Heather Tomlinson has over 30 years of experience in the biopharmaceutical and CDMO sectors and has extensive knowledge of quality requirements at early and late stage development. Heather has a strong background in sterile (aseptic) product manufacturing. 

In her current role Heather leads the Quality Assurance and Regulatory Affairs (CMC) activities at the Alnwick site and is responsible for maintaining a Quality Management System in compliance with GLP, GCP and GMP regulations.