Job Details

A company is looking for an Associate Director, Good Pharmacovigilance Practice (GVP) Audits.Key ResponsibilitiesLead risk-based quality auditing activities in compliance with international regulationsOversee the execution of GVP audits, including all phases from scheduling to follow-upDevelop and implement new audit standards and provide mentorship to audit teamsRequired Qualifications and EducationBachelor's degree requiredAt least 11 years of relevant experience, including 9+ years in GVP auditingStrong understanding of EU and FDA Pharmacovigilance regulationsExperience with regulatory inspections is desirableProven track record in audit and project management