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. Principal - Engineer - Automation (Small Molecule) This role is for a Sr. Principal Automation Engineer focused on the design and delivery of the DeltaV platform for a new API manufacturing facility. The position involves leading automation DCS functions, collaborating with various teams, and supporting GMP manufacturing operations post-project delivery. Experience with Emerson DeltaV and API/Drug Substance manufacturing is preferred. | — | 0 |
| Clinical Research Lead - Immunology, Investigator Engagement (West Coast) Clinical Research Lead responsible for driving clinical trial execution through investigator engagement and site performance management in the Immunology therapeutic area. This role requires deep therapeutic and scientific knowledge to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies. | — | 0 |
| Supervisor - Planning and Scheduling - Lilly Medicine Foundry Supervisor for Planning and Scheduling at Eli Lilly's Medicine Foundry, overseeing maintenance planning and craft scheduling in a cGMP and FDA-regulated environment. Responsibilities include managing a team, ensuring safety and quality compliance, and coordinating maintenance activities with operations. |
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| Deputy Project Controls Lead This role is for a Deputy Project Controls Lead at Eli Lilly, focusing on managing project controls for large capital programs in manufacturing facilities. The responsibilities include establishing cost and schedule baselines, managing resources, change control, risk management, and financial policy compliance. It requires experience in project controls on major industrial or manufacturing projects and proficiency with project management systems. | — | 0 |
| Principal Scientist/ Senior Principal Scientist, Large Molecule Biology This role focuses on designing and executing in vitro and ex vivo studies to advance oncology targets through the drug discovery pipeline. Responsibilities include performing biological assays, developing and validating bioanalytical methods, conducting flow cytometry, and collaborating cross-functionally. The role requires expertise in mammalian cell culture, pharmacology, and experience with biologic modalities. | — | 0 |
| Director - Clinical Research Scientist Director - Clinical Research Scientist at Eli Lilly (Verve subsidiary) to lead clinical trial efforts for gene editing therapies targeting cardiovascular disease. Responsibilities include developing clinical strategy, ensuring regulatory compliance, overseeing trial execution, analyzing data, and contributing to regulatory submissions and publications. The role requires deep understanding of clinical pharmacology, biomarkers, and regulatory guidelines (FDA, ICH, CPMP, GCPs). | — | 0 |
| Associate, Device Assembly / Packaging Associate, Device Assembly / Packaging role at Eli Lilly, a global healthcare leader. This position focuses on implementing and monitoring projects within the manufacturing process, leading improvement initiatives, and acting as a liaison between operations and support groups. The role requires a Bachelor's Degree in a science-based field and experience in Device Assembly/Packaging Operations, with a strong emphasis on safety and root cause analysis. | — | 0 |
| Associate Director – TS/MS Central Team Associate Director for a new central team supporting pharmaceutical manufacturing operations, focusing on components, materials, annual product review, and visual inspection qualifications. The role involves leading and mentoring technical staff, ensuring a safe work environment, providing technical guidance, managing GMP documentation, overseeing supplier interactions, and collaborating across functions to implement the technical agenda and business objectives. Requires a Bachelor's degree in a scientific discipline, 5+ years of pharmaceutical manufacturing experience, and 3+ years of team leadership experience. | — | 0 |
| Utilities Automation Engineer The Utilities Automation Engineer will be responsible for the maintenance, reliability, and optimization of utilities and facilities automation machine controls, integrations, and data at the Lilly Kenosha County campus. This hands-on role involves troubleshooting, root cause analysis, system improvements, and ensuring compliance with cGMP and HSE standards. The engineer will act as a Subject Matter Expert (SME) for various automation systems (BMS, EMS, QBMS, Clean Utility) supporting HVAC and utilities systems. | — | 0 |
| Utilities Process Engineer The Utilities Process Engineer will be a Subject Matter Expert (SME) for HVAC and Utilities systems (GMP and non-GMP) in a pharmaceutical manufacturing facility. Responsibilities include ensuring systems are in alignment with industry and company standards, supporting risk assessments, monitoring utility systems, providing technical assistance, troubleshooting equipment failures, and ensuring compliance with Health, Safety, and Environmental policies. The role requires a Bachelor's degree in Engineering or related field, technical understanding of HVAC and Utilities, knowledge of cGMP, and proficiency with relevant software and systems like TrackWise and CAPA. | — | 0 |
