Shawn Maxwell

Shawn Maxwell is a seasoned professional in regulatory affairs and pharmaceutical manufacturing with significant experience in the healthcare industry. Currently serving as a Senior Regulatory Affairs Specialist at AliveCor Inc. since November 2021, Shawn has been instrumental in managing compliance for various Class I and Class IIa medical software products under the European Union Medical Device Regulation (EU MDR). Previously, Shawn held positions at Cerner Corporation as a Regulatory Affairs Strategist and at Excite Pharma Services as VP of Manufacturing, where responsibilities included overseeing sterile manufacturing operations and ensuring adherence to safety regulations. Early career experience includes roles as a Clinical Data Coordinator at Quintiles and Laboratory Analyst at Pace Analytical. Shawn holds a Bachelor's Degree in Biology from Kansas State University and an MBA from MidAmerica Nazarene University.