Conducting both qualitative and quantitative analyses of Raw materials, Finished products,Stability samples,Validation and Cleaning validation samples utilising a range of analytical instrumentation.Organise work schedule to complete assigned tasks efficiently and on schedule.Proficient in analytical Method Evaluation, Development and Method Validation.Performed analytical laboratory data reviews for the release of intermediate and finished product lots, adherence to GMP/regulatory and internal SOP standard

Analysis of all laboratory and plant samples including In-process, Finished Product, Cleaning validation and Stability samples using analytical instruments.Method development, Method validation and Troubleshooting of different pharmaceuticals Solid dosage forms (Assay, RS, Dissolution, Moisture content, Disintegration, Hardness and Content Uniformity).Preparing and evaluating Method Development reports, Method Validation protocol and Method Validation summary reports.Documentation and Compilation of observations and data obtained from testing as per established SOPs Responsible for Calibration of Lab equipments as per GLP and GMP requirements.Maintain records of Calibration, Common instruments and Column inventories.

Carried out multistep organic reactions, extraction and purification.Worked on different projects for process development and cost reduction and validation. Impurity synthesis of API and its characterization.Good knowledge of data interpretation by NMR, Mass, LC-MS, HPLC.Proficient in Chem-draw software and SCR report preparation.Trouble shooting of plant batches.

Intern at Medicinal Chemistry Department.Specialised in Synthesis of NCE(New Chemical Entities), Separation, Isolation, Characterisation by different Spectrophotometric methods.Performed Various kind of Organic reactions like Oxidation, Reduction, Amination, Coupling reactions etc.Data interpretation of compounds by NMR, LC-MS, HPLC, IR ,TLC etc.Expertise in operating Rotavapour and Manual Column Chromatography.