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Pharmacovigilance Quality Officer - VAF228

ProductLife Group

France

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 4 jours
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Résumé du poste

A leading pharmaceutical group is seek a Pharmacovigilance Quality Officer to ensure high compliance standards within their Global Safety department. This role includes managing PV audits and enhancing quality processes. Candidates should possess a degree in Life Sciences or Pharmacy and relevant experience in pharmacovigilance.

Qualifications

  • Minimum 3-5 years experience in pharmacovigilance and quality assurance.
  • Fluency in English essential; French proficiency is a plus.
  • Strong understanding of GVP, ICH guidelines, and regulatory requirements.

Responsabilités

  • Management of pharmacovigilance audits of subsidiaries and partners.
  • Implementation and monitoring of PV KPIs.

Connaissances

Analytical skills
Communication skills
Organizational skills

Formation

Degree in Life Sciences, Pharmacy, or related field

Description du poste

Pharmacovigilance Quality Officer - VAF228
Client:

ProductLife Group

Location:

France

Job Category:

Other

EU work permit required:

Yes

Job Reference:

474a6305bf09

Job Views:

4

Posted:

28.06.2025

Expiry Date:

12.08.2025

Job Description:

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
Candidate 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)

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