Eli Lilly
Pharma · Pharma
- HQ
- Indianapolis, US
- Founded
- 1875
- Size
- 35,000+
- Website
- lilly.com
Eli Lilly currently has 36 active AI-related job listings. The majority of these roles, 56%, are focused on agents, with data-related positions making up another 28%. Engineering is the most frequent function for these hires. The company is primarily hiring in the United States and India. Frequent technology tags include agent orchestration, RAG, and model serving, indicating a focus on building and deploying AI systems.
Currently tracking 28 active AI roles, down 25% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $58k–$345k (avg $175k).
Eli Lilly currently has 36 active AI-related roles in our index. The most common open titles are: Director, Discovery Bioinformatics Oncology (2), Advisor - Agent Research, Advisor - Antibody Developability Validation & Benchmarking, Advisor - Data Architect, Data Foundry, Advisor - Lab Automation Software Engineer. Most positions are in Engineering and Research.
Eli Lilly's active AI hiring is concentrated in: agents (53%), data (25%), application (8%). These categories follow a seven-stage AI lifecycle: data, pre-training, post-training, serving infrastructure, agents, evaluation, and application.
Eli Lilly is hiring AI talent in: United States (29 roles), India (7 roles).
Job postings at Eli Lilly most frequently reference: agent orchestration, rag, model serving, llm observability, vector db.
In the past 30 days, Eli Lilly has posted 12 new AI-related roles. That is a -48% change versus the prior 30 days (23 → 12).
| Title | Stage | AI score |
|---|---|---|
| (Sr.) Manager-Medical Science Liaison-CMH The Medical Science Liaison (MSL) role at Eli Lilly is focused on scientific and clinical expertise within a therapeutic area. MSLs engage with healthcare professionals to provide in-depth scientific information, gather insights, and facilitate scientific exchange. The role requires continuous learning, strong communication skills, territory management, and strategic thinking to support Lilly's research and commercialization efforts. This is a customer-facing role that acts as a key interface between Lilly and external scientific experts. | — | 0 |
| (Sr.)Manager-Medical Science Liaison-Hema This role is for a Medical Science Liaison (MSL) in the Hematology therapeutic area at Eli Lilly. The MSL will serve as a scientific and clinical expert, providing in-depth information to healthcare professionals and researchers. Responsibilities include facilitating scientific exchange, synthesizing research, supporting clinical development, analyzing customer data, and communicating insights to internal teams. The role requires an advanced degree in health sciences and significant clinical or research experience. |
| — |
| 0 |
| (Sr.) Manager-Country Study Management This role is responsible for providing clinical operational expertise at the country level for study management. Key responsibilities include driving country initiation, meeting enrollment targets, ensuring quality oversight, and delivering study results on time. The role also involves contributing to process improvements and managing change within the business objectives. | — | 0 |
| Senior/Executive Director Global Medical Affairs - Breast Franchise Senior/Executive Director of Global Medical Affairs for the Breast Franchise at Eli Lilly, focusing on oncology. The role involves providing medical and scientific support for drugs in development and marketed products, engaging with external stakeholders (KOLs), shaping scientific strategy, and leading a team of medical affairs professionals. Requires strong leadership, strategic execution, therapeutic area expertise (breast cancer preferred), and scientific communication skills. | — | 0 |
| Intern - Finance (iNext) This internship focuses on supporting the global employee expense process using SAP Concur, ensuring accuracy, efficiency, and compliance with corporate policies and SOx controls. Responsibilities include Tier 1 support, issue resolution, credit card administration, audit support, and participation in system testing and process improvement projects. | — | 0 |
| Head of Medical Affairs / CRP (m/f/d) Head of Medical Affairs / CRP in Austria, providing medical and scientific leadership, overseeing the medical team, driving innovation, ensuring scientific excellence, regulatory compliance, and cross-functional collaboration for pre- and post-launch activities. Responsibilities include leadership, talent development, medical strategy, clinical oversight, scientific expertise, external engagement, and cross-functional collaboration. | — | 0 |
| Alternance 12 mois – Chargé(e) de Pharmacovigilance – F/H This is an apprenticeship role for a Pharmacovigilance Officer at Eli Lilly, focusing on managing and processing pharmacovigilance case information according to company procedures. The role involves data collection, translation, coding, data entry, and quality control of safety data. It requires a Master's degree in Pharmacovigilance, strong English skills, and proficiency in IT tools. | — | 0 |
