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 10 new AI-related roles. That is a -60% change versus the prior 30 days (25 → 10).
| Title | Stage | AI score |
|---|---|---|
| Advisor - Project Manager - Global Facilities Delivery Project Manager for Global Facilities Delivery at Eli Lilly, responsible for leading manufacturing capital projects from design to operational verification. Requires 10+ years of experience in capital project delivery in industrial or manufacturing facilities, with a focus on safety, quality, and compliance. | — | 0 |
| Engineer - MES - Lebanon LP1 This role is for an Engineer focused on Manufacturing Execution Systems (MES) in a pharmaceutical manufacturing setting. The primary responsibility is to design, develop, deliver, and qualify the MES solution for a new drug substance manufacturing site. The role involves partnering with automation and operations teams, ensuring operational readiness, adapting project roadmaps, and maintaining system validation. A key requirement is the ability to incorporate AI tools into daily workflows to improve MES recipes and activities, alongside a strong understanding of GMP and regulatory requirements. | — | 0 |
| Sr Director - Business Solutions MQ IT This role is for a Sr. Director of Business Solutions MQ IT at Eli Lilly, focusing on defining and deploying the digital strategy for a new manufacturing facility. It involves integrating various systems like SAP, MES, and Data Historian, ensuring cGMP compliance, and managing the IT/OT footprint. The role requires strong leadership in Pharma IT, with a focus on manufacturing operations and technology. |
| — |
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| Production Operator Lilly Medicine Foundry This role is for a Production Operator at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The operator will support the startup phase of the facility, bringing manufacturing equipment into service, and then oversee the production of API molecules. The role emphasizes safety, quality, and adherence to GMP practices in a pharmaceutical manufacturing environment. | — | 0 |
| Principal - Engineer - Automation (Data & Platforms integration) Principal Automation Engineer - Data & Platforms integration role at Eli Lilly, focusing on designing, delivering, and managing data historian and integration platforms for a new API manufacturing facility. Requires expertise in Aveva PI Data Historian, system integration, validation practices (cGMP, data integrity), and server administration within a pharmaceutical manufacturing context. | — | 0 |
| Principal - Engineer - Automation (DeltaV System Administrator) This role is for a Principal Automation Engineer specializing in DeltaV System Administration within a pharmaceutical manufacturing facility. It involves supporting the design, delivery, validation, and ongoing management of DeltaV DCS platforms, ensuring compliance with cGMP standards and data integrity. The position requires a deep understanding of process automation systems and Lilly's computer system validation practices, with responsibilities including hardware design, administrative procedures, and collaboration with various internal and external stakeholders. The role transitions from project delivery to site-based support for GMP manufacturing operations. | — | 0 |
| Lead Chemical Operator - Peptide Operations Lead Chemical Operator for API manufacturing operations at a new Eli Lilly facility, responsible for production, safety, quality, and compliance in a regulated pharmaceutical environment. | — | 0 |
| Manufacturing Chemical Operator - Peptide Operations This role is for a Manufacturing Chemical Operator at a new pharmaceutical API manufacturing facility. The operator will be responsible for the production of API molecules, maintaining compliance with regulatory requirements, and ensuring equipment is in good operating condition. The role involves monitoring, testing, cleaning, and responding to production issues, with a strong emphasis on safety and quality within a GMP environment. Experience in facility startups and pharmaceutical manufacturing is preferred. | — | 0 |
| Associate Director - Device, Assembly, and Packaging Associate Director of Operations for Device, Assembly, and Packaging in the pharmaceutical industry. Responsibilities include leading operations teams, ensuring production goals, managing cross-functional teams, and presenting to regulatory agencies. Requires experience in pharmaceutical manufacturing, leadership, and understanding of regulatory requirements. | — | 0 |
| Sr. Program Director - Global Facilities Delivery This role is for a Sr. Program Director in Global Facilities Delivery at Eli Lilly, focusing on managing large capital projects (>$1BN USD) in pharmaceutical manufacturing. The role requires extensive experience in project management, interface management, compliance, and safety/environmental execution within regulated facilities. It involves leading cross-functional teams and ensuring projects meet safety, cost, schedule, and quality objectives from planning through operational qualification. | — | 0 |
