Jobs at Eli Lilly and Company

Leads global regulatory strategy and execution for immunology medicines from candidate selection through end of lifecycle. Oversees FDA submissions and agency interactions, guides cross-functional regulatory teams, aligns regional plans, manages labeling and risk strategies, and supports global development and commercialization. Builds external stakeholder relationships, advises marketing and communications teams, mentors regulatory personnel, and represents regulatory affairs in governance forums.

Lead development of scalable digital health platform solutions, establishing software architecture and development standards while coordinating multiple technical teams. Evaluate designs, manage software delivery risks, support regulatory and medical device quality expectations, and drive platform innovation through proofs of concept. Mentor developers, influence architects and delivery teams, and guide Agile development across Lilly and external partners. The role requires expertise in cloud platforms, asynchronous systems, identity management, CI/CD, and software lifecycle delivery.

Lead architecture and technical direction for digital health software platforms while managing a team of 2–5 engineers. Responsibilities include approving system designs, guiding cloud and asynchronous integrations, managing performance and capacity, driving innovation roadmaps, supporting cybersecurity and regulatory compliance, establishing engineering standards, mentoring technical leaders, and coordinating delivery across product, design, operations, and business teams.

Develop and deploy analytical methods for small-molecule drug discovery across cheminformatics, computational biology, statistical modeling, and AI/ML. Translate scientific challenges into analyses supporting compound prioritization, design recommendations, and mechanism-of-action hypotheses. Collaborate across data, architecture, automation, and AI teams to create production-ready, agent-accessible capabilities. Evaluate emerging methods through benchmarking, address data gaps, publish research, present at conferences, and advise scientific teams.

Lead day-to-day small-molecule API manufacturing operations for a greenfield GMP site, overseeing frontline leaders, ensuring safety, quality, validated processes, staffing, continuous improvement, and cross-functional integration through startup to full-scale production.

The Advisor - Computational Modeling Engineer develops computational models to enhance manufacturing processes, supporting operations with simulation techniques and Digital Twin solutions.

Lead computational peptide discovery by integrating AI/ML and physics-based modelling to support hit identification through lead optimization for oral macrocyclic peptides. Provide assay and biochemistry expertise, develop/drive assay workflows (e.g., SPR), mentor junior scientists, collaborate across structural biology, medicinal chemistry, and therapeutic teams, and help build computational and automated discovery infrastructure.

As Engineering Leader, you will manage operations related to formulation, filling, and automated inspection, focusing on equipment reliability and team development.

Support the Cardiometabolic Health brand by coordinating with creative agencies, managing marketing materials and Veeva Vault uploads, assisting the Brand Manager with events and sales-force requests, and collaborating with team members to ensure successful program execution and operational tasks.

Lead design, automation, and operations of enterprise Linux platforms across on‑prem, cloud, and hybrid environments. Build and maintain Ansible Automation Platform content, IaC, CI/CD pipelines, patching, drift remediation, HA/disaster recovery, security hardening, and cloud integrations. Provide architecture guidance, mentoring, incident response, and ensure compliance and operational excellence.

Lead development, deployment, and validation of advanced analytical methods (e.g., cheminformatics, computational biology, AI/ML) to inform discovery decisions, integrate tools with data infrastructure and autonomous agents, mentor junior scientists, publish research, and collaborate across Data Foundry pillars to accelerate molecule discovery.

Support Pricing, Reimbursement & Access team by monitoring market access environment, preparing pricing/reimbursement materials, conducting secondary research, maintaining trackers and databases, assisting cross-functional projects, and producing presentations and reports while ensuring accuracy and compliance.

Lead and manage a team administering Medicaid Drug Rebate and copay payment obligations, ensuring accurate, timely, and compliant payments, operational controls, dispute resolution, system ownership, and cross-functional project leadership to minimize financial and legal risk.

Perform frontline cyber defense: monitor, detect, analyze, investigate, and respond to threats across functions (ETR, ASM, CTI, CDR, DAO, ITR). Develop detection capabilities, document analysis, prioritize and remediate incidents, recommend strategic improvements, and provide rotational on-call support.

Promote cardiometabolic products to healthcare professionals across the Chennai territory, develop and execute territory sales plans, meet sales targets, conduct HCP, pharmacy and nurse awareness programs, provide scientific support, liaise with stockists, submit sales reports and forecasts, and ensure compliance with industry and company ethics.

Leads a district sales team focused on immunology and specialty medicines. The Business Director coaches Territory Managers, develops sales strategies, manages key healthcare accounts, drives product adoption, implements approved technologies and analytics, and achieves sales and execution targets. The role also recruits and develops talent, fosters an inclusive performance culture, manages organizational change, and builds relationships with healthcare professionals, health systems, and internal partners.

Lead technical design, implementation, and lifecycle management of downstream purification and conjugation processes for GMP biologics. Provide engineering oversight for chromatography, filtration, control systems, tech transfers, risk assessments, regulatory support, audits, and mentor engineers while ensuring cGMP and quality system compliance.

Lead a regional pharma sales team: build area sales plans, coach and develop territory managers, manage KOL relationships, monitor performance and compliance, analyze reports, and coordinate cross-functionally to meet sales targets.

The Clinical Research Lead drives clinical trial execution by engaging investigators, managing sites, and collaborating cross-functionally to optimize enrollment and compliance with protocols in the immunology therapeutic area.

Author, configure, validate, and support MES recipes (GMBR/PMBR) on PharmaSuite or Werum PAS-X. Manage recipe migration across environments, execute IQ/OQ/PQ and test scripts, provide L2/L3 production support, ensure compliance with GxP/CSV/21 CFR Part 11/Annex 11 and data integrity (ALCOA+), and collaborate with manufacturing, quality, and validation teams for site go-lives and change control.