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Sr. Engineer, Automation Engineering, Controls Hardware - Lilly Medicine Foundry

Job in Lebanon, Boone County, Indiana, 46052, USA
Listing for: BioSpace
Full Time position
Listed on 2026-06-19
Job specializations:
  • Engineering
    Automation & Mechatronics Engineer, Electrical Engineering, Systems Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 64500 - 167200 USD Yearly USD 64500.00 167200.00 YEAR
Job Description & How to Apply Below

The Senior Engineer – Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry. The engineer will provide automation support for one or more operating areas across site and/or for capital projects, with primary focus on Instrumentation and Control Hardware. Process Automation is core to delivering the right first‑time facility start up and continued support of ongoing manufacturing operations into the future.

The Senior Engineer will collaborate and partner with cross‑functional peers to support successful delivery of robust control systems and instrumentation.

Key Objectives / Deliverables
  • Experience working with DeltaV Distributed Control System, Batch Process Automation.
  • Experience working with Rockwell Allen Bradley PLC’s, Factory Talk View.
  • Experience working with DeltaV control panels, DeltaV Remote I/O panels and Rockwell I/O’s.
  • Experience in performing automation engineering activities including design, development and commissioning of Process Automation projects using DeltaV DCS and/or Rockwell Allen Bradley PLC.
  • Experience with tuning and troubleshooting of control loops and Field Instruments.
  • Hands‑on experience in configuration and troubleshooting of Variable Frequency Drives (VFD’s).
  • Thorough understanding of P&’s and Instrument loop drawings.
  • Understanding of various process control communication protocols.
Operational Excellence
  • Site operation runtime support, enhance control system reliability and lifecycle management, in a GMP regulated environment.
  • Support capital project execution, commissioning and qualification.
  • Demonstrated ability to resolve complex technical challenges with instrument and control system hardware.
  • Work with Site Area leads and System Integrators.
  • Develop and review functional requirements, design specifications, and test specifications.
  • Demonstrated experience utilizing Master maintenance plans.
  • Familiarity with 21

    CFR Part 11, GMP processes.
  • Participate in design reviews and site system hardware reviews, attend equipment FATs.
  • Provide periodic status updates to Project Management.
  • Support electronic systems (such as plant historians) used to capture process automation related production data.
  • Maintain the validated state of the site control system hardware in line with Lilly quality standards, including development and execution of validation strategies and associated documentation.
  • Good planning and organizational skills, ability to prioritize tasks, and commitment to task completion and timelines.
Organizational Capability
  • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.
  • Engage with cross‑functional peers to strengthen technical capabilities and adopt best practices to enhance system reliability and business continuity.
Basic Requirements
  • Minimum B.S. in Engineering and experience in Automation Engineering, preferably in major pharmaceutical manufacturing.
  • 2+ years of experience in biopharma engineering, operations, or manufacturing.
  • Experience working in a highly automated Greenfield Pharmaceutical facility, using DeltaV DCS, Rockwell Allen Bradley PLC, BMS and Warehouse Monitoring from design through startup.
  • Possess a keen technical curiosity and have demonstrated strong problem‑solving skills with a desire for continuous improvement.
  • Good written and verbal communication skills for both technical and non‑technical audiences.
  • Knowledge of GMP, regulatory requirements, and computer system validation.
  • Qualified applicants must be authorized to work in the United States on a full‑time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1.

Lilly is dedicated to helping individuals with disabilities actively engage in the workforce. If you require accommodation to submit a resume, please complete the accommodation request form for further assistance.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $64,500 – $167,200. Full‑time employees are eligible for a comprehensive benefits program including a company‑sponsored 401(k), pension, vacation, medical, dental, vision, prescription drug benefits, flexible benefits, life insurance, and well‑being initiatives.

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