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Regulatory Affairs Specialist

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Reference Number: TS-6208416721
Date Posted: 06-21-22
Location: Pacific Northwest

Our client is a small, fast-growing surgical technology company in the Pacific Northwest. They are currently seeking a Regulatory Affairs Specialist to join their team.

What's in it for you...
  • Industry leader within their space
  • Make your mark - be the RA expert
  • Lots of variety - will get to wear multiple hats
  • Expanding into new countries - global submissions
  • Good team & nice group to work with
To be considered for an interview, the following experience/skills are desired:
  • Bachelor’s degree, Life Science preferred
  • 2+ years of medical device regulatory experience with FDA and ISO regulations
  • FDA 510(k) submission experience
  • Reviewing on-going changes and decide whether a FDA change needs to be filed
If you experience technical difficulty while applying to the position, please email your resume directly to MedicalDeviceTeam@MRIGlobalMedDevice.com