Overview Pharmacovigilance Quality Officer - VAF228 France Hybrid Life Cycle Quality & compliance, Safety and Vigilance Permanent contract 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. Responsibilities Management of pharmacovigilance audits of PV subsidiaries/subcontractors/distribution and licensing partners (preparation, conduct, CAPA monitoring) Implementation and monitoring of PV KPIs 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) #J-18808-Ljbffr Groupe ProductLife
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