Senior Scientist - promoted to Principal Scientist - Head of Quality Control and Quality Assurance @ (June 2011 - June 2014)
Analytical Development Chemist @ (November 2010 - June 2011)
Senior Research Associate @ (February 2008 - November 2010)
Process Measurement Scientist @ (April 2006 - December 2007)
Associate Scientist, promoted to Assistant Scientist, promoted to Scientist, Extractables and Leachables @ (January 2001 - April 2006)
Materials Technologist @ (August 1998 - December 2000)
Paul Berry Education
Northeastern University
MS (Chemistry with Chemical Biology)
BSc (Chemistry)
University of Hertfordshire
HNC Chemistry (Chemistry)
Paul Berry Skills
GMP
Validation
Analytical Chemistry
FDA
HPLC
Technology Transfer
Pharmaceutical Industry
CAPA
GLP
Regulatory Submissions
Drug Development
Drug Discovery
LC-MS
Sop
Quality Control
Chromatography
Change Control
Chemistry
Gas Chromatography
Good Laboratory Practice (GLP)
Outsourcing
Mass Spectrometry
Vendor Management
Quality System
Quality Assurance
Auditing
Biotechnology
Biopharmaceuticals
Strategic Partnerships
Communication
Drug Delivery
FTIR
NIR spectroscopy
GC-FID
Chemstation
Empower
Trackwise
USP
Regulatory Filings
OOS
Deviations
Outsourcing Management
Data Integrity
Quality Systems Design
CRO
GxP
Leadership
GCP
Paul Berry Summary
Paul Berry, based in California, United States, is currently a Vice President Quality Assurance at BlueRock Therapeutics. Paul Berry brings experience from previous roles at Checkmate Pharmaceuticals and Gilead Sciences. Paul Berry holds a MS in Chemistry with Chemical Biology @ Northeastern University. With a robust skill set that includes GMP, Validation, Analytical Chemistry, FDA, HPLC and more. Paul Berry has 2 emails and 2 mobile phone numbers on RocketReach.
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