Regulatory Affairs Specialist
A global Medical Device Company based in Switzerland with ambitious growth plans is currently recruiting for a Regulatory Affairs Specialist with proven regulatory skills focused on MDR to join their team in Zug, Switzerland.
This Medical Device company requires Regulatory Affairs professional to join the team for a 9-month fixed term contract with an option of a permanent position after the initial 9 months. You will work together with the Regulatory Affairs team on all general aspects of Regulatory Affairs and most importantly on MDR.
- 4 - 6 years of experience within Regulatory affairs
- Good knowledge of MDR
- Regulatory Affairs Technical files
- Good team player
- Good communication skills
- Fluent in English, German would be an asset
Disclaimer: Applicant Must have the Right to Work in Switzerland.