Lilly is building a new gene therapy manufacturing site (LP2) in Lebanon, Indiana. This role owns the Manufacturing Execution System (MES) end-to-end - from the Tulip application layer and Tulip Table data model, through MuleSoft integrations connecting SAP, QbDVision, and LabVantage, to the MQTT-based Unified Namespace driving real-time equipment communication. You will serve as both the technical authority over the platform’s architecture and the hands-on engineer responsible for its ongoing design, build, and validation., * Serve as Technical Lead/SME for LP2 MES architecture, design standards, and technical direction

• Design, build, and validate Tulip applications for GxP manufacturing workflows and electronic batch records

• Direct automation integrations with Automation Engineering (equipment commands, confirmations, process value subscriptions)

• Author/approve design specs ensuring compliance with ALCOA+ and 21 CFR Part 11

• Guide components through validated migration lifecycle (DEV * QA * Production)

• Participate in Change Control Board (CCB) and ServiceNow change management

• Partner with Manufacturing Operations, Automation Engineering, and Quality (BQA/CSQA)

• Mentor MES engineers; act as escalation point for complex issues

• Collaborate with MES Product Owner on ALM requirements/backlog

• Report system status and technical risk to site/IT leadership

• Bachelor’s degree in IT, Software/Computer Engineering or related field

• 5+ years with MES or pharma manufacturing IT platforms, including system integration (middleware/ERP/PLM) and Computer System Validation (CSV) in GMP settings

• 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 Skills/Preferences

• Modern software architecture and integration patterns

• MuleSoft/Anypoint, DataWeave for MES-ERP(SAP)-PLM integrations

• MQTT, Unified Namespace (UNS), OPC UA knowledge

• CSV experience: Validation/Test Plans, IQ/OQ/UAT, design specs under 21 CFR Part 11/ALCOA+

• Understanding of eBRs, non-terminal record controls, e-signatures

• Git/GitHub, GitHub Actions, MUnit, ALM/Jira

• Familiarity with MABL and ServiceNow

• Strong cross-functional communication and problem-solving skills

Additional Information:

• Position Location: Lebanon, Indiana, with potential travel to other U.S. and global Lilly sites as required.

• Travel Percentage (%): <10

• Shift Information: Role is Monday through Friday and based on-site. Must be flexible in providing support to accommodate production schedules, batch execution windows, and change control activities. Occasional extended hours and/or off-hour support may be required.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $129,000 - $211,200

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility 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; and 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, 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., Science has been our calling from the beginning. Colonel Eli Lilly founded the company in 1876 and charged employees to “take what you find here and make it better and better.” More than 147 years later, we remain committed to his vision through every aspect of our business and the people we serve, starting with discovering the best treatments for those who take our medicines and extending to health care professionals, employees and the communities in which we live. Moreover, you can also count on the team at Lilly to be incredibly civic-minded, supporting our communities through philanthropy, volunteerism, and a creative and innovative can-do spirit.