QC Analyst – Chemistry Stability & GMP Compliance

A leading pharmaceutical organization in Oxford seeks an experienced Quality Control Analyst to enhance its GMP laboratory team. The role involves performing routine analytical and stability testing, documentation, and compliance with FDA, EU, and ICH requirements. Candidates should possess a BSc in Chemistry and 5–7 years of pharmaceutical Quality Control experience, along with hands-on GMP testing expertise. The position values attention to detail and collaboration in a high-standard laboratory environment. #J-18808-Ljbffr