Jobs at Eli Lilly and Company

Supports MODA environmental monitoring and laboratory informatics systems across GMP-regulated manufacturing and quality laboratories. Responsibilities include system configuration, integrations, troubleshooting, validation, testing, documentation, compliance, CAPA, change control, reporting, and automation. The role collaborates with laboratory, quality, manufacturing, engineering, vendors, and IT teams while supporting platforms such as LabVantage, Empower, SAP, and MES systems.

Responsible for quality oversight of contract manufacturers in the pharmaceutical sector, ensuring compliance with regulatory standards and quality agreements, and participating in inspections and quality activities.

The HRBP Project Consultant leads HR projects, drives talent management, ensures employee engagement, and partners with business leaders to support organizational goals at Eli Lilly Japan.

Leads the invoicing and accounts payable function, managing team performance, end-to-end invoice operations, controls, compliance, KPIs, escalations, and supplier relationships. Drives finance transformation through automation, digital tools, process improvement, and data-led decision-making. Partners with Procurement, Treasury, Commercial Finance, IT, and senior leadership on system enhancements, reporting, audits, and strategic initiatives.

Leads the design, development, validation, and application of immunoassay-based biomarker methods for neuroscience and neurodegenerative disease clinical trials. Performs laboratory experiments, analyzes preclinical and clinical samples, reports assay results, and collaborates with internal stakeholders, CROs, and academic partners. Provides leadership and mentorship to biomarker research teams while supporting therapeutic molecule evaluation and clinical program integration.

Build and deploy agentic AI applications, document-intelligence pipelines, retrieval-augmented systems, and workflow automation for pharmaceutical sourcing and supply-chain decisions. Develop reliable agent skills, evaluations, guardrails, monitoring, and MLOps practices. Partner with sourcing, procurement, strategy, and technology teams to translate ambiguous business needs into production AI solutions, including the PRD Supply Chain Intelligence agent. Mentor colleagues and guide responsible AI adoption in a regulated environment.

Lead qualification and onboarding of CRO laboratories supporting ADME and bioanalytical assays. Provide scientific oversight for method development, validation, sample analysis, data quality, and regulatory compliance across diverse therapeutic modalities. Partner with Discovery, Clinical, Procurement, Quality, and Operations teams; build vendor relationships, troubleshoot methods, manage reagents, improve qualification processes, and mentor scientists.

Supports, develops, validates, deploys, and maintains manufacturing execution systems in a GMP pharmaceutical manufacturing environment. Translates business processes into technical solutions, manages electronic execution tickets, resolves system issues, coordinates releases and lifecycle activities, and ensures systems remain validated. Partners with business stakeholders, IT teams, third parties, and global MES teams to improve manufacturing processes, prioritize work, manage escalations, and deliver compliant digital solutions. This is an onsite role with occasional on-call work and 10%–15% travel.

Owns digital quality strategy for Catalyze360 systems and platforms. Leads QMS, design controls, risk assessments, change control, deviations, CAPAs, audits, and AI/ML governance. Serves as a software quality and CSQA subject-matter expert, embedding CSA and risk-based assurance into agile and CI/CD delivery. Advises internal teams and external partners on regulated software quality, CSV/CSA, IT controls, privacy, cybersecurity, and model governance while driving audit-ready execution and quality improvements.

Owns sales performance across a pharmaceutical territory by promoting Lilly’s portfolio to healthcare providers and hospital accounts. Builds relationships with key stakeholders, develops territory strategies, navigates payer and healthcare environments, uses analytics and approved AI tools to identify opportunities, and conducts patient-centered product discussions. The role requires meeting sales metrics, addressing on-label medical and market-access questions, and collaborating with internal and external partners while maintaining company compliance.

Leads global case management standards, policies, compliance monitoring, audits, training, regulatory inspection readiness, and corrective actions for pharmacovigilance and product complaint processes. Serves as a subject matter expert for cross-functional stakeholders, oversees compliance risks and metrics, supports case management system improvements, and ensures adherence to global regulations and internal policies.

Supports LabVantage LIMS master data, test methods, templates, specifications, scripts, reports, APIs, and laboratory integrations. Troubleshoots system issues, assists with configuration and platform support, and contributes to automated testing, upgrades, and releases. Performs validation documentation and testing under GxP, 21 CFR Part 11, and ALCOA++ requirements. Collaborates with laboratory, vendor, and technology teams while developing skills in scripting, automation, AI, integrations, and master data governance.

The role involves leading technical support and analytical development in protein synthesis, team management, ensuring safety, and promoting a culture of scientific excellence.

The Statistician collaborates on statistical analysis plans, conducts and justifies data analyses, and ensures compliance with regulatory requirements, while maintaining a focus on statistical programming proficiency and effective communication of results.

Implement next-generation MES across manufacturing sites: define and execute integrated deployment plans, align solutions with global standards and digital initiatives, serve as site/team point of contact, enable change management and user adoption, develop training and support models, and partner with site and global project leaders to ensure validated, compliant MES deployments.

Provide strategic patent counseling for key pharmaceutical assets: develop global patent filing and prosecution strategies, assess freedom-to-operate and IP risk, advise senior management, lead projects and task-directed teams, and drive continuous improvement in patent practice.

Architect and lead scalable cloud-native software systems across backend and frontend layers. Build production-grade Generative AI and LLM-powered capabilities, including multi-agent solutions. Establish architecture and engineering standards, champion observability, reliability, and security, and collaborate with product, data science, security, and infrastructure teams. Own the full software development lifecycle, use AI-assisted development tools, and mentor junior engineers.

Owns enterprise project controls governance across capital projects, including budgeting, cost control, earned value management, forecasting, change and risk management, scheduling, reporting, and performance measurement. Establishes standards, procedures, assurance programs, and system requirements; provides strategic guidance to project teams and service providers; leads training and capability development; and partners with Finance, Procurement, Engineering, and Project Delivery to improve portfolio performance and decision-making.

Leads competitive intelligence, market monitoring, strategic planning, and partnership evaluation for LillyDirect’s digital health platform. Advises senior leadership on industry trends, competitors, market expansion, new services, ecosystem partnerships, and potential acquisitions. Synthesizes customer and market insights, benchmarks best practices, and leads the annual strategic planning process. Requires 10+ years of experience in strategy, competitive intelligence, consulting, or comparable market analysis roles.

Owns enterprise project information management and document control for Lilly’s global capital project portfolio. Establishes governance, standards, workflows, metadata, Common Data Environment requirements, digital handover practices, and information lifecycle controls. Oversees project information systems, compliance assessments, audits, contractor documentation, and operational readiness. Leads continuous improvement, digital transformation, stakeholder adoption, training, and capability development across internal teams and external delivery partners.