Materials Management Scientist

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 pioneering center that integrates advanced manufacturing and drug development. As the first facility of its kind, the Foundry is designed to accelerate innovation in manufacturing processes, expand capacity for clinical trial medicines, and speed Lilly’s innovative medicine to clinics, and reduce both costs and environmental impact.

The Process Translation and Execution (PTE) team plays a critical role in this mission. PTE is responsible for leading technology transfers from lab or pilot scale to cGMP production, collaborating with Operations and cross‑functional teams to ensure reliable clinical supply and right‑first‑time production. The team also drives continuous improvement, advances the site technical agenda, and researches transformative technologies and champions the accelerated adoption of innovation in clinical and commercial manufacturing, ultimately delivering patient‑centric outcomes.

We are seeking enthusiastic scientists and engineers to join the PTE team and help bring the Lilly Medicine Foundry’s vision to life.

• Chemical and raw material management
  • Chemical of concern assessment and compliance with evolving federal and state regulations, including evaluation of materials subject to REACH, TSCA, or international restrictions.
  • Provide written technical opinions and risk summaries to support site‑level regulatory submissions, inspections, and internal audits.
• Technical interface and advisory to Supply Chain/Procurement organization
  • Support the creation and review of material specifications and liaise with supply chain, warehouse and analytical groups on sampling and testing plans.
  • Coordinate with supply chain on the completion of material qualification activities, including qualification of suppliers, technical review of regulatory documentation, certificates of analysis, and SDS accuracy.
  • Assess the impact of supplier changes in collaboration with PTE scientists and provide input to change control documentation.
  • Collaborate with PTE tech transfer lead and Procurement to identify preferred suppliers and flag single‑source risks or supply chain vulnerabilities.
  • Assist in developing and maintaining approved supplier lists (ASLs) for critical regulated materials in partnership with Process Development, Quality and Supply Chain.
  • Participate in lifecycle management reviews for existing materials.
• Provide Technical Support to Tech Transfer Teams
  • Evaluate new chemical entities and reagents introduced for regulatory and classification implications before first‑in‑site use.
  • Engage with Development early in technology transfer workflows to assess material management requirements for incoming programs across all Foundry modalities.
  • Author or contribute to chemical management sections of tech transfer packages, process descriptions, and facility fit assessments.
  • For process consumables, collaborate with process engineering on the site’s Extractables and Leachables program, risk assessments and support start‑up.
  • Prepare, review, approve relevant technical documents such as change controls, deviation investigations, plant trial protocols and summary reports, procedures, etc.
  • Lead material investigations working with process teams to assess/investigate material issues, implement material changes and…