Responsibilities Analysis and Reporting of In-process, Validation, Finished Product and Stability Study samples of ANDA project as per Production schedules on daily basis. Analysis of Swab sample / cleaning verification samples of area and equipment’s related to manufacturing of ANDA project. To maintain Good Laboratory Practices in the laboratory. To maintain the assigned Laboratory workplace, instruments and equipment. Should have good command on HPLC / GC / UPLC / IC Instruments and having an independent capacity of troubleshooting. To ensure compliance to the requirements of policy and procedures on Data Integrity. Analysis and Reporting of In-process, Validation, Finished Product and Stability Study samples of ANDA project (exhibit) as per Production schedules. Hands on the techniques / SOPs / instructions to be followed up as per the Good laboratory Practices. To participate in Method transfer and validation activities as per committed timelines of New Project. Reporting of Laboratory Investigation of OOS, OOT, Action Limit and Aberrant Analytical Test results, Chromatographic errors and Deviations (If any). Responsible for maintenance and upkeep of Sample storage area. Exposure to authorized regulatory audit agencies, e.g. USFDA, MHRA etc. To ensure timely disposition of samples.     Qualification & Experience B.Sc. / M.Sc. in Chemistry. 5 plus years relevant experience in Quality Control Laboratory. Hands on experience on Instruments viz., GC, HPLC, Ion Chromatography, UPLC, UV and Dissolution apparatus etc. Knowledge of regulatory requirements for different markets (US, EU, Canada etc.) Familier with Good Laboratory Practices