Regulatory Affairs Specialist
- Location
- Winston-Salem, NC
- Listed
- Today
About the role
Plans, organizes and implements strategies and activities required to procure regulatory approval for new and revised product lines. Coordinates and prepares regulatory submissions, including 510(k) premarket notifications, EU MDR Technical Files and other international registrations. Ensure compliance to all US, EU and international requirements and company policies and procedures regarding submissions and other requirements for market approval of medical devices.
From Solesis's careers page, first listed on Rolev.ai on November 12, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Regulatory Affairs Specialist job at Solesis located?
This Regulatory Affairs Specialist position at Solesis is located in Winston-Salem, NC. Always check Solesis's application page for specific state eligibility or relocation policies.
How do I apply for the Regulatory Affairs Specialist position at Solesis?
This listing links directly to Solesis's application page. You can apply directly on Solesis's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.