- To perform analytical method development of drug products for different tests like Assay/Dissolution/Degradation products/Residual solvents/water content by using advanced techniques like HPLC/GC/UV/KF
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- To perform documentation through the BIOVIA system to ensure data integrity, traceability, version control, audit trail compliance, and secure electronic record management in accordance with applicable quality and regulatory requirements.
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- Performing routine/initial analysis of drug products for market samples/query response.
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- Preparation of method development protocols, reports, method equivalency report and COA
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- To perform multimedia dissolution study and compatibility study and prepare report of the same.
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- Maintaining lab safety compliance during analysis
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- Maintaining GLP compliance in the laboratory.
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- Maintaining GDP in the laboratory.
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