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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.…
The Principal Scientist QA provides GMP quality oversight for early-phase clinical development assets, ensuring compliance and managing documentation for drug products and external partners. The role involves cross-functional collaboration, deviation investigations, and inspection readiness activities.
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.
Lead a team to design and implement end-to-end test automation for AI-powered healthcare systems, validating LLMs, RAG pipelines, and model outputs using frameworks like RAGAS and DeepEval.
Lead quality assurance for a new active pharmaceutical ingredient (API) manufacturing site, overseeing QA teams, cGMP compliance, and regulatory audits to ensure safe, high-quality drug production.
Quality Assurance Associate supporting GMP operations at a new biopharma manufacturing facility, reviewing documentation, ensuring compliance, and collaborating with cross-functional teams during startup and scaling phases.
Oversee quality for Lilly’s contract manufacturers producing solid oral drugs (tablets/capsules), ensuring cGMP compliance, batch release, and regulatory alignment while serving as the primary liaison between CMs and Lilly.
Quality Assurance Associate ensuring pharmaceutical cartridge filling meets cGMP standards and regulatory requirements at Eli Lilly’s manufacturing site in Sesto Fiorentino, Italy.
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