Pharmaceutical QC Analyst

Testing & Analysis Test raw materials, packaging materials, in-process samples, and finished products against BP/USP/EP and in-house specifications Perform analyses using HPLC, UV-Vis, Karl Fischer, dissolution, disintegration, pH, and other routine QC instruments Conduct stability studies and maintain stability records Prepare and review analytical reports and Certificates of Analysis (CoA) Water System Testing Collect daily samples of purified water from user points and the distribution loop Test conductivity, TOC, pH, and other chemical parameters per pharmacopoeia Collect microbiological samples and coordinate with micro testing Track water results, trend data, and report any excursions immediately Daily Lab Operations Perform daily instrument checks (balance verification, pH meter calibration, HPLC system suitability) Record and monitor lab temperature/humidity and fridge/incubator logs Receive, log, and store samples; maintain retention samples Prepare and label reagents, volumetric solutions, and mobile phases Manage reference standards, chemicals inventory, and expiry control Maintain lab cleanliness, glassware control, and safe chemical waste disposal Keep all logbooks and records complete and accurate daily (ALCOA+) Quality Support Support OOS/OOT investigations, deviations, and CAPA Support method validation/verification and regulatory submission data Participate in internal audits and PIC/S readiness activities Requirements Bachelor's degree in Chemistry, Pharmacy, or a related science field (required) 3–5 years of QC experience in a GMP pharmaceutical laboratory (required) Hands-on HPLC experience preferred (method running, system suitability, troubleshooting) Good knowledge of pharmacopoeial testing (BP/USP/EP) and GMP documentation Good written and spoken English Available to join within 4 weeks Candidates already in the UAE preferred