At Sun Pharma, I gained hands-on exposure to analytical method development and verification in a pharmaceutical R&D environment. I performed HPLC-based testing and prepared mobile phases, reagents, and standards.
I also supported instrument calibration and routine qualification checks, and assisted in evaluating method parameters against acceptance criteria. Under supervisor guidance, I reviewed raw data and chromatograms and maintained documentation in line with GLP practices.
My research project focused on developing and verifying an analgesic dosage form, with an emphasis on pharmaceutical quality control and chromatographic analysis. I’ve also co-authored review articles on analytical method development and chromatographic approaches.
