James C. Vetricek

James C.
Vetricek joined in January 2003 in connection with acquisition of AMO as Vice President of AMO and was promoted to Vice President of Operations for HEI in January 2004.
Prior to January 2003, Mr. Vetricek served as Vice President, Quality and Regulatory Affairs of CMED from February 2001 to January 2003.
Mr. Vetricek has over 20 years of experience as a medical device professional managing facilities with multi-site operations.
His responsibilities have included research and development, regulatory affairs, pilot manufacturing, and proprietary and contract manufacturing operations.
Mr. Vetricek's product experience includes sterile single use devices, implants, bio absorbable surgical materials, electromechanical surgical systems, anesthesia systems and cardiovascular monitoring devices.
Prior to joining CMED, Mr. Vetricek served as Vice President of Regulatory Affairs & Quality Management at Linvatec, a division of Conmed, a medical equipment manufacturer, from February 1999 to February 2001.
Mr. Vetricek also serve from September 1994 to June 1998 as Vice President of Regulatory Affairs & Quality Assurance and R&D at Ohmeda Medical Device, a division of BOC Group, an industrial producer of gases.