| Business Unit/Communications Senior Director／部長＜コミュニケーション部/Communications＞ Senior Director of Communications for Eli Lilly Japan, responsible for guiding and leading all product and environmental shaping communications efforts. This role involves developing disease state and consumer communications, supporting data and regulatory milestones, coordinating with global teams, and managing relationships with internal and external partners. The position also includes leading, coaching, and developing a team of communicators, providing media training, and managing issues preparedness. | — | 0 |
| Associate Director, Product Quality & Quality Information (PQQI) Associate Director, Product Quality & Quality Information (PQQI) at Eli Lilly Japan, responsible for setting strategy and leading teams focused on product quality and quality information management throughout the product lifecycle, ensuring compliance with GQP and Japanese regulatory requirements, driving operational excellence, and supporting product launches. | — | 0 |
| Lilly StarT HR Intern Internship role supporting the Human Resources team at Eli Lilly, focusing on core HR operations, employee lifecycle processes, recruitment support, HR metrics tracking, and contributing to HR process improvement, AI, and automation projects. | — | 0 |
| Associate Director - Digital & Data Lead Associate Director - Digital & Data Lead at Eli Lilly, responsible for overseeing and aligning digital programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. The role involves championing digital plant strategy, influencing senior leadership on technology direction, providing input to business and strategic financial plans, and ensuring GxP compliance for all digital solutions. This position requires a deep understanding of manufacturing, lab, and quality processes, and the ability to translate business needs into actionable digital strategies. | — | 0 |
| Regulatory Affairs Associate/Manager-Quality & Operation This role focuses on ensuring the quality and compliance of regulatory affairs activities in China for a global healthcare company. Responsibilities include managing regulatory documentation, implementing company SOPs, coordinating local processes, managing RA systems, and providing training. The role also involves collaboration with internal teams and external vendors, supporting technology development, and conducting compliance monitoring and audits. It requires a bachelor's degree, 1-3 years of experience, strong computer skills, and excellent English communication. | — | 0 |
| Lung Cancer - cMBA Launch Readiness Lead MBA intern role focused on developing a launch plan for a new lung cancer drug, requiring financial and commercial acumen to assess readiness and create an action plan with cross-functional teams. | — | 0 |
| Sr. Director, COO Strategy & Operations - GPS Capabilities This role is for a Sr. Director of COO Strategy & Operations within the Global Patient Safety (GPS) Capabilities function at Eli Lilly. The primary focus is on driving strategic execution, financial stewardship, and organizational effectiveness, with a key near-term objective of orchestrating the PV Affiliate Centralization initiative. The role also involves supporting broader GPS Capabilities pillars through cross-functional alignment, resource planning, stakeholder communications, and leadership meeting governance. It requires a blend of strategic thinking, operational rigor, change management, and executive communication skills within a healthcare context. | — | 0 |
| Medical Affairs Director Switzerland Medical Affairs Director for Switzerland, responsible for providing medical and scientific leadership, strategic direction, and oversight for Medical Affairs activities. This role involves leading and developing the medical team, driving innovation, ensuring scientific excellence, regulatory compliance, and cross-functional collaboration to support pre- and post-launch activities. The position requires an MD with clinical research and/or Medical Affairs experience, leadership skills, and fluency in English. | — | 0 |
| Medical Science Liaison, Oncology, Türkiye Medical Science Liaison (MSL) role focused on Oncology in Türkiye, requiring deep scientific knowledge of disease states and Lilly/competitor compounds. The role involves engaging with scientific experts to facilitate scientific exchange, gather insights, and inform Lilly's research and commercialization strategies. Responsibilities include maintaining scientific expertise, supporting medical/scientific information needs, strategic planning, and territory ownership, all while adhering to compliance and company policies. | — | 0 |
| Associate Director/Director, External Collaborations-1 This role leads pharmacovigilance (PV) strategy with alliance partnerships for Global Patient Safety (GPS). It involves evaluating business deals for safety operational risks and planning for PV system integration of acquisitions/divestitures, defining strategy, performing due diligence, leading negotiations, and ensuring compliance with GVP regulations. | — | 0 |
| Manager/ Senior Manager Medical Science Liaison Manager/Senior Manager Medical Science Liaison role at Eli Lilly, a global healthcare leader. The role focuses on engaging with scientific experts in oncology, providing deep scientific knowledge, and communicating clinical insights to inform Lilly's strategic direction. Requires advanced scientific expertise and strong communication and relationship-building skills. | — | 0 |
