Senior Research Associate

3 - 7 years

0 Lacs

Posted:1 day ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

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 verification methods - Evaluate and verify API methods - Assess API solubility studies - Qualify working standards - Develop and verify methods for drug product formulation - Release raw material and packaging material - Prepare test procedures for routine development analysis - Manage columns - Analyze TOC samples - Ensure compliance with in-house systems - Maintain hygienic conditions in the department - Follow GxP (GMP, GDP, GLP) for all processes Qualifications Required: - M. Pharm / M.Sc. in Chemistry/Analytical Chemistry,

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