About this role
Senior Quality Engineer (On site) at Cordis. Location: Santa Clara, California, United States. Role: maintaining QMS, conducting audits, leading investigations Requirements: Engineering bachelor's plus 5+ years relevant experience; expertise in FDA Medical Device Quality System Regulation, MDR, MDSAP, and ISO 13485; QMS, CAPA, audits, and root cause investigation experience. Category: Engineering Seniority: Senior Level Tools: FDA Medical Device Quality System Regulation, MDR, MDSAP, ISO 13485, Distributed Product Risk Assessments (DPRA) Commitment: Full Time Workplace: Onsite Languages: English