Regulatory Affairs Specialist

Stryker

Biberist, Switzerland
Hybrid
Regulatory submissions and registrations
Quality management system processes
Experience in highly regulated industry
As a RAQA Specialist, you will support Regulatory Affairs and Quality activities across Germany, Switzerland, and Austria

Job Summary

  • As a RAQA Specialist, you will support Regulatory Affairs and Quality activities across Germany, Switzerland, and Austria.
  • You will help ensure compliance with MDR 2017/745 and applicable Swiss legislation.
  • Collaborating with cross-functional stakeholders, you will contribute to a compliant and efficient RAQA organization.

Matching Summary

As a RAQA Specialist, you will support Regulatory Affairs and Quality activities across Germany, Switzerland, and Austria.

Skills & Requirements

Must-have

  • Regulatory submissions and registrations
  • Quality Management System processes
  • Experience in highly regulated industry

Nice-to-have

  • Knowledge of Swiss medical device legislation
  • Experience with Swiss regulatory tools
  • Confident stakeholder management skills

Key Requirements

  • Bachelor's degree in Engineering or Science
  • 2+ years of experience in Regulatory Affairs
  • Proficiency in English and German

Work Rights

Not specified

Tailored Resume

Cover Letter