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.