VADIM BODIK

Vadim Bodik is a Principal Quality Engineer at Roche with over 25 years of experience in the FDA regulated industry, specializing in Medical Devices, Diagnostics, and Pharmaceutical operations. They possess a working knowledge of 21 CFR Part 210, 211, 820, ISO 13485, and ISO 14971 standards. Vadim has successfully managed nonconformance root cause and failure investigations, developing corrective and preventive actions using Quality Engineering and Process Excellence tools. Earlier in their career, they held positions as a Quality Engineer at Feintool New York, a Quality Assurance Engineer at Schick Technologies and Micro Stamping Corporation, and a Senior Quality Engineer at Ortho Clinical Diagnostics. Vadim is currently pursuing a Master of Science in Technology Management at Stevens Institute of Technology.