Daniela Zaczek is the Director of Regulatory Affairs at Philips, where they plan and execute global regulatory submission activities and support new product development. Previously, they served as a Regulatory Affairs Manager at Rakuten Medical and DJO Global, managing clinical trial submissions and overseeing regulatory support for orthopedic products. Daniela has also held research positions at the University of Illinois at Chicago and the University of Pittsburgh, contributing to studies in biomedical engineering. They hold a Bachelor's degree in Biomedical Engineering and Chemistry from the University of Pittsburgh and are certified as a CQE and RAC-US.
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