SCIENTIST
PAR FORMULATION PVT LIMITED
Total years of experience :13 years, 11 Months
• Currently Working as a “Scientist-API” - Analytical Research and Development in “Par Formulation Research laboratory” Chennai.
• Industrial experience in Analytical R&D in API with expertise in Method development in HPLC, Method validation in HPLC and GC, , Preparing Working Standard, Stability studies, Routine analysis of Reaction Monitoring, Assay, Related Substance and Routine analysis in GC, Chemical analysis, Thermo gravimetric analysis.
• Attitude to work in teams lead the team towards the target .
• Highly motivated and result oriented professional with strong analytical team building skills.
• Willingness to learn new ideas and concepts.
1.)Qualification of Intermediate, raw materials and API molecules.
2.) Calibration of analytical instruments.
3.) Periodic calibration Schedule preparation and execution of calibrations for analytical instruments
4.) Establishing LOD and LOQ s and generating Cutoff data as a part of support to DMF filings.
5.) Method validation of intermediate and Final API in HPLC and GC method.
6.) Implementation of cGLP
7.) Evaluation of product stability with respect to various packing conditions and concluding it.
8.) Design of Experiments (DoE) studies for processing pharmaceutical products.
9.) Responsible for carrying out day to day work.
10.) Validation of analytical methods for active pharmaceutical ingredients.
11.) Stability study and hygroscopic study of finished products of all conditions.
12.) Method development and Validation method for all impurities and reagent absence study in active pharmaceutical ingredient for DMF filling activities.
13.) Practicing Electronic Note Book work (ELN) for Electronic online documentation
14.) Continuous support to synthesis R&D requirement for process and developing molecule.
15.) Currently working generic oncology drugs of Enzalutamide, and Pemetroxide tritromethamine molecule, process and development.
16.) Drafted all the development reports like Development strategy report, Feasibility report, DoE report and other documents required for the technology transfer.
17.) Analytical Laboratory Documentation simplification, lab maintenance as per CGLP, documents archival and easy retrieval for audit purposes.
18.) Quantification of final API molecules, analysis of related substances, assay
And purity of the compound.
Worked as a “Research Executive” - Analytical Research and Development in Orchid chemicals and Pharmaceuticals since June 2010 to June 2013.
Qualification of Intermediate, raw materials and API molecules.
1.) Calibration of analytical instruments.
2.) Continuous support to synthesis R&D.
3.) Quantification of final API molecules, analysis of related substances, Assay and Purity of compounds.
4.) Preparative HPLC- Isolation, Purification of impurity from API molecule.
5.) Isolation of New Chemical Entity (NCE) molecule using Preparative HPLC enriched to purity of the compound by using Preparative HPLC Techniques
M.Sc., Chemistry, Department of Chemistry, Thiyagarajar College of Art & Science, Madurai 2008-2010 Marks obtained– 73%
.Sc., Chemistry, Department of Chemistry, the American College of Art & Science, Madurai 2005-2008 Marks obtained– 71%
