Pharma Validation Specialist – CSV & GxP Expert
Listed on 2026-10-06
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Quality Assurance - QA/QC
IT QA Tester / Automation -
IT/Tech
IT QA Tester / Automation
Katalyst CRO is seeking a qualified professional for validation programs within the pharma/biotech/medical device space in New Jersey. The role emphasizes CSV, SDLC, GxP, and risk-based validation in FDA/global environments, with strong documentation skills and cross-functional collaboration.
The ideal candidate has 3+ years in CSV and 2+ years in SDLC, with exposure to QA methodologies, test plans, UAT, and traceability matrices. Remote collaboration is supported across projects.
The Pharma Validation Specialist – CSV & GxP Expert position in the IT & Technology field is open for applications.
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This posting is for the Pharma Validation Specialist – CSV & GxP Expert role at Katalyst CRO, based in Raritan, NJ, United States.
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