Associate Director GVP Audits

Job Summary

A company is looking for an Associate Director, Good Pharmacovigilance Practice (GVP) Audits.

Key Responsibilities

• Lead risk-based quality auditing activities in compliance with international regulations
• Oversee the execution of GVP audits, including all phases from scheduling to follow-up
• Develop and implement new audit standards and provide mentorship to audit teams

Required Qualifications and Education

• Bachelor's degree required
• At least 11 years of relevant experience, including 9+ years in GVP auditing
• Strong understanding of EU and FDA Pharmacovigilance regulations
• Experience with regulatory inspections is desirable
• Proven track record in audit and project management