Sr. Director, Quality Assurance @ (June 2019 - September 2021)
Quality Consultant @ Consultant (January 2014 - May 2019)
Head, US R and D QA @ Galderma R&D, LLC (June 2016 - February 2018)
Sr. Director, Quality and Regulatory Affairs @ Lux Biosciences, Inc. (August 2011 - June 2013)
Director, Quality @ Lux Biosciences, Inc. (January 2011 - August 2011)
Associate Director, Quality @ Lux Biosciences, Inc. (January 2010 - December 2010)
Manager, Quality @ Lux Biosciences, Inc. (May 2008 - December 2009)
Sr. QA Auditor @ Cephalon (November 2005 - January 2008)
QA Specialist @ (February 2004 - November 2005)
Sr. QA Specialist @ Par Pharmaceuticals, Inc (November 2002 - March 2003)
QA Manager @ (January 1993 - January 2001)
Pedro Gittens Education
Charter Oak State College
Bachelor of Science - BS (Chemistry & Math)
Pedro Gittens Skills
21 CFR Part 11
Auditing
Biopharmaceuticals
Biotechnology
CAPA
CRO
CTMS
Change Management
Clinical Development
Clinical Trials
Computer System Validation
Drug Development
FDA
GCP
GMP
GxP
IND
Life Sciences
Lifesciences
Management
NDA
Pharmaceutical Industry
Quality Assurance
Regulatory Affairs
Regulatory Submissions
SOP
Standard Operating Procedure (SOP)
Technology Transfer
U.S. Food and Drug Administration (FDA)
Validation
Pedro Gittens Summary
Pedro Gittens, based in United States, is currently a Sr. Director, Quality Assurance at Surrozen. Pedro Gittens brings experience from previous roles at Alkahest, Inc., Consultant, Galderma R&D, LLC and Lux Biosciences, Inc.. Pedro Gittens holds a Bachelor of Science - BS in Chemistry & Math @ Charter Oak State College. With a robust skill set that includes 21 CFR Part 11, Auditing, Biopharmaceuticals, Biotechnology, CAPA and more. Pedro Gittens has 2 emails and 1 mobile phone numbers on RocketReach.
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