Regulatory Affairs Manager
5+ years regulatory affairs experience in medical devices, experience leading 510(k) and EU technical file submissions, Bachelor's in life sciences/regulatory affairs, regulatory certification (RAC) preferred, strong leadership and technical writing skills.
Key Responsibilities
- developing strategies
- managing submissions
- mentoring staff
Skills & Tools
reputed company Office Suite, Regulatory software
Job Details
- Category: Research and Development (R&D)
- Seniority: Senior Level
- Commitment: Full Time
- Workplace: Remote — reputed company or Charlotte
- Languages: English
About reputed company
A global manufacturer of reputed company dental products and technologies providing solutions for dental and oral health. — Industry: Manufacturing
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