Certificate Completed December 2014 (Regulatory Affairs: Pharmaceuticals)
2014-2014
California Polytechnic State University-San Luis Obispo
BS (Microbiology)
1985-1990
Nancy Lewis Skills
21 CFR Part 11
Biopharmaceuticals
Biotechnology
CAPA
CMC Regulatory Affairs
Cell Culture
Change Control
Chromatography
FDA
Fermentation
GMP
Life Sciences
Lifesciences
Pharmaceutical Industry
Project Management
Protein Purification
Quality Assurance
Quality System
Regulatory Affairs
Regulatory Requirements
Regulatory Submissions
SOP
Standard Operating Procedure (SOP)
Technology Transfer
U.S. Food and Drug Administration (FDA)
Validation
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 21 CFR Part 11, Biopharmaceuticals, Biotechnology, CAPA, CMC Regulatory Affairs and more. Nancy Lewis has 3 emails and 2 mobile phone numbers on RocketReach.
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