Automation Developer Jobs in Indiana (NOW HIRING)

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.

We unify caring with discovery to make life better for people worldwide. We are a global healthcare leader headquartered in Indianapolis, Indiana, dedicated to discovering and delivering life‑changing medicines, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism. We put people first and strive to bring our best effort to everything we do.

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 will combine research and manufacturing in a single location, enabling us to develop innovative solutions that optimize manufacturing processes, increase capacity for clinical‑trial medicines, and reduce costs and environmental impact.

This role will serve as a member of the Automation Engineering Department at the Foundry. The engineer will provide automation support for one or more operating areas across site and/or for capital projects. Responsibilities include CSV support, validating systems critical to the manufacture of life‑changing products, ensuring compliant control applications, and influencing the technical agenda across the organization.

In the project delivery and startup phases (expected 2025‑2028), automation engineering will be fluid and dynamic as we build the new organization, develop and implement the necessary systems and business processes to support GMP operations, and cultivate a culture of collaboration, creativity, and resilience.

• Process control validation testing, implementation, and coordination
• Develop and implement the Automation Engineering Project Validation Plan
• Provide subject‑matter expertise for computer system validation and data integrity for automation systems across the site, including Process Automation Systems (DCS, SCADA, BMS, MES, Historian), Building Management System, Vendor‑Packaged Equipment, Data Historian, Automated Storage and Retrieval System, QMS
• Perform risk assessments for computerized systems and develop mitigation strategies
• Develop and execute validation protocols for computerized systems
• Ensure compliance with regulatory requirements and industry standards (GAMP, 21 CFR Part 11, Data Integrity) and corporate Lilly quality policies
• Generate and maintain validation documentation (plans and summary reports)
• Develop local site procedures (SOPs, Work Instructions, etc.) related to automation systems
• Manage change control and deviation management for CSV activities
• Collaborate with vendors to ensure third‑party systems and software meet validation requirements; conduct vendor audits as needed
• Provide training to personnel on CSV principles, procedures and best practices
• Stay informed of industry trends and advancements in CSV and automation technologies
• Represent the automation department during audits by regulatory agencies as assigned
• Act as functional owner for the Electronic testing system (Kneat, ALM, Valgenesis) managing CSV documents related to automation systems

• Review and oversee Design documentation, including Functional Requirements, Design Specifications, DCS Application Software, and Test Specifications
• Lead or participate in design reviews and Automation application software reviews to ensure compliance and standardization
• Provide periodic status updates to Project Management
• Devise CSV and quality strategies for control systems in collaboration with the Site Quality organization
• Implement and support electronic systems (e.g., 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 developing and executing validation strategies and documentation
• Provide Automation support for capital projects, including new product introductions
• Promote automation to improve productivity, operational efficiency, and compliance
• Develop a 'network' of corporate contacts and leverage corporate expertise when needed

• In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products
• Demonstrate initiative, good planning, and organizational skills; prioritize tasks and meet timelines
• Possess a keen technical curiosity and strong problem‑solving skills with a desire for continuous improvement
• Demonstrate ability to influence peers and business partners
• Possess strong written and verbal communication skills for both technical and non‑technical audiences
• Have knowledge of GMP, regulatory requirements, and computer system validation

• Minimum B.S. in Engineering or a related degree
• 2+ years of experience in FDA‑regulated environments
• Experience with design, development, commissioning, or qualification of computer systems
• Qualified applicants must be authorized to work in the United States on a full‑time basis; Lilly does not sponsor work authorization or visas

• Deep knowledge of GMP/GXP, regulatory requirements, computer system validation, and data integrity
• Experience in Automation Engineering, preferably in major pharmaceutical manufacturing
• Experience designing, developing, commissioning, and qualifying highly automated greenfield manufacturing sites utilizing SCADA, DCS, MES, LIMS, and Site Historian systems
• Experience commissioning, qualifying, and supporting interconnectivity among SCADA, DCS, MES, LIMS, Historian, and other applications
• Experience leading quality compliance and data integrity activities in a highly automated environment
• Experience facilitating and driving decision‑making at an organizational level

• Initial location: Carmel, IN
• Permanent location: new Lilly Medicines Foundry, Lebanon, IN
• Actual compensation will depend on education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600.
• Full‑time employees will be eligible for a company bonus (depending on company and individual performance) and a comprehensive benefit program, including 401(k), pension, vacation, medical, dental, vision, prescription drug, flexible benefits, life and disability insurance, time‑off and leave of absence benefits, and well‑being benefits.

Lilly is an EEO/Affirmative Action 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.