At Johnson & Johnson, I perform routine and non-routine quality control testing for raw materials, intermediates, and finished pharmaceutical products under cGMP and USP guidelines.
I use HPLC, UV-Visible spectroscopy, FTIR, Karl Fischer titration, and wet chemistry methods while maintaining test records, analytical reports, and documentation aligned with GDP and ALCOA+ principles. I also support stability studies, OOS/OOT investigations, CAPA implementation, audits, inspections, instrument calibration, and preventive maintenance.
Across US and Indian pharmaceutical environments, I've contributed to data tracking, compliance documentation, reporting, and quality-improvement initiatives focused on accuracy and operational efficiency.
