Your area of responsibility

  • Prepare national and international product approvals, particularly in the United States, registrations and notifications as well as subsequent maintenance and any changes to existing approvals.
  • Support the entire approval process from development of the product to final approval.
  • Maintain contact with authorities and consultants
  • Support us during implementation of applicable statutory requirements

Your qualifications

  • Completed law degree
  • Relevant professional experience
  • Experience working with the FDA and/or medical technology desirable
  • Very good spoken and written English and German
  • Independent work style and team player
  • Flexibility and a high stress tolerance

We offer

  • Attractive salary plan
  • Pleasant work environment
  • Exciting opportunity to work in a startup company in an international environment


Actual compensation will be based on the applicant’s qualifications and profile, especially relevant professional experience. Candidates with relevant professional experience will receive a yearly gross salary starting at €50,000.00 for full-time employment. Part-time is also an option.

Please contact us with any questions. If you are looking for a job with a varied range of responsibilities, then please send all relevant information, including curriculum vitae, photograph, and any certifications via e-mail to: