2019 -2025 Executive Director Cell Therapy Quality Systems and Compliance @
2018 -2019 Site Quality Head @
2016 -2018 Director, Quality Systems and Regulatory Compliance @
2015 -2016 Director, Compliance and Change Management @
2013 -2015 Director, QA @
2008 -2013 Sr. Compliance and QA Systems Specialist @
2006 -2008 Product Compliance Analyst @
2005 -2006 Quality Assurance Supervisor @
2004 -2005 Quality Systems Specialist @
2003 -2004 QC Lab Technician @
Heidi Davis Education
Arizona State University
Penn State University
Heidi Davis Skills
GMP
Quality Assurance
Pharmaceutical Industry
CAPA
Sop
Quality System
Quality Control
GxP
Validation
FDA
Change Control
GLP
Aseptic Processing
Cross-functional Team Leadership
Complaint Investigations
Deviation Management
21 CFR Part 11
U.S. Food and Drug Administration (FDA)
Standard Operating Procedure (SOP)
Good Manufacturing Practice (GMP)
Corrective and Preventive Action (CAPA)
Cell Therapy
Compliance
Project Management
Marketing
Cross Functional Team
Customer Service
Microsoft Word
Cross Functional Team Leadership
Change Management
Corrective And Preventive Action Capa
Good Manufacturing Practice Gmp
U.S. Food And Drug Administration Fda
Standard Operating Procedure Sop
Standard Operating Procedure
Corrective and Preventive Action
u.s. Food and Drug Administration
Good Manufacturing Practice
Heidi Davis Summary
Heidi Davis, based in Kirkland, WA, US, is currently a Executive Director, Corporate Quality QMS at Bristol Myers Squibb. Heidi Davis brings experience from previous roles at Bristol Myers Squibb, Novartis and AstraZeneca. Heidi Davis holds a Arizona State University. With a robust skill set that includes GMP, Quality Assurance, Pharmaceutical Industry, CAPA, Sop and more. Heidi Davis has 3 emails and 2 mobile phone numbers on RocketReach.
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