Kevin Charrier Par Pharmaceuticals Inc.

Kevin Charrier is currently Vice President of Quality at PAR Pharmaceutical in Irvine CA, he is responsible for all aspects of Quality Assurance and Quality Control for a high volume solid dose extended release drug manufacturing plant.  He oversees the testing and release of incoming materials through to manufacture, testing and release of final drug products.  He also oversees the research and development for products in early stages of FDA application for the plant, scale up, through to late stage commercialization.  Prior experience he has worked in Research and Development developing Active Pharmaceutical Ingredients by fermentation technology, developing chemical methods in the pesticide industry and has worked at multiple new companies developing new drugs.  He has a BSc in Chemistry from the University of Winnipeg in Manitoba, Canada.