Company: LUCENT Surgical Solutions
Location: Southfield, MI, United States
Type: Full-time | Quality & Regulatory
About the Role
Oversee development, implementation, and management of quality systems and regulatory compliance processes for medical devices.
Requirements
- 5+ years in QA/RA for medical devices
- ISO 13485 and FDA 21 CFR 820 expertise
- Experience with Class II and III devices
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