Regulatory Affairs CMC Lead - Cell & Gene Therapies

A biopharmaceutical company in the UK seeks an experienced Associate Director, Regulatory Affairs CMC, responsible for leading global CMC regulatory strategies for its innovative cell and gene therapy products. The ideal candidate will have 8-10 years of experience in Regulatory Affairs for biologics, excellent communication skills, and a proven track record in regulatory submissions and interactions with health authorities. This role offers a dynamic work environment focused on teamwork and advancing cancer therapies.