| QC Lab Technician QC Lab Technician at Eli Lilly responsible for technical support, testing, and quality systems within a device manufacturing laboratory, ensuring compliance with regulations and supporting product release. | — | 0 |
| Site Compliance Leader The Site Compliance Leader at Eli Lilly is responsible for managing compliance to all regulatory requirements for next-generation biotech facilities. This role involves overseeing quality systems and processes, providing quality and technical expertise, and ensuring adherence to corporate quality standards and initiatives. The position requires extensive experience in quality assurance within the biotechnology or pharmaceutical manufacturing environment and a strong understanding of regulatory compliance. | — | 0 |
| Process Technician - Formulation/Filling/Material Prep (Nights) This role operates highly automated equipment for filling syringes in a pharmaceutical manufacturing facility, ensuring compliance with Good Manufacturing Practices and safety standards. It involves learning formulation operations and potentially transitioning to Filling or Material Prep roles. The position requires adherence to safety policies, SOPs, and quality control, with a focus on troubleshooting, supporting leadership, and driving departmental objectives. | — | 0 |
| Engineer - Process This role supports the development of key solutions or process improvements for Lilly manufacturing processes or industry-defined subjects. The Engineer - Process is expected to bring expertise and knowledge to lead development processes through research, PEC laboratory experimental efforts, and direct interactions with manufacturing sites, development, and functional areas. The role provides technical leadership, guidance, and support to sites and external manufacturing organizations, supports major capital projects, and networks with the external community. Key responsibilities include providing engineering technical leadership globally in transport phenomena and fermentation engineering support, collaborating cross-functionally to direct discipline activities, new technology development, assessments, and deployment, and assisting with technical evaluations, technology assessment, and specific problem resolution. The role also involves developing experimental programs, protocols, and models, supervising laboratory experiments, preparing technical reports, and leveraging external resources to stay current in technology expertise. | — | 0 |
| Associate Director/Director – Risk Management Scientist Global Patient Safety Associate Director/Director role focused on risk management and patient safety within the pharmaceutical industry, requiring strategic guidance, development, and maintenance of risk minimization strategies, and collaboration with cross-functional teams and regulatory bodies. | — | 0 |
| Manager-Technology Implementation Specialist – Global Medical Information Contact Centers Manager-Technology Implementation Specialist for Global Medical Information Contact Centers at Eli Lilly. This role leads the deployment of digital technologies to improve customer experience and operational efficiency in contact centers worldwide. It involves bridging business strategy and technical execution, managing implementation projects, stakeholder relationships, budgets, and timelines, and ensuring technology adoption drives business outcomes and regulatory compliance. | — | 0 |
| Sr. Director, MSL Leader, CMH Mid Atlantic This role is for a Sr. Director, MSL Leader in the CMH Mid Atlantic region at Eli Lilly. The primary responsibility is to lead and manage a team of Medical Science Liaisons (MSLs), providing national field strategic leadership and ensuring effective interactions with Scientific and Clinical Experts. The role involves people leadership, field coaching, TA expertise, strategy integration, and operational excellence, ensuring compliance with all applicable policies and regulations. | — | 0 |
| Sr. Director, MSL Leader, CMH West This role is for a Sr. Director, MSL Leader in the CMH West region for Eli Lilly, a global healthcare company. The position focuses on leading and managing a team of Medical Science Liaisons (MSLs), providing strategic field leadership, and ensuring effective interactions with Scientific and Clinical Experts. Responsibilities include people leadership, development, field coaching, TA expertise integration, and operational excellence, ensuring compliance with regulations. | — | 0 |
| Senior Associate / Manager, Clinical Development Trial Lead (CDTL) This role leads the cross-functional study team in the development and execution of clinical trials, managing timelines, risks, and budgets. It requires knowledge of drug development processes, clinical trial leadership, and scientific expertise, with a focus on ensuring quality, timeliness, and adherence to budget and scope. The role also involves managing relationships with third-party organizations and ensuring compliance with global and regional regulations, Good Clinical Practice (GCP), and Lilly standards. | — | 0 |
