Senior Automation Engineer, MES & GMP (Rockwell)

Pharmadog

Durham, Northern (NC, KY)

Hybrid

USD 140,000 - 185,000

Full time

2 days ago
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Job summary

Beam Therapeutics is seeking a Sr. Engineer II/III, Automation & MES to design, install, configure, maintain and validate GMP automation systems at the Durham/RTP site. You will lead Rockwell PharmaSuite MES efforts and partner with IT, QA, manufacturing, and facilities to scale cell therapy processes.

The role requires hands-on GMP MES work, strong leadership, and collaboration across cross-functional teams to support clinical and commercial manufacturing and long-term automation strategy.

Qualifications

  • Bachelor's degree in engineering or related technical field.
  • 6+ years MES/automation experience; leadership in MES or automation programs.
  • Hands-on GMP MES design, configuration, testing, and validation.
  • Experience with electronic batch records and master recipes.
  • Knowledge of validation and data integrity (GAMP 5, 21 CFR Part 11, EU Annex 11).
  • Biotech/pharma manufacturing environment experience.

Responsibilities

  • Lead design, implementation, and lifecycle management of Rockwell PharmaSuite MES.
  • Own MES change control end-to-end including IQ/OQ/PQ and validation.
  • Support MES deployment across suites, processes, and products.
  • Interface MES with SAP, LIMS, CMMS, PI, and related systems.
  • Mentor junior engineers and contract resources; ensure cross‑functional collaboration.
  • Support safety, quality, compliance, and readiness for inspections.

Skills

Automation/MES experience
Technical leadership
Regulatory compliance

Education

BS degree in Engineering or related technical discipline

Tools

Rockwell PharmaSuite
Emerson Syncade
Korber PAS-X
Tulip
Apprentice
SAP
LIMS
CMMS
PI
Ignition
DeltaV

Job description

Beam Therapeutics is seeking a Sr. Engineer II/III, Automation & MES to design, install, configure, maintain and validate GMP automation systems at the Durham/RTP site. You will lead Rockwell PharmaSuite MES efforts and partner with IT, QA, manufacturing, and facilities to scale cell therapy processes.

The role requires hands-on GMP MES work, strong leadership, and collaboration across cross-functional teams to support clinical and commercial manufacturing and long-term automation strategy.

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