 Managing price control activity of pharmaceutical products in coordination with respective CFTs  Administering Form V, Form II, Form III, Form I, Form IV filing in compliance with NPPA  In compliance with submission of monthly details as well as quarterly return of price changes to NPPA  Studying and clarifying on concept of Design Analysis data, Reliability Data, Safety Data, Performance Data of Medical Device First of its kind application on Combi pack Initiation KIT which will serve the patients need in best way  Providing leadership for ensuring that compliant regulatory strategies are developed in alignment with business objectives and implemented professionally within timeline  Devising tactics for delivery of high quality regulatory COPP for CFT (World’s top most companies) filing for countries Help maintain an information network for monitoring domestic regulatory developments, followed by appropriate preventive communication and training Through the regulatory team, provide strategic direction and advice to project and company management regarding regulatory pathways and timelines for new and changed products/processes Liaising with external / internal customers to meet regulatory requirements with respect to drug formulations development, analysis and manufacturing Organize and plan regulatory activities in line with company’s business priorities, including budget management  Administering departmental planning and coordinating activities within the dept. as well as interface with other departments Reviewing R&D data, analytical data and other DMF related requirements with feedback capability to comply with the requirements during product development and registration Keeping knowledge up to date with regard to guidelines and regulatory Monitoring and ensuring appropriate ongoing company-wide regulatory compliance with applicable standards  Reviewing and assisting in the development of Company Quality Manual and Standards

Executing work as a analyst, in PoDER Process division. Neutralization of polyol after alkoxylation step with in specification is a tricky task.Once immediate after neutralization product will flow directly to the foaming. High temperature process with handling of ATS(acute toxic substances) and should know pressure and temperature behavior concept is important in this process. As we know safety is important , till date executed more than 50+ experiments with "Zero" accidents

Did work in AOTECH INDIA PVT LTD technical centre Banglore as a R&D Development Engineer in Electroless Nickel Department from March 30th 2015.2. Worked on the different base flow projects and promoting projects from lab scale to Alpha,Beta, customer scale trials.3 Know the concepts as well as operating knowledge of X-Ray Fluorescence, Vickers Hardness Tester, having good operating experience with qualification of project concepts and analysis methods.4. Successfully Completed Business Meet of 20 Days on Electroless Nickel, Analytical Lab Analysis, Material Science Lab Management at Berlin Germany from 18th October To 7th November 2015 5. Till date have a Industrial experience of 4+ years with ZERO incidents and accidents6. Secured Safety Award of the year 2015-2016

Worked as a Chemical Engineer at The Energy and Resources Institute(TERI), In the R&D Department of Center for Earth Science.2. Worked on projects, both in-house and outside lab. Provided field work s support for several base flow projects as well as research assistance.3. Assisted as environmental lab research studies including data management, g groundwater monitoring sampling, and analytical report writing.4. Had the experience of managing the instrumentation lab, and smoothly handling ionChromatography as well as Carbon Analyzer for water sample analysis and Carbon content analysis respectively.