Alternance Chargé Affaires Réglementaires H/f

29

Puteaux, France
Master 2 in regulatory affairs
Professional english proficiency
Knowledge of french and european regulations
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory lifecycle of medicines

Job Summary

  • You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory lifecycle of medicines.
  • The role involves collaborating with pharmacists and regulatory managers to prepare and submit marketing authorization variation dossiers.
  • Candidates must demonstrate rigor, organization, and a results-oriented approach while managing multiple regulatory files.

Matching Summary

You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory lifecycle of medicines.

Skills & Requirements

Must-have

  • Master 2 in Regulatory Affairs
  • Professional English proficiency
  • Knowledge of French and European regulations

Nice-to-have

  • Strong analytical and synthesis skills
  • Excellent organizational abilities
  • Team-oriented mindset with client focus

Key Requirements

  • Student in Pharmacy or Scientific Master 2
  • Minimum 12-month internship duration
  • Proficiency in Outlook, Teams, Word, Excel, PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter