Auditor - GVP

Role: GVP Auditor within global pharmacovigilance quality assurance, responsible for executing audits of external vendors and internal safety processes to ensure compliance with GVP and global regulations. Responsibilities: conduct audits, develop detailed reports, categorize findings by risk, identify systemic non-compliance trends, and support continuous improvement initiatives aligned with EMA and other regulatory standards. Maintain current knowledge of PV regulations, including EMA GVP modules, ICH guidelines, and CFR parts. Qualifications: BS in biological sciences, pharmacy, or related field; proven QA experience in GVP-regulated environments; expertise in PV audit and inspection management; excellent communication skills for cross-border stakeholder collaboration. HighValue: pharmacovigilance, GVP compliance, external vendor audits, risk-based assessments, EMA and CFR regulations, global PV quality systems. WorkSetup: up to 50% travel, remote or hybrid work possible.