Raphael Mohr is a Senior Project Manager in Regulatory Affairs at Stryker, with a focus on transitioning the Foot & Ankle and Upper Extremities product portfolio to comply with EU Medical Device Regulation (EU MDR) since June 2019. Prior experience includes leading a cross-functional cost reduction program across six manufacturing sites and managing EU MDR implementation for the Trauma & Extremities Division. Raphael also served as a Project Engineer, overseeing the EU MDR Cutover Project for the Selzach manufacturing site, and completed a Procurement Internship at Stryker. Academic credentials include a Master of Science and a Bachelor of Science in Technically-Oriented Business Administration from the University of Stuttgart.
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