About this role
Product Design Quality Sr Specialist I (11225) at Zimmer Biomet. Location: Warsaw, Indiana, United States. Role: ensuring compliance, supporting design, analyzing data Requirements: 3-5+ years quality engineering experience in medical devices, B.S. in engineering or related field, knowledge of FDA 21 CFR Part 820/ISO 13485/EU MDR, risk management (ISO 14971/FMEA), V&V, CAPA, and technical documentation. Category: Engineering Seniority: Mid Level Tools: Windchill, Codebeamer, Jira, Microsoft Office, Minitab, Github Certifications: cqe, cre, six sigma green belt Commitment: Full Time Workplace: Onsite Languages: English