Ryan Murray is a quality and manufacturing science Senior Consultant with ValSource, Inc. He is primarily focused in the areas of quality and regulatory compliance, facility design and control, technology transfer, process qualification, and aseptic risk management of both biologics and advanced therapy medicinal products (ATMPs). Ryan is an active member of the International Society for Pharmaceutical Engineering’s (ISPE) South Central Chapter and is a board member of the Parenteral Drug Association’s (PDA) Texas chapter and a member of the PDA ATMP Advisory Board. Ryan holds a BS in biomedical science and MS in biochemistry and biophysics from Texas A&M University and has authored several industry publications and presented internationally on contamination control strategies and aseptic processing risk management.