George Pasinski

George Pasinski possesses extensive experience in Quality Assurance and Regulatory affairs within the medical device and combination products sector. Since March 2017, George has held various leadership roles at AbbVie, currently serving as Director Therapeutic Combination Products & Medical Devices in R&D Quality Assurance, where responsibilities include setting the global vision and strategy for quality compliance across diverse medical devices. Previous positions at AbbVie involved managing global teams and providing QA support throughout the development lifecycle. Prior to AbbVie, George held senior roles at Hollister, GE Healthcare, and CareFusion, among others, contributing to quality management, design assurance, and regulatory compliance in the medical device arena. George holds a Bachelor of Science degree in Biochemistry from Northern Illinois University.