ABEY VARGHESE

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

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

adrmuz@r.postjobfree.com

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

​​​​​​​​​​​​​ Page 2

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

Contact this candidate