Divya Verlapally

Email: ad2zj9@r.postjobfree.com Cell: +1-215-***-**** Bensalem, PA,19020.

Professional Overview:

Seeking an opportunity to utilize my skills and abilities in the Industry that can offer professional growth while being resourceful, innovative and flexible.

Education:

Master of Sciences in Pharmacy [M.Pharm] Jun 2013 – May 2015

C.M.R College of Pharmacy,

Jawaharlal Nehru Technological University, Hyderabad, India.

Bachelor in Pharmaceutical Science [B.Pharm] April 2009 – May 2013

St. Mary’s College of Pharmacy,

Jawaharlal Nehru Technological University, Hyderabad, India.

Work Experience:

Pharma Benefit Analyst, Optum Global Solutions: June 2017 – Dec 2017

Resolution of Customer Queries and complaints based on healthcare service order.

Processing and delivery center with 100% quality, safety and efficiency.

Responding to inbound calls transferring the data to electronic sources.

Ensure high level of customer satisfaction without any delay in order delivery, processing good and order in taking process

Having Knowledge on COBRA health care insurance and processing the prescriptions of customer with COBRA Policies and Procedures.

Having hands on experience on order delivery process of Prescription for US based insurance policies.

Providing 100% quality to the work.

Research Associate, Excelra Knowledge Solutions: May 2016 – June 2017

Worked in Formulations department in which I have to map the forms in the preparation of pharmaceutical formulations like topical, parental formulations.

Have to research through the paper to find out the forms for the preparations and map them appropriately.

Research Associate, G.V.K Bioscience: Sept 2015 – May 2016

Worked on two projects the CAS (Chemical Abstract Services) project which was a project that mapped the reactions of transcript files and captured the data with the help of supporting PDF files. The CAS project documented on the reaction by doing research activities

Worked on the Formulation project which was used to develop a strategy that was based on in-depth studies of patents, scientific literature, and compendia information to capture data to produce a final medicinal product.

Worked on a team, handling functions such as allocating requests of others, assisting them in quality checks and finding root causes and analysis.

Maintained SLAs, AHT and have initiated and established smooth glow of projects by effectively managing resources.

Academic Experience:

Formulation and Evaluation of Aceclofenac Floating Tablets Project

The aim of this investigation was to design and evaluate gastro retentive floating tablets of acelofenac to increase the efficiency and stability of the drug in the stomach.

Aceclofenac is a newer derivative of the diclofenac group of NSAIDs that exhibits analgesic and anti-inflammatory activities. It has less gastro-intestinal complications. Aceclofenac is having rapid absorption and shorter half-life (3 to 4 hrs.) and hence necessitate for modified release formulation.

The purpose of study was to develop and optimize Gastric Floating Drug Delivery System (GFDDS) containing aceclofenac as a model drug by using various proportion of polymer such as HPMC. This was employed to enhance the bioavailability and therapeutic efficiency of the drug.

Optimization of formulation was done by studying effect of drug to polymer ratio on drug release. Five formulations were released. The tablet was evaluated for its hardness friability and other in-vitro evaluation tests. All parameters compiled with IP limits.

Industrial Training

Undergone industrial training at “NEULAND LABORATORIES LIMITED” from 25-12-2012 to 24-01-2013. During this training period I interacted with the department Preclinical and acquired relevant basic knowledge.

The Preclinical Study is to test a drug, a procedure, or another medical treatment in animals. The aim of preclinical study is to collect the data in support of the safety of the new treatment. Preclinical studies are required before clinical trials in humans can be started.

Achievements:

Received a certificate from a national conference on reforms & innovations which was given towards my pharmaceutical education and it’s the global standards.

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