Informatics Engineer - Lilly Medicine Foundry

About the role

Lilly is seeking an Informatics Engineer to join the Lilly Medicine Foundry team. The Foundry is a new center for advanced manufacturing and drug development in Lebanon, IN, where Lilly will optimize manufacturing processes, increase capacity for clinical trial medicines, reduce costs, and decrease environmental impact.

Responsibilities

• Partner with Process Translation and Analytical Laboratories functional areas and site, group, and global IT teams to implement and support digital laboratory solutions.
• Drive and support system design, configuration, validation, and release for key lab systems such as LIMS, LES, ELN, CDS, and EM platforms.
• Translate business and scientific processes into validated technical solutions for LIMS, LES, ELN, and CDS platforms.
• Develop and implement IQ, OQ, and PQ protocols in compliance with 21 CFR Part 11 and EU Annex 11.
• Ensure data integrity requirements across lab systems and audit readiness for regulatory inspections.
• Coordinate instrument integration and data flows between lab equipment and LIMS/LES platforms.
• Support site deployment and upgrade of analytical laboratory IT systems throughout the facility’s startup and operational phases.

Validation & Compliance

• Produce and maintain Computer System Validation (CSV) documentation, SOPs, and validation plans in alignment with applicable regulatory frameworks.
• Ensure systems remain in a validated state and lead their lifecycle through releases, recapitalization, and retirement.
• Build and maintain awareness of regulatory, legal, and quality requirements impacting the quality control laboratory, ensuring solution requirements comply.

Collaboration & Readiness

• Collaborate with site and global IT system teams to ensure operational readiness of laboratory systems supporting the Foundry’s release objectives.
• Act as a key IT SME for analytical laboratory IT systems, organizing and educating peers on system use and best practices.
• Support audits and provide oversight for management reviews, laboratory metrics, equipment records, and laboratory documentation.

Qualifications

• Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or related field.
• 1+ year of relevant experience in information technology, engineering, computer system validation, quality control support, or a related area.
• Experience with Computer System Validation (CSV) methodology.
• Qualified applicants must be authorized to work in the United States on a full-time basis.

Additional Skills / Preferences

• Strong working knowledge of analytical laboratory IT systems including: LIMS, ELN, CDS, and EM platforms.
• Experience working in a GMP-regulated environment (pharmaceutical, biotech, or equivalent).
• Demonstrated ability to prepare and implement IQ/OQ/PQ protocols and associated documentation.
• Experience with API/middleware integration and instrument connectivity between lab equipment and informatics platforms.
• Familiarity with data integrity frameworks applicable to GMP lab environments.
• Understanding of Agile or iterative delivery methodologies in a regulated setting.
• Demonstrated learning agility and curiosity; ability to analyze, anticipate, and resolve complex issues through sound problem-solving.
• Effective communicator across diverse forums and audiences, including technical peers, QA, and business customers.
• Certification in relevant IT areas (e.g., ITIL, cloud, AI) is a plus.