Director Of Quality @ (October 2021 - October 2025)
Sr. Manager Regulatory Affairs and Compliance @ (January 2021 - January 2022)
Supplier Quality Engineer @ (January 2019 - January 2021)
Quality Assurance Supervisor @ (October 2013 - January 2019)
Compliance Specialist @ (September 2011 - October 2013)
cGMP Compliance Coordinator @ (September 2010 - September 2011)
Quality Assurance Specialist @ (September 2008 - September 2010)
Robert Waldron Education
Northwestern University
M.S. (Quality Assurance & Regulatory Science)
2011-2015
BS (Management)
Robert Waldron Skills
FDA
Pharmaceutical Industry
GMP
CAPA
Regulatory Affairs
Change Control
Validation
21 CFR Part 11
Quality System
Technology Transfer
Cleaning Validation
GxP
Computer System Validation
Quality Auditing
Sop
Standard Operating Procedure (SOP)
Corrective and Preventive Action (CAPA)
Quality Assurance
Good Laboratory Practice (GLP)
Good Manufacturing Practice (GMP)
Standard Operating Procedure Sop
Good Laboratory Practice Glp
Good Manufacturing Practice Gmp
Corrective And Preventive Action Capa
Good Manufacturing Practice
Standard Operating Procedure
Corrective and Preventive Action
Good Laboratory Practice
Robert Waldron Summary
Robert Waldron, based in Evanston, IL, US, is currently a Sr. Director, Quality – Americas | Clinical Trials Division at Thermo Fisher Scientific. Robert Waldron brings experience from previous roles at Thermo Fisher Scientific, Flex and Wockhardt. Robert Waldron holds a 2011 - 2015 M.S. in Quality Assurance & Regulatory Science @ Northwestern University. With a robust skill set that includes FDA, Pharmaceutical Industry, GMP, CAPA, Regulatory Affairs and more. Robert Waldron has 2 emails and 2 mobile phone numbers on RocketReach.
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