About this role
The Quality Engineer Level 3 - Risk Management is an experienced individual contributor responsible for performing and maintaining product and process risk management activities in support of medical device and/or in-vitro diagnostic products. This role supports cross-functional teams throughout the product lifecycle by developing, reviewing, and updating risk management documentation, including, but not limited to new product development, sustaining, manufacturing non-conformances, supplier-related activities, post-market surveillance, complaints, CAPA, and change management.