| Manager - Discovery Operations, Early-Stage Oncology Manager in Discovery Operations (Operational Project Manager) experienced in external contract enablement, licensed biological material procurement/transfer, vendor relationship management, and domestic and international supply chain coordination, with some knowledge of third-party qualification processes. The role supports Oncology discovery portfolio by managing contractual and procurement enablement, prioritizing requests, and identifying operational risks. | — | 0 |
| Lead Process Technician - QA Floor Support This role provides daily quality assurance support and oversight for GMP operations in pharmaceutical manufacturing, focusing on ensuring adherence to quality systems, reviewing documentation, and supporting production functions. | — | 0 |
| Principal/Sr. Principal Logistics Engineer The Principal/Sr. Principal Logistics Engineer at Eli Lilly will support the design, implementation, and continuous improvement of logistics and material flow systems at a manufacturing site. This role involves working with automated systems like ASRS and AMRs, SAP EWM integration, and developing business processes to create a digitally enabled logistics environment. Responsibilities include managing material flow, system performance monitoring, developing SOPs, and supporting operational readiness and ongoing operations. | — | 0 |
| Director Process Chemistry SMDD Director of Process Chemistry at Eli Lilly, focusing on the development, optimization, and commercialization of synthetic active pharmaceutical ingredients (APIs) and drug products. The role involves leading cross-disciplinary teams, managing external R&D, overseeing tech transfer, and ensuring regulatory compliance within the pharmaceutical sector. | — | 0 |
| Process Systems Engineer Seeking a Process Systems Engineer to apply computerized model-based solutions to accelerate the development of new medicines. Responsibilities include designing and optimizing pharmaceutical manufacturing processes using modeling, simulation, and data analysis, developing computational tools, and training others. The role involves collaborating with multidisciplinary teams, managing external manufacturing networks, and ensuring compliance with regulations. | — | 0 |
| Sr. Director - Quality, Concord Senior Director of Quality responsible for overseeing the Quality Management System, ensuring compliance with cGMPs, policies, and standards for parenteral manufacturing, device assembly, and packaging. The role involves strategic direction, quality objectives, continuous improvement projects, and leading/responding to regulatory inspections. | — | 0 |
| Scientist, Dissolution & Biopharmaceutical Modeling Scientist role focused on developing analytical methods and conducting experiments for early clinical formulation development of synthetic drug molecules, collaborating with formulation scientists and biopharmaceutical modeling scientists to guide drug product development from research through commercialization. Emphasizes safety, quality, regulatory, GLP/GMP, and authoring regulatory documents. | — | 0 |
| Director, Vaccine Formulation Development The Director, Vaccine Formulation Development at Eli Lilly will lead the formulation and process development of vaccines, including recombinant protein antigens, emulsion- or aluminum-based co-formulated vaccines, and antigen-display nanoparticles. This role involves supporting drug product development, bringing in new formulation technologies, and working with cross-functional teams to ensure immunogenic, stable, and patient-centric vaccine drug products. The position requires a PhD, 10 years of experience in vaccine drug product development, and demonstrated leadership in program management and regulatory submissions. | — | 0 |
| Director, Analytical Chemistry Extended Characterization This role is for a Director of Analytical Development at Eli Lilly's subsidiary, Verve Therapeutics, focusing on building and leading a team to develop next-generation analytical methods for RNA drug substances and LNP drug products. The position involves hands-on experience with biophysical techniques and supporting late-stage development and commercialization of gene editing programs, including regulatory submissions and GMP validation. | — | 0 |
| Sterility Assurance Scientist , Technical Services / Manufacturing Sciences This role focuses on sterility assurance within pharmaceutical manufacturing, ensuring cleanliness and contamination control in manufacturing processes. Responsibilities include environmental monitoring, aseptic processing, cleaning and sanitization, and data analysis to identify trends and improve strategies. The Principal level involves technical leadership, mentoring, and supporting broader company initiatives. This is not an AI/ML role. | — | 0 |
| Scientific Director — Synthetic Process Chemistry (Peptides & Small Molecules) Scientific Director for Synthetic Process Chemistry at Eli Lilly, focusing on peptide and small molecule drug substance development. The role involves hands-on bench work, leading a team, optimizing synthetic routes, implementing green chemistry solutions, and transferring processes to manufacturing facilities. Requires expertise in Liquid Phase Peptide Synthesis (LPPS) and a strong publication record. | — | 0 |
