Auditor - GVP

Role: Serve as GVP Auditor within the pharmacovigilance quality audit program, ensuring compliance and data accuracy. Responsibilities: conduct external audits of PV vendors and internal safety processes, produce detailed audit reports, categorize findings by risk, and develop CAPAs; analyze trends for systemic risks, support SOP improvements, and maintain knowledge of global GVP regulations. Requirements: BS in biological sciences, pharmacy, or related field; experience in GVP-regulated QA environments; audit and inspection expertise; strong communication skills; proficiency with ICH GVP guidelines, FDA/EMA regulations, and pharmacovigilance standards. HighValue: pharmacovigilance, GVP compliance, audit management, PV safety systems, EMA and FDA regulatory knowledge. WorkSetup: up to 50% travel.