Marguerite Thomlinson

Marguerite is a regulatory and quality leader with over 20 years of medical device expertise. She has led hundreds of FDA and international regulatory submissions for instrument and software devices (SaMD) including wearable technology, hospital connectivity, critical-care patient monitoring, and IVD diagnostics.

Prior to Whiterabbit, Marguerite was Senior Director of Regulatory Affairs for Masimo Corporation, specializing in hospital automation and noninvasive medical innovation. Before that she was Director of Regulatory Affairs for Edwards Lifesciences, focusing on cardiovascular technology. She also worked in product development and engineering management at B. Braun Medical, CareFusion, Teledyne, and Boeing.

Marguerite holds a Bachelor of Science in Mechanical Engineering from California State Polytechnic University and a Juris Doctorate from Western State College of Law.