Auditor - GVP

Role: GVP Auditor within global pharmacovigilance quality assurance, responsible for executing audits to ensure safety data accuracy and compliance with GVP and global regulations. Responsibilities: conduct external audits of PV vendors and internal safety functions, produce detailed reports with risk assessments and CAPAs, identify systemic non-compliance trends, and support continuous improvement initiatives aligned with EMA and other global standards. Maintain up-to-date knowledge of pharmacovigilance regulations and industry trends. Requirements: BS in biological or pharmaceutical sciences; extensive QA experience in GVP-regulated environments; proven audit and inspection skills; excellent communication and stakeholder management abilities. High-Value: expertise in pharmacovigilance regulations (ICH E2 series, 21 CFR Parts, EMA GVP modules), experience in audit management, and knowledge of complex safety systems. Work setup: involves up to 50% travel; location flexible.