Kevin is a chartered biochemical engineer with over 30 years’ experience in the design of biopharmaceutical manufacturing facilities. He is an expert in biotechnology process design and aseptic fill-finish manufacturing. Kevin is a patient safety-driven leader in the application of QRM/QBD principles in the design of drug product and drug substance facilities. As an active member of the Parenteral Drug Association and International Society of Pharmaceutical Engineering Ireland Affiliate, he chairs and organizes technical seminars in Ireland for both organizations.