Jobs at Eli Lilly and Company

Promote Lilly's cardiometabolic health products, build relationships with healthcare professionals, travel regionally, maintain customer satisfaction, and comply with standards.

The Scientific Lead will drive oncology target discovery using genetic medicine technologies, design experimental strategies, collaborate with teams, and contribute to innovative cancer therapies.

As an Engineer - MES, you will design and implement MES solutions for a new pharmaceutical manufacturing site, ensuring compliance with regulatory requirements and driving operational excellence.

The role involves overseeing clinical study operations, driving country initiation activities, managing enrollment targets, and ensuring quality oversight of deliverables.

The role involves leading technical integration and maintenance of SAP EWM systems in manufacturing logistics, collaborating across teams to ensure operational excellence and data system readiness.

The role involves serving as a senior Ethics and Compliance Business Partner, managing E&C risks, advising on program design, leading monitoring strategies, and partnering with stakeholders to enhance compliance execution.

The HPC Platform Engineer will lead the design, build, and maintenance of scalable HPC platforms while enabling analytical capabilities and optimizing workflows for researchers.

The role involves overseeing process engineering for drug manufacturing, optimizing lab processes, conducting experiments, ensuring safety compliance, and collaborating across functions to enhance operational efficiency.

As a Principal Application Support Engineer, you lead complex incident resolutions, improve system reliability, mentor engineers, and collaborate with teams to enhance operational standards.

Promote and educate clinicians about cardiovascular/metabolic products within an assigned territory, execute company product strategy and sales plans, develop and maintain hospital customer relationships, provide product information, report market/competitive insights, support cross‑department collaboration, and protect company confidentiality.

The Principal Automation Engineer will lead the design, delivery, and administration of data historian and integration platforms in pharmaceutical manufacturing, ensuring compliance with cGMP standards and successful project implementation.

Design and govern an AI-ready data architecture for a greenfield pharmaceutical manufacturing site. Define data models, integrations (MES/LIMS/DCS/SAP), cloud platform standards (Azure/AWS), and AI platform design for regulated GMP contexts. Establish data and AI governance, ensure compliance (ALCOA+, GxP, GDPR, EU AI Act), support CSV/GAMP5 validation, mentor teams, and influence site and network architecture for deployable, auditable AI capabilities.

The role involves promoting pharmaceutical products, executing marketing strategies, maintaining relationships with clients, and providing accurate drug information.

Support the efficiency and accuracy of the employee expense process globally by ensuring compliance with policies and resolving system queries, while providing analysis and project participation.

Lead industrial design for drug delivery devices, driving human-centered design, cross-functional research, ideation, prototyping, and design language development. Advocate user needs, ensure brand-consistent, manufacturable solutions, build team capabilities, align design strategy with business priorities, and communicate design vision across stakeholders.

Manage adverse event notifications: receipt, entry into pharmacovigilance database, regulatory reporting, follow-ups, filing, and related administrative tasks within the PV department.

The Clinical Research Physician provides medical expertise in drug development, collaborates globally on clinical trials, and engages with health authorities while enhancing the patient journey and commercial strategies.

Manage legal needs for the India commercial organization, providing day-to-day legal support, compliance, and risk management. Lead legal strategy and training programs, ensuring adherence to laws and regulations.

Lead design and build of an end-to-end SaaS product that wraps Lilly's AI/ML and LLM models for biotech customers. Architect frontend, backend, data and integrations, implement federated learning, establish engineering practices (testing, releases, on-call), mentor hires, recruit, and coordinate with internal platform, security, and customer stakeholders.

Promote and educate on company cardiovascular and metabolic products within an assigned territory. Execute product strategy and business plans, build and maintain hospital and key customer relationships, communicate drug features/safety, report market/competitive intelligence, support team collaboration, and protect company confidentiality.