| Bioinformatics Platform Engineer The Bioinformatics Platform Engineer will operate, improve, and scale scientific computing infrastructure for production bioinformatics workflows in AWS. This role involves supporting and troubleshooting NGS workflows, managing Linux environments, and contributing to infrastructure automation and platform reliability. The engineer will collaborate with scientists to translate workflow needs into scalable solutions and participate in architecture decisions. | — | 0 |
| Lead Calibration Technician Lead Calibration Technician responsible for performing and documenting routine and non-routine instrument calibrations, including maintenance, testing, troubleshooting, and repairs on manufacturing equipment in a GMP/regulated environment. | — | 0 |
| Engineer - Plant Engineering Automation This role focuses on the automation aspects of plant engineering for HVAC, Utilities, and Facilities within pharmaceutical manufacturing. The engineer will develop, implement, and improve process automation solutions, ensuring systems are in-control, capable, and compliant. Responsibilities include defining user requirements, designing system architectures, developing and testing code, managing change control, and ensuring validation documentation is maintained. The role requires experience as a process automation engineer and ideally pharmaceutical and computer system validation experience. | — | 0 |
| QA Manager-Night Shift QA Manager for Night Shift at a new pharmaceutical manufacturing site, focusing on device assembly and packaging. Responsibilities include technical oversight, document approvals, cross-functional collaboration, team management, and ensuring GMP compliance. The role transitions from commissioning and qualification to supporting routine manufacturing operations. | — | 0 |
| Senior/Principal Manufacturing Scientist - Peptides - Lebanon API Senior/Principal Manufacturing Scientist role at Eli Lilly focused on peptide API manufacturing. Responsibilities include providing technical support, executing experimental projects, modeling, data analysis to improve process control, yield, purity, and productivity within a cGMP environment. Requires experience in peptide synthesis or purification technologies. | — | 0 |
| Associate Director Process Engineering - Small Molecule API Associate Director of Process Engineering for Small Molecule API manufacturing, responsible for leading and developing a team of process engineers to ensure compliant and reliable operations in a new, advanced manufacturing facility. The role involves building the organization, implementing business systems, and supporting project delivery during the startup phase, transitioning to operational oversight and continuous improvement post-startup. | — | 0 |
| Senior Director of Engineering – Facilities and Utilities Senior Director of Engineering role focused on facilities and utilities for pharmaceutical manufacturing operations, ensuring infrastructure and leadership support site startup and long-term operations. Responsibilities include guiding GMP systems, building operational readiness, managing evolving responsibilities, and ensuring safety and quality standards. | — | 0 |
| Sr Director - Engineering (Automation, Maintenance, Process) Senior Director of Engineering at Eli Lilly, responsible for leading process engineering, automation, and maintenance for site startup and long-term manufacturing goals in a healthcare/pharmaceutical setting. Focuses on organizational development, functional strategy, safety leadership, and ensuring system readiness for GMP manufacturing. | — | 0 |
| Senior Director - TS/MS Senior Director of Technical Services/Manufacturing Science (TS/MS) overseeing site operations, new product introduction, process development, and optimization within a pharmaceutical manufacturing context, ensuring compliance with cGMP and regulatory standards. This role involves strategic leadership, cross-functional engagement, and people development within a global healthcare company. | — | 0 |
| Sr Director - Operations Senior Director of Operations for a new API manufacturing facility at Eli Lilly, responsible for leading manufacturing operations, building the organization, and ensuring compliance with GMP and regulatory requirements during startup and post-startup phases. | — | 0 |
| Lead Operator Small Molecule - Lilly Medicine Foundry Lead Operator for Eli Lilly's new Medicine Foundry, focusing on advanced manufacturing and drug development for small molecules. This role supports the startup phase of a new facility, ensuring operational readiness, training teams, and eventually providing on-the-floor leadership for API production. Responsibilities include adhering to safety and quality compliance, operating equipment, troubleshooting process upsets, and promoting a strong safety culture within a GMP environment. | — | 0 |
