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# Senior MES Engineer (Pharma)

- **Company:** Manpower
- **Location:** Durham, NC, United States
- **Experience:** Expert
- **Salary:** $124,800.0 - $145,600.0
- **Contract:** Permanent contract
- **Skills:** Cloud Computing, Dassault Systèmes DELMIA (Software), SAP (Applications), Plex, Information Technology, Syncade, Epicor ERP, Trackwise, Infor, Oracle Cloud Infrastructure, GXP
- **Published:** June 12, 2026
- **Apply:** https://www.juju.com/job/00000000g7ftey

## About the Role

+ 5+ years of experience supporting Manufacturing Execution Systems (MES) within pharmaceutical manufacturing industry.

 + Experience with **Recipe Authoring** for PFS (prefilled syringe) or similar Parenteral pharmaceuticals

 + Hands-on experience with **PMX or Plex or FactoryTalk PharmaSuite** in a pharmaceutical manufacturing environment (or other MES platforms such as: Siemens Opcenter, SAP Digital Manufacturing, NoMuda VisualFactory, Infor MES, Tulip Platform, iBase-t Solumina MES, Oracle Cloud Manufacturing, Dassault Systems DELMIA Apriso, DELMIAWORKS, HYDRA X, GE Vernova Proficy Smart Factory, L2L (Leading2Lean), Werum PAS-X MES Suite by Korber Pharma, iTAC.MOM.Suite by iTAC Software, ProManage, TrakSYS by Parsec, 42Q, AVEVA Manufacturing Execution System, Trackwise by Honeywell, Honeywell Forge Operations Management, PINpoint MES, Emerson Syncade,MasterControl Manufacturing Excellence, Aegis Software FactoryLogix, Epicor Advanced MES, Sepasoft MES, ABB Ability Manufacturing Operations Management Suite, Tempo Manufacturing Cloud, Aptean Process Manufacturing OEE, Accevo MES, DeltaV Manufacturing Execution System by Emerson, AspenONE MES, Nexplant MESplus, Cantier MES, or Vimachem Pharma MES)

 + Familiarity with GAMP 5, 21 CFR Part 11, and Annex 11

 + Working knowledge of GMP, CSV, and regulated systems

 + Bachelor's degree in Engineering, Computer Science, IT, or equivalent experience

## Description

We are looking for a talented **Senior MES Engineer (Pharma)** to support and enhance Manufacturing Execution Systems used in regulated pharmaceutical manufacturing environments., + Support and maintain **PMX or Plex or FactoryTalk PharmaSuite MES** systems in GMP manufacturing operations

 + Troubleshoot MES issues and act as a Tier 2 escalation point for production support

 + Assist with MES deployments, upgrades, and functional enhancements across manufacturing sites

 + Develop, configure, and support Electronic Batch Records (EBRs) and Master Batch Records (MBRs)

 + Partner with engineering, manufacturing, IT, and quality teams to deliver compliant MES solutions

 + Maintain validation documentation throughout the system lifecycle (CSV)

 + Contribute to MES standardization and site-to-site replication initiatives


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