The Quality Engineer II will support the manufacturing of medical devices. This individual will with work Product Development, Service and Manufacturing to resolve product quality issues. The Quality Engineer II will also support manufacturing process changes, continuous improvement initiatives and establishing/meeting in-process performance metrics. Primary responsibilities include working in Quality Operations, Quality Engineering and with other functional groups in support of day-to-day activities relating to legacy products. Calibration Management utilizing Maximo Software Nonconformance Management utilizing Trackwise. Reviewing Incoming Inspection Records, Travelers and DHR’s f
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