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About Me
To obtain challenging and rewarding full time position in a company with growth and learning opportunities in supportive, challenging work environment.....
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Description
- 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 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.