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Click here or scroll down to respond to this candidateCandidate's Name
3 Spur Drive, Nanuet, NY Street Address
PHONE NUMBER AVAILABLE, Street Address -4061EMAIL AVAILABLESUMMARYTECHNICAL EXPERIENCEAnalytical 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 ElmerViscometer (Brookfield)Dissolution Apparatus- Varian, Distek, Rotating BottleNicolet FTIR Impact 400 D, Malvern Particle Size AnalyzerHPLC Alliance system from Waters Empower softwareGas Chromatography techniquePROFESSIONAL EXPERIENCECHARTWELL Pharmaceutical, 77 Brenner Dr. Congers, NY 10920 2015 -NowChemistPerforming HPLC and UPLC for finished drug products, stability samples and QA release samplesWorking on chromatographic purity, assay, dissolutions profile, forced degradation studiesProduct testing on UV visible spectrometer, FTIR SpectrophotometersWorking on Raw material AnalysisPAR Pharmaceutical, Inc, Spring Valley. NY (Corporate Brokers Agency) 2013-2014ScientistPerformed HPLC for finished drug products, stability samples and QA release samplesWorked on chromatographic purity, assay, dissolutions profile, forced degradation studiesProduct testing on UV visible spectrometer, FTIR Spectrophotometers.Worked on Nasal Spray productsFamiliar with Laboratory Information System (LIMS)Glatt Air Technique Inc. Pharmaceutical Division, 20 Spear Rd, Ramsey, NJ. 2011-2013Research ChemistPerformed HPLC for finished drug products, stability samples, process validationand QA release samplesWorked on impurity, assay, dissolutions profile, forced degradation studiesBIOREFERENCE LABORATORIES, INC., Elmwood Park, New Jersey 07407 2011- 2011TechnologistSample preparation for GC/MS AnalysisDerivatization of drugAnalysis of specimen using GC/MSCandidate's Name
Page 2BARR PHARMACEUTICALS (Teva), Pomona, NY 2006-2009Research ChemistA 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 1999-2005Research ChemistConducted 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.EDUCATIONAttended Masters in Industrial Pharmacy (36 credits), Long Island University, 2008-2010Brookline, New York.Master of Science in Chemistry, Safia College of Science, 1993-1995Bhopal, IndiaMajor in Organic ChemistryBachelor of Science, St. Alberts College, Kochin, India 1990-1993Major in ChemistryACTIVITYTrained in Good Manufacturing Practices/Good Laboratory PracticeMember of eVionyx Company Safety CommitteeCertification for Dissolution trouble shooting from EAS |
