Stevens Pharmaceutical Research Center
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Stevens Pharmaceutical Research Center Employees
Employee
Years
Job
Industry
Sanjay Thapa Sanjay Thapa's Stevens Pharmaceutical Research Center Experience January 2013 - December 2013
Job Cleaning Validation Engineer
Industry Pharmaceuticals
Experience
JLL April 2015 - Present
Merck September 2014 - April 2015
Janssen, Pharmaceutical Companies of Johnson and Johnson January 2014 - July 2014
Stevens Pharmaceutical Research Center January 2013 - December 2013
SR Drug Laboratories Pvt. Ltd September 2007 - December 2009
Lomus Pharmaceuticals June 2007 - September 2007
Skills
GMP, Validation, CAPA, Sop, Pharmaceutics, Minitab, Design of Experiments, Change Control, Root Cause Analysis, Formulation, Microsoft Office, PowerPoint, Formulation and Process..., Windows, Design of Experiment..., Gage R & R, Aseptic Technique, TrackWise, LIMS, SOP, Cleaning Validation, Quality Assurance, Regulatory Affairs, Pharmaceutical Industry, FDA
Education
Stevens Institute of Technology 2012 — 2013
Master of Science (MS), Pharmaceutical Manufacturing Engineering (PME), 3.867
Kathmandu University 2003 — 2007
Undergraduate, Bachelor in Pharmacy (B.Pharm)
JLL April 2015 - Present
Merck September 2014 - April 2015
Janssen, Pharmaceutical Companies of Johnson and Johnson January 2014 - July 2014
Stevens Pharmaceutical Research Center January 2013 - December 2013
SR Drug Laboratories Pvt. Ltd September 2007 - December 2009
Lomus Pharmaceuticals June 2007 - September 2007
Skills
GMP, Validation, CAPA, Sop, Pharmaceutics, Minitab, Design of Experiments, Change Control, Root Cause Analysis, Formulation, Microsoft Office, PowerPoint, Formulation and Process..., Windows, Design of Experiment..., Gage R & R, Aseptic Technique, TrackWise, LIMS, SOP, Cleaning Validation, Quality Assurance, Regulatory Affairs, Pharmaceutical Industry, FDA
Education
Stevens Institute of Technology 2012 — 2013
Master of Science (MS), Pharmaceutical Manufacturing Engineering (PME), 3.867
Kathmandu University 2003 — 2007
Undergraduate, Bachelor in Pharmacy (B.Pharm)
Sonali Sharma Sonali Sharma's Stevens Pharmaceutical Research Center Experience September 2010 - June 2012
Job Manufacturing Process Engineer Pfizer
Industry Pharmaceuticals
Experience
Hospira October 2014 - Present
Johnson & Johnson January 2013 - September 2014
Johnson & Johnson - Janssen Supply Chain June 2012 - January 2013
Stevens Pharmaceutical Research Center September 2010 - June 2012
Stevens Institute of Technology August 2011 - December 2011
Stevens Pharmaceutical Research Center August 2011 - December 2011
Adman Formulations July 2008 - August 2010
Skills
TOC Analyzer, Tablet..., M-files, Track pro,..., Six sigma tools,..., SOP, Pharmaceuticals, Validation, Minitab, Root Cause Analysis, Quality Systems, Six Sigma, Cleaning Validation, cGMP, GLP, CAPA, GMP, HPLC, Quality Assurance, FMEA, Quality Management, Design of Experiments, Chromatography, 21 CFR Part 11, DOE, Process Development, Risk Analysis, Documentation, Pharmaceutical Industry, Sop, TOC, Quality System, Process Optimization, Process Simulation, Pharmaceutics, Cell Culture, Quality Control, V&V, Regulatory Affairs, Software Documentation, Medical Devices
Education
Stevens Institute of Technology 2010 — 2012
Master's in Pharmaceutical Manufacturing, Pharmaceuticals
Women In Pharma Club 2010 — 2012
President, Organizational Leadership
Oxford College of Pharmacy 2005 — 2009
B. Pharmacy, Pharmacy
Hospira October 2014 - Present
Johnson & Johnson January 2013 - September 2014
Johnson & Johnson - Janssen Supply Chain June 2012 - January 2013
Stevens Pharmaceutical Research Center September 2010 - June 2012
Stevens Institute of Technology August 2011 - December 2011
Stevens Pharmaceutical Research Center August 2011 - December 2011
Adman Formulations July 2008 - August 2010
Skills
TOC Analyzer, Tablet..., M-files, Track pro,..., Six sigma tools,..., SOP, Pharmaceuticals, Validation, Minitab, Root Cause Analysis, Quality Systems, Six Sigma, Cleaning Validation, cGMP, GLP, CAPA, GMP, HPLC, Quality Assurance, FMEA, Quality Management, Design of Experiments, Chromatography, 21 CFR Part 11, DOE, Process Development, Risk Analysis, Documentation, Pharmaceutical Industry, Sop, TOC, Quality System, Process Optimization, Process Simulation, Pharmaceutics, Cell Culture, Quality Control, V&V, Regulatory Affairs, Software Documentation, Medical Devices
Education
Stevens Institute of Technology 2010 — 2012
Master's in Pharmaceutical Manufacturing, Pharmaceuticals
Women In Pharma Club 2010 — 2012
President, Organizational Leadership
Oxford College of Pharmacy 2005 — 2009
B. Pharmacy, Pharmacy
Pranav Siddhapura Pranav Siddhapura's Stevens Pharmaceutical Research Center Experience August 2011 - April 2013
Job Validation Engineer at Abbott Lab.
