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 |
|---|---|---|
| PRINCIPAL OPERATIONS ENGINEER - IGA This role is for a Principal Operations Engineer focused on Identity Governance platforms within a healthcare company. The primary responsibilities include managing incident, change, and problem resolution for these platforms, ensuring compliance, and supporting 24/7 operations through on-call rotations. The role requires experience in Identity and Access Management (IAM) and Identity Governance and Administration (IGA), with preferred experience in IT service management, security principles, specific IAM technologies, and scripting languages. | — | 0 |
| Snr. Principal Operations Engineer – IGA Tech lead Senior Principal Operations Engineer to lead and direct the IGA Cork team in the day-to-day management and resolution of identity incidents, ensuring secure and timely access to enterprise resources. This role involves on-call rotation and technical leadership for Identity Governance platforms and services, focusing on incident, change, and problem management, compliance, and risk reduction. | — |
| 0 |
| Senior Associate/ Manager - Clinical Pharmacokinetics Operations Associate (PK/PD) This role supports the operational aspects of drug discovery and clinical development programs by overseeing key PK/PD deliverables, ensuring high quality and on-time delivery. Responsibilities include managing timelines, performing quality checks, overseeing Non-Compartmental Analysis (NCA) activities, providing end-to-end operational support for Phase 1-3 clinical studies, and contributing to process improvement and automation initiatives. Experience with Phoenix WinNonlin or Monolix and clinical pharmacokinetics is required. | — | 0 |
| Analytical QA Senior Associate (QA for QC) This role is for an Analytical QA Senior Associate in a biotechnology manufacturing facility. The primary focus is on providing QA oversight for Quality Control (QC) laboratories and digital systems, ensuring compliance with cGMP, FDA/EMA regulations, and Data Integrity principles. Responsibilities include managing deviations, change controls, risk assessments, and supporting audits and inspections. The role requires a degree in a related scientific discipline and at least 3 years of QA experience in the pharmaceutical or biotech industry. | — | 0 |
| Sr. Manager - Bioanalytical Laboratory This role is for a Senior Manager in the Bioanalytical Laboratory within the Quality Control Laboratory team at Eli Lilly's new Biologics Manufacturing Facility in Limerick, Ireland. The role involves leadership, oversight of the Bioanalytical team, meeting customer goals for cycle time and compliance, developing and maintaining training and performance plans, and reviewing quality documents. It also includes designing, building, and maintaining digital systems for the lab in collaboration with site and external digital teams. Requires a BSc, MSc or PhD in Analytical Sciences with pharmaceutical/biotechnology supervisory experience and knowledge of cGMPs, data integrity, and analytical techniques. | — | 0 |
| Microbiologist - Technical Services/Manufacturing Sciences Microbiologist role focused on contamination control in GMP production areas, supporting microbiological, viral, and environmental monitoring programs. Responsibilities include technical support for facility startup, EMPQ, contamination FMEA, response plans, and product protection control strategy. Requires expertise in microbiology, data-driven decision-making, and continuous process improvement using new technologies and data analytics. | — | 0 |
| Sr Associate - Clinical Laboratory Science This role focuses on clinical laboratory science within the pharmaceutical industry, specifically at Eli Lilly. The Sr. Associate will be involved in the early stages of clinical trial development, coordinating vendor activities, and resolving issues related to clinical laboratory and diagnostic services. They will also provide expertise on assay development, validation, and manage clinical testing plans and study risk oversight. The role requires collaboration with study teams, business partners, and sourcing organizations to ensure high-quality, combinable data in a cost-effective and timely manner. The position is based in Cork, Ireland, and contributes to Eli Lilly's global healthcare initiatives. | — | 0 |
| Associate Director - Clinical Development - Neuroscience Associate Director for Clinical Development in Neuroscience at Eli Lilly, focusing on leadership and direction for clinical trials, ensuring high performance, and driving cross-functional collaboration. The role involves business planning, resource management, trial management expertise, and ensuring training and compliance with GCPs and SOPs within a regulated healthcare environment. | — | 0 |
| Apprenticeship - Electrical Instrumentation (QQI Level 6) Apprenticeship role focused on electrical instrumentation maintenance within a regulated GMP environment at a pharmaceutical manufacturing site. Responsibilities include supporting repair, replacement, installation, and maintenance of equipment, working with industrial control systems, interpreting schematics, and analyzing system faults. | — | 0 |
| Apprenticeship - Mechanical Automation & Maintenance Fitting (QQI Level 6) Apprenticeship role focused on mechanical automation and maintenance fitting within a regulated GMP environment to support production activities. Responsibilities include installation, repair, and maintenance of plant and machinery, working with various machine tools, and understanding technical drawings. | — | 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 |
| 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 |
| 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 |
