Certificate (Clinical Research Conduct and Management)
2009-2010
University of California, Berkeley
B.S (Chemical Biology)
2001-2005
Denise Lee Skills
GMP
Column Chromatography
SOP
Purification
Validation
Technical Writing
cGMP
Aseptic Processing
Excel
Protein Purification
SDS-PAGE
PCR
PowerPoint
Biotechnology
Trackwise
Microsoft Excel
Chromatography
HPLC
Aseptic Technique
Downstream Processing
Cleaning Validation
Deviations
Filtration
UV/Vis
SOP development
cGMP manufacturing
Quality System
cGMP practices
Spectrophotometry
Root Cause Analysis
Electrophoresis
Pharmaceutical Industry
Analytical Chemistry
Gel Electrophoresis
Pharmaceutical Manufacturing
UV
Cell Culture
DNA
GxP
Chemistry
Biopharmaceuticals
CAPA
Standard Operating Procedure (SOP)
Data Validation
Clinical Research
QC
Sds Page
Manufacturing
Pharmaceutical
Standard Operating Procedure Sop
Research
Standard Operating Procedure
Denise Lee Summary
Denise Lee, based in California, United States, is currently a Associate Director External Quality Control at Sutro Biopharma, Inc.. Denise Lee brings experience from previous roles at Sutro Biopharma, Inc., Revance, Maverick Therapeutics and Portola Pharmaceuticals contracted by Precision Global Consulting. Denise Lee holds a 2017 - 2019 Master of Science - MS in Data Science @ University of the Pacific. With a robust skill set that includes GMP, Column Chromatography, SOP, Purification, Validation and more. Denise Lee has 3 emails and 2 mobile phone numbers on RocketReach.
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