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Click here or scroll down to respond to this candidateCandidate's Name
PHONE NUMBER AVAILABLECurrent Location: Newark, NJ Street Address
Work Authorization: US CitizenAvailable to interview with prior noticeSummary of Experience:Fifteen years of Flavor and Fragrance Quality, Analytical, Evaluation, and Testing of Raw and Finished Flavor and Fragrance products.Used analytical techniques: UPLC, HPLC, GC, Wet Chemistry, spectroscopy, KF ACID/BASE titrations requiring software, Electronic Notebook, Empower.Experience working in the Pharmaceutical Industry as a Quality Assurance Laboratory Technician and Chemist.Gained valuable experience having worked for Givaudan Flavors as a Sr. Laboratory Technician for roughly eight of those years.Aseptic technics experienceRegulatory Manufacturing Environment experienceManufacturing Execution SystemsCore Competencies Include:Quality Control/Testing Flavor/Fragrance Raw Materials and Finished ProductsOperation/Calibration/Maintenance of Laboratory Equipment/Instrumentation relative to Flavor & Fragrance Industry/ Sensory Science Including: GC (Gas Chromatograph), HPLC, UPLC TLC, pH Meter, IR, UV Spec, Titration, Viscometer, Polarimeter, Refractometer, Karl Fisher, sensory/ odor evaluation Etc.Performing analysis and testing of fragrance samples, stability and sensoryRaw material extraction and extraction analysisCommunication, Organizational Skills.Education:Associates degree in chemistry, Essex County College, Newark, NJ 2017Technical Training Project Inc., Essex County College, Newark, NJ 2001Certificate in Chemical TechnologyGHS Mundemba-CAMEROONG.C.E. A-Level in Chemistry 89-91ROBERTET USA, Mt Olive, NJ 12/2022 Present.ChemistCarry out QC analysis on flavor raw materials and finished productsPerform all analysis using GC, GC-MS, Densitometer, Refractometer, UV/VIS, FTIR, Karl Fisher, Melting Point, OpenLab software for GC analysis.Report all results and logged them in LIMS. Sample Manager Laboratory Information Management System (LIMS)Planning, coordinating and executing the successful transition of the Sample Manager systemUpgrading in-scope Sample Manager instances from the existing version 11.1 to version 12.3. Carry investigations and corrective actions for out of specification results.Sensory/Olfactory/Color evaluations of both Fragrance and Flavor raw materials and Finished productsSensory/Food Science experience: Physiological and psychological bases for sensory evaluation and consumer testingMethods, theories and approaches used in sensory evaluation and consumer testingTools for managing sensory evaluation resources and activities and their interaction with other business unitsApplied business skills to advance sensory initiatives and develop successful new products.Report all results to QC managementSRIDES PHARMACEUTICAL, Chestnut Ridge, NY 2022Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, OpenLab. GC, UV/VIS, FTIR, dissolution apparatus, particle size analyzer, etc.Responsible for the timely execution of lab analysis and related documentation. Concurrent documentation of all the raw data, observations in the worksheets/templates/notebooks.Compile the analytical data and notify the results to supervisor.Adhere to safety, DEA procedures, and department SOPPerform calibration of analytical instruments.Keep the working place clean and tidy.Create and maintain clear and concise lab records and documentation (notebooks and computer-based)Perform routine maintenance of lab equipment as needed.BERJE INC, Carteret, NJChemist 02/2022-06/2022Carry QC analysis on flavor raw materials and finished product.Perform all analysis using GC, GCMS, Densitometer, Refractometer, UV/VIS, FTIR, Karl Fisher, Melting Point, OpenLab,/ Total Chrom for GC analysis.Report all results and logged them in LIMSCarry investigations and corrective actions for out of specification results.Sensory/Olfactory/Color evaluation of both Fragrance and Flavor raw materials and Finished productsReport all results to QC managementSOLGAR VITAMINS AND HERBS, LEONIA, NJ 08/2017-05/2021CHEMIST 11Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, Empower software. GC, UV/VIS, FTIR, dissolution apparatus, particle size analyzer, etc.Responsible for the timely execution of lab analysis and related documentation. Concurrent documentation of all the raw data, observations in the worksheets/templates/notebooks.Compile the analytical data and notify the results to supervisor.Adhere to safety, DEA procedures, and department SOPPerform calibration of analytical instruments.Keep the working place