Digital Engineer – POMS MES

Posted Aug 19

This is a fully remote position, open to applicants in Illinois.

πŸ“‹ Description

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.


⛳️ Requirements

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.


🏝️ Benefits

β€’ Employees have the option to work remotely.

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