Director, Central Quality Audit, Pharmacovigilance

📋 Description Develop, implement, and maintain a global PV audit strategy aligned with regulatory requirements. Own and execute audit programs for internal audits, affiliates, and service providers. Identify compliance risks and provide actionable recommendations to senior leadership. Define and monitor audit performance indicators and quality risks. Lead, coach, and develop a team of auditors for operational excellence. Partner with Pharmacovigilance, Quality, and Regulatory teams to drive continuous improvement. 🎯 Requirements Minimum of 5 years leading teams with coaching and performance management. Active certification as a qualified Lead Auditor. Master’s degree with 5+ years in pharmacovigilance/pharma, or Bachelor’s with 10+ years of related Proven experience managing global programs focused on quality and compliance. Strong knowledge of QMS and regulatory requirements: cGMP, GDP, GPvP, GCP, GLP. Experience with medical device quality systems and ISO 13485; familiarity with Veeva and TrackWise 🎁 Benefits Competitive salary range aligned with experience and location. Performance-based incentives, including potential bonuses and LTIs. Comprehensive healthcare benefits (medical, dental, vision). Retirement plan with employer contributions. Paid time off and additional employee support programs. Tuition reimbursement and professional development opportunities.