We are a world leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting our partners in the biopharmaceutical industry with the development and production of their biologic, vaccines and advanced therapies.
With over 25 years of experience in process development and cGMP manufacturing, a dedicated staff of over 1,200 and a reputation for excellent customer service, flexibility and responsiveness, we’ve become a trusted partner to some of the most prominent biotech developers and pharmaceutical companies in the industry. Our Process Development experience includes the development of processes for molecules expressed via fermentation (e.g., E. coli, P. pastoris), cell culture systems including CHO, and insect cells, and from transgenic sources.
Our network expands within three development and manufacturing facilities located in Billingham, United Kingdom, Redcar, United Kingdom, Research Triangle Park, North Carolina, USA, College Station, Texas, USA, and Hillerod, Denmark. Our UK sites are currently undergoing expansion and are recruiting graduates across R&D (MCC, USP Microbial, Downstream Processing, Analytical Development), Manufacturing, QA and QC