Jim Clossick
Vice President, Quality Assurance and Regulatory A
Pharmaceutical Management
OrbusNeich
Hong Kong
Biography
Jim Clossick's background includes over 30 years of medical device experience. He specializes in international regulatory affairs, design control, process validation engineering, design of experiments, failure mode and effects analysis, customer requirements analysis, and quality functional deployment (QFD).Clossick provides leadership for seeking regulatory approvals for cardiovascular devices, including combination products. He holds two U.S. patents for device design. Clossick is a certified quality engineer, a certified Six Sigma Black Belt, and a certified QFD facilitator. In addition to his BS degree in Mechanical Engineering from the Missouri University of Science and Technology-Rolla, he has undertaken additional studies in Biomedical Engineering.
Research Interest
Biomedical Engineering