Sterling Pharma: A versatile CDMO you can depend on; Sterling combines a full-service offering with expert knowledge and technical agility to offer API development and cGMP contract manufacturing capabilities. They can support your projects through the entire product lifecycle from grams to tons.
Their 700+ strong team across our facilities in the UK and the US are capable of handling even the most hazardous chemical processes safely. Industry-leading compliance culture and performance are part of their day-to-day work, and they work hard to maintain the Sterling standards.
Dedicated to adding value through continuous improvement, they constantly explore new and improved ways of doing things as part of their Technology and Innovation Program.
With over 50 years of experience, their exceptionally talented team combines their unrivaled knowledge with first-class customer service to ensure high-quality project delivery every time. That’s the Sterling way!
Bio Highlights: Adam holds a B.S. in Chemistry and Biochemistry from Carroll University, and joined Sterling as part of the Germantown acquisition. He has worked in the global CDMO space for over 17 years in both API and drug product, most recently as Senior Director, Technical Operations, where he was responsible for all site R&D, operations, facilities, engineering, and supply chain.