CY Partners are excited to be supporting a leading CRO/CDMO in Durham who are looking for a Quality Control Analyst to join their QC team. This is a fantastic opportunity to work across pharmaceuticals, biotech and fine chemicals, contributing to GMP manufacture of novel APIs and other specialist materials. The Role Routine and non-routine analysis of raw materials, intermediates and finished products Use of HPLC, GC, UV-Vis, FTIR, NMR and wet chemistry techniques Method development, validation and stability studies Supporting equipment qualification and GMP compliance Clear communication of results to colleagues and management About You Degree in Chemistry (or equivalent experience) Prior experience in an analytical/GMP testing environment Strong knowledge of analytical techniques and method validation Excellent attention to detail, communication, and IT/data integrity skills If you d like further information, please contact Graham at CY Partners.