HuFriedyGroup
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.
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HuFriedyGroup
HuFriedyGroup, a STERIS company, is a global leader in dental instrument manufacturing, infection prevention and instrument reprocessing workflows. With over 200 years of collective experience in the dental industry, HuFriedyGroup helps dental professionals be the best in practice by providing a complete circle of protection in the dental suite, bringing together world class products, services, education, and communities that result in superior clinician performance, superior clinical outcomes, and safety for clinicians and patients. Headquartered in Chicago, HuFriedyGroup products are distributed in more than 100 countries, and the dental division maintains offices in Germany, Italy, China, Singapore, and Japan.