QA Lead – Cell Therapy & MHRA Compliance

A leading biotechnology company in Stevenage seeks an ambitious Quality Assurance Lead to drive the company toward MHRA Manufacturing and Import Authorisation for its automated CDMO. You will establish quality processes and ensure compliance while collaborating with industry experts. Ideal candidates have substantial QA experience in GxP environments, particularly in ATMPs or cell therapy. The role offers competitive salary and benefits in a fast-paced, innovative environment, contributing to significant healthcare solutions. #J-18808-Ljbffr