Matt Quirk

Matt Quirk is a seasoned professional with extensive experience in regulatory affairs and clinical quality assurance within the medical device industry. Currently serving as the Director of Regulatory Affairs at Abbott since April 2017, Matt leads the Global Regulatory Operations team and focuses on building a shared service function to enhance operational efficiencies and tools across regulatory functions. Previous positions include Associate Director of Clinical Quality Assurance at St. Jude Medical (2006-2016) and Sr. Manager of Clinical QA at Guidant (1996-2006), where Matt held various roles including Clinical Research Manager, Director of Information Systems, Manufacturing Manager, and Information Systems Manager. Matt Quirk holds an MBA in Operations from the University of Minnesota (1990-1991) and a BBA in Information Systems from the University of Wisconsin-Whitewater (1983-1986).