We are currently seeking an experienced Pharmacovigilance Quality Officer to support our client, a leading pharmaceutical group, in ensuring high standards of compliance within their Global Safety department. This role will be instrumental in managing PV audits and enhancing quality processes.

Group 10
Responsibilities

  • Management of pharmacovigilance audits of PV subsidiaries/subcontractors/distribution and licensing partners (preparation, conduct, CAPA monitoring)

  • Implementation and monitoring of PV KPIs

Group 12
Profile

  • Degree in Life Sciences, Pharmacy, or a related field

  • Minimum of 3 to 5 years of experience in pharmacovigilance and quality assurance within the pharmaceutical industry

  • Demonstrated expertise in pharmacovigilance systems, audit management, and quality metrics

  • Strong understanding of GVP, ICH guidelines, and international regulatory requirements

  • Proactive, autonomous, and organized professional with strong analytical and communication skills

  • Fluency in English is essential; proficiency in French is a plus

  • Flexibility to work remotely with occasional travel to Clermont-Ferrand (1 to 2 days per month or every two months)

Pharmacovigilance Quality Officer - VAF228