Automation Engineer — GMP Biotech Manufacturing

Socket.dev

Lebanon (IN)

On-site

USD 66,000 - 172,000

Full time

14 days+

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Benefits offered by this job

Annual bonus
401(k) plan
Comprehensive benefits

Job summary

Lilly’s Automation Engineering role supports the new Medicines Foundry, delivering automation solutions for a cutting-edge manufacturing center in Indiana. The engineer will work across site operations and capital projects to ensure robust control systems, validation, and lifecycle management while partnering with cross-functional teams for GMP compliance and continuous improvement.

The position entails startup involvement through 2025–2028, with responsibilities spanning design reviews,

Qualifications

  • BS in Engineering or related field with ≥2 years in automation engineering, operations, or manufacturing.
  • Authorized to work in the United States on a full-time basis.
  • Experience with DeltaV DCS, Rockwell PLCs, and FactoryTalk View.
  • GMP knowledge and regulatory/compliance experience.
  • Experience in design, development, commissioning and qualification of automated manufacturing sites.

Responsibilities

  • Provide automation support across operating areas and capital projects.
  • Support robust control systems and instrumentation to achieve first-time facility startup success.
  • Participate in design reviews and site control system reviews; attend/support FATs.
  • Tune and troubleshoot control loops and VFDs.
  • Maintain validated state of site control systems and document validation strategies.

Skills

Automation design
Troubleshooting
Cross-functional collaboration
Regulatory compliance
Documentation

Education

Bachelor of Science in Engineering or related field

Tools

DeltaV DCS
Rockwell PLCs
FactoryTalk View
MES systems
SCADA/DCS integration

Job description

Lilly’s Automation Engineering role supports the new Medicines Foundry, delivering automation solutions for a cutting-edge manufacturing center in Indiana. The engineer will work across site operations and capital projects to ensure robust control systems, validation, and lifecycle management while partnering with cross-functional teams for GMP compliance and continuous improvement.

The position entails startup involvement through 2025–2028, with responsibilities spanning design reviews,

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