Industry Pharmaceuticals
Experience
Abbott Laboratories April 2013 - Present
Stevens Pharmaceutical Research Center August 2011 - April 2013
Sunrise Remedies October 2009 - October 2010
Carewin Pharmaceuticals Guj Ltd April 2009 - September 2009
Skills
Statistical Process..., Minitab (Statistical..., M-Files (Electronic..., Internal Audit, Root Cause Analysis, CAPA, Quality System..., Total Organic Carbon..., HPLC, Cleaning Validation, Change Control
Education
Stevens Institute of Technology 2011 — 2012
Master of Science, Pharmaceutical Manufacturing, 4.0
Gujarat University 2006 — 2010
Bachelor of Pharmacy
Abbott Laboratories April 2013 - Present
Stevens Pharmaceutical Research Center August 2011 - April 2013
Sunrise Remedies October 2009 - October 2010
Carewin Pharmaceuticals Guj Ltd April 2009 - September 2009
Skills
Statistical Process..., Minitab (Statistical..., M-Files (Electronic..., Internal Audit, Root Cause Analysis, CAPA, Quality System..., Total Organic Carbon..., HPLC, Cleaning Validation, Change Control
Education
Stevens Institute of Technology 2011 — 2012
Master of Science, Pharmaceutical Manufacturing, 4.0
Gujarat University 2006 — 2010
Bachelor of Pharmacy
Evangelos Kustubardis Evangelos Kustubardis's Stevens Pharmaceutical Research Center Experience August 2012 - May 2013
Job Engineer at Azzur Group
Industry Biotechnology
Experience
Azzur Group June 2015 - Present
Zimmer October 2014 - June 2015
Hyde Engineering + Consulting November 2013 - August 2014
Stevens Pharmaceutical Research Center August 2012 - May 2013
Stevens Institute of Technology May 2010 - May 2011
Skills
Titrations, Spectrofluorometry, Polarimetry, Preparing Solutions, Gas Chromatography, Fourier Transform..., Atomic Absorption..., Microinjection of Cells, Agarose Gel..., PCR, HPLC, Matlab, Minitab, M-Files, Titration, Pharmaceutical Industry, Laboratory, Protein Chemistry, Antibodies, Cleaning Validation, Recruiters, FTIR, Quality Control, Formulation, GLP, Design of Experiments, UV/Vis, Chromatography, GMP, TOC, Sop, Gage R&R, FMEA, Process Capability, Risk Management, GAMP, Atomic Absorption, Validation, SOP, FDA
Education
Stevens Institute of Technology 2011 — 2013
Master of Science (M.S.), Pharmaceutical Manufacturing
Stevens Institute of Technology 2009 — 2013
Bachelor of Science (B.S.), Chemical Biology
Azzur Group June 2015 - Present
Zimmer October 2014 - June 2015
Hyde Engineering + Consulting November 2013 - August 2014
Stevens Pharmaceutical Research Center August 2012 - May 2013
Stevens Institute of Technology May 2010 - May 2011
Skills
Titrations, Spectrofluorometry, Polarimetry, Preparing Solutions, Gas Chromatography, Fourier Transform..., Atomic Absorption..., Microinjection of Cells, Agarose Gel..., PCR, HPLC, Matlab, Minitab, M-Files, Titration, Pharmaceutical Industry, Laboratory, Protein Chemistry, Antibodies, Cleaning Validation, Recruiters, FTIR, Quality Control, Formulation, GLP, Design of Experiments, UV/Vis, Chromatography, GMP, TOC, Sop, Gage R&R, FMEA, Process Capability, Risk Management, GAMP, Atomic Absorption, Validation, SOP, FDA
Education
Stevens Institute of Technology 2011 — 2013
Master of Science (M.S.), Pharmaceutical Manufacturing
Stevens Institute of Technology 2009 — 2013
Bachelor of Science (B.S.), Chemical Biology
Charulatha Papineni Charulatha Papineni's Stevens Pharmaceutical Research Center Experience August 2010 - Present
Job Quality Engineer at Medefil, Inc.
