Current Job Responsibilities;1.Review and monitor analytical method development for new formulations and existing redevelopment products for various analytical tests such as (Assay, RS, Dissolution, CU etc.) 2.Routine analysis monitoring and trouble shooting during analysis.3.Review of calibration documents for various instruments.4. Monitoring of analysis for market complaints, and regulatory queries.5. Daily work allocation for team members and monitoring the execution of… Show more Current Job Responsibilities;1.Review and monitor analytical method development for new formulations and existing redevelopment products for various analytical tests such as (Assay, RS, Dissolution, CU etc.) 2.Routine analysis monitoring and trouble shooting during analysis.3.Review of calibration documents for various instruments.4. Monitoring of analysis for market complaints, and regulatory queries.5. Daily work allocation for team members and monitoring the execution of the same.6. Preparation and execution of documents like - Method development Reports, Standard test procedures, Product Development Reports.7.Preparation of Validation Protocol and review of validation reports. 8.Ensure and maintain GLP, GDP and quality compliance in laboratory.9.Imparting training to subordinate/Team member as and when required.10.Literature search for new and existing products as and when required. Show less

1. Development of Analytical Methods for Finished Drug Products (Assay, Related Impurities and Dissolution) for Regulated markets.2. Analysis of stability samples and routine developmental samples.3. Pre-formulation studies, compatibility studies, solubility studies, for formulation.4. Preparation and execution of documents like - Method development strategies, reports, Standard test procedures and stability data compilation.5. Dissolution profiling for Bio equivalency studies… Show more 1. Development of Analytical Methods for Finished Drug Products (Assay, Related Impurities and Dissolution) for Regulated markets.2. Analysis of stability samples and routine developmental samples.3. Pre-formulation studies, compatibility studies, solubility studies, for formulation.4. Preparation and execution of documents like - Method development strategies, reports, Standard test procedures and stability data compilation.5. Dissolution profiling for Bio equivalency studies (Multimedia & Bio relevant media. Show less

1. Development of Analytical Methods for Finished Drug substances (Assay, Related Impurities and Dissolution) for products of Regulated markets and Domestic Market.2. Analytical method development and validation of analytical test procedures.Pre-formulation studies, compatibility studies, solubility studies, stability studies for formulation.3. Preparation and execution of documents like - Method development strategies, reports, Standard test procedures and stability data… Show more 1. Development of Analytical Methods for Finished Drug substances (Assay, Related Impurities and Dissolution) for products of Regulated markets and Domestic Market.2. Analytical method development and validation of analytical test procedures.Pre-formulation studies, compatibility studies, solubility studies, stability studies for formulation.3. Preparation and execution of documents like - Method development strategies, reports, Standard test procedures and stability data compilation.4. Dissolution profiling for Bio equivalency studies (Multimedia & Bio relevant medias). Show less

PhD Dissertation: “Study of Degradation Behavior of Active Pharmaceutical Ingredients.” Summary of Research Investigated: Systematic degradation behavior was studied for selected drugs as per ICH guidelines to evaluate their intrinsic stability. Stability indicating assay method was developed and validated for selected drugs. Possible mechanism of degradation for selected drugs were proposed after the characterization of degradation products formed during stress degradation studies… Show more PhD Dissertation: “Study of Degradation Behavior of Active Pharmaceutical Ingredients.” Summary of Research Investigated: Systematic degradation behavior was studied for selected drugs as per ICH guidelines to evaluate their intrinsic stability. Stability indicating assay method was developed and validated for selected drugs. Possible mechanism of degradation for selected drugs were proposed after the characterization of degradation products formed during stress degradation studies using LC-MS/MS study. Show less

1. Conducted periodic lectures for B. Pharm. and M. Pharm. students on various topics related Pharmaceutical analysis and Quality Assurance.2. Conducted periodic Practicals for B. Pharm. and M. Pharm. students on various topics related Pharmaceutical analysis and Quality Assurance.3. Evaluated and graded B. Pharm. Students for theory papers and practical examination in the subject of Pharmaceutical Analysis.4. Advised M. Pharm. students for their minor and major dissertation… Show more 1. Conducted periodic lectures for B. Pharm. and M. Pharm. students on various topics related Pharmaceutical analysis and Quality Assurance.2. Conducted periodic Practicals for B. Pharm. and M. Pharm. students on various topics related Pharmaceutical analysis and Quality Assurance.3. Evaluated and graded B. Pharm. Students for theory papers and practical examination in the subject of Pharmaceutical Analysis.4. Advised M. Pharm. students for their minor and major dissertation projects. Show less

Method Development of Pharmaceuticals By HPLC.Assay, RS, CU,Blend, etc. By HPLCAnalysis of Stability Samples.Dissolution Studies by HPLC and UVValidation of Developed Methods.Prepared Validation Protocols, Finished Product Specification, Method of Analysis, Stability Reports etc.