CSV Engineer for GMP pharma validation and OT systems remediation in Visp.
Conduct risk-based validation assessments and remediation for operationally critical systems in a pharmaceutical manufacturing environment. You'll design validation strategies, execute testing on control systems (DeltaV, SCADA, PLC), manage deviations, and assemble compliant documentation. This role requires 8+ years of CSV experience in GMP pharma with hands-on OT/automation systems knowledge, deep familiarity with GAMP 5 and regulatory frameworks, and willingness to travel to the site two days monthly.
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Found at a specialist agency · listed 21 October 2026 · InsideJobs links you to the original posting.