Industry Pharmaceuticals
Experience
Medefil, Inc. August 2012 - Present
Stevens Pharmaceutical Research Center August 2010 - Present
Stevens Pharmaceutical Research Center June 2011 - June 2012
Stevens Pharmaceutical Research center January 2012 - May 2012
NATCO Pharma ltd. January 2010 - April 2010
SMS Pharmaceuticals ltd. June 2009 - April 2010
Skills
Tablet punching..., TOC Analyzer, HPLC, M-Files, Minitab, Preparing SOP,..., Root Cause Analysis,..., Validation, Design of Experiments..., Process Development, Gantt Charts, Risk Analysis, FMECA, Documentation, 21 CFR Part 11, Bioprocessing-..., Media and culture..., TOC, Design of Experiments, CAPA
Education
Stevens Institute of Technology 2010 — 2012
Master of Science (MS), Pharmaceutical Manufacturing, 3.8
SRM College of Pharmacy 2005 — 2009
Bachelor of Pharmacy (B.Pharm.), Pharmacy, Pharmaceutical Sciences, and Administration, 8.7/10.0
Medefil, Inc. August 2012 - Present
Stevens Pharmaceutical Research Center August 2010 - Present
Stevens Pharmaceutical Research Center June 2011 - June 2012
Stevens Pharmaceutical Research center January 2012 - May 2012
NATCO Pharma ltd. January 2010 - April 2010
SMS Pharmaceuticals ltd. June 2009 - April 2010
Skills
Tablet punching..., TOC Analyzer, HPLC, M-Files, Minitab, Preparing SOP,..., Root Cause Analysis,..., Validation, Design of Experiments..., Process Development, Gantt Charts, Risk Analysis, FMECA, Documentation, 21 CFR Part 11, Bioprocessing-..., Media and culture..., TOC, Design of Experiments, CAPA
Education
Stevens Institute of Technology 2010 — 2012
Master of Science (MS), Pharmaceutical Manufacturing, 3.8
SRM College of Pharmacy 2005 — 2009
Bachelor of Pharmacy (B.Pharm.), Pharmacy, Pharmaceutical Sciences, and Administration, 8.7/10.0
Ankit Chovatia Ankit Chovatia's Stevens Pharmaceutical Research Center Experience August 2010 - June 2012
Job Validation Consultant at Regeneron Pharmaceuticals
Industry Pharmaceuticals
Experience
Regeneron Pharmaceuticals (Intracom LLC) April 2013 - Present
Genzyme (Intracom LLC) September 2012 - April 2013
Stevens Pharmaceutical Research Center August 2010 - June 2012
Stevens Institute of Technology June 2011 - May 2012
ISPE February 2011 - May 2012
Stevens Institute of Technology August 2010 - May 2012
Rise Remedies Ltd. May 2009 - August 2010
Bluecross laboratories Ltd September 2009 - March 2010
Skills
Minitab, Validation, GMP, Root Cause Analysis, Quality Assurance, Quality Control, TOC analyzer, Track-Pro, M-files, Qualification, CAPA, Installation..., Operational..., Performance..., Cleaning Validation, Calibration Protocol..., Risk Management tools..., Process Simulation and..., Design of Experiments, Quality by Design (QbD), Six Sigma and..., Fishbone, TOC, Chart, Commissioning, Quality Management, CIP, SIP, Calibration, Software Documentation, Biotechnology, Regulatory Affairs, Pharmaceutical Industry, HPLC, Sop, 21 CFR Part 11, SOP
Education
Stevens Institute of Technology 2010 — 2012
Master of Science in Pharmaceutical Manufacturing, Commissioning, Qualification and Validation, 3.7
M.S.University of Baroda 2005 — 2009
B.Pharm, Pharmacy, 3.63
Regeneron Pharmaceuticals (Intracom LLC) April 2013 - Present
Genzyme (Intracom LLC) September 2012 - April 2013
Stevens Pharmaceutical Research Center August 2010 - June 2012
Stevens Institute of Technology June 2011 - May 2012
ISPE February 2011 - May 2012
Stevens Institute of Technology August 2010 - May 2012
Rise Remedies Ltd. May 2009 - August 2010
Bluecross laboratories Ltd September 2009 - March 2010
Skills
Minitab, Validation, GMP, Root Cause Analysis, Quality Assurance, Quality Control, TOC analyzer, Track-Pro, M-files, Qualification, CAPA, Installation..., Operational..., Performance..., Cleaning Validation, Calibration Protocol..., Risk Management tools..., Process Simulation and..., Design of Experiments, Quality by Design (QbD), Six Sigma and..., Fishbone, TOC, Chart, Commissioning, Quality Management, CIP, SIP, Calibration, Software Documentation, Biotechnology, Regulatory Affairs, Pharmaceutical Industry, HPLC, Sop, 21 CFR Part 11, SOP
Education
Stevens Institute of Technology 2010 — 2012
Master of Science in Pharmaceutical Manufacturing, Commissioning, Qualification and Validation, 3.7
M.S.University of Baroda 2005 — 2009
B.Pharm, Pharmacy, 3.63
Dhaval Bhanushali Dhaval Bhanushali's Stevens Pharmaceutical Research Center Experience January 2013 - May 2014
