About this role

  • Posted on

  • Location


  • Salary

    CHF66631.20 - CHF99946.80 per annum

  • Type


  • Division

    Pharmaceutical Regulatory Affairs Jobs

  • Reference

    BB - 13018.1_1599119913

  • Start date


  • Managing this role

Executive Consultant

Brieuc Baeckeroot

+44 203 8540 263


Source Group International GmbH, Bosch 106, 6331 Hunenberg, Switzerland


Being part of a growing company where you will have the responsibility to register one of their products with the FDA. This is a great step where you can work closely with the top management to define the Regulatory strategy from the development to the registration.

The company has been evolving and growing for the last decades, this will be a place of growth for yourself personally as well as professionally. This is a great step to move forward in your career.

Your task:

  • Define the Regulatory Strategy to register a Class III MD with the FDA
  • Working closely with the Development teams to ensure the best regulatory strategy regarding the country targeted
  • Being the support for all the regulatory matters: Audit, Regulatory monitoring…

Your experience:

  • 5 Years of experience in the Medical Device Industry.
  • Experience with the FDA, and their registration process.
  • English speaking, French is a bonus

Do you think you would be a good fit? Do you want to know more about the role? Do not hesitate to be in touch.


Feel free to reach me even if the position is not exactly what you are looking for.
Please share it with your network or any person you think you might be interested in.

You can send me your CV, Resume with your contact details through the link OR you can contact me on Linkedin.

Apply Back to search Xplore News
Upload your CV/resume or any other relevant file. Max. file size: 1 MB.
Don’t have access to your CV? Apply with your LinkedIn profile.
I consent to storing and processing my personal data as outlined on the 'How Xplore Life Science manages and uses your personal data' page.