Design Quality Engineer, Medical Devices

Zimmer Biomet in Bogotá, Colombia, is seeking a Design Quality Engineer to support design control across new product development and sustaining engineering for the iovera line. You will ensure regulatory compliance (21 CFR 820, ISO 13485, EU MDR), manage risk, and contribute to continuous improvement in quality documentation and processes. You will...

Zimmer Biomet is seeking a Design Quality Engineer to uphold robust design controls and regulatory compliance for the iovera product line in Bogotá. You will partner with R&D and cross-functional teams to ensure product development adheres to ISO 13485, 21 CFR 820, and EU MDR while supporting risk management, documentation, and continuous improvement...

Zimmer Biomet in Bogotá is seeking a Quality Assurance professional to ensure products meet established requirements through audits, inspections, and testing. The role collaborates with multiple departments and suppliers to uphold quality goals and compliance. Ranked for process validation experience (IQ/OQ/PQ) and a strong background in medical devices,...

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life...

Zimmer Biomet is seeking a Design Quality Engineer to support robust design control practices across new product development and sustaining engineering for the iovera product line. You will act as the quality representative in cross-functional teams, ensuring regulatory alignment and quality deliverables. The role involves design changes, risk management,...

Zimmer Biomet is seeking a Quality Engineer to ensure products meet established requirements through audits, inspections, and testing. The role interfaces with multiple departments, suppliers, and external experts to drive quality goals. The ideal candidate will hold a B.S. in engineering with CQE certification, have at least 1 year of relevant experience,...

Job Summary The Technical Program Manager coordinates the development of a medical device across hardware, optics, software, imaging, systems engineering, quality, regulatory, clinical and manufacturing workstreams. The role owns the integrated program plan and the engineering operations processes that support development, testing and early manufacturing,...

Job Summary The Technical Program Manager coordinates the development of a medical device across hardware, optics, software, imaging, systems engineering, quality, regulatory, clinical and manufacturing workstreams. The role owns the integrated program plan and the engineering operations processes that support development, testing and early manufacturing,...

Plutus21 Capital, L.L.C. is seeking a Technical Program Manager to coordinate the development of a medical device across hardware, optics, software, imaging, systems engineering, quality, regulatory and manufacturing workstreams. The role owns the integrated program plan and supports design controls, change management and manufacturing transfer, with on-site...