
Digital Engineer β POMS MES
Posted Aug 19

Posted Aug 19
This is a fully remote position, open to applicants in Illinois.
β’ Act as a techno-functional subject matter expert for POMS MES in pharmaceutical manufacturing.
β’ Facilitate collaboration between business, quality, validation, and IT departments.
β’ Configure, maintain, and deploy MES solutions.
β’ Ensure adherence to compliance standards and promote operational excellence.
β’ Diagnose and document MES solutions effectively.
β’ 8 to 12 years of experience in Pharma/Life Sciences.
β’ Over 5 years of experience with POMS MES.
β’ In-depth knowledge of MES and Electronic Batch Records (EBR).
β’ Familiarity with workflow processes.
β’ Understanding of Good Manufacturing Practices (GMP) and Good Automated Manufacturing Practice (GxP).
β’ Experience with Computer System Validation (CSV).
β’ Strong troubleshooting abilities.
β’ Experience in documentation and compliance practices.
β’ Knowledge of FDA 21 CFR Part 11 and GAMP 5 guidelines.
β’ Employees have the option to work remotely.
Mercor
RTX
Expel
Qualus
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