Job Quality Engineer at Zimmer
Industry Pharmaceuticals
Experience
Hologic, Inc. August 2015 - Present
Zimmer October 2014 - Present
Stevens Pharmaceutical Research Center January 2013 - May 2014
Ronak Life Care Private ltd. September 2009 - August 2012
Skills
Microsoft Office, Microsoft Word, Microsoft Excel, Quality Assurance, GMP, Validation, Change Control, Regulatory Affairs, CAPA, Cleaning Validation, Process Validation, FMEA, Sop, SOP, FDA, V, Six Sigma, Pharmaceutical Industry
Education
Stevens Institute of Technology 2013 — 2014
Master of Science (MS), Pharmaceutical Manufacturing, 3.21
Rajiv Gandhi University of Health Science, Karnataka 2004 — 2009
Bachelor of Pharmacy, Pharmacy, 3.1
Hologic, Inc. August 2015 - Present
Zimmer October 2014 - Present
Stevens Pharmaceutical Research Center January 2013 - May 2014
Ronak Life Care Private ltd. September 2009 - August 2012
Skills
Microsoft Office, Microsoft Word, Microsoft Excel, Quality Assurance, GMP, Validation, Change Control, Regulatory Affairs, CAPA, Cleaning Validation, Process Validation, FMEA, Sop, SOP, FDA, V, Six Sigma, Pharmaceutical Industry
Education
Stevens Institute of Technology 2013 — 2014
Master of Science (MS), Pharmaceutical Manufacturing, 3.21
Rajiv Gandhi University of Health Science, Karnataka 2004 — 2009
Bachelor of Pharmacy, Pharmacy, 3.1
Rupen Shah Rupen Shah's Stevens Pharmaceutical Research Center Experience August 2010 - May 2012
Job validation engineer at Colgate Palmolive
Industry Pharmaceuticals
Experience
Colgate Palmolive November 2012 - Present
Stevens Pharmaceutical Research Center August 2010 - May 2012
Rucha Pharmaceutical April 2009 - June 2010
Skills
Validation, GMP, Sop, Microsoft Office, HPLC, Microsoft Excel, CAPA, Regulatory Affairs, PowerPoint, Quality Assurance, Microsoft Word, Minitab, 21 CFR Part 11, Biotechnology, Design of Experiments, Quality System, Research, Manufacturing, FMEA, Cleaning Validation, Root Cause Analysis, Protocol, Analysis, Quality Control, Data Analysis, Change Control, R&D, Teamwork, Lean Manufacturing, Auditing, FDA, Pharmaceutical Industry, GLP, Quality Management, Chromatography, Six Sigma, Pharmaceutics, Microbiology, Process Improvement, ISO, Calibration, SPC, Aseptic Technique, Team Leadership, Process Engineering, DMAIC
Education
Stevens Institute of Technology 2010 — 2012
MS, Pharmaceutical Manufacturing, 3.5/4.0
Rajiv Gandhi University of Health Sciences 2005 — 2009
Bachelor of Pharmacy (B.Pharm.), Manufacturing Engineering
Colgate Palmolive November 2012 - Present
Stevens Pharmaceutical Research Center August 2010 - May 2012
Rucha Pharmaceutical April 2009 - June 2010
Skills
Validation, GMP, Sop, Microsoft Office, HPLC, Microsoft Excel, CAPA, Regulatory Affairs, PowerPoint, Quality Assurance, Microsoft Word, Minitab, 21 CFR Part 11, Biotechnology, Design of Experiments, Quality System, Research, Manufacturing, FMEA, Cleaning Validation, Root Cause Analysis, Protocol, Analysis, Quality Control, Data Analysis, Change Control, R&D, Teamwork, Lean Manufacturing, Auditing, FDA, Pharmaceutical Industry, GLP, Quality Management, Chromatography, Six Sigma, Pharmaceutics, Microbiology, Process Improvement, ISO, Calibration, SPC, Aseptic Technique, Team Leadership, Process Engineering, DMAIC
Education
Stevens Institute of Technology 2010 — 2012
MS, Pharmaceutical Manufacturing, 3.5/4.0
Rajiv Gandhi University of Health Sciences 2005 — 2009
Bachelor of Pharmacy (B.Pharm.), Manufacturing Engineering
Dhruval Balar Dhruval Balar's Stevens Pharmaceutical Research Center Experience February 2010 - December 2011
Job Validation Specialist at QSP LLC (Sanofi Pasteur)
Industry Pharmaceuticals
Experience
QSP LLC (Sanofi Pasteur) January 2013 - Present
Aerotek (Mindray North America) March 2012 - November 2012
Stevens Institute of Technology August 2011 - February 2012
Stevens Pharmaceutical Research Center February 2010 - December 2011
Stevens Institute of Technology January 2011 - November 2011
Prayas Pharmaceuticals June 2008 - November 2009
Prayas Pharmaceuticals December 2007 - May 2008
Skills
Process Validation, Validation, Cleaning Validation, GMP, Quality Assurance, Pharmaceuticals, Manufacturing, cGMP, Regulatory Affairs, CAPA, Minitab, Root Cause Analysis, FMEA, Documentation, DOE, Document Management, V&V, Design of Experiments, ClearCase, ClearQuest, RequisitePro, Sop, Pharmaceutical Industry, Pharmaceutics, Software Documentation, Sterilization, Dry Heat Sterilization, Moist Heat Sterilization, Lethality, SIP, Fermentation, Kaye Validator, Lives Datalogger, FDA, Medical Devices, SOP
