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Research Associate

Cadila Pharmaceuticals Ltd

Dholka, GujaratOn-siteassociateNot disclosed
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About the role

1) Method development and report preparation. 2) Routine F&D and stability sample analysis. 3) Method development and report preparation 4) Analytical method verification of assigned products. 5) To perform the forced degradation studies. 6) To develop and validate the cleaning method. 7) To Perform partial method validation for new develop method. 8) Characterization and analysis of reference product. 9) To perform the multimedia dissolution and preparation of CDP report. 10) Preparation of working standard as per SOP. 11) Analytical method transfer to QC Lab. 12) Cleaning and maintenance of laboratory equipment.

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