Responsibilities   • • Ensuring good laboratory practices (GLP), good documentation practices (GDP) and good manufacturing practices (GMP). • To follow the laboratory safety standards and practices. • To perform activities related to LCMS instrument and analysis. • To ensure that analysis was conducted as per the respective SOP or STP or GTP. • For Calibration and Standardization of Analytical instruments. • For ensuring the preparation and standardization of Volumetric Solutions, reagents and mobile phase preparations. • To report/Highlight discrepancies in- procedures / products / materials /People practices/ Systemic issues to the group leader and functional head on time. • To ensure that the documentation done in online and error free. • To ensure that only calibrated instruments / equipment’s are used for analysis. • To ensure that only valid working / reference / impurity standards are used for analysis. • For ensuring the Disposal of samples after the completion of analysis. • To ensure that the instruments / equipment’s are used with utmost care and as instructed in the relevant SOP. • To report incidents / OOS/OOT on time to the group leader. • To ensure Instruments/ Equipment’s and work area should be clean. • For maintenance of registers, logbooks used for analysis. • Testing of analytical samples as per schedule and submit the reports online to the concern. • Responsible for result posting and other SAP and LIMS related activities for sample analysis. • For sending the samples to contract laboratory for testing. • For documents tagging and submission to QA. • For conduct investigation related to notifications. • For initiation of change controls and implementation of CAPA and notifications closure on time. • Chromatographic data processing in Analyst Software. • To ensure the compliance with respect to LCMS instrumental handling and analysis of respective samples. • To coordinate during internal / external inspections along with necessary action plans. • Ensure to comply any other responsibility given by the reporting authority. M.Sc./M Pharma. Experience: 6 to 10 Years