Mary A. Mayka

Mary A. Mayka, Ph.D., is currently the Associate Director of Regulatory Affairs at Baxter, bringing over 15 years of experience in the medical device sector. Previously, they served as Associate Director at Abbott, overseeing global regulatory strategies for Neuromodulation devices, and held several managerial roles at GE Healthcare, focusing on regulatory compliance and research operations. With extensive expertise in EU MDR and a proven ability to navigate complex regulatory landscapes, Mayka has demonstrated a commitment to developing effective regulatory strategies that align with business objectives. They earned a Ph.D. in Bioengineering from the University of Illinois Chicago, with a focus on Neural Engineering.