Detail-oriented Quality Control Analyst with 2 years of experience in pharmaceutical cGMP environments. Expertise in HPLC, FTIR, KF, and UV-Vis spectroscopy, ensuring product quality and regulatory compliance. Skilled in managing stability studies (ICH guidelines), analytical troubleshooting, chromatography data systems, and technical documentation (SOPs, protocols, reports). Dedicated to maintaining high QA/QC standards, process improvements, and cross-functional collaboration.