Cencora seeks a Pharmacovigilance Auditor in Madrid to lead GVP audits, conduct mock inspections, and assess pharmaceutical safety systems. The role requires extensive PV expertise, audit planning capabilities, and regulatory compliance knowledge to support clients across Europe.

Responsibilities

- Lead or co-audit GVP compliance across process, system, and document reviews
- Conduct mock inspections and support pharmaceutical companies during regulatory inspections
- Assess pharmacovigilance systems, processes, and cross-departmental interfaces
- Develop audit strategy, risk assessments, and audit programs; manage corrective action plans
- Advise clients on Good Pharmacovigilance Practices and regulatory compliance requirements

Requirements

- Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related discipline
- Minimum 10 years pharmacovigilance experience
- Minimum 5 years GVP auditing experience
- Demonstrated audit planning, execution, documentation, and follow-up skills
- Strong knowledge of integral and local pharmacovigilance regulations and GVP
- Fluent in English; additional languages preferred
- Availability to travel at least 30% of the time

📌 PHARMACOVIGILANCE AUDITOR (España)
🏢 Cencora
📍 España