Jun 2010 to 2000 Pharmaceutical QA / Compliance Consultant and InstructorValidant Scientific Staffing (Contractor) at Patheon Pharmaceuticals Cincinnati, OH Jun 2011 to Aug 2011 AuditorAerotek Scientific Staffing (Contractor) at Schering-Plough / Merck
Jun 2009 to May 2010 Aerotek Scientific Staffing (Contractor)QPSI LLC - Steritek Division
2008 to 2009 Manager, Quality AssuranceElite Laboratories / Pharmaceuticals
2006 to 2008 Manager / Group Leader / QA Associate IV, Quality Assurance and ComplianceGlatt Air Techniques Inc
2000 to 2006 Group Leader / Sr. QA Associate - Quality Assurance and ComplianceSmithKline Beecham
1992 to 2000 Analytical Chemist / Technician - Analytical Research and DevelopmentSmithKline Beecham - now Glaxo-SmithKline Parsippany, NJ 1995 to 1995 Analytical ChemitsSmithKline Beecham
1994 to 1994 Publication and Method Development "SimultaneousSmithKline Beecham
1993 to 1993 Analytical ChemistEthicon, Inc
1991 to 1992 ContractorART International, Inc
1989 to 1991 Project Manager / Analytical Lab Supervisor / QA Engineer / OSHA Coordina tor - R & DJ. L. Prescott Company
1981 to 1988 Facility Quality Control Laboratory Manager / Corporate Quality Assurance Supervisor
Education:
Thomas Edison State College Trenton, NJ Jan 1999 BA in - Chemistry ConcentrationMorris County College Township of Randolph, NJ Jan 1988 AS in ChemistryRutgers College, Rutgers University New Brunswick, NJ Pre - Med
Medicine Doctors
Dr. David H Stern, New York NY - MD (Doctor of Medicine)
Faculty Practice Associates 17 E 102Nd St, New York, NY 10029 (212)2416585 (Phone)
Mt Sinai Primary Care 17 E 102Nd St Suite D, New York, NY 10029 (212)2416585 (Phone)
Certifications:
Internal Medicine, 2009
Awards:
Healthgrades Honor Roll
Languages:
English
Education:
Medical School Perelman School of Medicine University of Pennsylvania Graduated: 1996 Medical School Hospital Of The University Of Pennsylvania Graduated: 1996
Dr. David T Stern, New York NY - MD (Doctor of Medicine)
Faculty Practice Associates 17 E 102Nd St, New York, NY 10029 (212)2416585 (Phone)
Mt Sinai Primary Care 17 E 102Nd St Suite D, New York, NY 10029 (212)2416585 (Phone)
Certifications:
Internal Medicine, 2002
Awards:
Healthgrades Honor Roll
Languages:
English
Education:
Medical School Vanderbilt University School Of Medicine Graduated: 1989 Medical School Tufts New England Mc Graduated: 1990 Medical School Tufts New England Mc Graduated: 1992 Medical School Palo Alto Va/Stanford Graduated: 1992
Dr. David A Stern, Bronx NY - MD (Doctor of Medicine)
Palm Beach Medical Group 4601 N Congress Ave, West Palm Beach, FL 33407 (561)8404600 (phone), (561)8404680 (fax)
Palm Beach Medical Group 500 University Blvd STE 106, Jupiter, FL 33458 (561)7479600 (phone), (561)8404680 (fax)
Education:
Medical School Philadelphia College of Osteopathic Medicine Graduated: 1979
Procedures:
Allergen Immunotherapy Destruction of Benign/Premalignant Skin Lesions Electrocardiogram (EKG or ECG) Pulmonary Function Tests Vaccine Administration
Conditions:
Abdominal Hernia Acne Anxiety Dissociative and Somatoform Disorders Atherosclerosis Atrial Fibrillation and Atrial Flutter
Languages:
English Spanish
Description:
Dr. Stern graduated from the Philadelphia College of Osteopathic Medicine in 1979. He works in West Palm Beach, FL and 1 other location and specializes in Internal Medicine. Dr. Stern is affiliated with John F Kennedy Medical Center North Campus and Jupiter Medical Center.
Medical School Kansas City University of Medicine and Biosciences College of Osteopathic Medicine Graduated: 2002
Procedures:
Electrocardiogram (EKG or ECG)
Conditions:
Intervertebral Disc Degeneration Spinal Stenosis
Languages:
English
Description:
Dr. Stern graduated from the Kansas City University of Medicine and Biosciences College of Osteopathic Medicine in 2002. He works in Omaha, NE and specializes in Anesthesiology. Dr. Stern is affiliated with CHI Health Bergan Mercy.
