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

Seqirus France

Paris, France
On-site
Regulatory document control
Marketing authorization dossiers
Pharmacovigilance system management
Play a key role in regulatory compliance and quality of laboratory activities

Job Summary

  • Play a key role in regulatory compliance and quality of laboratory activities.
  • Manage regulatory affairs including promotional material control, marketing authorization dossiers, and legal mentions.
  • Oversee pharmacovigilance activities, ensuring compliance with national regulations and safety management.

Matching Summary

Play a key role in regulatory compliance and quality of laboratory activities.

Skills & Requirements

Must-have

  • Regulatory document control
  • Marketing authorization dossiers
  • Pharmacovigilance system management
  • Adverse event reporting
  • Risk management systems
  • Transparency and link disclosure

Nice-to-have

  • Proactive regulatory monitoring
  • Cross-functional collaboration
  • Continuous process improvement

Key Requirements

  • Doctor of Pharmacy degree
  • Master's in pharmaceutical regulation or DU in pharmacovigilance
  • Minimum 5 years of experience in Regulatory Affairs and Pharmacovigilance
  • Registered with the French Order of Pharmacists (Section B)

Work Rights

Not specified

Tailored Resume

Cover Letter