| Principal - QA API External Manufacturing Peptides This role provides Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for products manufactured by third-party partners. Responsibilities include leading quality aspects of external sites, conducting audits, reviewing documents, collaborating cross-functionally, providing QA guidance, developing quality agreements, investigating incidents, and representing Lilly during regulatory inspections. | — | 0 |
| Senior Engineer – Intralogistics System Integration Lead Senior Engineer role focused on technical project management and delivery oversight for intralogistics system deployments in manufacturing. This involves integrating various systems like SAP/EWM, MES, and automation hardware (AGVs, ASRS) to enable autonomous material flow. The role requires developing integrated schedules, coordinating dependencies, and ensuring system requirements are met. | — | 0 |
| Associate Director - Operational Readiness Associate Director of Operational Readiness for a new API manufacturing facility in the pharmaceutical industry. This role involves developing and managing an integrated project plan for facility startup, leading a cross-functional team, and establishing Lean principles for operational excellence. The position requires experience in GMP operations and project leadership within the pharmaceutical sector. | — | 0 |
| Scientist - Sample Management Scientist role focused on developing and maintaining operations for sample preparation, organization, and tracking within a drug discovery environment. Involves managing compound libraries, designing plate preparation, collaborating with global sample management networks, and troubleshooting lab automation systems. The role emphasizes process improvement, data integrity, and safety in a laboratory setting. | — | 0 |
| Sr. Principal Scientist - MES Data and Integration Lead The Sr. Principal Scientist, MES Data and Integration Lead will support the design, deployment, and operation of the Manufacturing Execution System (MES)/Electronic Batch Record (EBR) for a new API manufacturing facility. This role focuses on translating manufacturing requirements into MES solutions, ensuring data governance, and integrating MES with other enterprise systems to support compliant and efficient GMP operations. The role involves working with process data for continuous improvement and performance analytics. | — | 0 |
| Sr. Principal Scientist - MES Process Area Lead This role focuses on the Manufacturing Execution System (MES) and Electronic Batch Record (EBR) for a new, digitally native API manufacturing facility. The Sr. Principal Scientist will lead the MES technical agenda, translate manufacturing requirements into MES solutions, and ensure compliant, data-driven production. The role involves system ownership, support, risk assessment, and developing best practices for MES-enabled operations within a GMP environment. | — | 0 |
| Principal Scientist - Contamination Control Strategy This role supports the design, deployment, and operation of a contamination control strategy in a new pharmaceutical manufacturing facility. It involves ensuring strategies align with technical, quality, and regulatory guidance, applying data-driven decision-making, and improving contamination control performance through innovative technologies. Responsibilities include authoring technical documents, monitoring environmental conditions, investigating contamination events, analyzing trending data, and training staff. | — | 0 |
| PPM Engineer - Packaging - Dry External Manufacturing This role focuses on managing printed packaging materials (PPMs) for contract manufacturers in the pharmaceutical space, ensuring they meet technical and company standards. Responsibilities include managing layouts, metadata, artwork development, and technical changes, as well as participating in testing, investigations, and projects, including digital transformation initiatives within packaging. | — | 0 |
| Advisor – Operations Optimization – Lilly Medicine Foundry This role focuses on operational readiness and continuous improvement in pharmaceutical manufacturing, specifically within the new Lilly Medicine Foundry. It involves analyzing processes, implementing Lean and OpEx principles, managing projects, and ensuring safety and quality in a regulated environment. The role requires strong leadership and cross-functional collaboration to optimize manufacturing processes and support the startup and production phases of the facility. | — | 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 |
| Director - BRD Analytical Development This role is for a Director in Analytical Development within the Bioproduct Research and Development organization at Eli Lilly. The position focuses on leading analytical efforts for pharmaceutical drug substance and drug product development, commercialization, clinical trials, and regulatory submissions. Responsibilities include developing analytical methods, designing stability studies, authoring regulatory documents, and providing technical guidance for external analytical activities. The role requires a strong foundation in analytical sciences and experience in the pharmaceutical industry, with a focus on ensuring the quality and control strategies for various therapeutic modalities. | — | 0 |
