Sr. Manager, Document Control @ (December 2021 - May 2025)
Sr. Document Control Specialist, Quality Assurance @ (July 2019 - December 2021)
Sr. Associate, QADC @ (February 2016 - July 2019)
Sr. QA Associate @ (November 2015 - January 2016)
Quality Assurance Consultant, Quality Compliance and Systems @ (June 2013 - March 2015)
QA Specialist @ Affymax (February 2008 - April 2013)
Sr. QC Analyst @ (January 2005 - February 2007)
D'Andre Lopez Education
Capella University
Master Of Business Administration (Project Management)
2006-2008
University Of California - Santa Cruz 1994-2003
D'Andre Lopez Skills
FDA
GMP
Validation
Sop
Biotechnology
Change Control
Computer System Validation
GLP
Pharmaceutical Industry
21 CFR Part 11
Quality Assurance
CAPA
IND
Biopharmaceuticals
Quality Control
Quality Auditing
GCP
GxP
Aseptic Processing
HPLC
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
U.S. Food And Drug Administration Fda
Standard Operating Procedure Sop
Standard Operating Procedure
u.s. Food and Drug Administration
D'Andre Lopez Summary
D'Andre Lopez, based in United States, is currently a Quality Assurance Consultant at Smart Pharma Solutions, Inc.. D'Andre Lopez brings experience from previous roles at Telios Pharma, Inc., Revance Therapeutics, Inc., Intarcia Therapeutics, Inc. and Carbylan Therapeutics. D'Andre Lopez holds a 2006 - 2008 Master Of Business Administration in Project Management @ Capella University. With a robust skill set that includes FDA, GMP, Validation, Sop, Biotechnology and more. D'Andre Lopez has 2 emails and 1 mobile phone numbers on RocketReach.
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