Us Patents
Method For Inhibiting Thrombosis In A Patient Whose Blood Is Subjected To Extracorporeal Circulation
This invention provides a method for inhibiting thrombosis in a patient whose blood is subjected to extracorporeal blood circulation which comprises contacting the extracorporeal circulating blood with a Factor IXa compound in an amount effective to inhibit thrombosis in the blood of a patient and under conditions such that the Factor IXa compound circulates in the patient. The Factor IXa compound may include an active site-blocked Factor IXa compound or Glu-Gly-Arg chloromethyl ketone-inactivated human factor IXa compound. This invention also provides that the effective amount may be from about 0. 1 g/ml plasma to about 250 g/ml plasma or from about 0. 5 g/ml plasma to about 25 g/ml plasma. The patient may be subjected to extracorporeal blood circulation during transplant surgery or cardiopulmonary bypass surgery. This invention further provides for a method for inhibiting thrombosis in a patient whose blood is subjected to extracorporeal blood circulation, which comprises contacting the extracorporeal circulating blood with an agent capable of inhibiting a step of the intrinsic pathway of coagulation in an amount effective to inhibit thrombosis in the blood of a patient and under conditions such that the Factor IXa compound circulates in the patient.
Jeffrey S. Beck - Burlington NJ Vinaya A. Kapoor - Kirkwood Voorhees NJ David L. Stern - Mount Laurel NJ John H. Thurtell - Glen Mills PA
Assignee:
Exxon Mobil Oil Corporation - Fairfax VA
International Classification:
C10G 3506
US Classification:
208 65, 208 63, 208 66, 208134, 208137, 208138
Abstract:
The patent application discloses an integrated process for reformate upgrading. Such a process enables production of a high value product slate, by incorporating the step of reforming along with reaction/diffusion with a zeolite.
Jeffrey S. Beck - Burlington NJ Carrie L. Kennedy - Turnersville NJ Wieslaw J. Roth - Sewell NJ David L. Stern - Mount Laurel NJ
Assignee:
ExxonMobil Oil Corporation - Fairfax VA
International Classification:
C07C 552
US Classification:
585475, 585481
Abstract:
A synthetic porous crystalline material has the structure of ZSM-5 and a composition involving the molar relationship: wherein X is a trivalent element; Y is a tetravalent element; and n is less than 25, and wherein the slope of the nitrogen sorption isotherm of the material at a partial pressure of nitrogen of 0. 4 to 0. 7 and a temperature 77Â K is greater than 30. The material has a mesoporous surface area (MSA) greater than 45 m /g and is useful as a catalyst in the liquid phase isomerization of xylene.
David Stern - Great Neck NY Shi Du Yan - New York NY Ann Marie Schmidt - Franklin Lakes NJ Ira Lamster - Wyckoff NJ
Assignee:
The Trustees of Columbia University in the City of New York - New York NY
International Classification:
A61K 3800
US Classification:
530324, 530300
Abstract:
The present method provides for an isolated peptide having an amino acid sequence corresponding to the amino acid sequence of a V-domain of a receptor for advanced glycation endproduct (RAGE). The present invention also provides for an isolated peptide having an amino acid sequence A-Q-N-I-T-A-R-I-G-E-P-L-V-L-K-C-K-G-A-P-K-K-P-P-Q-R-L-E-W-K (SEQ. ID No: 1). The present invention provides for a pharmaceutical composition comprising a therapeutically effect amount of an isolated peptide having an amino acid sequence corresponding to the amino acid sequence of a V-domain of RAGE. The present invention also provides for a method for inhibiting interaction of an amyloid- peptide with a receptor for advanced glycation end product which is on the surface of a cell, which comprises contacting the cell with the peptide or a functionally equivalent agent, wherein the peptide or agent is capable of inhibiting interaction of the amyloid- peptide with the receptor for advanced glycation end product, and the peptide or agent is present in an amount effective to inhibit interaction of the amyloid- peptide with the receptor for advanced glycation endproduct.
