Auditor - GVP

Role: Serve as GVP Auditor within global pharmacovigilance quality assurance, executing audits to ensure safety data accuracy and compliance with regulatory standards. Responsibilities: conduct external audits of PV vendors and internal safety processes, develop comprehensive audit reports, identify non-compliance trends, support continuous improvement of SOPs, and maintain up-to-date knowledge of GVP regulations. Requirements: BS in biological sciences, pharmacy, or related field; proven QA experience in GVP-regulated environments; expertise in PV audit management; strong communication skills for multinational stakeholder engagement. HighValue: GVP audit expertise, pharmacovigilance operations, regulatory compliance (EMA, FDA), risk assessment, trend analysis, up to 50% travel. WorkSetup: Not specified.