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Manufacturing Execution Systems Specialist

Intellectt Inc
Greenville, NC Contractor
POSTED ON 8/5/2025 CLOSED ON 9/3/2025

What are the responsibilities and job description for the Manufacturing Execution Systems Specialist position at Intellectt Inc?

Hello,

One of my clients is currently seeking a MES Designer. If this role aligns with your experience or interests, I’d love to connect with you. Please share your updated resume with me at sushma@intellectt.com, or feel free to call me directly at (732) 838-4956 to discuss further.


Position Title: MES Designer

Location: Greenville, NC (On-site)


Job Overview:

We are seeking a skilled MES Designer to support manufacturing execution system (MES) activities, focusing on MBR (Master Batch Record) design, system integration, and validation. The ideal candidate will have hands-on experience with Rockwell MES, strong technical understanding of manufacturing environments, and a proven ability to support digital manufacturing solutions from design through implementation.


Key Responsibilities:

  • Design and develop Master Batch Records (MBRs) within the Rockwell MES platform.
  • Perform system design verification and validation activities in compliance with regulatory and quality standards.
  • Integrate MES with shop-floor equipment, machines, and automation systems.
  • Provide post-implementation support, including troubleshooting and resolving issues related to MES functionality or integration.
  • Collaborate with cross-functional teams including IT, Quality, and Manufacturing Engineering to ensure successful MES deployment and operation.
  • Ensure all system changes are documented according to change control processes.


Preferred Qualifications:

  • Bachelor’s degree in Engineering, Computer Science, or a related technical field.
  • Experience with Rockwell MES platforms (e.g., PharmaSuite, FactoryTalk ProductionCentre).
  • Hands-on experience with MBR design and configuration.
  • Strong understanding of equipment integration, automation systems, and data communication protocols (e.g., OPC, PLC).
  • Experience in regulated environments such as pharmaceutical or biotech manufacturing.
  • Familiarity with GMP, GAMP5, and CSV (Computer System Validation) practices.

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