Joseph Musto has over 30 years of experience in the pharmaceutical industry. He has held different responsibilities and positions, both in large pharmaceutical enterprises and and small startups, ranging from supervisory roles in manufacturing to VP in Quality and Regulatory Affairs. This involved mostly quality and regulatory affairs—as applied to product development—within projects from both academic settings and those from more experienced organizations and seasoned teams. The technologies included vaccines, cellular processing, biologics, small molecules and medical devices in different therapeutic areas. Joseph obtained his BSc at McGill University in Montreal and a B. Pharm at Université Laval in Quebec City, Canada.