Terumo Aortic is seeking a dedicated quality assurance professional to analyze, investigate, and resolve external customer complaints in line with FDA, ISO, EU MDR, and other regulatory requirements.
You will drive complaint investigations, adverse-event reporting support, trending, and post-market surveillance activities while helping improve complaint processes and team capability across cross-functional groups. Strong knowledge of medical-device regulations is essential.
#J-18808-LjbffrQuality Complaints Engineer II – Medical Devices in town of florida at Unknown Company
This position is listed as full time and onsite.