Education
Stevens Institute of Technology 2010 — 2011
Master, Pharmaceutical Manufacturing, Quality assurance, Regulations in Pharmaceuticals, Validation
South Gujarat University 2005 — 2009
Bachelor of Pharmacy, Pharmacy
QSP LLC (Sanofi Pasteur) January 2013 - Present
Aerotek (Mindray North America) March 2012 - November 2012
Stevens Institute of Technology August 2011 - February 2012
Stevens Pharmaceutical Research Center February 2010 - December 2011
Stevens Institute of Technology January 2011 - November 2011
Prayas Pharmaceuticals June 2008 - November 2009
Prayas Pharmaceuticals December 2007 - May 2008
Skills
Process Validation, Validation, Cleaning Validation, GMP, Quality Assurance, Pharmaceuticals, Manufacturing, cGMP, Regulatory Affairs, CAPA, Minitab, Root Cause Analysis, FMEA, Documentation, DOE, Document Management, V&V, Design of Experiments, ClearCase, ClearQuest, RequisitePro, Sop, Pharmaceutical Industry, Pharmaceutics, Software Documentation, Sterilization, Dry Heat Sterilization, Moist Heat Sterilization, Lethality, SIP, Fermentation, Kaye Validator, Lives Datalogger, FDA, Medical Devices, SOP
Education
Stevens Institute of Technology 2010 — 2011
Master, Pharmaceutical Manufacturing, Quality assurance, Regulations in Pharmaceuticals, Validation
South Gujarat University 2005 — 2009
Bachelor of Pharmacy, Pharmacy
Vinod Borsadiya Vinod Borsadiya's Stevens Pharmaceutical Research Center Experience October 2009 - June 2011
Job Class II & Class III Medical Devices, Sterile Operations, Packaging Operations
Industry Pharmaceuticals
Experience
Synthes January 2015 - Present
PharmaBio Compliance, Inc February 2011 - February 2015
McNeil Consumer Healthcare February 2014 - January 2015
Protocol Link, Inc./NYCOMED June 2011 - November 2013
Stevens Pharmaceutical Research Center October 2009 - June 2011
Stevens Institute of Technology August 2010 - April 2011
Beatle Healthcare November 2008 - June 2009
Skills
Method..., Process Validation &..., Equipment Qualification..., Technical Writing: SOP..., Operation,..., Use of..., Thorough knowledge of..., Use of..., Performing CAPA & Audit..., Cleaning Validation, Sop, V&V, Validation, CAPA, GMP, Quality Assurance, HPLC, Regulatory Affairs, Quality Control, 21 CFR Part 11, Six Sigma, Quality System, Pharmaceutical Industry, FDA, GLP, Change Control, Manufacturing, Minitab, FMEA, Design of Experiments, SOP
Education
Stevens Institute of Technology 2009 — 2011
Master of Science, Pharmaceutical Manufacturing Engineering
Rajiv Gandhi University of Health Sciences 2004 — 2008
Bachelor of Science (BS), Pharmacy
Synthes January 2015 - Present
PharmaBio Compliance, Inc February 2011 - February 2015
McNeil Consumer Healthcare February 2014 - January 2015
Protocol Link, Inc./NYCOMED June 2011 - November 2013
Stevens Pharmaceutical Research Center October 2009 - June 2011
Stevens Institute of Technology August 2010 - April 2011
Beatle Healthcare November 2008 - June 2009
Skills
Method..., Process Validation &..., Equipment Qualification..., Technical Writing: SOP..., Operation,..., Use of..., Thorough knowledge of..., Use of..., Performing CAPA & Audit..., Cleaning Validation, Sop, V&V, Validation, CAPA, GMP, Quality Assurance, HPLC, Regulatory Affairs, Quality Control, 21 CFR Part 11, Six Sigma, Quality System, Pharmaceutical Industry, FDA, GLP, Change Control, Manufacturing, Minitab, FMEA, Design of Experiments, SOP
Education
Stevens Institute of Technology 2009 — 2011
Master of Science, Pharmaceutical Manufacturing Engineering
Rajiv Gandhi University of Health Sciences 2004 — 2008
Bachelor of Science (BS), Pharmacy
Hiren Italia Hiren Italia's Stevens Pharmaceutical Research Center Experience August 2009 - December 2010
Job QC technologist II Caladrius Bioscience
Industry Pharmaceuticals
Experience
Caladrius Biosciences September 2012 - Present
PCT, a Caladrius company September 2012 - December 2012
ITC medical device company March 2011 - June 2012
Stevens Pharmaceutical research center August 2009 - December 2010
Sanofi-Aventis pharmaceutical January 2008 - December 2008
Skills
CAPA, Sop, Six Sigma, Cleaning Validation, Internal Audit, Quality Control, V&V, Quality Assurance, Stability Studies, identity test, Change Control, ISO, Laboratory, SOP, GLP
