MES SME — Pharma GMP & Digital Manufacturing
Listed on 2026-10-11
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Manufacturing / Production
Validation Engineer
Validation & Engineering Group in the United States seeks a Manufacturing Execution Systems (MES) Subject Matter Expert to support pharmaceutical manufacturing operations and digital initiatives. You will lead MES configuration, integration with PAS-X, DeltaV and SAP, and ensure compliant system performance across engineering, quality, IT/OT, and validation teams.
The role emphasizes lifecycle management, troubleshooting, and creating documentation for GMP-compliant MES solutions in a regulated
We invite applications for the MES SME — Pharma GMP & Digital Manufacturing position located in Wilson, NC, United States.
All applications are reviewed carefully by our team.
The position is based in Wilson, NC, United States.
This opportunity is part of our work in Management & Operations, IT & Technology.
The advertised compensation is 120..
We aim to respond to suitable candidates as soon as possible.
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