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, EMA, and global regulations. Responsibilities: conduct and report on safety audits, identify non-compliance trends, develop CAPAs, and support continuous process improvement aligned with regulatory standards. Qualifications: BS in biological sciences, pharmacy, or related field; proven QA experience in a GVP-regulated environment; strong audit and inspection skills; excellent stakeholder communication. High-Value: pharmacovigilance, GVP compliance, audit management, EMA and FDA regulations (e.g., ICH E2 series, 21 CFR, EU directives), risk-based assessments, and trend analysis. Work setup: up to 50% travel, global stakeholder engagement.