Swiss Medtech Regulatory Affairs Specialist

Swiss medtech

Swissmedic

MDR

CE marking

Basel

Zurich

High Salary

AT

CH

DE

We seek an experienced Regulatory Affairs Specialist with deep expertise in Swiss and European medical device regulations to ensure compliance and facilitate market approval for innovative medtech products. This role requires managing regulatory submissions, liaising with authorities, and maintaining up-to-date knowledge of evolving regulatory frameworks in the Swiss healthcare landscape.