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# Sr. MES Engineer

- **Company:** TechDigital Corporation
- **Location:** Greenville, NC, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Application Programming Interfaces (APIs), Computing Platforms, Unit Testing, Databases, Software Debugging, File Transfer Protocol (FTP) SSL Extension, Supervisory Control and Data Acquisition (SCADA), SAP (Applications), Software Deployment, Software Engineering, Systems Integration, Web Services, Sql Optimization, Restful APIs
- **Published:** October 16, 2026
- **Apply:** https://www.careerbuilder.com/job-details/sr-mes-engineer-greenville-nc--563805e4-752b-4885-9f8f-5adaccd1916b

## About the Role

Notes from HM: We have some flexibility with MES - FTPS skill set/ FactoryTalk PharmaSuite experience preferred; however, candidates with any MES experience in Life Sciences environments will be considered, * Platform Expertise: Hands-on development experience with Rockwell FactoryTalk PharmaSuite (FTPS).

 * Database & APIs: Advanced SQL, database management, and RESTful API or webservices development.
 * Life Sciences Domain: Deep working knowledge of Good Manufacturing Practices (GMP) and Software Development Life Cycle (SDLC) methodologies.

## Description

Notes from HM: We have some flexibility with MES - FTPS skill set/ FactoryTalk PharmaSuite experience preferred; however, candidates with any MES experience in Life Sciences environments will be considered * System Design & Configuration: Develop, deploy, and maintain Rockwell FactoryTalk PharmaSuite (FTPS) and FTPC MES applications. * EBR Authoring: Design, configure, and validate Electronic Batch Records (EBR) to enforce manufacturing workflows. * Integrations: Integrate MES solutions with ERP systems (e.g., SAP) and plant-floor control equipment/SCADA systems. * Troubleshooting: Debug system defects, resolve data gaps, and perform unit testing before production deployments. * Compliance: Ensure all system architectures adhere to 21 CFR Part 11, GAMP, and cGMP regulatory standards within validated environments. Technical Requirements * Platform Expertise: Hands-on development experience with Rockwell FactoryTalk PharmaSuite (FTPS). * Database & APIs: Advanced SQL, database management, and RESTful API or webservices development. * Life Sciences Domain: Deep working knowledge of Good Manufacturing Practices (GMP) and Software Development Life Cycle (SDLC) methodologies.
Notes from HM: We have some flexibility with MES - FTPS skill set/ FactoryTalk PharmaSuite experience preferred; however, candidates with any MES experience in Life Sciences environments will be considered * System Design & Configuration: Develop, deploy, and maintain Rockwell FactoryTalk PharmaSuite (FTPS) and FTPC MES applications. * EBR Authoring: Design, configure, and validate Electronic Batch Records (EBR) to enforce manufacturing workflows. * Integrations: Integrate MES solutions with ERP systems (e.g., SAP) and plant-floor control equipment/SCADA systems. * Troubleshooting: Debug system defects, resolve data gaps, and perform unit testing before production deployments. * Compliance: Ensure all system architectures adhere to 21 CFR Part 11, GAMP, and cGMP regulatory standards within validated environments. Technical Requirements * Platform Expertise: Hands-on development experience with Rockwell FactoryTalk PharmaSuite (FTPS). * Database & APIs: Advanced SQL, database management, and RESTful API or webservices development. * Life Sciences Domain: Deep working knowledge of Good Manufacturing Practices (GMP) and Software Development Life Cycle (SDLC) methodologies.