Education
Stevens Institute of Technology 2009 — 2010
Master Degree, Pharmaceutical manufacturing, 3.56
Stevens Institute of Technology 2009 — 2010
Master's degree, pharmaceutical manufacturing
N.E.T pharmacy college
N.E.T pharmacy college
N.E.T pharmacy college
Caladrius Biosciences September 2012 - Present
PCT, a Caladrius company September 2012 - December 2012
ITC medical device company March 2011 - June 2012
Stevens Pharmaceutical research center August 2009 - December 2010
Sanofi-Aventis pharmaceutical January 2008 - December 2008
Skills
CAPA, Sop, Six Sigma, Cleaning Validation, Internal Audit, Quality Control, V&V, Quality Assurance, Stability Studies, identity test, Change Control, ISO, Laboratory, SOP, GLP
Education
Stevens Institute of Technology 2009 — 2010
Master Degree, Pharmaceutical manufacturing, 3.56
Stevens Institute of Technology 2009 — 2010
Master's degree, pharmaceutical manufacturing
N.E.T pharmacy college
N.E.T pharmacy college
N.E.T pharmacy college
priya patel priya patel's Stevens Pharmaceutical Research Center Experience January 2013 - December 2013
Job QC Chemist at Novel Laboratories
Industry Pharmaceuticals
Experience
Novel Laboratories, Inc. July 2014 - Present
Stevens Institute of Technology December 2013 - Present
Stevens Pharmaceutical Research Center January 2013 - December 2013
Sidmak Laboratories (I) Pvt. Ltd. May 2010 - July 2011
Skills
Validation, Cleaning Validation, SOP development, GMP, CAPA, Change Control, Quality Assurance, Quality Control, Aseptic Processing, Regulatory Requirements, HPLC, Microsoft Excel, Microsoft Word, PowerPoint, Research, Teamwork, Photoshop, Social Media, Sop, GLP, Dissolution, UV/Vis, 21 CFR Part 11, Pharmaceutical Industry, FDA, Regulatory Affairs, Minitab, Biotechnology
Education
Stevens Institute of Technology 2013 — 2014
Master of Science (M.S.), Pharmaceutical Manufacturing
Novel Laboratories, Inc. July 2014 - Present
Stevens Institute of Technology December 2013 - Present
Stevens Pharmaceutical Research Center January 2013 - December 2013
Sidmak Laboratories (I) Pvt. Ltd. May 2010 - July 2011
Skills
Validation, Cleaning Validation, SOP development, GMP, CAPA, Change Control, Quality Assurance, Quality Control, Aseptic Processing, Regulatory Requirements, HPLC, Microsoft Excel, Microsoft Word, PowerPoint, Research, Teamwork, Photoshop, Social Media, Sop, GLP, Dissolution, UV/Vis, 21 CFR Part 11, Pharmaceutical Industry, FDA, Regulatory Affairs, Minitab, Biotechnology
Education
Stevens Institute of Technology 2013 — 2014
Master of Science (M.S.), Pharmaceutical Manufacturing
Ashish Patel Ashish Patel's Stevens Pharmaceutical Research Center Experience August 2010 - June 2012
Job Validation and Compliance Consultant
Industry Biotechnology
Experience
Sanofi Pasteur Biologics Co / Hyde EC February 2013 - Present
- Johnson & Johnson June 2012 - February 2013
Stevens Pharmaceutical Research Center August 2010 - June 2012
Stevens Institute of Technology January 2011 - May 2011
Relax Pharmaceuticals September 2008 - August 2010
The Oxford College of Pharmacy November 2006 - June 2008
Mahalaxmi Industrial Corporation June 2004 - July 2005
Skills
Validation, CAPA, V&V, GMP, Cleaning Validation, 21 CFR Part 11, HPLC, Change Control, Quality System, GLP, Computer System..., Minitab, Root Cause Analysis, Sop, FDA, SPC, Pharmaceutics, Design of Experiments, Data Analysis, Process Capability, Quality Control, Process Validation, Statistical Software, FMEA, Calibration, cGMP, Quality Auditing, Chromatography, Quality Systems, Cell Culture, Process Development, Six Sigma, Manufacturing, Risk Analysis, Validations, DOE, Quality Management, Biopharmaceuticals, Aseptic Technique, Quality by Design, Aseptic Processing, Process Optimization, Fermentation, Purification, GAMP, DMAIC, Continuous Improvement, Lean Manufacturing, Equipment Qualification, Trackwise
Education
Stevens Institute of Technology 2010 — 2012
Master of Science, Pharmaceutical Manufacturing Engineering, 3.9
Rajiv Gandhi University of Health Sciences 2005 — 2009
Bachelor in Pharmacy, Microbiology, Clinical Pharmacy and Toxicology, Pharmaceutical Technology and Microbiology., 4.0
Bharati Vidyapeeth
Sanofi Pasteur Biologics Co / Hyde EC February 2013 - Present
- Johnson & Johnson June 2012 - February 2013
