Swiss Regulatory Affairs Specialist

Brenntag

Basel, Switzerland
Knowledge of pharmaceutical regulations
Experience in regulatory documentation
Fluent in english and german/swiss german
You will be supporting the EMEA divisions on topics around the supply of raw materials into the pharmaceutical industry

Job Summary

  • You will be supporting the EMEA divisions on topics around the supply of raw materials into the pharmaceutical industry.
  • Your responsibilities will include completion of technical and regulatory documentation and collaborating with various teams.
  • Brenntag provides equal employment opportunities to create a workplace where difference is valued.

Matching Summary

You will be supporting the EMEA divisions on topics around the supply of raw materials into the pharmaceutical industry.

Skills & Requirements

Must-have

  • Knowledge of pharmaceutical regulations
  • Experience in regulatory documentation
  • Fluent in English and German/Swiss German

Nice-to-have

  • Good collaborator and communicator
  • Ability to adapt to changing regulations
  • Experience in training on regulatory topics

Key Requirements

  • Degree in life sciences
  • Knowledge of Swiss Medic requirements
  • Experience in resolving compliance issues

Work Rights

Not specified

Tailored Resume

Cover Letter