About Me

• Handling of sophisticated instruments like HPLC.

• Analysis & reporting of In-process (Blend/Bulk), finished products , Stability & RM.

• Drawn up plans for the sampling and analysis of the Packing Material and raw material...M.

• Drawn up plans for the sampling and analysis of the Packing Material and raw materials, ensuring problem free operations.

• Assisting in the organisation of the Quality Control Laboratory workload in a safe manner to meet the requirements specified by the Quality department and the QC Manager.

• Completing accurate analysis of In-process (Blend/Bulk), finished products , Stability ,RM & PM compliance with authorized test procedures and relevant reference literature (i.e. Pharmacopoeias).

• Management of samples and report writing as well as the investigation of samples showing nonconformance to a specification and arranging for contract analysis at external test facilities.

• Preparation of SOP and Specifications.

• Reporting change control and OOS.

• Calibration of Instruments.

• Exposure to CDSCO Audit Nov-2016 and GSK External Supply Audit Apr-2017& 2019.