GxP CSV Engineer — Validation Lead Gene Therapy
Listed on 2026-10-06
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Quality Assurance - QA/QC
Quality Engineering
Katalyst CRO is seeking a CSV Engineer to validate GxP computerized systems at client sites in the United States. The role leads validation activities for systems such as Veeva QMS, BMRAM, and analytical instruments, ensuring data integrity, quality, and inspection readiness.
Responsibilities include authoring validation plans and protocols, performing risk assessments, and managing change controls and CAPAs within Forge's quality system.
We would love to welcome a new GxP CSV Engineer — Validation Lead for Gene Therapy to our group in Seattle, WA, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the GxP CSV Engineer — Validation Lead for Gene Therapy role in the description above.
We appreciate your interest in this position.
Join Katalyst CRO and contribute to our ongoing work.
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