Mr. Quintenz serves as Global Scientific & Professional Affairs Manager for Bio-Rad Laboratories Quality Systems Division. He works to promote an understanding of laboratory regulations and best practices, as they pertain to QC and EQA/PT programs.
With over 20 years of medical device industry experience, his work has focused on improving the quality of laboratory testing worldwide by promoting an understanding of quality control/quality assurance best practices and laboratory regulations. Prior to joining the Board, he was a member on CLSI's Consensus Council and worked on various committees. He is the current chair of the US TAG to ISO TC212 (Clinical Lab Testing and IVD Testing), a member of the AACC Corporate Advisory Board, a member of the CLIAC US federal advisory committee, and a member of the AdvaMed Diagnostic Task Force.