Alternance Chargé Affaires Réglementaires H/f

Merck & Co., Inc., Rahway, NJ, USA

Puteaux, France
Regulatory affairs france and europe
English professional written and oral
Microsoft outlook, teams, word, excel, powerpoint
You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle

Job Summary

  • You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle.
  • You will participate in the preparation and submission of variations to Marketing Authorizations, and follow up on dossiers under evaluation by authorities.
  • You will be involved in the management of modifications and creation of packaging components, SmPCs, and legal mentions.

Matching Summary

You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle.

Skills & Requirements

Must-have

  • Regulatory Affairs France and Europe
  • English professional written and oral
  • Microsoft Outlook, Teams, Word, Excel, Powerpoint
  • Database usage

Nice-to-have

  • Open and curious mindset
  • Results and internal client oriented
  • Good analytical and synthesis skills
  • Teamwork and interpersonal skills

Key Requirements

  • Student in Pharmacy or scientific Master 2
  • Regulatory Affairs / Registration focus
  • Minimum 12 months duration

Work Rights

Not specified

Tailored Resume

Cover Letter