Education
NEW JERSEY INSTITUTE OF TECHNOLOGY – BACHELORS OF SCIENCE SEPT 2007- DEC 2010
School of Engineering/Albert Dorman Honors College
Major: Biomedical Engineering with a concentration in Tissue Eng. /Biomaterials
Graduated Early in December 2010 with a 3.0 GPA
Related Coursework:
Biomedical Computing
Biotransport
Biomaterials Characterization Biomaterials & Biocompatibility
Static & Strength of Materials
Materials Science Industrial Engineering- Human Factors
Engineering Optics
Senior Project – Medtrainer- Built a system that uses a pump and synthetic tubing to simulate in-vivo flow in an atherosclerotic artery to simulate an endarterectomy specifically the carotid artery. Designed and tested pump and circulation system with a flowmeter and a pressure gauge to make quantifiable measurements pre and post practice surgical procedure to ensure proper surgical method. Created and tested experimental set-ups with an instron machine to characterize and assess functional performance of possible arterial stenosis material, synthetic tubing (artery), and synthetic invivo environment to match properties of the carotid artery and surrounding tissue. Gained experience in technical writing and GMP standards with proposals, progress reports, SOP’s, final reports, FDA research, and technical presentations to a large audience.
Skills Summary
INFORMATION TECHNOLOGY-Proficient in Microsoft Office (Excel, Word, PowerPoint) Adobe, Statistical Analysis Software (Matlab), Basic Computer Programming, Labview, Oracle, Visual Basic, AutoCAD ( introductory level)
LABORATORY TOOLS- Techniques of simple recrystallization, distillation, extraction, and chromatography; analysis of IR and GC spectra, oscilloscope, function generator, Instron machine (stress-strain, mechanical testing), microscopy, and gel electrophoresis, ECG, Signal processing
OTHER SKILLS- CPR and First Aid Certified Hindi (basic), Guajarati (conversational), Spanish (limited)
Experience
DENDREON- CELL PROCESSING ASSOCIATE 1 APRIL 2011- CURRENT
Working in Aseptic GMP manufacturing of clinical and commercial human blood therapeutics in a clean-room environment with biological safety cabinets in ISO 5/class 100 clean rooms.
Weigh, measure, and check raw materials to ensure batches manufactured contain proper ingredients and quantities
Maintain standard operating procedures (SOP’s), batch records, and other applicable documentation to comply with regulatory requirements and good manufacturing practices (GMP’s). As well as assisting the validation department in executing applicable protocols effecti...
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