Swiss Regulatory Affairs Specialist

bcd-chemie.de

Basel, Switzerland
On-site
Support emea divisions on raw material supply
Technical and regulatory documentation
Sourcing information internally and from suppliers
The Swiss Regulatory Affairs Specialist position at BCD Chemie in Basel, Switzerland, involves supporting the EMEA divisions with regulatory, compliance, and quality responsibilities related to the supply of raw materials in the pharmaceutical industry. The ideal candidate should have a background in life sciences, knowledge of pharmaceutical regulations, and fluency in English and German/Swiss German

Job Summary

  • Working in a Pharma team, you will be supporting the EMEA divisions on topics around the supply of raw materials into the pharmaceutical industry including regulatory, legal, compliance, quality and product safety responsibilities.
  • You will have knowledge of pharmaceutical industry requirements and regulations on APIs, excipients, biopharma, and traditional pharma raw materials.
  • You will work in an European team with members all over Europe, and will be working from preferably our Ballerup office.

Matching Summary

Match Score: 85

The Swiss Regulatory Affairs Specialist position at BCD Chemie in Basel, Switzerland, involves supporting the EMEA divisions with regulatory, compliance, and quality responsibilities related to the supply of raw materials in the pharmaceutical industry. The ideal candidate should have a background in life sciences, knowledge of pharmaceutical regulations, and fluency in English and German/Swiss German.

Skills & Requirements

Must-have

  • Support EMEA divisions on raw material supply
  • Technical and regulatory documentation
  • Sourcing information internally and from suppliers
  • Reporting and documenting customer requests via KPIs
  • Collaborate with QHSE & supply chain teams
  • Creation and management of product regulatory information

Nice-to-have

  • Proactively leading and managing regulatory topics
  • Collaborating on global business unit projects
  • Providing training on regulatory topics
  • Supporting commercial success of Pharma business unit

Key Requirements

  • Degree or considerable experience in life sciences
  • Knowledge of Swiss Medic and European NCA requirements
  • Fluent in English & German/Swiss German
  • Understanding of current regulations around raw materials
  • Ability to resolve compliance issues and respond to complex queries

Work Rights

Not specified

Tailored Resume

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