2024 -now Associate Director, Quality Engineering and Validation (QEV) @
2022 -2024 Sr. Manager II, Computer Systems Validation @
2021 -2022 Sr. Manager, Computer Systems Validation @
2019 -2021 Manager, CSV @
2018 -2019 Manager, CSV @
2016 -2018 Validation Supervisor @
2015 -2016 Sr. Validation Engineer, Computer Systems @
2013 -2015 Validation Engineer III (CSV) @
2012 -2013 Validation Engineer II (CSV) @
2009 -2012 Validation Engineer III (CSV) @
2007 -2008 IS Staff Analyst - Quality, Validation and Documentation @
2006 -2007 Validation Engineer II (CSV) @
2005 -2005 Validation Engineer @
2000 -2005 Validation Contractor @
1995 -2000 Project Manager @
Robert Ewing Skills
Computer System Validation
GMP
Process Validation
Data Validation
Change Control
Software Documentation
Regression Testing
Validation
Process Improvement
Quality Assurance
Engineering
V&V
Program Management
Document Management
Customer Service
U.S. Food And Drug Administration Fda
System Integration Testing
Business Process Improvement
Documentation
Standard Operating Procedure Sop
Database Design
Pharmaceutical Industry
CAPA
FDA
Sop
21 CFR Part 11
Biopharmaceuticals
Verification And Validation V&V
Corrective And Preventive Action Capa
Standard Operating Procedure
u.s. Food and Drug Administration
Verification and Validation
Corrective and Preventive Action
Robert Ewing Summary
Robert Ewing, based in Seattle, WA, US, is currently a Associate Director, Quality Engineering and Validation (QEV) at Bristol Myers Squibb. Robert Ewing brings experience from previous roles at Bristol Myers Squibb and Celgene. With a robust skill set that includes Computer System Validation, GMP, Process Validation, Data Validation, Change Control and more. Robert Ewing has 2 emails and 2 mobile phone numbers on RocketReach.
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