Result oriented professional with a master’s degree in biology and over 7 years of Pharmaceutical industry experience in positions of increasing responsibilities in cGMP production under sterile conditions, quality assurance, and quality control and process development. Skilled at leading multiple projects, as well as developing and managing laboratory operations and budgets. Familiar with both the US and Health Canada’s organizational structure. Responsible for the preparation of several audits (USDA, CFIA and Novartis) and acted as a liaison officer with the Head Office of regulatory affairs in Charlottetown, P.E.I, Canada. Broad diverse technical background with experience in cell culture technology, immunology, bacteriology and virology in a cGMP environment.
Description
