Pharmacovigilance Quality Officer - VAF228

ProductLife Group; France; Hybride; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading pharmaceutical group in France seeks an experienced Pharmacovigilance Quality Officer to ensure compliance within their Global Safety department. This role involves managing PV audits, implementing KPIs, and enhancing quality processes. Candidates should have a degree in Life Sciences, 3-5 years of experience in pharmacovigilance, and strong skills in audit management and quality metrics. Fluency in English is essential, with French proficiency as a plus. Remote work is possible with occasional travel to Clermont-Ferrand.

Qualifications

• Minimum of 3 to 5 years of experience in pharmacovigilance and quality assurance within the pharmaceutical industry.
• Demonstrated expertise in managing pharmacovigilance audits.
• Strong understanding of GVP, ICH guidelines, and regulatory requirements.

Responsabilités

• Management of pharmacovigilance audits and compliance.
• Implementation and monitoring of PV KPIs.

Connaissances

Pharmacovigilance systems

Audit management

Quality metrics

Analytical skills

Communication skills

Formation

Degree in Life Sciences, Pharmacy, or related field

Description du poste

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)