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Paul Berry Location
California, United States
Paul Berry Work
2022 -now Vice President Quality Assurance @
2021 -2022 Vice President, Quality @
2020 -2021 Senior Director Quality @
2018 -2020 Director CMC QA @
2015 -2018 Research Scientist promoted to Sr Manager Analytical Outsourcing @
2014 -2015 QC Manager - Contract Labs @
2011 -2014 Senior Scientist - promoted to Principal Scientist - Head of Quality Control and Quality Assurance @
2010 -2011 Analytical Development Chemist @
2008 -2010 Senior Research Associate @
2006 -2007 Process Measurement Scientist @
2001 -2006 Associate Scientist, promoted to Assistant Scientist, promoted to Scientist, Extractables and Leachables @
1998 -2000 Materials Technologist @
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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