| Associate Director, TS/MS Manufacturing CMC Project Management Associate Director, TS/MS Manufacturing CMC Project Management role at Eli Lilly, focused on integrating Manufacturing CMC elements for molecule commercialization and managing the development and implementation of technical plans for commercially manufactured molecules. The role leads cross-functional teams to ensure integrated CMC plans, accelerate medicine delivery, and coordinate Global Product Assessments. It requires strong project management, leadership, and communication skills within the pharmaceutical manufacturing context. | — | 0 |
| Associate Director - Medical Science Liaison (Cardiometabolic) - Nashville, TN The Associate Director - Medical Science Liaison (Cardiometabolic) role at Eli Lilly is responsible for engaging with scientific and clinical experts in a specific therapeutic area to provide in-depth scientific and clinical information. This role involves synthesizing research, responding to medical information needs, and communicating insights to inform Lilly's strategic direction. It requires deep content knowledge, strategic thinking, and field execution. | — | 0 |
| Sr. Director - Medical Affairs Oncology Senior Director, Medical Affairs – Oncology (solid tumor and hematology) is a senior scientific and strategic leader responsible for setting the medical vision and driving cross-functional execution across the oncology therapeutic area (TA). This individual serves as the primary medical authority for the oncology business unit, leading a team of Medical Affairs professionals to deliver evidence-based, patient-centric medical strategies that support peri-launch and lifecycle commercialization of oncology assets. This role combines deep oncology expertise with organizational leadership, requiring the ability to influence at the executive level, partner effectively with Commercial, Regulatory, Clinical Development, Market Access, and external stakeholders, and shape a high-performance culture grounded in scientific rigor, inclusion, and continuous learning. | — | 0 |
| Supply Chain Associate - API EM This role is for a Supply Chain Associate in the External Manufacturing organization, focusing on ensuring reliable supply of medicines through effective supply chain processes. Responsibilities include forecasting, supply planning, purchase order generation, inventory management, and data stewardship within a GMP regulated environment, primarily using SAP. | — | 0 |
| Quality Intern The Quality Intern will support the Quality Department by performing administrative tasks related to product complaints, sample management, and documentation. This role involves translation, sample handling, cargo arrangements, permit drafting, and reconciliation of complaint data. The intern will also assist with archiving and ensuring compliance with global policies and local procedures. | — | 0 |
| Director (m/w/d) Medical Affairs Allgemeinmedizin Cardiometabolic Health Director of Medical Affairs for Cardiometabolic Health in Primary Care, focusing on strategic planning, medical education, and scientific exchange within the German healthcare system. | — | 0 |
| Alternance 12 mois - Chargé(e) de Communication – F/H This is an internship position for a Communications Officer at Eli Lilly in France. The role involves contributing to communication strategy, creating external and internal communication materials, organizing events, and updating institutional information. The ideal candidate is a student in communication with a strong interest in the healthcare field, social media savvy, and good organizational and writing skills. | — | 0 |
| Executive Assistant and Chief of Staff Executive Assistant and Chief of Staff supporting the head of diabetes at Lilly, who is also the VP and site head of Lilly’s Protomer site in Los Angeles. This role provides critical administrative support, manages site initiatives, tracks projects, schedules meetings, and supports visitor arrangements. Requires strong organizational and communication skills. | — | 0 |
| Clinical Design Physician Neuroscience (M.D.) Physician role focused on designing Phase II to Phase IV clinical programs and studies within the neuroscience therapeutic area at Eli Lilly. Responsibilities include translating strategy into clear objectives, representing design optionality, informing protocol design, contributing to asset strategy, and collaborating with cross-functional teams. The role also involves scientific data dissemination, evaluating medical literature, and contributing to organizational learning on clinical design best practices. | — | 0 |
| Senior Director ADME Operations Seeking a Senior Director Operational Leader with strong project management, portfolio operations, and budget governance experience to transform how the DMPK/ADME organization plans, forecasts, tracks, and delivers its book of work. This role involves leading a team, optimizing operational workflows, ensuring accurate forecasting, tracking results, managing budgets, and collaborating cross-functionally. | — | 0 |
