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Principal - Engineer – Automation; Utility Systems

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Eli Lilly and Company
Full Time position
Listed on 2026-02-17
Job specializations:
  • Engineering
    Systems Engineer, Electrical Engineering, Automation Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Principal - Engineer – Automation (Utility Systems)

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life‑changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first.

We’re looking for people who are determined to make life better for people around the world.

Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Houston, TX. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the site technical team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Responsibilities:

The Principal – Engineer – (Automation – Utility Systems) is a mid‑level automation engineering position that will support the design and delivery of the automation platforms and associated system integration as part of Lilly’s manufacturing expansion. This role is intended to support one or more project work streams including central utility systems and process utility systems in the manufacturing and lab areas.

Key responsibilities include system design, hardware/software selection, delivery strategy, factory acceptance testing, and installation and testing. Lilly Houston is part of Lilly’s Drug Substance (Active Pharmaceutical Ingredient) network.

During the design and delivery (startup expected 2029 to 2030) of the project this role will be integrated into the corporate automation team GPACE (Global Process Automation & Control Engineering) and then transition fully to a site‑based process team position. During delivery, this role will collaborate with A&E firms, system integrators, corporate and site engineering peers, and Tech@Lilly (Lilly’s corporate IT team) to develop and manage software/hardware design, testing, startup, commissioning, and qualification.

Post‑project delivery, this role will support GMP manufacturing operations in the central engineering function supporting one or more process teams. This role will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing site through start‑up.

Key Deliverables:
  • Champion a strong safety culture, mentor and coach others, and utilize engineering and automation fundamental principles in design and problem solving.

  • Collaborate with Lilly Engineering, A&E firms, and system integrators to develop requirements and specifications that will be the foundation for software development, hardware design, and system architecture.

  • Manage one or more system integrators and partners with utility OEMs to fully deliver utility process equipment.

  • Collaborate with Tech@Lilly to deliver a fully integrated Automation solution that is scaled for the needs of business if applicable.

  • Participate in basic and detailed design that also includes staffing, statements of work, supplier management, and delivery strategies for automation systems.

  • Participate in developing computer system validation strategies.

  • Develop and build capabilities within the Houston site automation team.

  • Develop site procedures for automation platforms and associated administration activities.

  • Provide engineering support for Process Safety Management (PSM) and Process Hazard Reviews (PHRs).

  • Provide technical oversight during development of equipment and process system User Requirements and related Design Review/Qualification documentation to ensure equipment and systems are appropriate for intended purpose.

Basic Qualifications:
  • Bachelor’s degree in engineering or related applicable discipline required.

  • 3+ years of experience in GMP pharmaceutical utility systems automation including water, steam, and air generation and distribution is preferred. Related manufacturing experience will be…

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