Jean is Vice President of Analytical Development & Quality Control. She was awarded a PhD in Analytical Chemistry from McGill University, Canada, and has over 20 years experience in Analytical and Bioanalytical Chemistry.Â Jean started her postdoc training with a Fellowship from National Research Council. Then she worked as a project officer at NIOSH and as a NIH Fellow at Einstein Medical School in New York. Before joining IriSys, she worked at Frontage Laboratories in a GLP compliant lab. In January 2009, Jean joined IriSys and worked in a cGMP compliant facility. She has many years of experience in analytical/bioanalytical method development and extensive knowledge of various analytical technologies/ devices such as HPLC, GC/MS, ELISA, SDS-PAGE, UV/VIS, FT/IR, SFE-AAS, NMR, MALDI-TOF MS, and LC-ESI-MS/MS systems etc. She designed, planned, managed, and executed many projects that involved the analyses of both small molecular drugs, and large peptide and protein products, in addition to supervising technicians, and junior scientists. She published a book chapter and more than 20 peer-reviewed journal articles, as well as owns a US patent for a novel assay method. Jean has over 10 years experience in project management and excellent expertise in analytical method development/validation for contract service that covers all stages of drug development and pharmaceutical contract manufacturing.