Alternance Chargé Affaires Réglementaires H/f

med-in.at

Puteaux, France
Master 2 degree 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 to prepare and submit variation dossiers for marketing authorizations.
  • Candidates must possess rigorous organizational skills and proficiency with standard office tools like Outlook, Teams, and Excel.

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

Nice-to-have

  • Strong analytical and synthesis skills
  • Excellent interpersonal abilities
  • Results-oriented mindset

Key Requirements

  • Student in Pharmacy or Scientific Master 2
  • Minimum 12-month contract duration
  • No visa sponsorship available

Work Rights

Not specified

Tailored Resume

Cover Letter