Junior Regulatory Affairs Consultant
A global Medical Device Company based in Switzerland with ambitious growth plans is currently recruiting for a Junior Regulatory Affairs consultant with proven regulatory skills focused on MDR for their Swiss site.
This Medical Device company requires a consultant to join the team for 6 months or more to successfully work together with the Regulatory Affairs team on technical files, to review them and update them for MDR submission.
- 2 - 5 years of experience within Regulatory affairs
- Good knowledge of MDR
- Good work experience with Technical files
- Good team player
- Fluent in English, German would be an asset
Disclaimer: Applicant Must have the Right to Work in Switzerland.