Description
The Quality Engineer will support New Product Introduction and new product development for implantable and non-implantable spinal surgery devices in a regulated medical-device environment. Responsibilities include design controls, OEM and supplier qualification, nonconformance and CAPA activities, inspection planning, change-order reviews, validation, risk management, audits, and technical collaboration with contract manufacturers and suppliers. The role requires a bachelor’s degree in a relevant engineering discipline, mechanical inspection and GD&T knowledge, regulated medical-device quality experience preferred, and strong analytical, technical writing, communication, and project-management abilities.