| Advisor Process Analytical Technologies for Biologics Lilly Medicine Foundry The Process Analytical Technology (PAT) Advisor will lead PAT strategies for biologic drug substance production at the Lilly Medicine Foundry, focusing on implementing and utilizing PAT tools for in-line monitoring and process control. This role involves collaborating with development and manufacturing teams, supporting automation integration, and ensuring cGMP compliance. | — | 0 |
| Associate Director - eCOA Delivery Associate Director for eCOA Delivery at Eli Lilly, responsible for end-to-end planning, coordination, and delivery of electronic Clinical Outcome Assessment (eCOA) activities for clinical trials. This role involves managing project plans, cross-functional hand-offs, vendor deliverables, and risk mitigation to ensure timely and quality execution of eCOA builds and go-lives on the eCOA platform, adhering to GCP and 21 CFR Part 11 regulations. | — | 0 |
| Manufacturing Associate - Advanced Manufacturing Eli Lilly is seeking a Manufacturing Associate for a new, cutting-edge facility focused on advanced therapies like Gene Therapy. This role involves performing routine manufacturing activities in GMP areas, supporting equipment qualification, developing procedures, and ensuring safe and quality production. The position is crucial for the startup of a greenfield manufacturing site, contributing to both clinical and commercial supply. | — | 0 |
| Associate Director - Quality Assurance - Device Assembly Associate Director, Quality Assurance for Device Assembly at Eli Lilly, responsible for leading the QA team, overseeing process development, operational readiness, qualification, and validation of combination product device assembly and operations. Focus on building a strong quality culture and ensuring compliance. | — | 0 |
| Supply Chain Operations/OSSCE/Project Management Eli Lilly is seeking a Supply Chain Operations Specialist to manage projects, drive continuous improvement using Lean/Six Sigma, act as a SAP WM Classic SME, coordinate OSSCE, and steward Power BI analytics for warehouse and supply chain functions. | — | 0 |
| Associate/Sr. Associate/Manager - Lilly Ventures Tech Investing Associate to support and execute Lilly Ventures Tech Investing strategy, focusing on direct equity investments, fund-of-funds investments, and value pull-through. Responsibilities include data analytics, opportunity triage, reporting, and process optimization within the biotech and health tech innovation space. | — | 0 |
| Operator-Filling/Manufacturing (Night Shift)-2 Operator role in pharmaceutical manufacturing (filling/aseptic operations) on night shift, focusing on safety, quality, and productivity. Requires high school diploma, computer proficiency, and ability to troubleshoot. Experience in GMP, aseptic filling, and automated equipment is preferred. | — | 0 |
| Lead Specialist - Operations Training (Nights) This role is for an Operations Training Specialist at Eli Lilly, a healthcare company. The primary focus is on developing, creating, and implementing training programs for parenteral operations, particularly aseptic filling. Responsibilities include evaluating existing employees, onboarding new hires, and ensuring personnel are trained to perform tasks. The role emphasizes safety, quality, and continuous improvement in the training environment. | — | 0 |
| Manager - Operational Readiness Manager role focused on operational readiness for a new advanced API manufacturing facility in Houston, TX. Responsibilities include leading cross-functional teams, defining scope, managing schedules, and ensuring alignment with project master schedules and GMP startup requirements. Requires project management experience and a background in manufacturing, preferably in pharmaceuticals or biotechnology. | — | 0 |
| Sr. Director - eCOA Program Lead This role is a Sr. Director level Program Lead for eCOA (electronic Clinical Outcome Assessments) within a specific therapeutic area at Eli Lilly. The role involves leading the strategy, delivery, governance, and continuous improvement of eCOA capabilities, serving as a senior point of contact between eCOA teams and clinical development stakeholders. Responsibilities include advising leadership, anticipating needs, resolving complex issues, managing escalations, contributing to platform strategy and roadmap, ensuring inspection readiness, and driving capability development. The role requires a strong background in clinical data management or drug development within the pharmaceutical/biotech/CRO industry, with preferred qualifications including experience with modern data technologies like AI/ML, RPA, and cloud systems, as well as familiarity with regulatory requirements like GCP and 21 CFR Part 11. | — | 0 |