| Cyber Intelligence Analyst The Cyber Intelligence Analyst role at Eli Lilly focuses on active defense within Global Cyber Defense Operations (GCDO). Responsibilities include monitoring, analyzing, investigating, and responding to cybersecurity events and incidents, managing the attack surface, producing threat intelligence, and ensuring readiness and detection capabilities. The role involves supporting various cybersecurity functions, developing capabilities, documenting analysis, identifying security issues, prioritizing threats, and recommending strategic changes. Rotational on-call availability is required. | — | 0 |
| Process Cleaning Representative This role is responsible for supporting the cleaning program for process equipment and ancillary components in a new Biotech Drug Substance Manufacturing Facility. Responsibilities include developing cleaning strategies, authoring validation plans and protocols, executing protocols, authoring procedures, and troubleshooting cleaning processes. The role requires a BSc in Engineering or Science with 2 years of experience in a pharmaceutical/biopharmaceutical manufacturing site. | — | 0 |
| Senior Manager - QC Support Senior Manager for Quality Control Support in a pharmaceutical setting, focusing on team leadership, GMP compliance, and digital system management within QC operations. | — | 0 |
| Senior Associate/Lead - Competitive Continuous Improvement (CCI) Coach This role focuses on driving continuous improvement and operational excellence within a pharmaceutical manufacturing setting, primarily using Lean principles and digital tools. It involves facilitating the implementation of daily management systems, leading system design and governance, and partnering on improvement initiatives to enhance safety, quality, productivity, and cost. | — | 0 |
| Sr Director - Project Management - Global Facilities Delivery This role is for a Sr. Director of Project Management within Global Facilities Delivery at Eli Lilly, focusing on delivering large capital assets for medical innovation and medicine supply chains. The position requires leading cross-functional teams to manage projects from conceptual design through operational qualification, ensuring safety, cost, schedule, and quality. Key responsibilities include stakeholder communication, compliance with company policies, and developing safety/environmental execution plans. The role is based in various locations including the Netherlands and US, with travel flexibility required. | — | 0 |
| Senior Application Security Engineer Senior Application Security Engineer responsible for integrating security testing tools into the SDLC, partnering with engineering teams on secure coding, and coordinating vulnerability remediation. The role involves developing and implementing application security strategies, performing threat analysis, and ensuring secure configurations for containers. | — | 0 |
| Sr. Principal Scientist - Regulatory GRA-CMCD This role focuses on developing and executing post-approval CMC regulatory strategies for Eli Lilly's global commercial portfolio, ensuring compliance with global CMC regulatory requirements for pharmaceutical manufacturing and product registrations. It involves strategic planning, submission preparation, and providing technical and regulatory expertise to manufacturing and quality teams. | — | 0 |
| Process Permitting This role is for a Process Permitting role at a new biotech manufacturing facility. The primary responsibility is to provide safety leadership and expertise for the permit to work program, including drafting, reviewing, and authorizing various types of permits. The role also involves reviewing hazards and controls, ensuring personnel competence, and supporting emergency response and maintenance activities. Basic requirements include a trade qualification and experience in GMP manufacturing and operations/engineering. | — | 0 |
| Sr Associate / Manager - Clinical Development Trial Lead Oncology This role leads cross-functional study teams in the development and execution of clinical trials, focusing on quality, timeliness, and budget adherence. It requires strong project management, operational knowledge, and scientific expertise within the drug development process. | — | 0 |
| Sr Associate / Manager - Clinical Development Trial Lead (Immunology) This role leads cross-functional study teams in the development and execution of clinical trials, ensuring quality, timeliness, and adherence to scope and budget. It requires strong project management, regional operational knowledge, and scientific expertise within the drug development process. | — | 0 |
| Sr. Associate / Manager - Clinical Development Trial Lead (Cardiometabolic Health) This role leads cross-functional study teams in the development and execution of clinical trials, ensuring quality, timeliness, and adherence to scope and budget. It requires project management, regional operational knowledge, and scientific expertise to drive trial deliverables and manage risks. | — | 0 |
| Supervisor - Production Supervisor for a Next Generation Biotech Drug Substance Manufacturing Facility, focusing on leadership, people management, and ensuring compliance with GMP manufacturing standards. The role involves direct supervision of production operators, employee relations, team development, and promoting a culture of quality and safety. | — | 0 |
| Senior Principal/Principal Bioprocess Engineer Senior Principal/Principal Bioprocess Engineer role at Eli Lilly in Limerick, Ireland, supporting the expansion of a Next Generation Biotech Drug Substance Manufacturing Facility. The role involves providing engineering subject matter expertise for design, construction, and startup, focusing on process engineering fundamentals, continuous improvement, and root cause analysis. | — | 0 |
| Operator Logistics Centre 23 Month Contract | — | — |
| Associate / Sr. Associate/Manager – CTRS - | — | — |