Job Description
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 & finished products Use of HPLC, GC, UV-Vis, FTIR, NMR & wet chemistry techniques Method development, validation & stability studies Supporting equipment qualification and GMP compliance Clear communication of results to colleagues & management About You
Degree in Chemistry (or equivalent experience) Prior experience in an analytical/GMP testing environment Strong knowledge of analytical techniques & method validation Excellent attention to detail, communication, and IT/data integrity skills
If you’d like further information, please contact Graham at CY Partners.