Jobs at Eli Lilly and Company

Lead the global Reliability discipline for plant equipment and systems, driving process and technology improvements, supporting sites and CMOs, mentoring engineers, influencing capital projects, ensuring cGMP compliance, and delivering productivity and uptime improvements.

Lead Technical Services/Manufacturing Science team for a greenfield API manufacturing site startup. Oversee technical reviews, validations, investigations, process optimizations, regulatory interactions, staffing, and cross-functional implementation to achieve GMP compliance, process control, yield, and productivity during project delivery and startup.

Responsible for reviewing batch records and performing final disposition of semi-finished products to ensure GMP compliance. Reviews and approves GMP documents, supports site readiness and e-release process, and helps ensure systems and quality controls meet regulatory standards. Provides technical guidance and supports inspection readiness.

The Configuration Sr. Associate will develop, configure, and support manufacturing applications on the Tulip platform, collaborating globally to eliminate paper-based processes and improve efficiency.

Manage and implement hardware and software application upgrades for process control and automation, ensuring compliance with GMP standards and meeting project timelines.

The Operation Associate Manager will oversee Visual Inspection operations, lead improvement projects, ensure safety compliance, and support cross-functional initiatives while monitoring metrics in a manufacturing environment.

The Senior Director leads manufacturing operations for API production, ensuring operational readiness, compliance, and cultural development during startup. The role includes developing strategic and operational plans and managing compliance risks post-startup.

Lead and mentor a technical team supporting cGMP API commercial manufacturing. Oversee technology transfer, process validation, process control and capability, GMP compliance, investigations, and cross-functional technical initiatives to enable GMP startup and continuous improvement.

The Sr Principal Engineer - MES Systems will develop and integrate MES solutions for new API facilities, ensuring compliance and operational excellence in a regulated environment.

Lead project controls for large ($500M+) pharmaceutical capital programs from planning through qualification. Establish and monitor cost, schedule, resource baselines; manage change control, risk, forecasts, cashflows, contracts, and compliance. Coach and train project controls teams and ensure application of finance policies.

Support site readiness and startup of a new parenteral/device manufacturing site. Perform final batch disposition for semi-finished and finished combination products, review/approve GMP documents, ensure inspection readiness and GMP compliance, and support electronic batch records and quality systems.

The Postdoctoral Scientist will manage and analyze CNS neuroimaging datasets, optimize imaging strategies, and collaborate on drug delivery strategies within a pharmaceutical research context.

Promote Lilly oncology portfolio to HCPs and hospital accounts within the Miami territory using account-based selling. Build relationships, use data/analytics and company selling models, achieve sales targets, manage customer interactions (on‑label questions), and adopt company technologies to drive utilization and patient-centered dialogues.

Lead and deliver capital projects for pharmaceutical manufacturing from design through operational verification. Manage scope, budget, schedule, procurement, construction, commissioning, qualification, and compliance. Coordinate site teams, contractors, and stakeholders, ensure HSE and GMP adherence, and support facilities planning and continuous improvement initiatives.

Manage brand strategy and marketing initiatives for Cardiometabolic portfolio; develop market insights, foster cross-functional collaboration, and maintain KOL relationships.

The Senior Scientist in BioAnalytical Research focuses on developing and applying bioanalytical methods for drug molecules using mass spectrometry and collaborating on drug discovery projects.

The role involves designing and optimizing automation strategies for peptide synthesis, ensuring compliance with cGMP standards, and providing technical leadership in the implementation of automated systems.

Lead and supervise engineering teams delivering major capital projects (> $10M) for the Indianapolis API manufacturing plant. Oversee project execution, compliance (health, safety, environmental, quality), staff development, resource planning, stakeholder alignment, and continuous improvement. Ensure project management deployment and readiness for manufacturing operations.

The Manufacturing Finance Intern will support finance operations through cost control, cost analysis, investment management, and developing digital tools, while gaining exposure to strategic projects.

Oversee quality assurance for API external manufacturing, ensuring compliance with cGMP and regulatory norms while managing quality documents and audits.