Sherry has over a decade of designing pharmaceutical and biopharmaceutical facilities. Her specialties include process and critical utility design, equipment specification, architectural programming, procurement, construction support, and start-up/commissioning. Sherry’s broad spectrum of experiences in facility design makes her an asset to clients through all stages of a project. Her focus is to meet regulatory requirements through CGMP process system design and to align with the client’s business goals. She is actively involved with the ASME Bioprocess Equipment Standards and aims to bring the latest trends and best practices to meet clients’ needs. 

View Bio

Tim has over 25 years of extensive bioprocess engineering, project management, and start-up experience. His experience includes scale-up of fermentation processes, process design, large-scale cell culture, vaccines, isolation, recovery, purification, facility design, critical utility system design, start-up, and commissioning. He has considerable experience in vaccine facility and process design.

View Bio