Eli Lilly
Pharma · Pharma
- HQ
- Indianapolis, US
- Founded
- 1875
- Size
- 35,000+
- Website
- lilly.com
Currently tracking 36 active AI roles, up 67% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $58k–$345k (avg $175k).
| Title | Stage | AI score |
|---|---|---|
| Associate Director - Source to Pay Center of Excellence - Data and Analytics This role leads a data and analytics team focused on the Source to Pay (S2P) value chain within a healthcare company. The responsibilities include delivering actionable insights, building scalable data products, enabling self-service analytics, and evolving the S2P data strategy using Microsoft Fabric. The role involves applying advanced analytical methods, developing predictive and prescriptive capabilities, and leading a team of data professionals. While AI is mentioned as an area to explore for future capabilities, the core focus is on data strategy, architecture, and analytics delivery for procurement, P2P, and TPRM processes. | — | 2 |
| Laboratory Analyst Laboratory Analyst role in a Next Generation Biotech Drug Substance Manufacturing Facility, focusing on cell-based assay quality control. Responsibilities include executing analytical procedures, maintaining cell cultures, managing digital systems, reporting results, instrument qualification, methodology development/validation, deviation investigations, and inventory management. Requires expertise in GMP/GLP, cell culture, virology, bioassays, and instrument platforms. |
| — |
| 0 |
| Senior Laboratory Analyst (Sr. Specialist - Analytical) Senior Laboratory Analyst role at Eli Lilly focused on executing analytical procedures, maintaining digital systems, reporting results, and validating methodologies in a pharmaceutical manufacturing environment. Requires a BSc in Analytical Sciences with pharmaceutical experience and knowledge of various analytical techniques and instrument platforms. | — | 0 |
| Associate / Senior AssociateGlobal Regulatory Affairs-Cork-Regulatory Delivery & Excellence-Global Publisher This role is responsible for executing and maintaining global regulatory submissions throughout the product lifecycle, coordinating the creation and legalization of submission documents, and ensuring adherence to regulatory agency electronic common technical document (eCTD) specifications. The role requires technical proficiency in publishing tools like RIM, Adobe Acrobat, Lorenz, and ISIToolbox, and involves collaboration with various internal and external stakeholders to ensure timely and compliant submissions. | — | 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 |
| Expert Specialist - Clinical Development This role provides technical and project administrative support for clinical trial execution at Eli Lilly. Responsibilities include managing study budgets, ordering and tracking supplies, tracking enrollment data, maintaining study files and documentation for regulatory inspections and submissions, and managing clinical trial systems by inputting and updating study timelines and generating reports. The role requires a two-year degree or equivalent experience and proficiency in various software packages. | — | 0 |
| IAM SecOps Engineer - PKI & Encryption This role is for an IAM SecOps Engineer focused on Public Key Infrastructure (PKI) and encryption services within a large enterprise. The engineer will be responsible for designing, implementing, and securing these technologies, managing certificate lifecycles, key management, and cryptographic standards. The role involves partnering with various stakeholders to ensure secure and compliant operations. | — | 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 Associate/Manager - Clinical Trial Project Management, Exploratory Medicine This role is a Senior Associate/Manager for Clinical Trial Project Management within Exploratory Medicine at Eli Lilly. The primary focus is on leading cross-functional teams to develop and execute clinical trials, ensuring quality, timeliness, and adherence to budget and scope. Responsibilities include project planning, timeline and risk management, budget oversight, investigator training coordination, enrollment strategy, vendor management, and ensuring the Trial Master File is up-to-date. The role requires a strong understanding of the drug development process and clinical trial operations. | — | 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 |
| Associate Director/Director, GRA-CMCD Diagnostics Regulatory Scientist - IVD Studies and Clinical Trial Support This role is responsible for assessing, establishing, and operationalizing the regulatory strategy and execution plan for assigned IVD performance studies and for clinical trials that use IVDs, ensuring compliance with EU IVDR and applicable national requirements. The role involves developing regulatory documents, supporting interactions with regulatory agencies, and providing expertise on IVD regulations for clinical trials. | — | 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 |
