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

CSL

Paris, France
On-site
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
  • Adverse event reporting
  • Risk management plan implementation
  • Regulatory intelligence monitoring

Nice-to-have

  • Cross-functional collaboration
  • Training delivery
  • Quality system management
  • Audit preparation

Key Requirements

  • Pharmacist degree
  • Experience in regulatory affairs
  • Experience in pharmacovigilance
  • Knowledge of French regulations (CSP, ANSM)

Work Rights

Not specified

Tailored Resume

Cover Letter