Paul Swift

Paul Swift currently serves as the Head of Regulatory and Clinical Affairs for the Americas at ZEISS Medical Technology, a position held since April 2021. Prior to this role, Paul held various director-level positions in Global Regulatory Affairs at Alcon from January 2016 to April 2021, where responsibilities included developing regulatory strategies for high-risk intraocular lens products. Paul’s regulatory experience began at BD from January 2009 to January 2016, focusing on molecular diagnostics and regulatory project management. Earlier career highlights include managing regulatory affairs at Care Products, Inc., where Paul led medical device submissions and obtained significant product clearances. Paul holds a Master's Degree in Biotechnology from The Johns Hopkins University and a Bachelor's Degree in Biology from Loyola University Maryland, complemented by executive education from Northwestern University's Kellogg School of Management. Professional contributions include co-authoring regulatory publications and serving as a speaker at notable industry conferences.