Mumbai, Maharashtra, India
Conducted qualitative and quantitative analysis of raw materials, in-process samples, and finished products as per pharmacopeial standards (IP, BP, USP). ● Performed HPLC, UV-Vis spectroscopy, and titration-based assays for drug content and purity. ● Ensured compliance with cGMP, GLP, and regulatory guidelines during analysis and documentation. ● Calibrated and maintained analytical instruments