Stevens Pharmaceutical Research Center August 2010 - June 2012
Stevens Institute of Technology January 2011 - May 2011
Relax Pharmaceuticals September 2008 - August 2010
The Oxford College of Pharmacy November 2006 - June 2008
Mahalaxmi Industrial Corporation June 2004 - July 2005
Skills
Validation, CAPA, V&V, GMP, Cleaning Validation, 21 CFR Part 11, HPLC, Change Control, Quality System, GLP, Computer System..., Minitab, Root Cause Analysis, Sop, FDA, SPC, Pharmaceutics, Design of Experiments, Data Analysis, Process Capability, Quality Control, Process Validation, Statistical Software, FMEA, Calibration, cGMP, Quality Auditing, Chromatography, Quality Systems, Cell Culture, Process Development, Six Sigma, Manufacturing, Risk Analysis, Validations, DOE, Quality Management, Biopharmaceuticals, Aseptic Technique, Quality by Design, Aseptic Processing, Process Optimization, Fermentation, Purification, GAMP, DMAIC, Continuous Improvement, Lean Manufacturing, Equipment Qualification, Trackwise
Education
Stevens Institute of Technology 2010 — 2012
Master of Science, Pharmaceutical Manufacturing Engineering, 3.9
Rajiv Gandhi University of Health Sciences 2005 — 2009
Bachelor in Pharmacy, Microbiology, Clinical Pharmacy and Toxicology, Pharmaceutical Technology and Microbiology., 4.0
Bharati Vidyapeeth
Pooja Talsania's Stevens Pharmaceutical Research Center Experience January 2011 - December 2011
Job Validation Engineer at West Ward Pharmaceuticals
Industry Pharmaceuticals
Experience
West-Ward Pharmaceuticals April 2012 - Present
Stevens Pharmaceutical Research Center January 2011 - December 2011
Sun Pharmaceutical Ltd June 2009 - December 2009
Skills
Document Management, Internal Communications, Process Validation, Cleaning Validation, Regulatory Affairs, Quality Assurance, Minitab, M-files (Electronic..., FMEA, FMECA, GMP, GLP, Root Cause Analysis, CAPA, Risk Assessment, Equipment Qualification, Process Capability Study, Statistical Process..., Validation, V&V, Quality Control, Chromatography
Education
Stevens Institute of Technology 2010 — 2011
Master of Science, Pharmaceutical Manufacturing and Engineering
Gujarat University 2005 — 2009
B.Pharmacy, Pharmaceutical Science
West-Ward Pharmaceuticals April 2012 - Present
Stevens Pharmaceutical Research Center January 2011 - December 2011
Sun Pharmaceutical Ltd June 2009 - December 2009
Skills
Document Management, Internal Communications, Process Validation, Cleaning Validation, Regulatory Affairs, Quality Assurance, Minitab, M-files (Electronic..., FMEA, FMECA, GMP, GLP, Root Cause Analysis, CAPA, Risk Assessment, Equipment Qualification, Process Capability Study, Statistical Process..., Validation, V&V, Quality Control, Chromatography
Education
Stevens Institute of Technology 2010 — 2011
Master of Science, Pharmaceutical Manufacturing and Engineering
Gujarat University 2005 — 2009
B.Pharmacy, Pharmaceutical Science
Dipesh Amin's Stevens Pharmaceutical Research Center Experience August 2012 - December 2013
Job Quality Assurance Analyst at AbbVie
Industry Pharmaceuticals
Experience
AbbVie June 2015 - Present
Target February 2009 - Present
Cambridge Major Laboratories, Inc. April 2014 - June 2015
AIDS Resource Center of Wisconsin December 2011 - April 2014
Stevens Pharmaceutical Research Center August 2012 - December 2013
Torrent Pharmaceuticals Ltd August 2007 - September 2008
Bioplus Lifesciences May 2006 - June 2007
Skills
GMP, Pharmaceutical Industry, SOP, Regulatory Affairs, Pharmaceutics, CAPA, Validation, Change Control, Quality Control, Quality Assurance, HPLC, Cleaning Validation, GLP, FDA
Education
Stevens Institute of Technology 2012 — 2013
Master of Science (M.S.), Pharmaceutical Manufacturing, 4.0
Rajiv Gandhi University of Health Sciences 2001 — 2006
Bachelor's degree, Pharmacy, 3.45
AbbVie June 2015 - Present
Target February 2009 - Present
Cambridge Major Laboratories, Inc. April 2014 - June 2015
AIDS Resource Center of Wisconsin December 2011 - April 2014
Stevens Pharmaceutical Research Center August 2012 - December 2013
Torrent Pharmaceuticals Ltd August 2007 - September 2008
Bioplus Lifesciences May 2006 - June 2007
Skills
GMP, Pharmaceutical Industry, SOP, Regulatory Affairs, Pharmaceutics, CAPA, Validation, Change Control, Quality Control, Quality Assurance, HPLC, Cleaning Validation, GLP, FDA
Education
Stevens Institute of Technology 2012 — 2013
Master of Science (M.S.), Pharmaceutical Manufacturing, 4.0
