Supports released cardiovascular medical devices throughout their post-market lifecycle. Responsibilities include engineering and process changes, design transfer, complaint investigations, root cause analysis, CAPA, verification and validation, manufacturing support, post-market data analysis, audits, documentation, supplier coordination, and continuous improvement. The role collaborates with cross-functional teams, contract manufacturers, suppliers, service teams, distributors, and customers while coordinating project plans, risks, budgets, and timelines.

Engineering Interns will assist in product design, development, compliance with regulations, and support R&D and quality engineering teams under supervision.