Team Member - QC (LCMS)

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