Transgenic Mice Over-Expressing Receptor For Advanced Glycation Endproduct (Rage) And Mutant App In Brain And Uses Thereof
David M. Stern - Great Neck NY Ann Marie Schmidt - Franklin Lakes NJ Shi Du Yan - New York NY
Assignee:
The Trustees of Columbia University in the City of New York - New York NY
International Classification:
G01N 3300
US Classification:
800 3, 800 12, 800 18
Abstract:
The invention provides for a non-human transgenic animal whose cells contain a recombinant DNA sequence comprising: (a) a nerve tissue specific promoter operatively linked to a DNA sequence which encodes human receptor for advanced glycation endproducts (RAGE), and (b) a nerve tissue specific promoter operatively linked to a DNA sequence encoding a mutant human amyloid precursor protein hAPP695, hAPP751 and hAPP770 bearing mutations linked to familial Alzheimers disease in humans, wherein said non-human transgenic animal exhibits at least one phenotype from the group consisting of: increased expression of M-CSF gene in cerebral cortex; increased expression of IL-6 gene in cerebral cortex; increased neuronal stress; increased neurotoxicity; neuron loss; increased level of activated form of caspase 3 in brain; and increased level of phosphorylated tau protein in brain.
Jeffrey S. Beck - Lawrenceville NJ Jane C. Cheng - Clarksburg NJ Sharon B. McCullen - Newtown PA David H. Olson - Pennington NJ David L. Stern - Lawrenceville NJ
Assignee:
ExxonMobil Oil Corporation - Fairfax VA
International Classification:
B01J 2906
US Classification:
502 71, 502 63, 502 64, 502 77, 502 85
Abstract:
There is provided a substantially binder-free catalytic molecular sieve which has been modified by being ex situ selectivated with a silicon compound. The ex situ selectivation involves exposing the molecular sieve to at least two silicon impregnation sequences, each sequence comprising an impregnation with a silicon compound followed by calcination. The catalyst may be used in a hydrocarbon conversion process, such as toluene disproportionation.
A process and system is disclosed for removing sulfur from tail-gas emitted from a Claus sulfur recovery process. First, the tail-gas is oxidized so as to convert sulfur therein to sulfur oxides. Oxidized tail-gas is directed into an absorber where a solid absorbent absorbs substantially all the sulfur oxides thereon. After allowing sufficient time for a desired amount of sulfur oxides to be absorbed, absorption is ceased. Next, the solid absorbent containing the absorbed sulfur oxides is contacted with a reducing gas so as to release an off gas containing hydrogen sulfide and sulfur dioxide. Upon releasing sulfur from the solid absorbent, the solid absorbent is regenerated and redirected into the absorber. Sulfur in the off gas emitted by regeneration is concentrated to an extent sufficient for use within a Claus sulfur recovery process for conversion to elemental sulfur. By combining this process with a Claus sulfur recovery process, sulfur dioxide emissions can be reduced to less than about two parts per million.
John Scott Buchanan - Lambertville NJ Xiaobing Feng - Houston TX Gary David Mohr - Houston TX David L. Stern - Annandale NJ
Assignee:
ExxonMobil Chemical Patents Inc. - Houston TX
International Classification:
C07C 527
US Classification:
585481, 585480, 585482, 585314
Abstract:
In a process for isomerizing a feed comprising ethylbenzene and a mixture of xylene isomers, the feed is first contacted under xylene isomerization conditions with a first catalyst composition to produce an intermediate product having a higher para-xylene concentration than the feed, and then the intermediate product is contacted under ethylbenzene isomerization conditions with a second catalyst composition. The second catalyst composition comprises a hydrogenation-dehydrogenation component and a molecular sieve having 10-membered ring pores and is effective to selectively isomerize at least part of the ethylbenzene in the intermediate product to para-xylene and thereby produce a further product having a para-xylene concentration greater than the equilibrium concentration of para-xylene at said ethylbenzene isomerization conditions.
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Googleplus
David Stern
Lived:
Bloomington, IN Bloomington, IL New York City Tempe, AZ Richmond, VA Champaign, IL Frreport, NY Stamford, CT New Haven, CT Providence, RI Alta, UT
Work:
Illinois State University - Associate Dean of Public Services (2011)
Education:
Indiana University - History & Philosophy of Science
David F. Stern has concentrated his practice in the area of workers’ compensation litigation since graduation from The University of Pittsburgh School of Law. Mr. Stern has been representing injured w...
Tagline:
The Unmistakable Choice in Workers' Compensation and Social Security Disability Law
David Stern
Work:
Slate Magazine - Senior Product Manager
Education:
London School of Economics, Cornell University
David Stern
Work:
Self-Employed (1995) USC - Sr. Mgr. of Operations/Hospitality (2009-2011)
Education:
Culinary Institute of America - Hospitality Management