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.