Pharmaziepraktikant*in Im Bereich Regulatory Affairs Für Mai 2027

Sanofi UK

Frankfurt Am Main, Germany
Hybrid
Regulatory affairs
Pharmaceutical quality
Product information texts
You will be working in Research & Development within the Regulatory Affairs department, contributing to the market access of new medicines and maintaining existing drug approvals

Job Summary

  • You will be working in Research & Development within the Regulatory Affairs department, contributing to the market access of new medicines and maintaining existing drug approvals.
  • You will support the team in preparing, creating, and processing variations for pharmaceutical quality and changes to informative texts, as well as reviewing professional and patient information for printing.
  • Sanofi offers diverse opportunities for talent development and career advancement, comprehensive health and social benefits, and a hybrid work model.

Matching Summary

You will be working in Research & Development within the Regulatory Affairs department, contributing to the market access of new medicines and maintaining existing drug approvals.

Skills & Requirements

Must-have

  • Regulatory Affairs
  • pharmaceutical quality
  • product information texts
  • regulatory databases
  • document management systems
  • service requests
  • research activities

Nice-to-have

  • customer-oriented mindset
  • team player
  • high motivation
  • strong initiative
  • collaborative team
  • future-oriented team

Key Requirements

  • 2nd section of pharmaceutical training
  • MS-Office proficiency
  • German and English language skills

Work Rights

Not specified

Tailored Resume

Cover Letter