Engineer - Automation Engineering Historian Admin and Data Architect - Lilly Medicine Foundry
Job
Eli Lilly and Company
Lebanon, IN (In Person)
$115,850 Salary, Full-Time
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Job Description
Engineer
- Automation Engineering
- Historian Admin and Data Architect
- Lilly Medicine Foundry Employer Eli Lilly and Company Location Lebanon, Indiana Start date Mar 30, 2026 View more categories View less categories Discipline Administration , Engineering , Automation Engineer Required Education Bachelors Degree Position Type Full time Hotbed BioMidwest , Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job.
- Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry.
Key Objectives/Deliverables:
- Technical Expertise
- 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 collaborate with Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications to ensure Data historization and architecture is considered.
- Provide periodic status updates to Project Management
- Work with Engineering, Operations and many cross functional groups to trouble shoot issues, making changes to the site data historian system (OSI PI) in line with site change control procedures and site standards, responding to system events and performing routine system maintenance checks
- Maintain Data Historian System health and respond to issues as they arise
- Develop standard operating procedures, work instructions and other job aids to ensure the appropriate level of documentation is in place to train on, maintain and operate OSI PI, alarm management and alarm notification systems.
- Provide subject matter expertise on data historian systems design, development, installation, testing, validation, and lifecycle support.
- Ensure solutions are delivered by system Integrators, equipment vendors and others that can be integrated to the site data historian per the site standards and data management strategies. This includes developing requirements for the system in line with industry and Lilly standards.
- Design, configuration, and testing of the platform (OSI PI).
This includes:
OSI PI Server Infrastructure OSI PI Integration with Emerson DeltaV DCS solution OSI PI Interfaces with other systems (e.g. BMS, PLCs, Remote IO) OSI PI Asset Frame design and build Other OSI PI related solutions such as PI Vision- Implement and support electronic systems (such as plant historians) 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
- Promote 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 major pharmaceutical manufacturing.
- 5+ 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.
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 and MES systems (DeltaV, Rockwell, Syncade, etc).
- Experience with: OSI PI and related applications Cybersecurity and IOT considerations when managing systems Awareness of integrating other process automation systems such as DeltaV, BMS, PLC/HMI and similar control systems in a manufacturing environment Industrial communication protocols such as BACnet/IP, modbus, HART, OPC DA & UA, Profibus, Ethernet/IP, RIO Systems performing backup and restore, disaster recovery Experience of developing documents with electronic document management system (Kneat, Valgenesis, ALM) Configuration and support of alarm management systems such as LogMate, Win911 • Experience with Root Cause Analysis methodologies Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions.
Our current groups include:
Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. 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 equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
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