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RONALD NEWMAN
949-378-6191
Newbaker21@aol.com
Experience
Irvine Pharmaceutical Services Irvine, CA Jan 2013 – April 2016
R&D Team Lead
 Supervising a team of 5 chemists
 Proficient with IC, GC, HPLC, and a variety of detectors
 Working with clients to resolve scientific and scheduling issues
 Reviewing work performed in the department
 Documentation of OOT/OOS incidents, including reports
 Update, write methods and reports
Par Pharmaceuticals Inc. Irvine, CA Nov 2011 – Jul 2012
R&D Scientist
 Provided formulation support for solid dose drugs
 Validated analytical test methods, Assay, Degradants and Dissolution
 Performed development and validation of cleaning validations
 Prepared validation protocols, reports
 Performed ongoing Stability Testing to support ANDA’s
NexGen Pharma Irvine, CA Jul 2010 – Nov 2011
R&D Chemist
 Development of HPLC methods, Assay and Degradants
 Performed HPLC calibrations, maintenance and OQ/PQ
 Developed/validated cleaning validations, prepared validation protocols, reports and SOP’s
TEVA Parenteral Medicines Irvine, CA Jun 2000 – Jun 2009
R&D Scientist (2007-2009)
 Reviewed and analyzed stability data and monitored stability data trends
 Conducted investigations and generate OOS and OOT reports
 Performed HPLC, GC, Particle Size, Dissolution, Osmolality and Hunter Color
 Reviewed and approved analytical data
 Introduced lean manufacturing concepts to improve lab efficiency
 Reduced turn-around times for analytical chemistry projects
QC Chemist (2000-2007)
 Worked under pressure to meet turn-around times for in-process samples and finished products
 Improved efficiency by properly maintaining and calibrating analytical instruments
 Designated trainer for the use of Agilent ChemStation software
 Saved resources by quickly and correctly troubleshooting HPLC instruments and methods
 Consistently surpassed department goal of 95% on time completion of analytical work
 Interim supervisor of QC stability group
 Trained new employees on company procedures and instruments
 Familiar with HPLC, GC, AA, UV/Vis, FTIR, Dissolution, Particle size and sedimentation
RONALD NEWMAN
949-378-6191
Newbaker21@aol.com
Allergan Irvine, CA Mar 1999 – Mar 2000
Staff Scientist – Preformulations Dept.
 Performed Compendial testing of raw materials using USP/EP/JP/BP
 Performed Titrations, Karl Fischer, Coulometer, UV/Vis, LOD, pH, IR and Extractions
Information Technology and Software Systems
 HP ChemStation
 Empower
 Nugenesis
 LIMS
 Master Control
 Word, Excel, PowerPoint
 Chromeleon Analytical Software
 Sotax, Agilent and Distek Dissolution
systems
Education
California State University, Long Beach
Long Beach, CA
B.S., Ecology and Environmental Studies – Cum Laude
Chemeketa Community College
Salem, OR
A.A., Liberal Studies

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Resume Ron Newman

  • 1. RONALD NEWMAN 949-378-6191 Newbaker21@aol.com Experience Irvine Pharmaceutical Services Irvine, CA Jan 2013 – April 2016 R&D Team Lead  Supervising a team of 5 chemists  Proficient with IC, GC, HPLC, and a variety of detectors  Working with clients to resolve scientific and scheduling issues  Reviewing work performed in the department  Documentation of OOT/OOS incidents, including reports  Update, write methods and reports Par Pharmaceuticals Inc. Irvine, CA Nov 2011 – Jul 2012 R&D Scientist  Provided formulation support for solid dose drugs  Validated analytical test methods, Assay, Degradants and Dissolution  Performed development and validation of cleaning validations  Prepared validation protocols, reports  Performed ongoing Stability Testing to support ANDA’s NexGen Pharma Irvine, CA Jul 2010 – Nov 2011 R&D Chemist  Development of HPLC methods, Assay and Degradants  Performed HPLC calibrations, maintenance and OQ/PQ  Developed/validated cleaning validations, prepared validation protocols, reports and SOP’s TEVA Parenteral Medicines Irvine, CA Jun 2000 – Jun 2009 R&D Scientist (2007-2009)  Reviewed and analyzed stability data and monitored stability data trends  Conducted investigations and generate OOS and OOT reports  Performed HPLC, GC, Particle Size, Dissolution, Osmolality and Hunter Color  Reviewed and approved analytical data  Introduced lean manufacturing concepts to improve lab efficiency  Reduced turn-around times for analytical chemistry projects QC Chemist (2000-2007)  Worked under pressure to meet turn-around times for in-process samples and finished products  Improved efficiency by properly maintaining and calibrating analytical instruments  Designated trainer for the use of Agilent ChemStation software  Saved resources by quickly and correctly troubleshooting HPLC instruments and methods  Consistently surpassed department goal of 95% on time completion of analytical work  Interim supervisor of QC stability group  Trained new employees on company procedures and instruments  Familiar with HPLC, GC, AA, UV/Vis, FTIR, Dissolution, Particle size and sedimentation
  • 2. RONALD NEWMAN 949-378-6191 Newbaker21@aol.com Allergan Irvine, CA Mar 1999 – Mar 2000 Staff Scientist – Preformulations Dept.  Performed Compendial testing of raw materials using USP/EP/JP/BP  Performed Titrations, Karl Fischer, Coulometer, UV/Vis, LOD, pH, IR and Extractions Information Technology and Software Systems  HP ChemStation  Empower  Nugenesis  LIMS  Master Control  Word, Excel, PowerPoint  Chromeleon Analytical Software  Sotax, Agilent and Distek Dissolution systems Education California State University, Long Beach Long Beach, CA B.S., Ecology and Environmental Studies – Cum Laude Chemeketa Community College Salem, OR A.A., Liberal Studies