Responsible for RM sample analysis- review. Troubleshooting related to sophisticated analytical instruments.Preparation of COA. Preparation of in-house and outside Calibration planner for laboratory instruments and execution as per schedule. compilation of the Calibration data and review.Lab Chemicals, Reference standards, working standards maintenance as per SOP.Reporting of Laboratory events like OOS, OOT, incidents. Investigation and preparation of investigation report with the help of Lab Manager.To Ensure data integrity, cGMP, GDP, GLP, ALCOA+ at workplace.

Responsible for analysis of RM, FP, Stability samples by instrumental method of analysis by GC and GC-HS. Chromatographic Integration as per GCP, Online reporting and documentation of the data by following GDP.Instruments Calibration and verification activities. Column, chemicals and solvents management. To maintain all testing records, raw data and logbooks as per SOP.To follow data integrity, cGMP, GDP, ALOCA, ALCOA+ principles at workplace.

Responsible for Physico-Chemical analysis of RM, FG, Stability samples. Online reporting and documentation in compliance with the SOP and GLP. To maintain all testing records, raw data, log books as per SOP.Preparation and standardization of volumetric solutions, preparation of reagents and indicators, stock solutions as per requirement and as per set frequency.To assist Lab Manager for efficient and smooth functioning of QC lab through QC analysis and by following GDP, GLP practices.Routine instrumental analysis of RM, FG. Stability sample analysis by use of GC, HPLC, UV instruments as per planned frequency. Working knowledge of chromatographic practices, Integration, calibration & verification activities and troubleshooting related to sophisticated instruments like GC, HPLC, UV etc.Laboratory chemicals, reference standards, working standards management and documentation as per SOP and GDP guidelines.

Got an opportunity to work during plant setup. Attended several trainings such as 5S, Safety, First aid, Process flow, Process implementation, Validation, Health and hygiene, QMS, GMP, GDP, GLP, GWP, SAP, concepts of Pharmaceutical analysis.Involved in DM water plant validation and monitoring activities. DM plant charging and regeneration process. DM treatment by antiscalent, Gramicid dosing, Chlorine and fungal treatment. DM plant sample collection for microbial and Physico-Chemical testing.Actively participated in Process implementation, Batch coding, artwork checking, In-process quality checks, Dispensing activity, Line clearance, online observations and records.Sampling of RM, PM, IP, FP, stability samples and analysis by use of applicable method of analysis and analytical instruments as per GLP. Calculation and recording of the analytical data and results in the respective work sheet by following GDP.