Sue Bottomley

Sue Bottomley has over 30 years of experience in the pharmaceutical and biotechnology industries, with a strong focus on regulatory affairs and quality control. Most recently, Sue served as Director of CMC Global Regulatory Affairs Biopharm R&D at GSK from February 2006 to April 2022, where responsibilities included strategy execution. Prior roles at GSK included Associate Director and Scientific Director, as well as Head of QCNDA Analytics. Earlier experience was gained at Charles River Laboratories as a QA/QC Manager and at Shionogi & Co., Ltd and Abbott as a Microbiologist. Sue holds a BSc (Honors) in Biology from the University of the West of England and an A level in Chemistry from Burton Technical College.