Analytical Chemist Product Testing

ABEY VARGHESE

* **** *****, ******, ** *****

845-***-****, 200-4061

*******@*****.***

SUMMARY

TECHNICAL EXPERIENCE

Analytical Chemist with over 10 years experience in Research and Development in Generic Pharmaceutical company (cGMP) environment and Energy research firm – analyzing Solid dosage- Tablets, Capsules, beads, Ophthalmic solutions, Control drugs, Cytotoxic, Extended and Delayed release products.

●UV Visible Spectrophotometer, Shimadzu UV 160, Perkin Elmer

●Viscometer (Brookfield)

●Dissolution Apparatus- Varian, Distek, Rotating Bottle

●Nicolet FTIR Impact 400 D, Malvern Particle Size Analyzer

●HPLC Alliance system from Waters Empower software

●Gas Chromatography technique

PROFESSIONAL EXPERIENCE

CHARTWELL Pharmaceutical, 77 Brenner Dr. Congers, NY 10920 2015 -Now

Chemist

●Performing HPLC and UPLC for finished drug products, stability samples and QA release samples

●Working on chromatographic purity, assay, dissolutions profile, forced degradation studies

●Product testing on UV visible spectrometer, FTIR Spectrophotometers

●Working on Raw material Analysis

PAR Pharmaceutical, Inc, Spring Valley. NY (Corporate Brokers Agency) 2013-2014

Scientist

●Performed HPLC for finished drug products, stability samples and QA release samples

●Worked on chromatographic purity, assay, dissolutions profile, forced degradation studies

●Product testing on UV visible spectrometer, FTIR Spectrophotometers.

●Worked on Nasal Spray products

●Familiar with Laboratory Information System (LIMS)

Glatt Air Technique Inc. Pharmaceutical Division, 20 Spear Rd, Ramsey, NJ. 2011-2013

Research Chemist

●Performed HPLC for finished drug products, stability samples, process validation

and QA release samples

●Worked on impurity, assay, dissolutions profile, forced degradation studies

BIOREFERENCE LABORATORIES, INC., Elmwood Park, New Jersey 07407 2011- 2011

Technologist

●Sample preparation for GC/MS Analysis

●Derivatization of drug

●Analysis of specimen using GC/MS

ABEY VARGHESE

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BARR PHARMACEUTICALS (Teva), Pomona, NY 2006-2009

Research Chemist

A Generic Pharmaceutical Company working in a FDA Regulated GMP Environment.

●Performed in-vitro bio-indicative, rotating bottle, dose dumping, bio- dissolution and fast and fed simulated dissolution profiles for IR, DR and ER products.

●Developed and validated analytical procedures for products in the pipeline.

●Worked on impurity profile, assay, dissolutions, forced degradation studies.

●Analyzed Capsules, beads, Ophthalmic solutions, Control drugs, Cytotoxic, IR, ER and DR products under c-GMP compliance.

●Method transfer.

●Prepared Gx-pharma documentation such as test methods, method validation protocol and reports.

●Performed HPLC for finished drug products, stability samples, process validation and QA release samples.

EVIONYX, INC., Hawthorne, NY 1999-2005

Research Chemist

●Conducted synthesis and coating of polymer precursors for membrane Separator production.

●Processed and characterized oxygen reducing catalyst for porous Carbon electrode.

●Supervised DSC, TGA, Particle size analyzer, Rheometer, Porometer and FTIR.

●Improved porous electrode lifetime by optimizing physical and chemical Properties.

●Performed electrochemical testing, slurry formulation and QC testing with GC.

EDUCATION

Attended Masters in Industrial Pharmacy (36 credits), Long Island University, 2008-2010

Brookline, New York.

Master of Science in Chemistry, Safia College of Science, 1993-1995

Bhopal, India

Major in Organic Chemistry

Bachelor of Science, St. Albert’s College, Kochin, India 1990-1993

Major in Chemistry

ACTIVITY

Trained in Good Manufacturing Practices/Good Laboratory Practice

Member of eVionyx Company Safety Committee

Certification for Dissolution trouble shooting from EAS

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