Certificate Completed December 2014 (Regulatory Affairs: Pharmaceuticals)
2014-2014
Cal Poly San Luis Obispo
BS (Microbiology)
1985-1990
Nancy Lewis Skills
CMC Regulatory Affairs
Regulatory Submissions
Regulatory Affairs
Biotechnology
Project Management
Protein Purification
GMP
FDA
Quality Assurance
Change Control
CAPA
21 CFR Part 11
Cell Culture
Biopharmaceuticals
Chromatography
SOP
Lifesciences
Technology Transfer
Fermentation
Validation
Pharmaceutical Industry
Quality System
Regulatory Requirements
Life Sciences
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Microsoft Word
u.s. Food and Drug Administration Fda
Public Speaking
Standard Operating Procedure Sop
Continuous Improvement
Research
Standard Operating Procedure
u.s. Food and Drug Administration
Nancy Lewis Summary
Nancy Lewis, based in Thousand Oaks, CA, US, is currently a Regulatory Affairs CMC Manager at Atara Biotherapeutics, Inc.. Nancy Lewis brings experience from previous roles at Shire, Baxter International Inc., Jewelry Creations By Nancy and Amgen. Nancy Lewis holds a 2014 - 2014 Certificate Completed December 2014 in Regulatory Affairs: Pharmaceuticals @ RAPS: Regulatory Affairs Certificate: Pharmaceuticals. With a robust skill set that includes CMC Regulatory Affairs, Regulatory Submissions, Regulatory Affairs, Biotechnology, Project Management and more. Nancy Lewis has 3 emails and 2 mobile phone numbers on RocketReach.
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