| Senior Director Regulatory Strategy Senior Director of Regulatory Strategy at Eli Lilly, focusing on gene-editing programs in early development. Responsibilities include planning, developing, and implementing regulatory strategy, submissions, and compliance activities to support regulatory approvals. The role involves leading regulatory affairs for assigned programs, interacting with global health authorities, and ensuring compliance with regulatory standards. | — | 0 |
| Qualified Person (QP) - (m/w/d) The Qualified Person (QP) is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility, ensuring compliance with GMP, marketing authorization, and current regulations. This role involves continuous quality and regulatory monitoring, analysis of corporate standards, participation in regulatory updates, and oversight of imported products. | — | 0 |
| Sr. Director / Executive E&C Core Capabilities This role is for a Sr. Director/Executive Director of E&C Core Capabilities at Eli Lilly in Shanghai, China. The primary function is to serve as a senior Ethics and Compliance (E&C) Business Partner, providing expert leadership in managing E&C risks and advising on program design, process controls, and risk management. The role involves leading Centers of Excellence for Monitoring & Data Intelligence and Third-Party Organization (TPO) Management, and partnering with business leaders to strengthen controls through risk-based oversight and data-driven insights. The ideal candidate will have over 10 years of experience in ethics and compliance within highly regulated industries, strong analytical capabilities, and the ability to influence senior leaders. Fluency in Mandarin and English is required. | — | 0 |
| Master Planner This role is a Master Planner responsible for creating and managing production plans, inventory, and material requirements within SAP for a pharmaceutical manufacturing facility. It involves close collaboration with regulatory, production, and quality departments to ensure compliance and optimize capacity, with a focus on meeting demand while minimizing inventory costs. The role also includes managing change control and reporting on key supply chain metrics. | — | 0 |
| Alternance 12 mois – Apprenti(e) Associé(e) Affaires Médicales Oncologie– F/H This is an apprenticeship role in Medical Affairs Oncology at Eli Lilly, focusing on supporting medico-marketing activities, scientific literature analysis, and participation in medical unit activities. The role requires a scientific background, autonomy, organizational skills, and proficiency in English and Microsoft Office. | — | 0 |
| Associate Director - Clinical Development Neuroscience Associate Director for Clinical Development Neuroscience at Eli Lilly, responsible for leading and directing teams involved in clinical trials. The role focuses on operational oversight, resource management, and ensuring compliance with regulations and best practices in drug development. | — | 0 |
| CDI-Responsable QA Système Qualité (F/H) This role is for a Quality Assurance System Manager at Eli Lilly's Fegersheim production site. The primary focus is on managing a team, ensuring adherence to quality and safety procedures, managing documentation and quality systems, and resolving operational and technical issues within a pharmaceutical manufacturing environment. It involves leadership, team management, and ensuring compliance with regulations. | — | 0 |
| Alternance - Associé(e) Assurance Qualité - H/F This is an Associate Quality Assurance role within a pharmaceutical company, focusing on maintaining compliance with pharmaceutical regulations, managing product complaints, and contributing to the quality management system. It involves preparing for inspections and audits, and managing documentation. The role requires a background in pharmacy or quality management and proficiency in MS Office and English. | — | 0 |
| Associate Director, Global Intake and Triage Leader Associate Director/Director, Global Intake and Triage Leader at Eli Lilly, responsible for operational leadership of end-to-end intake and triage processes for Individual Case Safety Reports (ICSRs) globally. This role ensures timely, accurate, and compliant receipt, acknowledgment, and initial assessment of adverse event information from all sources, managing global operations, triage, acknowledgment, invalid case assessment, literature screening, and escalation pathways. It requires collaboration with various internal teams and technology partners, people management of manager-level leaders, and support for regulatory inspections. The role demands a strong understanding of global pharmacovigilance regulations and experience with safety databases. | — | 0 |
| Sr. Manager - PRA Senior Manager role in the pharmaceutical industry focused on developing and implementing pricing and reimbursement strategies for the China market. Responsibilities include new product strategy, payer engagement, health economic outcomes research, and cross-functional collaboration. | — | 0 |
| Alternance 12 mois – Chargé(e) des Affaires Médicales en Immunologie - F/H This is an internship position in Medical Affairs for Immunology at Eli Lilly, focusing on supporting medico-marketing activities, scientific literature analysis, and participation in medical unit activities. The role requires a scientific background, autonomy, organizational skills, and proficiency in English and Microsoft Office. | — | 0 |
