Description
The role leads manufacturing quality activities, including structured problem-solving, technical-drawing interpretation, nonconformance disposition, defect and complaint investigations, CAPA implementation, validation and test-data review, continuous improvement, audits, and regulatory compliance. It requires a bachelor’s degree in science, engineering, or a related field, at least nine years of manufacturing experience with strong operations-quality exposure, and experience in process validation, root-cause analysis, quality operations, and ISO 13485 or QMSR. Medical-device experience and people-management experience are preferred.
