Jobs at Eli Lilly and Company

Provide high-level administrative support within Product Research & Development, coordinating multiple functions, complex calendars, meetings, travel arrangements, and fostering communication.

The Senior Scientist will provide technical oversight in peptide manufacturing, ensuring compliance with regulations, resolving technical issues, and supporting continuous improvement. The role involves close collaboration with internal and external partners, requiring strong communication and project management skills.

The Sr. Regulatory Affairs Manager will oversee product registration procedures, ensure compliance with regulations, liaise with global teams, and mentor junior staff in a pharmaceutical setting.

The role involves adhering to safety policies, training requirements, following operational procedures, and ensuring good documentation in a manufacturing environment.

The role involves promoting pharmaceutical products, executing business strategies, establishing relationships with clients, and providing accurate drug information. Participation in team building and maintaining a professional image are also key responsibilities.

As a Finance Intern at Lilly, you will support invoice validation and invoicing tasks, assist with vendor communications, and help with compliance and process improvements in the accounts payable department.

The BioProcess R&D Automation Engineer develops automation solutions and supports bioprocess systems, ensuring data management, system integrity, and process improvement in GMP manufacturing environments.

The Director leads clinical pharmacology and translational modeling strategies for gene editing therapeutics, overseeing all stages from preclinical to regulatory submission.

The Process Permitting role involves authorizing safety permits, ensuring safe operations, and supporting maintenance and HSE activities at Lilly's Limerick facility.

The Associate Director - TSMS oversees technical services in pharmaceutical manufacturing, ensuring compliance, managing staff, and driving operational excellence during the startup of a new facility.

The Alzheimer’s Ecosystem Manager will map the diagnostic and treatment landscape for Alzheimer's disease, enhance pathways, address infusion capacity, build alliances, and engage stakeholders to optimize patient outcomes.

The Senior Director of Strategic Alliances will lead external collaborations to advance drug development, ensuring operational excellence and alignment with strategic goals across teams and partners.

The Senior/Principal Process Engineer will support facility startup and operations for API production, focusing on process engineering and safety. Responsibilities include developing operational readiness plans and leading tech transfers to improve batch and continuous production capabilities.

The Territory Manager will drive account management and sales strategies to improve care for Alzheimer's patients, managing multiple healthcare stakeholders and promoting products effectively.

Lead the sales and marketing strategies for the Oncology portfolio, ensuring business objectives are met through effective team management and cross-functional collaboration.

The Senior Director HSE manages HSE programs at a manufacturing facility, ensuring compliance and safety during startup and operations. They lead teams, engage with regulatory agencies, and develop organizational capabilities to support GMP operations.

The Director of Statistics leads statistical projects in clinical research, implements innovative methodologies, designs trials, and collaborates with teams to analyze results, ensuring regulatory compliance and contributing to cardiovascular disease treatments.

Lead Methods4Insight to define, validate, and deploy analytical and computational methods for molecule discovery. Build/guide a multidisciplinary team, set evaluation frameworks, prioritize build-vs-buy decisions, fill strategic data gaps, and integrate agent-ready AI capabilities across Data Foundry.

Provide technical leadership for small-molecule/peptide API production: mentor process engineers, sustain process knowledge, support equipment qualification, drive process optimization, integrate modeling/statistics, and support tech transfer and GMP startup activities.

The role involves statistical analysis planning, methodology selection, programming in SAS, and collaboration for regulatory submissions and results communication.