clean and tidy.Create and maintain clear and concise lab records and documentation (notebooks and computer-based)Perform routine maintenance of lab equipment as needed.Examine product deviation records and results, OOSsCarry out deviation investigationCAPA participationMerck Sharp & Dohme Corp., Rahway, NJ 11/2016-03/2017 Scientist 1 (Assistant)Provide analytical support to pilot plant operations for synthetic development and scale-up of clinical drug substance processes.Use analytical techniques: HPLC, GC, Wet Chemistry, spectroscopy, KF ACID/BASE titrations requiring software, Electronic Notebook, Empower.QC testing and release of finished and raw material. Review of test procedures, and batch record for compliance.Planet Pharma (Hoffman La-Roche Molecular System), Branchburg, NJ 01/2014-11/2016Laboratory TechnicianPreparing Batch record/SOP Buffer Solutions of varied PH and concentrations for the production and purification of Oligonucleotides.Assist in ordering and requesting of production suppliesPerform filter integrity test on filters used in various phases of the purification ofOligonucleotides. Adhere to all aseptic/sterile gowning procedures of the production floor and c GMPs.Set-up and operate BUFFER/SOLVENT delivery equipment/system as per SOP.Operate electric Pallet jack.Take and track inventories.Frutarom, North Bergen, NJ (contract) 02/2013-05/2013Laboratory TechnicianQuality control analysis of Flavor Raw and Finished products.Performed all tests using HPLC, PH Meter, LOD, VOC, FCC, Brooker field, Viscometer, etc.Micro Media Prep., Serial Dilution, and testing of incubated samples.Carried out raw material extractions and extract analysis.Work closely with the R&D Lab to evaluate experiments and new product formulation under supervision.Sensory/Olfactory/Color evaluation of both Fragrance and and Flavor raw materials and Finished productsGivaudan Flavors, East Hanover NJ. 02/2005-10/2012 Sr. Laboratory TechnicianBuffer solution, test solution prep.Quality Control testing of raw and finished flavor products.Adjustment of Out of Specification products and instructing compounders of required ingredients and amount to be added for the adjustment.Performed QC tests using GC, HPLC, IR, UV-Spec. PH Meter, Titration, Viscometer, Coulter Counter Particle Size Analyzer, Simple and Fractional Distilleries, VOC, Analytical balances, Karl Fisher, etc.Record all test results in SAP.Performed analyses using USP, FCC test methods.Calculates and records results, and often develops conclusions.Familiarity with SOPs, GMP, GLP, and stability and sensory tests when preferredPrepare and stage new product formulas in the R&D Lab for evaluationSensory/Olfactory/Color evaluation of both Fragrance and and Flavor raw materials and Finished productsGlaxo Smith Kline, NJ 08/03-04/04Laboratory TechnicianTested and released both intermediate and finished, Pharmaceutical Solid Dosage Products (TOMS).Performed and carried out analysis as per written analytical procedures.Performed other duties as required e.g. - sampling of intermediate products and supply to micro lab, preparation of micro buffer solutions, etc.Calibrated Laboratory Analytical Equipment.Entered data and test results into LIMS.Unilever Cosmetics, Budd Lake, NJ 11/02-07/03Quality Control Laboratory TechnicianWorked in a QC Lab in the QA/QC department.Evaluated samples for customers, raw materials, and finished products.Performed analysis and testing of fragrance samples.Adjusted and advised product batches to equal/meet standards.Tested raw materials, calibrated equipment, and prepared stock solutions as neededRecorded data on lab sheets and maintained accurate records and notebooks.Abided by cGMP/SOP and company standards.Reported results to QC management on a daily basis.Pfizer Inc., Parsippany, NJ 01/02-11/02ChemistTested raw materials, in-process and finished products, Solid dosage forms for release using a variety of instruments, wet and dry chemistry and USP methods.Demonstrated Familiarity with USP analytical procedures.Performed other duties as assigned e.g. - sampled raw materials and supplied to QO Lab.Assisted in ordering and maintaining laboratory supplies.Kept good records and generated reports according to cGMPs.Documented test procedures and entered results into LIMSUsed HPLC, GC, UV/VIS, IR, Karl Fischer, Viscometer,TOC Analyzer, Polarimeter, Refractometer, Specific Gravity Meter,Purification, Reflux, for testing / analyzing raw materials.Demonstrated knowledge of FDA guidelines on release testing ofpharmaceutical raw materials.Operate and maintain laboratory instruments/equipment. |
