CSV Specialist: GxP System Validation for Pharma

ECHO Consulting Group is seeking a CSV Specialist to plan, execute, and document computer system validation activities for GxP-regulated systems in a pharmaceutical manufacturing environment. You will ensure systems comply with FDA 21 CFR Part 11, GAMP 5, and data integrity throughout the lifecycle.

Responsibilities include developing validation deliverables, applying risk-based validation, and collaborating with IT, QA, Engineering, and end users to support audits and system improvements.