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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.…
QA Senior Specialist overseeing daily statistical sorting operations, syringe defect kit management, deviation investigations, and GMP document review at a pharmaceutical manufacturing site in Wisconsin.
Analyze U.S. payer formulary data (MMIT) to track drug coverage and restrictions, then build AI-powered dashboards and reports for market-access strategy at a global pharmaceutical company.
Build and maintain Databricks/AWS pipelines and lakehouse architectures to power consumer analytics and AI-driven insights for a global pharmaceutical company.
Leads the design and automation of privacy, AI, and data governance controls for a large healthcare company, translating regulations into auditable, scalable systems while partnering with cybersecurity teams.
Lead multi-billion-dollar capital projects for pharma manufacturing facilities, coordinating global teams to deliver safe, compliant, and high-quality assets from design through qualification.
Lead Lilly Japan’s ethics and compliance program, ensuring adherence to laws and company standards while supporting new business initiatives in a regulated healthcare environment.
Lead supply chain, warehousing, and logistics for a new GMP API manufacturing site, planning production, managing inventory, and ensuring regulatory compliance while building the startup team and systems.
Leads global communications and consumer campaigns for Lilly’s cardiometabolic medicines (e.g., Mounjaro, Zepbound) across 40+ markets, managing media relations, issues management, and medical meeting communications.
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