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The Principal Process Engineer leads process knowledge development, tech transfers, and continuous improvement in API manufacturing, ensuring safety, quality, and operational excellence.

Lead technical vision and execution for AI capabilities in drug discovery, build a multidisciplinary team, and drive organizational alignment with research priorities.

The Associate Director PV Systems Strategy and Implementation leads technology and analytics strategies in pharmacovigilance, enhancing data quality and compliance. They collaborate on system development, project oversight, and regulatory compliance, while promoting efficiency and operational excellence in PV processes.

The Sr. Director of Parenteral Engineering leads strategic projects, operational excellence, and effective communication across manufacturing sites while ensuring safety and quality.

Embed with discovery teams to translate scientific workflows into production AI systems. Rapidly prototype and deploy LLM/RAG-based solutions for multi-omics problems, run evaluation loops, ensure data provenance and reliability, and distill learnings into reusable platform components to drive adoption across therapeutic areas.

The Engineering Associate Director leads engineering teams supporting process development, equipment optimization, maintenance, and compliance, contributing to the startup of a new manufacturing facility.

The Process Safety Lead provides technical support in process safety for manufacturing, focusing on safety evaluations, hazard analysis, and engineering practices to ensure compliance across Lilly's global operations.

The role involves statistical analysis, collaborating on analysis plans, maintaining SAS proficiency, ensuring quality compliance, and leading projects with innovative programming techniques.

The Senior Director of Supply Chain leads operations to ensure product delivery, manages planning and procurement, oversees logistics, and develops team capabilities in a GMP manufacturing environment.

The Clinical Project Statistician develops statistical methods for clinical study protocols, analyzes data, collaborates on regulatory submissions, and communicates results effectively.