Auditor - GVP

Role: GVP Auditor within a global pharmacovigilance quality audit program, responsible for executing audits of external vendors and internal safety functions to ensure data accuracy and compliance with global GVP guidelines. Responsibilities: conduct risk-based audits, prepare detailed reports, identify non-compliance trends, and support continuous improvement initiatives aligned with EMA and global regulatory standards. Requirements: BS in biological sciences, pharmacy, or related field; extensive QA experience in GVP-regulated environments; audit management expertise; strong communication skills for cross-regional stakeholder engagement. High-Value: pharmacovigilance (PV), GVP compliance, external vendor audits, risk assessment, EMA GVP Modules, 21 CFR Parts, and global pharmacovigilance regulations. Work Setup: hybrid with up to 50% travel.