Masters degree in Management of Drug Development, Biology, Microbiology, or Molecular Microbiology or closely related discipline with 2 years of related experience OR Bachelors degree in Management Of Drug Development, Biology, Microbiology, Or Molecular Microbiology or closely related discipline with 5 years of related experience Prior experience to includebr direct regulatory experience in the medical device and in vitro diagnostic device areas, interpretation of regulatory requirements, compliance, and effectively communicating this information to stakeholders; US IVD regulation , Qsubs, IDE, 510k and PMA. Ability to work remotely with manager approval
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