Quality Control Chemist

Role Analytical Chemist responsible for chromatographic testing and method development within a biopharma or related regulated environment. Responsibilities perform analytical testing using HPLC, GC, and related instruments develop and evaluate formulations support validation, technical transfers, stability studies, and troubleshooting prepare technical reports and documentation collaborate with cross-functional teams and train colleagues communicate project status and resource needs Qualifications bachelor's or master's degree in chemistry or life sciences minimum two years industry experience hands-on expertise with chromatography techniques, including HPLC and GC working knowledge of ISO 9001, ISO/IEC 17025, ISO 17034 standards Preferred experience in GLP/GMP or ISO-regulated settings familiarity with chromatographic detectors (UV-Vis, RI, ELSD, FID) knowledge of quality systems in pharma or medical device sectors High-value expertise in analytical chemistry for biopharma applications, supporting formulation development, validation, and compliance in regulated environments.