Ray Murphy is a computer system validation subject matter expert with 30 years experience in quality engineering, quality auditing, quality management, regulatory compliance, and software validation. For the past 14 years, he has worked for Boston Scientific where he has responsibility for non-device software validation lifecycles for equipment qualification, IT validation and spreadsheet validation. His responsibilities include the implementation of strategic quality initiatives and corporate quality policies and standards. While improving the agility of these processes, he supports teams in developing compliant and value-add CSV solutions. He has been a valued contributor to the FDA Industry CSA team since 2017.