Engineer - Automation Engineering – Small Molecule API- Lilly Medicine Foundry

100 Eli Lilly and Company

Lebanon (IN)

On-site

USD 66,000 - 172,000

Full time

4 days ago
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Benefits offered by this job

401(k)
Pension
Vacation benefits
Medical, dental, vision

Job summary

Eli Lilly and Company is seeking an Engineer - Automation Engineering to join the Automation Engineering Department at the Lilly Medicine Foundry in Lebanon, Indiana. The role focuses on providing automation support across site operations and capital projects while ensuring GMP-compliant control systems and reliable performance.

The ideal candidate will mentor the process control team, lead design reviews, and drive project plans to start up new and existing manufacturing processes in a

Qualifications

  • Minimum B.S. in Engineering and experience in Automation Engineering, preferably in Small Molecule API manufacturing.
  • A minimum of 2+ years working experience in Biopharma engineering, operations, or manufacturing.
  • Authorized to work in the United States on a full-time basis. Lilly will not provide sponsorship for work authorisation or visas.

Responsibilities

  • Provide automation support for one or more operating areas across site and/or for capital projects.
  • 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.
  • Lead/ oversee DeltaV/DCS/SCADA design, coding, testing and FAT activities.
  • Maintain validated state of site control systems and support validation strategies and documentation.
  • Promote automation to improve productivity, operational efficiency and compliance.

Skills

Automation engineering
Biopharma experience
GMP knowledge
Leadership
Troubleshooting

Education

Bachelor of Science in Engineering

Tools

DeltaV
Rockwell
SCADA
DCS
MES

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work— but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first‑ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.

The 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. Process Automation is core to delivering a right first time facility start up and continued support of ongoing manufacturing operations into the future. The Engineer is also responsible for the productivity and mentorship of the employees with the purpose of ensuring that reliable and compliant control applications and systems are used in the manufacturing at Foundry. Additionally, the Senior Principal Engineer as a key technical expert with partners to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives. In the project delivery phase and startup phase of the project (startup expected 2025 to 202 8 ), automation engineering roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.

Key Objectives/Deliverables
  • Technical Leadership
  • 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.
Operational Excellence
  • Technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications.
  • Lead/ Participate in design reviews and DeltaV application software reviews, attend equipment and software FATs
  • Lead a team of automation engineers supporting commissioning
  • Provide periodic status updates to Project Management
  • Devising functional requirements and process control strategies for control systems in collaboration with Process Engineering
  • DCS and SCADA software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.)
  • Perform automation engineering activities including design, tuning and troubleshooting of control loops
  • Implement and support electronic systems (such as plant historians, applications and software integration) used to capture process automation related production data
  • Maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation
  • Automation support for capital projects including new product introductions
  • Promoting the use of automation to improve productivity, operational efficiency and compliance
  • Developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed
Organizational Capability
  • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products.
  • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines.
  • Possess a keen technical curiosity and has demonstrated strong problem‑solving skills and a desire for continuous improvement
  • Demonstrated ability to influence peers and business partners
  • Good written and verbal communication skills for both technical and non‑technical audiences
  • Knowledge of GMP, regulatory requirements, computer system validation
Basic Requirements
  • Minimum B.S. in Engineering and experience in Automation Engineering, preferably in Small Molecule API manufacturing.
  • A minimum of 2 + years working experience in Biopharma engineering, operations, or manufacturing.
  • 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.
Additional Preferences
  • Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, PLC and MES systems (DeltaV, Rockwell, Syncade, etc ).
  • Experience in facilitating and driving decision‑making at an organizational level.
Other Information

Initial location at Parkwood West, Indianapolis, Indiana. Permanent location at the new Lilly Medicine Foundry in Lebanon, Indiana.

#WeAreLilly Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).

  • eligible to participate in a company-sponsored 401(k)
  • pension
  • vacation benefits
  • eligibility for medical, dental, vision and prescription drug benefits
  • flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • life insurance and death benefits
  • certain time off and leave of absence benefits
  • well‑being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe! #WeAreLilly

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