Description
The Quality Engineer will resolve complex manufacturing exceptions, investigate defects and customer complaints, make product-release decisions, support CAPA and validation activities, and drive quality improvements in a regulated medical-device environment. The role requires an undergraduate degree in science, material engineering, or a related discipline, at least three years of quality-engineering experience in regulated manufacturing, and expertise in incoming and outgoing inspection, equipment and test-method validation, material issue management, stakeholder communication, and regulatory quality standards.