| Director/ Senior Director/ Executive Director – Translational PKPD Project Leader This role focuses on leading PKPD project strategy for genetic medicines programs, developing and implementing modeling strategies to enhance decision-making in drug discovery and development. It involves designing, analyzing, and interpreting quantitative pharmacology studies, collaborating with cross-functional teams, and mentoring junior scientists. The role requires expertise in PK/PD and PBPK modeling, experience with relevant software, and a PhD in a related field. | — | 0 |
| Engineer - Data Movement Platforms Administrator This role is responsible for administering, maintaining, securing, and optimizing core data movement and integration platforms like IBM MQ, IBM App Connect Enterprise, Aspera, and Axway B2Bi. The individual will ensure high availability of messaging and file transfer services, automate operational tasks, and provide expert support for data exchange within the organization and with external partners. Key responsibilities include managing IBM MQ environments, supporting integration flows, administering file transfer solutions, configuring secure data exchange, developing automation scripts, implementing security configurations, and troubleshooting complex data flow issues. | — | 0 |
| Reliability Technician - Lilly Medicine Foundry Reliability Technician role at Eli Lilly's new Medicine Foundry, focusing on ensuring equipment availability and performance through predictive maintenance, data analysis, and continuous improvement in a cGMP-regulated manufacturing environment. | — | 0 |
| Automation Technician The Automation Technician is responsible for the performance of automated equipment, providing first-line support to production processes, and supporting area engineering initiatives, process improvements, and project implementation within a pharmaceutical manufacturing environment. This role requires expertise in production processes, commissioning, qualification, and validation requirements, as well as equipment-specific code and control system technologies. | — | 0 |
| Advisor, Project Controls - GFD This role is for an Advisor, Project Controls at Eli Lilly, focusing on managing project controls for large capital programs (>$500MM USD) in global facilities delivery. The responsibilities include leading project controls teams, establishing cost and schedule baselines, managing resources, change control, risk management, and ensuring compliance with finance policies. It requires significant experience in project controls on major industrial or manufacturing projects. | — | 0 |
| Associate Director - Project Controls - GFD Associate Director for Project Controls in Global Facilities Delivery (GFD) at Eli Lilly, focusing on manufacturing network projects. Responsibilities include budgeting, cost control, earned value management, change and risk management, forecasting, and planning. The role involves process improvement, governance, mentoring, and ensuring compliance with finance policies for capital projects. | — | 0 |
| Senior Director - Oncology and Peripheral Imaging Clinical Development This role is for a Senior Director in Oncology and Peripheral Imaging Clinical Development at Eli Lilly. The primary focus is on leading the clinical development of imaging strategies for oncology, immunology, and cardiometabolic diseases, spanning early to late-phase trials. While the role involves evaluating AI in imaging, its core function is in clinical research and development within the healthcare domain, not in building or shipping AI models. | — | 0 |
| Associate Director - TSMS Laboratory Associate Director for a Technical Services & Manufacturing Sciences (TSMS) Laboratory focused on small molecule and oligonucleotide API process troubleshooting and continuous improvement. Responsibilities include leading laboratory staff, designing and executing experiments, managing a safe work environment, hiring and developing staff, and collaborating with cross-functional teams for technology transfer, process validation, and manufacturing operations. The role also involves commissioning new equipment and defining the technical agenda for process capability and yield improvement. | — | 0 |
| Engineer - Automation This role is for an Automation Engineer at Eli Lilly's new manufacturing site in Concord, NC. The engineer will be responsible for automation design, managing system integrators, supporting corporate initiatives like lifecycle management and cybersecurity, and driving automation governance. The role involves evaluating new technologies and innovation trends for application within Lilly. | — | 0 |