| Principal Statistician - Manufacturing This role is for a Principal Statistician in Manufacturing at Eli Lilly, a global healthcare leader. The primary focus is on applying statistical expertise to support the manufacturing of current and new products and processes. Key responsibilities include designing experiments, establishing control strategies and regulatory specifications, evaluating process capability, and collaborating with cross-functional teams. The role requires a Master's degree in Statistics and at least 3 years of experience in industrial statistics, with a strong preference for CMC experience and proficiency in statistical software. | — | 0 |
| Quality Assurance Representative – Commissioning, Qualification & Commercialization (CQC-Q) Quality Assurance Representative with 5-7+ years of experience in medical device and combination product manufacturing, technical transfer, and contract manufacturer oversight. Responsibilities include QA oversight for manufacturing process design, validation, and readiness, ensuring compliance with global regulations and standards (FDA, ISO, EU MDR, etc.). Requires experience with contract manufacturers, cross-functional team influence, and strong communication skills. Computer System Validation (CSV) support and participation in risk management and audits are also key. | — | 0 |
| Scientist, TS/MS - Device Assembly Scientist role supporting the implementation of technical objectives for automated device assembly lines in a pharmaceutical manufacturing facility. Responsibilities include analyzing equipment/process data, monitoring production metrics, authoring protocols, process improvement, and root cause investigations. | — | 0 |
| Associate Director - IT Systems Delivery Lead The Associate Director - IT Systems Delivery Lead at Eli Lilly will oversee and align multiple programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. This role involves program management, release train engineering, GxP compliance, stakeholder management, risk management, and resource allocation within a pharmaceutical manufacturing context. The position requires a strong understanding of project management methodologies and experience in Pharma and GMP Manufacturing. | — | 0 |
| Senior Director/Executive Director - SMDD Late Stage Small Molecule Chemistry This role is for a Senior Director/Executive Director in Late Stage Small Molecule Chemistry at Eli Lilly, focusing on drug substance process development, scale-up, and commercialization. It involves leading a team, managing resources (including CMOs), ensuring safety, and providing strategic guidance on synthetic technologies. The role requires a Ph.D. or BS with equivalent experience in a relevant field and 10+ years of CMC experience in late-phase development and commercialization. | — | 0 |
| Process Technician - Filling (Days) This role is for a Process Technician responsible for the safe operation of automated filling equipment and performing area cleaning in a pharmaceutical manufacturing setting. The technician must adhere to Good Manufacturing Practices and safety standards, support leadership in operator development, and identify operational improvements. Experience in regulated industries, particularly pharmaceuticals, is preferred. | — | 0 |
| Engineer - Automation This role focuses on developing and implementing automation solutions and process control engineering for bioprocess systems within a healthcare/pharmaceutical setting. The engineer will leverage process automation and IT technologies, with a strong emphasis on data historians (AVEVA PI System) and data integration, to enable data flow for process development, manufacturing, and tech transfer. Responsibilities include system administration, troubleshooting, change control, and ensuring compliance in a GMP environment. | — | 0 |
| Facilities Coordinator - Lilly Medicine Foundry The Facilities Coordinator at Eli Lilly's Medicine Foundry is responsible for providing engineering and maintenance coordination support, overseeing contractor resources, managing work orders, and ensuring facilities meet safety and business needs within a regulated GMP environment. This role involves project management for small capital or maintenance projects and ensuring compliance with CGMP policies. | — | 0 |
| Validation Engineer/Scientist The Validation Engineer/Scientist role at Eli Lilly is responsible for developing and supporting the validation of production equipment and systems, with a focus on temperature mapping, cleaning, and sterilization validation strategies for parenteral drug products. This role involves technical support for manufacturing processes, data analysis using statistical principles, and ensuring compliance with cGMP manufacturing standards within the healthcare domain. | — | 0 |
| Senior Director, Commercial Insights & BD Forecasting This role is for a Senior Director of Business Development Forecasting & Analytics in the healthcare industry. The primary focus is on leading end-to-end commercial assessments for licensing, acquisition, and partnership opportunities, and building forecasting infrastructure. This involves developing expertise in new therapeutic areas, leading primary market research, and building flexible forecasting models. The role requires strong financial modeling skills and the ability to influence senior executives. | — | 0 |