QA Specialist and Document Control(Contract) @ Carbylan Therapeutics Inc. (formerly Carbylan BioSurgery Inc.) (June 2013 - August 2013)
CMC Documentation Specialist @ Medivation, Inc. San Francisco, CA. (August 2012 - May 2013)
Medical Regulatory Affairs Manager @ (February 2012 - July 2012)
Document Control Manager and Sr. Documentation Specialist @ Myriad Genetics ( formerly Crescendo Bioscience Inc.) (July 2011 - December 2011)
Sr. Documentation Specialist, RA and EH and S @ (December 2010 - April 2011)
QA Documentation Manager @ (April 2008 - May 2010)
RA and QA Documentation Manager @ (January 2006 - January 2008)
Documentation Manager @ BAS Medical, Inc (January 2005 - January 2006)
Sr QA Assoc Documentation Specialist and Training Program @ Gilead Sciences (formerly CV Therapeutics) (July 2001 - September 2005)
Doc. Control Specialist @ AESCULAPS (January 2000 - January 2001)
Sr. Assoc. Document Control @ Genelabs, Inc. (January 2000 - January 2001)
Sr. QA Document Control @ (January 1987 - January 1999)
Jenny Craytor Education
Notre Dame de Namur University, Belmont, CA
BS (Business Admin with Conc. Econ/Finance)
2002-2005
Notre Dame de Namur University
Bachelor of Science (Finance, General)
Jenny Craytor Skills
Onboarding
Troubleshooting
Training Material
Software Testing
Change Management
Test Scripts
Problem Solving
21 CFR Part 11
Sop
FDA
CAPA
Change Control
Quality System
GxP
GMP
Computer System Validation
Validation
Pharmaceutical Industry
Medical Devices
Regulatory Affairs
Biotechnology
V&V
Quality Assurance
Document Management
LIMS
ISO 13485
Clinical Trials
21 CFR Part 820
Document Control Expert
21 CFR
Software Documentation
Quality Control
GLP
Biopharmaceuticals
GCP
Clinical Development
Protocol
Regulatory Submissions
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Good Clinical Practice (GCP)
Corrective and Preventive Action (CAPA)
Microsoft Excel
u.s. Food and Drug Administration Fda
SQL
Computer System
Microsoft Office
Sales
Clinical Protocols
Standard Operating Procedure Sop
Clinical Operations
Corrective and Preventive Action Capa
Good Clinical Practice Gcp
Operations
Technical Documentation
u.s. Food and Drug Administration
Standard Operating Procedure
Good Clinical Practice
Corrective and Preventive Action
Jenny Craytor Summary
Jenny Craytor, based in California, United States, is currently a Sr. QA Specialist and Document Control at Zogenix, Inc.. Jenny Craytor brings experience from previous roles at Tenaya Therapeutics, Nuvation Bio, Takeda and TAKEDA PHARMACEUTICALS. Jenny Craytor holds a 2002 - 2005 BS in Business Admin with Conc. Econ/Finance @ Notre Dame de Namur University, Belmont, CA. With a robust skill set that includes Onboarding, Troubleshooting, Training Material, Software Testing, Change Management and more. Jenny Craytor has 1 emails and 1 mobile phone numbers on RocketReach.
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