RA Specialist

Are you looking for a career to make a difference? Are you interested in working for a global leader? My client is looking for a Regulatory Affairs Specialist to help their goal.

Their goal is to enable patients to get their diagnosis within 24 hours from biopsy. They are striving towards, a goal that will guide their future strategies, and you can be apart of this!

Key Qualifications:

  • Global Medical Device Registrations
  • Medical Device Company/Product Experience
  • Preparation and Submission of Declaration of Conformity
  • Knowledge of Certificate of Foreign Government (C of G), preparation and submission to FDA
  • Experience navigating and using FDA website
  • Management of submissions for Apostille approval


  • Minimum 2-4 years of experience in the Medical Device industry
  • Knowledge of the process to get licenses approved
  • Bachelors in a science field

Sthree US is acting as an Employment Business in relation to this vacancy.