Description
The Quality Engineering Manager leads product quality and quality assurance activities in a regulated medical device manufacturing environment. The role owns nonconforming-product disposition, root-cause and CAPA investigations, customer complaint analysis, validation engineering, regulatory compliance, technical review of operational and test data, supplier and customer quality issues, and continuous improvement. The manager also provides technical guidance to quality engineers and other staff, supports environmental impact goals, and collaborates with engineering, EHS, suppliers, and customers. The position requires a bachelor's degree or higher, preferably in engineering, and at least nine years of operations quality experience, with medical device experience preferred.
