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Executes site-level training in a GxP-regulated manufacturing environment, including onboarding, OJT, qualification activities, delivery tracking, LMS documentation, audit readiness, and GMP compliance. The role assesses frontline training effectiveness, identifies competency gaps, coordinates with site stakeholders, and feeds execution needs back to learning and platform leaders. It requires a bachelor's degree and at least two years of regulated manufacturing experience, preferably in pharmaceutical or biotech settings.

Leads Lilly’s global data and AI strategy, architecting scalable AWS and Databricks foundations for agentic AI, machine learning, and advanced analytics across US and international markets. Responsibilities include designing semantic data structures, APIs, ML pipelines, MLOps practices, and multi-agent architectures; driving AI adoption and automation; coordinating enterprise technology roadmaps; and mentoring data engineering, analytics, and AI practitioners.

Provides legal counsel to Lilly’s China business, advising on corporate, commercial, regulatory, compliance, competition, anti-bribery, sanctions, advertising, transactions, and litigation matters. Drafts and negotiates agreements, monitors legal developments, supports compliance programs and investigations, trains business teams, and partners with internal and external stakeholders. Serves as the primary legal contact for assigned business units while contributing to committees, projects, and strategic decisions.

Build and own Lilly’s PR&D semantic layer, ontologies, knowledge graphs, vector retrieval systems, and multi-agent AI architecture. Develop ingestion, triplet engineering, hybrid Graph-RAG retrieval, MCP integrations, orchestration, evaluation, observability, and governance for regulated scientific workflows. Lead technical direction for engineers, mentor teams, partner with science and business stakeholders, own the roadmap, and ensure compliance with GxP, FDA 21 CFR Part 11, privacy, security, and data integrity requirements.

Leads financial planning, forecasting, budgeting, business-case evaluation, pricing strategy, profitability analysis, and management reporting for Lilly India. Partners with commercial and corporate functions to support data-driven decisions, develops annual and long-range plans, evaluates strategic initiatives, and provides financial governance. Also drives FP&A transformation through automation, AI, and Power BI analytics.

Leads end-to-end quality engineering for software products, including test strategy, execution, automation, CI/CD integration, defect management, release readiness, and SIT/UAT coordination. Manages globally distributed QE teams, drives shift-left and AI-assisted testing, monitors quality metrics, mitigates risks, and communicates decisions across technical and business stakeholders. The role requires hands-on testing during deployment windows and leadership across multiple Agile delivery teams.

Lead end-to-end quality engineering for software products, including test strategy, execution, automation, defect management, CI/CD integration, release readiness, and risk mitigation. Coordinate SIT and UAT across multiple teams, guide a globally distributed QE team, report quality metrics, and partner with developers, product managers, and business stakeholders. Drive shift-left testing, modern automation, and AI-assisted quality practices while contributing hands-on during critical deployment windows.

Design, develop, deliver, qualify, and support MES solutions for a pharmaceutical manufacturing facility. Integrate MES with other systems, translate business requirements into technical solutions, maintain validated systems, manage releases and changes, support audits, and ensure compliance with GMP and quality requirements. Partner with automation, operations, and global technology teams while developing documentation and training materials.

Supports finance site readiness and ongoing cost accounting activities. Responsibilities include business planning and forecasting, month-end and year-end close, journal entries, standard cost establishment, account reconciliations, financial reporting, grants, asset capitalization, audit support, policy compliance, and finance project implementation. The role partners with business teams and global finance organizations and is fully onsite in Limerick, Ireland.

The Clinical Data Associate will program and test clinical trial data collection systems, collaborate with data analytics teams, and enhance data management processes in trials.