About this role
Usability and Regulatory Affairs Specialist at Sentec. Location: Lincoln, Rhode Island, United States. Role: planning studies, documenting usability, supporting submissions Requirements: 3+ years in human factors/usability or regulatory affairs in medical devices; Bachelor's in biomedical engineering or related; strong technical and analytical skills; familiarity with FDA and EU MDR preferred; ability to travel ~5 trips/year. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English