Offer summary
Qualifications:
Graduate degree in Scientific Discipline/Life Sciences or related field, 7+ years pharma industry experience, 5+ years in Pharmacovigilance QA, regulatory inspection background, good knowledge of GVP, CFR, GCP regulations, SOPs, CAPA programs.
Key responsabilities:
- Provide PV consultancy, lead inspections, develop and maintain Global PVRQA Audit Program, analyze audit observations, manage qualification of service providers, oversee PV-related BT systems, support continuous improvement of PVRQA processes, contribute to strategic vision, travel domestically and internationally