Zimmer Biomet seeks a Design Quality Engineer to strengthen design control practices across new product development and sustaining engineering for the iovera line. You will ensure regulatory compliance (21 CFR 820, ISO 13485, EU MDR) and lead risk management, documentation, and continuous improvement.
Collaborating with R&D;, Regulatory Affairs, and Manufacturing, you will review changes, support CAPA investigations, and prepare regulatory submissions while maintaining traceability and product
📌 Design Quality Engineer, Medical Devices (Bogotá)
🏢 Pta
📍 Bogotá