About this role
Quality Engineer at Remedy Robotics. Location: San Francisco, California, United States. Role: Own documentation, Lead risk, Define V&V Requirements: 7+ years of hands-on quality work in a medical device environment; experience with IDE, 510(k), or PMA submissions; strong ISO 14971, IEC 62304, ISO 13485 knowledge; able to author technical documents for FDA scrutiny; collaborates with engineering teams. Category: Quality Assurance Seniority: Senior Level Tools: ISO 14971, IEC 62304, ISO 13485, FDA submission guidance Commitment: Full Time Workplace: Onsite Languages: English