or Munich, is critical for ensuring BioNTech's pharmacovigilance activities adhere to global regulations and quality standards. The successful candidate will oversee safety compliance tracking, manage procedural documents, and actively prepare for and participate in GxP regulatory inspections and audits. This position requires an individual with a strong background in life sciences, expert knowledge of pharmacovigilance regulations, and a proactive, collaborative approach to ensure audit and inspection readiness. It offers an opportunity to contribute significantly to patient safety and regulatory adherence within a leading biotech company.
Required Skills
Education
Advanced degree in life sciences/healthcare (or clinically relevant degree)
Experience
- At least 5 years of experience in Pharmacovigilance and/or Quality Assurance in the biotech or pharmaceutical industry
- Experience with GxP audits and inspections
- Experience with deviation and CAPA management
- Expertise in authoring procedural documents
Languages
Additional
- Not specified
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