Rajiv Gandhi University of Health Sciences 2001 — 2006
Bachelor's degree, Pharmacy, 3.45
Vignya Shah's Stevens Pharmaceutical Research Center Experience December 2010 - September 2011
Job Regulatory Affairs Associate
Industry Pharmaceuticals
Experience
International Pharmaceutical Generics March 2014 - Present
Emcure Pharmaceuticals USA, Inc October 2011 - April 2012
Stevens Pharmaceutical Research Center December 2010 - September 2011
Stevens Institute of Technology August 2010 - December 2010
Unicure Remedies Pvt. Limited June 2009 - October 2009
Skills
Pharmaceutical Industry, Quality Assurance, Quality Control, Six Sigma, Cleaning Validation, HPLC, GLP, Sop, Laboratory, GMP, Validation, Regulatory Affairs, FDA, V&V, CAPA, Analytical Chemistry, Microbiology
Education
Stevens Institute of Technology 2009 — 2010
Masters, Pharmaceutical Manufacturing
Bharati Vidyapeeth University 2004 — 2008
Bachelor, Pharmacy
International Pharmaceutical Generics March 2014 - Present
Emcure Pharmaceuticals USA, Inc October 2011 - April 2012
Stevens Pharmaceutical Research Center December 2010 - September 2011
Stevens Institute of Technology August 2010 - December 2010
Unicure Remedies Pvt. Limited June 2009 - October 2009
Skills
Pharmaceutical Industry, Quality Assurance, Quality Control, Six Sigma, Cleaning Validation, HPLC, GLP, Sop, Laboratory, GMP, Validation, Regulatory Affairs, FDA, V&V, CAPA, Analytical Chemistry, Microbiology
Education
Stevens Institute of Technology 2009 — 2010
Masters, Pharmaceutical Manufacturing
Bharati Vidyapeeth University 2004 — 2008
Bachelor, Pharmacy
preksha shah's Stevens Pharmaceutical Research Center Experience January 2012 - December 2013
Job Contract Engineer at Merck
Industry Pharmaceuticals
Experience
Merck April 2014 - Present
Women In Pharma August 2013 - December 2013
Stevens Pharmaceutical Research Center January 2012 - December 2013
om laboratories October 2009 - July 2011
Skills
Validation, CAPA, SOP, Minitab, Quality System, Quality Assurance, V&V, 21 CFR Part 11, Root Cause Analysis, quality
Education
Stevens Institute of Technology 2012 — 2013
MS in Pharmaceutical Manufacturing, 3.5
Krupanidhi College Of Pharmacy 2005 — 2009
Bachelor of Pharmacy (B.Pharm.)
Merck April 2014 - Present
Women In Pharma August 2013 - December 2013
Stevens Pharmaceutical Research Center January 2012 - December 2013
om laboratories October 2009 - July 2011
Skills
Validation, CAPA, SOP, Minitab, Quality System, Quality Assurance, V&V, 21 CFR Part 11, Root Cause Analysis, quality
Education
Stevens Institute of Technology 2012 — 2013
MS in Pharmaceutical Manufacturing, 3.5
Krupanidhi College Of Pharmacy 2005 — 2009
Bachelor of Pharmacy (B.Pharm.)
Lan Huo's Stevens Pharmaceutical Research Center Experience September 2013 - December 2013
Job Validation Specialist, Pharmaceutical/Biopharma Industry
Industry Pharmaceuticals
Experience
Hemispherx Biopharma, Inc. June 2014 - Present
Stevens Institute of Technology September 2013 - May 2014
Stevens Pharmaceutical Research Center September 2013 - December 2013
Beaufour Ipsen Tianjin Pharmaceutical Co., Ltd. March 2012 - July 2012
Skills
GMP, HPLC, Six Sigma, Quality Assurance, Minitab, Root Cause Analysis, CAPA, FMEA, Gage R&R, Design of Experiment, cGMP, TOC, M- Files, Process Capability, Equipment Qualification, FDA, ICH, Lean Manufacturing, Change Control, SOP, Validation, Microsoft Office, Teamwork, Design of Experiments
Education
Stevens Institute of Technology 2012 — 2014
Master's degree, Pharmaceutical Manufacturing, 4.0
Tianjin University 2007 — 2011
Bachelor of Science (BS), Pharmaceutical Science and Technology, 3.6
Hemispherx Biopharma, Inc. June 2014 - Present
Stevens Institute of Technology September 2013 - May 2014
Stevens Pharmaceutical Research Center September 2013 - December 2013
Beaufour Ipsen Tianjin Pharmaceutical Co., Ltd. March 2012 - July 2012
Skills
GMP, HPLC, Six Sigma, Quality Assurance, Minitab, Root Cause Analysis, CAPA, FMEA, Gage R&R, Design of Experiment, cGMP, TOC, M- Files, Process Capability, Equipment Qualification, FDA, ICH, Lean Manufacturing, Change Control, SOP, Validation, Microsoft Office, Teamwork, Design of Experiments
Education
Stevens Institute of Technology 2012 — 2014
Master's degree, Pharmaceutical Manufacturing, 4.0
Tianjin University 2007 — 2011
Bachelor of Science (BS), Pharmaceutical Science and Technology, 3.6