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3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

You will be responsible for following standard practices cGLP during lab experiments, cleaning verification method development, API method evaluation and verification, API solubility study assessment, working standard qualification, method development and verification of drug product formulation, ARF release of raw material and packaging material, preparation of test procedures for routine development analysis, column management, TOC sample analysis, ensuring in-house compliance system, maintaining hygienic conditions in the respective department, and following GxP (GMP, GDP, GLP) for all processes. Key Responsibilities: - Follow cGLP during lab experiments - Develop and verify cleaning veri...

Posted 2 days ago

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