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Medical Devices Regulatory Affairs Specialist II; US​/EU

Job in Irvine, Orange County, California, 92713, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Medical Science Liaison, Healthcare Compliance
Job Description & How to Apply Below
Position: Medical Devices Regulatory Affairs Specialist II (US/EU)
A medical device regulatory firm is seeking a Regulatory Affairs Specialist II to prepare and support regulatory submissions required for medical devices in both the U.S. and Europe. The ideal candidate will have 2-5 years of medical device experience, working knowledge of FDA guidance, and at least 2 years in regulatory affairs. Strong analytical skills, attention to detail, and proficiency in Microsoft Office are essential for this mid-senior level contract position.
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