Alternance - Affaires Réglementaires (h/f) – 12 À 24 Mois

GlaxoSmithKline

Rueil Malmaison, France
Regulatory affairs dossier preparation
Product information management
Regulatory compliance activities
Contribute to regulatory activities within the Regulatory Affairs department, interacting with various internal and external teams across different therapeutic areas

Job Summary

  • Contribute to regulatory activities within the Regulatory Affairs department, interacting with various internal and external teams across different therapeutic areas.
  • Analyze, prepare, and follow up on pharmaceutical and clinical MAA/variation dossiers (national and European procedures).
  • Participate in regulatory compliance activities such as deviations, CAPAs, and Product Quality Reviews.

Matching Summary

Contribute to regulatory activities within the Regulatory Affairs department, interacting with various internal and external teams across different therapeutic areas.

Skills & Requirements

Must-have

  • Regulatory Affairs dossier preparation
  • Product Information management
  • Regulatory compliance activities
  • Regulatory monitoring and analysis

Nice-to-have

  • Team collaboration
  • Initiative and interpersonal skills
  • Interest in drug regulation

Key Requirements

  • Master II student or pharmacy intern
  • Fluent English

Work Rights

Not specified

Tailored Resume

Cover Letter