RONALD NEWMAN 949-378-6191 [email protected] 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

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RONALD NEWMAN

949-378-6191

[email protected]

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