1)Prepare and Review the ANDA, CTD, Domestic and Export documents of method validation, verification data, protocol & report. 2)Perform analytical method validation/verification as per the protocol. 3)Proper utilization of laboratory equipment and scientist day to day 4)To perform daily calibration of Instruments. 5)Proper archival of validation books and reports for ANDA, CTD, Domestic and Export products. 6)Trouble shooting during day to day analysis with proper instrument care. 7)Response to regulatory and customer queries. 8)Pharmacopeias and regulatory compliance. 9)Documentation as per the GLP requirement. 10)Task/activity assigned by reporting manger.
