4 years of regulated industry experience that includes, but not limited to, FDA, ISO 13485, ISO 14971, MDSAP and European MDDMDR requirements.br 4 years of experience working on projects with plastic injection molding, textile, andor converting part design and implementation.br 2 years of experience in single use disposable or reusable medical devices.br 2 years of sterile facility development experience supporting ISO Classified clean rooms.
Categories: eb3
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