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Michael Kilday has extensive experience in the field of quality assurance and regulatory compliance. Michael currently serves as the Vice President of Quality Assurance and Compliance at NextPhase Medical Devices, where they are responsible for developing and implementing effective quality assurance and quality control systems. Prior to this, they held the position of Director of Regulatory Affairs and Quality Assurance at Meridian Bioscience Inc., where they played a key role in developing and improving the company's quality and regulatory systems. Michael also served as the Head of Design and Postmarket Quality at Cardinal Health, overseeing product quality assurance for medical device products. Before that, they held leadership positions at Vention Medical, Nypro, Cabot, and Saint-Gobain Performance Plastics, where they led various quality and regulatory compliance initiatives. Overall, Kilday's work experience demonstrates their expertise in driving quality performance, developing compliance goals, and integrating quality with business objectives.

Michael Kilday holds a Bachelor of Science (BS) degree in Industrial Technology from the University of Massachusetts Lowell. Michael also has a Master's Graduate Certificate in Regulatory Affairs, specifically in the field of Medical Device, from Northeastern University. Additionally, Michael has obtained a certification as a Regulatory Affairs Certified Professional from RAPS (Regulatory Affairs Professionals Society), although the specific month and year of obtaining this certification are not mentioned.