Swiss Regulatory Affairs Specialist

BRENNTAG

Ballerup, Denmark
Competitive salary; good pension plan; health insu...
Fluent in english and german/swiss german
Knowledge of swiss medic regulations
Experience with ipec gmp and excipact standards
The role involves supporting EMEA divisions on the supply of raw materials into the pharmaceutical industry with a focus on regulatory, legal, and compliance responsibilities

Job Summary

  • The role involves supporting EMEA divisions on the supply of raw materials into the pharmaceutical industry with a focus on regulatory, legal, and compliance responsibilities.
  • Candidates will be responsible for completing technical documentation, managing customer requests, and collaborating with QHSE teams to ensure adherence to standards like GDP and EXCiPACT.
  • The position offers the opportunity to work within a European team based in Ballerup with competitive compensation, pension plans, and health insurance benefits.

Matching Summary

The role involves supporting EMEA divisions on the supply of raw materials into the pharmaceutical industry with a focus on regulatory, legal, and compliance responsibilities.

Salary

Competitive salary; Good pension plan; Health insurance

Skills & Requirements

Must-have

  • Fluent in English and German/Swiss German
  • Knowledge of Swiss Medic regulations
  • Experience with IPEC GMP and EXCiPACT standards
  • Ability to manage regulatory documentation
  • Understanding of API and excipient requirements

Nice-to-have

  • Proactive collaboration across functions
  • Training delivery experience
  • Adaptability to changing regulations
  • Strong communication skills

Key Requirements

  • Degree or considerable experience in life sciences
  • Fluency in English and German/Swiss German
  • Knowledge of European National Competent Authority requirements

Work Rights

Not specified

Tailored Resume

Cover Letter