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Regulatory Affairs Specialist

Are you looking to advance your regulatory career at a rapidly growing device company in South Central LA?

I am exclusively working with a class II device company in Long Beach that is actively looking for a Regulatory Affairs Specialist that is familiar with the MDR transition and able to help lead the transition for the organization.

Applicants must have:

  • Experience with MDR gap analysis and/or 510(k)/international submissions
  • >2 years of Regulatory experience in the medical device industry
  • A collaborative, team oriented mind-set
  • Strong written and verbal communication skills

While this opportunity offers

  • A competitive base salary with fantastic benefits
  • A high visibility role leading the MDR transition

If this is an opportunity you would be interested in, please apply as I will be contacting top applicants to schedule phone screenings

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