| Sr Associate / Manager - Clinical Development Trial Lead (Neuroscience) This role leads the cross-functional study team in the development and execution of clinical trials, accountable for delivering trials with quality, on time, and within scope and budget. It requires leveraging project management, regional operational knowledge, clinical trial process leadership, and scientific expertise. | — | 0 |
| Associate - QA API EM This role provides quality oversight of Quality Control activities at Contract Manufacturing organizations (CMs) for Active Pharmaceutical Ingredients (API) External Manufacturing. It involves ensuring compliance with cGMPs, supporting method validation/transfer, and managing quality-related issues with testing. | — | 0 |
| MSL Manager, Türkiye This role is for an MSL Manager in the pharmaceutical industry, responsible for leading a team of Medical Science Liaisons, overseeing their performance, training, and strategic implementation within assigned therapeutic areas. The position requires a health science degree, experience in the pharmaceutical industry, and strong people management and communication skills. | — | 0 |
| Director - Medical, Cardiometabolic Health, Türkiye Director of Medical Affairs for Cardiometabolic Health in Turkey, responsible for providing clinical and scientific input to brand teams, supporting medical launch activities, developing promotional materials, and engaging with healthcare professionals. The role involves responding to customer inquiries, managing thought leader engagement, and contributing to the medical affairs plan. Requires an advanced degree in health sciences with relevant experience, strong communication and interpersonal skills, and fluency in English. Experience in Cardiometabolic Health is preferred. | — | 0 |
| Lilly EnAble Internship Opportunity Internship opportunity for university students with a disability rate of 40% or above, registered with İŞ-KUR, to gain experience in various business functions within the pharmaceutical industry. | — | 0 |
| 〈研究開発・ﾒﾃﾞｨｶﾙｱﾌｪｱｰｽﾞ統括本部〉薬事本部 Policy and Excellence／担当・担当課長・専門課長／神戸本社・東京支社 This role focuses on regulatory affairs within the pharmaceutical industry, specifically managing Japan's regulatory policy and intelligence, ensuring compliance with drug and medical device laws, and driving operational excellence within the regulatory affairs department. It involves building relationships with regulatory bodies, contributing to policy strategy, managing submission processes, and enhancing compliance. | — | 0 |
| Program Manager - GFD Program Manager for Global Facilities Delivery (GFD) at Eli Lilly, responsible for managing large capital asset programs (>$500MM USD) from planning through operational qualification. Focuses on safety, cost, schedule, and quality assurance in pharmaceutical manufacturing facilities, requiring strong project management, communication, and compliance skills. | — | 0 |
| Associate Director - QMS Lifecycle Management (R&D) Associate Director role focused on Quality Management System (QMS) Lifecycle Management within R&D at a pharmaceutical company. The role involves partnering with Global Process Owners to support the integrity and evolution of QMS processes, monitor health, report on metrics, identify improvements, and ensure alignment with global regulatory standards and internal requirements for R&D processes. | — | 0 |
| Associate Vice President, Regulatory Strategy Associate Vice President, Regulatory Strategy role at Eli Lilly (Verve Therapeutics) focused on providing strategic regulatory leadership for gene editing therapies. Responsibilities include overseeing global regulatory strategies, managing regulatory activities (clinical trial applications, IND amendments, safety reporting), providing strategic regulatory input, resolving regulatory issues, advising product teams, and mentoring direct reports. Requires advanced degree, 15+ years of industry experience, and strong regulatory expertise in a fast-paced, innovation-focused environment. | — | 0 |
| Sr. Manager of Regulatory Affairs CMC This role is for a Sr. Manager of Regulatory Affairs CMC at Eli Lilly, focusing on new product registrations and life-cycle maintenance from a Chemistry, Manufacturing, and Controls (CMC) perspective. The individual will drive CMC strategy, prepare dossiers, oversee testing, manage queries, and shape the regulatory environment in China. It requires deep technical expertise in CMC drug development and compliance, with a strong understanding of China's regulations and ICH guidelines. | — | 0 |
| ＜コミュニケーション本部/Communications＞ Corporate Communications, Sr. Manager/課長(P3)/神戸本社/東京支社 This role is a Senior Manager/Manager in Corporate Communications with a digital focus at Eli Lilly, a global healthcare leader. The position is responsible for leading digital-focused corporate communications, managing the corporate website and social media channels, and developing digital content to enhance the company's reputation and brand. It requires strong experience in digital communications, website management, and social media, with a preference for experience in the pharmaceutical or regulated healthcare industry. The role also emphasizes collaboration, agility, and innovation. | — | 0 |