Summary from listing
The Quality Engineering Manager leads product quality and quality assurance activities in a regulated medical device manufacturing environment. The role covers defect disposition, root-cause analysis, CAPA and NCEP investigations, failure-mode investigations, validation engineering, regulatory compliance, customer complaint handling, supplier and customer quality issues, and technical guidance to quality and inspection staff. The position requires a bachelor's degree or higher, at least nine years of operations quality experience, and familiarity with QSR, ISO, and medical device regulatory requirements.
