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Senior Regulatory Affairs Specialist

My client is a class III device company in Northern LA that specializes in neurology and pain management. They are urgently searching for a Regulatory team member at either the Senior Specialist or Principal Specialist level to help lead their upcoming submissions and assist with the MDR transition. This is a full-time direct hire role with a very competitive compensation package along with relocation for non-local candidates.

Candidates must have:

  • Exposure to 510(k)s/PMAs/OUS submissions
  • Full life cycle regulatory submission experience
  • A desire to learn and get involved in every regulatory project

Nice to haves:

  • Class III experience
  • A master in Regulatory Science
  • Authorship of domestic or international submissions
  • Experience in a clinical regulatory setting

If this seems like an opportunity that would interest yourself or someone in your network please reach out as I will be qualifying top candidates for an initial phone screening.

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