Jason Rossi

AST Inc.
Principal Commissioning, Qualification, and Validation Engineer
Jason Rossi has over 29 years of operational expertise and leadership in various capacities throughout the pharmaceutical manufacturing industry. His experience includes project management, GMP facility and equipment design and installation, technology transfer, targeted drug manufacturing, and onsite CQV program development. Jason has been at the forefront of drug development, playing pivotal roles in bringing innovative new products to market, including first-generation gene-based hemophilia therapeutics.
At AST, Jason leads team efforts to ensure that AST’s products, systems, and processes meet the highest standards of quality and compliance, and spearheads on-site CGMP strategies in line with the latest regulations, technological advancements, and best practices for documentation, quality risk management, and validation.
Prior to AST, Jason held operational and leadership roles at leading pharmaceutical companies, including serving as Fill-Finish Manager at Pfizer, Head of Microbial Contamination Control at Lonza, and, most recently, Global Assistant Director of Engineering at Catalent, where he led Cell and Gene Therapy development initiatives.