Michelle Taylor is a seasoned professional in the field of medical device quality management and regulatory compliance. Currently serving at BSI since April 2019 as part of the Global Quality & Accreditation team, Michelle focuses on technical and regulatory aspects of ISO 13485 certification and medical device QMS audits on a global scale. Key responsibilities include supporting the implementation of policy decisions, delivering certification decisions, and providing technical support during regulatory audits. Prior to BSI, Michelle worked at STERIS Corporation from 2012 to April 2019, where responsibilities included managing FDA inspections and overseeing CAPA and complaint management processes. Michelle holds a Bachelor of Science in Biology from Lycoming College and further education from Kent State University College of Podiatric Medicine.
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