| Director - Engineering - Purification & Conjugation Technologies - BR&D Director of Engineering role focused on purification and conjugation technologies within Bioproduct Research and Development (BRD) at Eli Lilly. Responsibilities include providing technical expertise for GMP manufacturing of drug substance, focusing on chromatography, filtration, and bulk unit operations. The role involves developing control systems, performing risk assessments, collaborating with development scientists and manufacturing, evaluating new technologies, supporting tech transfers, mentoring engineers, and ensuring compliance with quality systems and cGMP requirements. Requires a Ph.D. or MS/BS in Chemical Engineering with significant experience in biopharmaceutical downstream processing and equipment design/qualification. | — | 0 |
| Associate Director - TSMS (Oligonucleotides) Associate Director for Technical Services/Manufacturing Support (TSMS) in an oligonucleotide API manufacturing facility. Responsibilities include leading a team, managing production support, implementing technical projects, process optimization, technical transfer, validation, and ensuring GMP compliance. Requires a Bachelor's or Master's in a science field and 5+ years of cGMP commercial API manufacturing experience. | — | 0 |
| Lab IT Systems Lead — Validation & Data Integrity This role focuses on ensuring the validation and data integrity of laboratory IT systems and computerized instruments within a pharmaceutical manufacturing environment. It involves implementing and maintaining systems according to regulatory requirements (cGMP, CSV) and collaborating with various quality and IT teams to ensure compliance and continuous improvement. | — | 0 |
| Director/Senior Director/Executive Director - AAV R&D This role is for a Director/Senior Director/Executive Director in AAV R&D at Eli Lilly, focusing on inventing, characterizing, and advancing novel genetic reagents for clinical applications. The responsibilities include developing AAV therapies, driving data-based decisions, implementing strategic vision, leading screening of AAV technologies, ensuring best practices in model development and validation, and leading a team. The role requires a PhD with 10+ years of industry experience, with a mastery of ophthalmology gene therapy and proven experience in leading gene therapy programs. | — | 0 |
| Instrument Technician - Lilly Medicine Foundry The Instrument Technician role provides process instrumentation maintenance support for the Lilly Medicine Foundry, focusing on equipment availability, calibration, troubleshooting, and reliability in a cGMP-regulated environment. Responsibilities include performing preventative and corrective maintenance, troubleshooting instrumentation, operating test equipment, and supporting new equipment installations. | — | 0 |
| In Vivo Imaging Scientist This role focuses on leading and executing in vivo and PET imaging studies, including experimental design, advanced image analysis, and data interpretation within the healthcare domain. The scientist will integrate cutting-edge imaging technologies and novel agents into research pipelines, collaborate with global leaders, and disseminate findings through publications and presentations. The role requires a Bachelor's or Master's degree with at least 7 years of experience in molecular imaging and a strong publication record. | — | 0 |
| Sr. Advisor - Statistics This role focuses on statistical trial design and analysis within clinical research and development in the healthcare domain. The primary responsibilities include developing protocol designs, writing protocols, selecting statistical methods, analyzing clinical study data, and communicating results. The role requires a Ph.D. in Statistics or Biostatistics with experience in clinical R&D and proficiency in statistical programming languages. | — | 0 |
| Lead Automation Technician Lead Automation Technician role at Eli Lilly, a global healthcare leader, focusing on automated equipment performance, production support, and process improvements in a new state-of-the-art parenteral manufacturing site. Responsibilities include ensuring equipment is maintained, safe, and operated according to cGMPs, investigating production delays, and supporting engineering initiatives. Requires an Associate's Degree or equivalent experience, with preferences for GMP manufacturing, PLC/HMI programming (Studio 5000, FactoryTalk View SE, B&R), and experience with automated equipment and maintenance management systems. | — | 0 |
| Utilities / High Voltage Electrician / Instrumentation This role is for a Utilities / Medium Voltage Electrician / Instrumentation at Eli Lilly, responsible for servicing, troubleshooting, and maintaining electrical and instrumentation equipment within utility systems. The position involves preventative and corrective maintenance on high and low voltage electrical equipment, process instrumentation, and ensuring compliance with safety and cGMP standards. It requires strong electrical and mechanical aptitude, with experience in utility systems and troubleshooting being preferred. | — | 0 |