MES Specialist

Intellectt Inc

Holly Springs (NC)

On-site

USD 41,328 - 68,880

Full time

14 days+
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Job summary

A leading technology firm in Holly Springs, North Carolina, is seeking an experienced MES Specialist to support a critical project within the GxP environment. The ideal candidate will have automation engineering experience and a strong understanding of cGMP regulations and DeltaV MES (Syncade) platforms. This contract role requires meticulous debugging and documentation skills.

Qualifications

  • Experience supporting an Emerson DeltaV MES (Syncade) project.
  • Understanding of cGMP regulations and FDA requirements.
  • Skills in debugging and troubleshooting workflows.

Responsibilities

  • Support critical Emerson DeltaV MES (Syncade) project.
  • Ensure compliance with cGMP regulations.
  • Document and debug manufacturing systems.

Skills

Automation engineering
cGMP environment experience
Debugging configuration items
Troubleshooting workflows
GMP documentation

Job description

Base pay range: $30.00/hr - $50.00/hr

Job Title

MES Specialist

Location

Holly Springs, North Carolina

Duration

6-12 Months contract

Work Type

Onsite

Description

We are seeking a highly skilled and experienced Automation Engineer to support a critical Emerson DeltaV MES (Syncade) project within our GxP environment. The ideal candidate will have a strong background in pharmaceutical or biotech manufacturing, a deep understanding of cGMP regulations, and hands‑on experience with the DeltaV and Syncade platforms. This role requires a meticulous approach to debugging, troubleshooting, and documentation to ensure the integrity and compliance of our manufacturing systems.

Required Skills
  • Previous experience as an automation engineer supporting an Emerson DeltaV MES (Syncade) project
  • Previous experience working in a cGMP environment or working with FDA regulations
  • Prior experience with debugging configuration items and behaviors within DeltaV (Syncade)
  • Previous experience troubleshooting workflows and identifying the point of failure (Tracing Activity)
  • Experience reviewing and reconciling engineering documentation, specifically during site technology or design transfers.
  • Prior experience reviewing and creating GMP documentation for a DeltaV MES project.
Seniority Level

Associate

Employment Type

Contract

Industries

HVAC and Refrigeration Equipment Manufacturing, Aviation and Aerospace Component Manufacturing, and Medical Equipment Manufacturing

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