Regulatory Affairs Specialist


CASCINATION AG is an award-winning medical technology company dedicated to the development, manufacturing and commercialization of innovations in computer-assisted and image-guided surgery. Our trailblazing navigation systems and surgical robots are designed to improve outcomes for patients undergoing surgical or interventional procedures and offer new perspectives to patients worldwide.

For our headquarters in Bern, Switzerland we are looking for a

Regulatory Affairs Specialist

Your mission

  • Create and update technical files and support the transition from MDD to MDR
  • Support global regulatory activities
  • Collect, analyse and evaluate post-market surveillance data and ensure information exchange between stakeholders
  • Support internal audits and health authority inspections

Your profile

  • Experience in medical device regulations - minimum three years
  • Regulatory background and scientific understanding
  • Proficient in English speaking and writing
  • Hands-on mentality and proactive personality


We offer a challenging role in a multinational, innovative, fast growing and dynamic environment. In our company you can create, shape and take on responsibility. Our unique company culture is shaped by our passion and values.

CASCINATION winning the Swiss Medtech Award 2019 Video

We are looking forward to receiving your application documents including CV, work references, diplomas etc. via email at Show us your motivation by being creative, no motivation letter required.

Contact for questions: Anja Reischmann, +41 31 306 26 03


Regulatory Affairs Specialist