Experienced Quality Control (QC) Analyst with expertise in pharmaceutical laboratory testing, analytical instrumentation, and GMP compliance. Skilled in performing raw material, in-process, finished product, and stability testing using HPLC, UV-Visible Spectrophotometer, Dissolution Apparatus, pH Meter, FTIR, and other laboratory equipment. Proficient in method execution, documentation, data analysis, SOP compliance, and investigation of out-of-specification (OOS) results. Strong knowledge of USP, BP, and regulatory requirements with a commitment to ensuring product quality, safety, and compliance. Dedicated to maintaining laboratory accuracy, integrity, and continuous improvement in pharmaceutical manufacturing environments.