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.
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Level
Lead L6
Location
Florida, NY
Occupation
Validation Engineers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing