Alternance Chargé Affaires Réglementaires H/f

Merck Merck · Pharma · Ile-de-France, France

This is an alternating contract (internship) position for a Regulatory Affairs Officer at Merck, focusing on the regulatory aspects of drug lifecycle management. The role involves participating in the preparation and submission of variation dossiers, monitoring evaluations by health authorities, and managing changes to packaging and labeling. It requires a scientific or pharmacy background with a Master's degree in Regulatory Affairs and proficiency in English and relevant IT tools.

What you'd actually do

  1. Participation à la constitution et au dépôt des dossiers de variations d’AMMs,
  2. Respect des timings proposés par le Bureau Européen,
  3. Suivi des dossiers en cours d’évaluation par les autorités (ANSM et EMA),
  4. Participation à la gestion des modifications et création des articles de conditionnement, des RCP et mentions légales,
  5. Participation à la coordination réglementaire de la mise en place des nouveaux libellés de RCP et notices,

Skills

Required

  • Rigor, excellent organizational and priority management skills
  • Interpersonal skills and teamwork
  • Proficiency in English
  • Proficiency in IT tools

Nice to have

  • Database Management
  • Data Entry
  • Document Management
  • Email Management
  • Event Planning
  • File Management
  • Inventory Management
  • Office Management
  • Payment Handling
  • Processing Expense Reports
  • Project Coordination
  • Purchase Order Management
  • Researching
  • Travel Coordination
  • Vendor Management

What the JD emphasized

  • professional English
  • knowledge in French and European regulatory affairs
  • structure of health authorities and organization of a pharmaceutical laboratory
  • rigor and organization
  • familiarity with Outlook, Teams, Word, Excel, Powerpoint, Internet and database usage
  • results and internal clients oriented
  • analytical and synthesis skills
  • interpersonal and teamwork skills