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Mid Atlantic

Regulatory Affairs Specialist

MRI Global Search

Our client is a regenerative medicine / medical device company. They are currently seeking a Regulatory Affairs Specialist to join their team in the Mid Atlantic.

What’s in it for you…

  • Implantable, class III medical device
  • Fast-paced, well-established company with deep pockets
  • Strong financial backing
  • High visibility opportunity – make a large impact on the business

To be considered for an interview, the following experience/skills are desired:

  • Bachelor’s degree, Science related
  • 3+ years medical device regulatory affairs experience
  • Domestic and/or international submissions experience

Salary: $100K to $110K base

If you experience technical difficulty while applying to the position, please email your resume directly to MedicalDeviceTeam@MRIGlobalMedDevice.com

  • Max. file size: 300 MB.

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