Research Scientist

• Preparation and review of test procedure, development reports, method validation protocol and LNBs.
• Perform calibration of the analytical instruments as per calibration schedule.
• Follow the standard practices-cGLP during lab experiments.
• Analytical method development and validation for quantification of genotoxic impurities by LCMS, GCMS and ICPMS.
• Analytical method development, validation, and sample analysis for Extractables and Leachables using HPLC, LCMS, GCMS and ICPMS.
• Identification and characterization of unknown impurities by LCMS.
• Follow the GxP (GMP, GDP, and GLP) for all processes.
• Maintain hygienic condition in respective department.
• Standard management.
• Review of routine analytical activity (Peer Reviewer)
• Ensure use of personal protective equipment, attend EHS training, send waste to concerned person, and comply EHS requirement.

B. Pharm / M. Pharm, BSc/MSc