Performed dissolution testing of acetaminophen tablets using USP Apparatus II and analyzed drug release profiles through UV-Vis spectrophotometry. Ensured compliance with USP standards, validated analytical results, and developed statistical models to evaluate consistency, accuracy, and pharmaceutical quality control parameters.

Executed bacterial transformation using pGLO plasmid and optimized experimental conditions to analyze GFP expression in E. coli. Conducted controlled experiments, protein analysis, and validation processes, ensuring accurate results, reproducibility, and compliance with laboratory protocols while enhancing understanding of gene expression mechanisms.