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Stephanie Wasielewski is an accomplished professional in the regulatory and quality assurance sectors of the medical device industry. Currently serving as Director of Regulatory Affairs at Hu-Friedy Mfg. Co., LLC, since July 2019, Wasielewski has extensive experience, having previously worked as a Regulatory/Quality Consultant at Medical Device Consultant from March 2018 to July 2019. Before that, Wasielewski held the position of VP of Regulatory Affairs/Quality Assurance at CORPAK MedSystems, Inc. for over two decades, from May 1996 to October 2017. Earlier in career, Wasielewski worked as a Validation Engineer at Pharmaceutical Systems from 1994 to 1996. Wasielewski holds a Bachelor's Degree in Biomedical Engineering from Marquette University.