Automation Engineer, Biopharma: Data & Controls

BioSpace

Lebanon (IN)

On-site

USD 65,000 - 167,000

Full time

14 days+

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Benefits offered by this job

Company bonus
401(k) plan
Pension
Vacation benefits
Medical, dental, vision
Flexible benefits
Life insurance
Time off and leave

Job summary

Lilly is seeking an Engineer – Automation Engineering to support the Automation Engineering Department at Lilly Foundry in Lebanon, Indiana. The role focuses on providing automation support across operating areas and capital projects, with a data-centric approach to historian systems and process control.

The engineer will collaborate with cross-functional teams to implement systems, maintain GMP compliance, and expand the site’s automation capabilities through the project delivery and startup

Qualifications

  • Minimum B.S. in Engineering.
  • 5+ years working experience in Biopharma engineering, operations, or manufacturing.
  • Authorized to work in the United States on a full-time basis.

Responsibilities

  • Mentor process control team, including design, controls philosophy, implementation and commissioning.
  • Process control work implementation and coordination.
  • Develop and implement the Automation Engineering Project Plan.
  • Maintain Data Historian System health and respond to issues as they arise.
  • Design, configuration, and testing of the platform (OSI PI).
  • Automation support for capital projects including new product introductions.

Skills

Automation Engineering
OSI PI
DCS
SCADA
Validation
Root Cause Analysis
Cybersecurity
BMS/PLC/HMI integration

Education

B.S. in Engineering

Tools

DeltaV
Rockwell
PI Vision
Kneat
Valgenesis
ALM
LogMate
Win911

Job description

Lilly is seeking an Engineer – Automation Engineering to support the Automation Engineering Department at Lilly Foundry in Lebanon, Indiana. The role focuses on providing automation support across operating areas and capital projects, with a data-centric approach to historian systems and process control.

The engineer will collaborate with cross-functional teams to implement systems, maintain GMP compliance, and expand the site’s automation capabilities through the project delivery and startup

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