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Develop scientific software for AI-native drug discovery, building data pipelines, APIs, and lab automation integrations while collaborating with scientists.

Responsible for promoting and marketing company products in the clinical setting, building relationships with clients, and providing detailed information on drug characteristics and effects. Engage in team collaboration and maintain company professionalism while adhering to business strategies.

The Data Scientist will lead the development of data products that enable AI-driven insights, ensuring compliance and optimizing processes across CMC workflows.

The Production Supervisor leads production operators, manages performance and development, ensures compliance with quality and safety, and supports team goals while promoting a positive culture.

The Sr. Director - QC Laboratories will lead quality laboratory operations, ensuring compliance, managing personnel, and developing strategic capabilities. Responsibilities include building a high-quality organization and maintaining GMP compliance while coordinating inspections and budget management.

Lead laboratory teams in Neuroscience focusing on psychiatric and neurodevelopmental disorders. Develop preclinical biomarker assays, supervise lab scientists, and present findings to leadership.

The position oversees technical aspects of commercial molecule manufacturing, ensures adherence to GMP, leads problem-solving, and manages process documentation.

The Senior Director for Strategy will lead external innovation efforts in the Asia-Pacific region, assess potential partnerships, and develop strategic relationships with external organizations to enhance Lilly's portfolio.

Design and develop software for automated laboratory workflows, build data pipelines, implement machine learning models, and integrate various systems to enhance biotherapeutics discovery.

This role involves designing and executing process studies for RNA-LNPs, leading process development, collaborating across functions, and ensuring regulatory compliance for genetic medicines.