Description
The role performs final functional testing, product and material release inspections, QA documentation maintenance, nonconformance investigation, defect analysis, CAPA support, quality reporting, and regulatory compliance in a manufacturing environment. It requires a diploma in science, engineering, or a related field, 3–8 years of manufacturing experience, and familiarity with testing, inspection, manufacturing systems, and quality regulations; medical device or regulated-industry experience is preferred. The role may guide junior team members and contribute to process improvements.
