Sk Chung

SK Chung is an experienced quality compliance professional with extensive expertise in computer system validation and laboratory management within the pharmaceutical industry. Currently a QC Specialist and Subject Matter Expert at Taro Pharmaceuticals Canada since February 2010, SK Chung supports analytical systems by providing user functional requirements and conducting risk assessments. As President and Consultant at Chung Quality Compliance Support, since September 2009, SK Chung offers consultancy on procedural processes with a focus on FDA 21 CFR Part 11 compliance. Previously, roles at Sanofi Pasteur, Pharma Medica Research Inc., Eli Lilly Canada Inc., and Teva - Novopharm showcased skills in SOP development, laboratory systems management, and analytical method development. SK Chung holds a Bachelor of Science in Biochemistry from McMaster University.