Built hands-on proficiency in pharmaceutical QC testing, evidenced by successfully performing dissolution and disintegration tests on finished dosage forms, by working directly within the Quality Control department for one month. Developed working competency in core analytical instrumentation, demonstrated by independently operating HPLC, UV-Visible Spectroscopy, and IR Spectroscopy for finished product analysis, by assisting senior QC analysts on daily sample testing. Strengthened understanding of regulatory compliance, reflected in accurate completion of pharmaceutical documentation and quality records, by applying GMP standards and QA protocols during routine testing cycles. Gained cross-functional insight into pharmaceutical manufacturing quality systems, shown through the ability to connect QC test outcomes to broader QA processes, by observing and documenting both departments' workflows.