A growing biotechnology company in the UK seeks a QA Manager (Consultant) to lead GCP quality assurance across clinical trials. The ideal candidate will have over 7 years of experience in Quality Assurance and a strong GCP background. Responsibilities include overseeing GCP compliance, conducting audits, and preparing for regulatory inspections with MHRA and FDA. This is a part-time, contract role offering flexible engagement and an estimated workload of 0.4–0.5 FTE, remote or hybrid work, initially for 12 months with a chance for extension. #J-18808-Ljbffr