Responsable Affaires Réglementaires Et Pharmacovigilance (rpv/lso) - Pharmacien Responsable Intérimaire

Seqirus France

France
Regulatory compliance
Pharmacovigilance system management
Promotional material control
You will play a key role in the regulatory compliance and quality of the laboratory's activities

Job Summary

  • You will play a key role in the regulatory compliance and quality of the laboratory's activities.
  • Manage and draft legal mentions for specialties, and participate in the realization and approval of packaging articles.
  • Implement and manage the pharmacovigilance system on national territory, ensuring compliance with national regulations and GSPV policies.

Matching Summary

You will play a key role in the regulatory compliance and quality of the laboratory's activities.

Skills & Requirements

Must-have

  • Regulatory compliance
  • Pharmacovigilance system management
  • Promotional material control
  • Submission to Health Authorities
  • Legal mentions management
  • Regulatory intelligence

Nice-to-have

  • Quality system management
  • Audit participation
  • CAPA implementation
  • Cross-functional collaboration
  • Training delivery

Key Requirements

  • Doctor of Pharmacy degree
  • Master's in Pharmaceutical Regulation and/or DU in Pharmacovigilance
  • Minimum 5 years of experience in Regulatory Affairs and Pharmacovigilance
  • Eligible for registration with the French Pharmacist Order (Section B)

Work Rights

Not specified

Tailored Resume

Cover Letter