San Francisco, California
•
Today
Provide QA oversight for computer system validation activities across Veeva Vault, LIMS, ERP, Clinical Systems, and other GxP-regulated applications.Review and approve validation lifecycle documents including Validation Plans, URS, FRS, Configuration Specifications, Risk Assessments, Test Plans, IQ/OQ/PQ protocols, UAT scripts, RTM, and Validation Summary Reports.Ensure validation deliverables are complete, accurate, traceable, and aligned with approved procedures, regulatory expectations, and b
Easy Apply
Contract
65 - 70













