Masters degree in Bioengineering Innovation and Design, Biomedical Engineering or related technical field plus 24 months of experience as a job offered, Product Manager for medical devices, or related occupation. Experience must include 1 Regulatory Writing interaction with the FDA to run clinical trials, and get product approval, 2 GLP Preclinical Testing, 3 Interventional Oncology Knowledge, 4 GLP Clinical Testing, and 5 Medical Device Quality System ISO.
Categories: eb3
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