| Upstream Bioprocess Scientist (Senior/Principal) - Technical Services/Manufacturing Sciences Senior/Principal Upstream Bioprocess Scientist at Eli Lilly in Limerick, Ireland, focusing on technical support for manufacturing processes, data-driven decision-making, and continuous process improvement in upstream bioprocessing. Requires expertise in cell culture, process monitoring, statistical methodologies, and regulatory compliance within the biopharmaceutical industry. | — | 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 |
| Associate - Delivery Lead Team Associate role focused on the end-to-end coordination, execution, and quality oversight of Recruitment & Retention (R&R) materials and appreciation item workflows in support of clinical trials. Responsibilities include managing vendors, overseeing documentation and approvals, and ensuring timely delivery of trial-ready materials. | — | 0 |
| Associate Director Procurement - API External Manufacturing Associate Director of Procurement for API External Manufacturing at Eli Lilly, responsible for managing contract manufacturing organizations (CMOs) for API production. The role involves developing category strategy, leading negotiations, managing contracts, and ensuring supply chain risks are addressed within the pharmaceutical industry. | — | 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 |
| Associate / Senior Associate - Trial Capabilities - Spanish Speaking Associate/Senior Associate role focused on clinical trial site initiation and management, requiring regulatory document submission, budget negotiation, contract management, and ensuring site compliance. The role involves communication with sites, regulatory authorities, and internal teams, with a strong emphasis on compliance with regulatory, data privacy, financial, and legal requirements. Fluency in both English and Spanish is required. | — | 0 |
| Senior Associate - QA Materials Management This role is a Senior Associate in QA Materials Management within a pharmaceutical manufacturing facility. It focuses on overseeing quality assurance for material receipt, batch disposition, and related processes, ensuring compliance with GMP regulations. Responsibilities include managing change controls, deviations, CAPAs, documentation, and participating in audits, with a strong emphasis on quality systems and regulatory requirements in the pharmaceutical/biotechnology sector. | — | 0 |
| Analyst Purchase to Pay Global Disbursements (Spanish / Portuguese) This role is an Analyst in Purchase to Pay (P2P) for Global Disbursements, focusing on managing payment processes, bank relations, and accounting for rejected/returned payments. It requires fluency in English and Spanish or Portuguese, with experience in SSC/GBS P2P (Treasury & payments). The role involves supporting team members, owning processes like Cash In Transit, liaising with global project teams, and ensuring compliance with SOx and other regulations. | — | 0 |
| Purchase to Pay Invoicing (Spanish/ Portuegues) - 12 month Fixed Duration Contract This role is for a Purchase to Pay (P2P) Analyst specializing in invoicing, responsible for processing third-party invoices, resolving vendor issues, and ensuring compliance with company policies and KPIs. The role requires fluency in English and Spanish or Portuguese, and experience in accounts payable or a similar operations environment. Desirable skills include SAP, ARIBA, and e-invoicing experience. | — | 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 |
| Warehouse Supervisor Warehouse Supervisor role at a new Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. Responsibilities include leading Warehouse Operators, ensuring safe and efficient daily operations, optimizing workflows, supporting continuous improvement, and developing the team. The role involves direct supervision, oversight of inbound/outbound activities, inventory management, and ensuring compliance with GMP, safety, and environmental standards. | — | 0 |
| Snr Associate/Manager - People Development This role supports the management, implementation, and maintenance of a cross-functional learning strategy to enhance organizational capabilities within GBS, aligning with emerging business needs. It involves the full HRD cycle (design, development, implementation, evaluation) and focuses on leadership and people development, including adapting to AI-enabled environments. | — | 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 |
| Operator Logistics Centre Operator for a logistics center in a biopharmaceutical manufacturing environment, responsible for materials management, inventory control, and shipping compliance within a regulated setting. Requires experience with SAP/MES systems and adherence to GMP/GDP standards. | — | 0 |
| SecOps Engineering – Identity Governance Tech Lead This role is for a Technical Lead in Security Operations Engineering focusing on Identity Governance and Identity Operations within a global healthcare company. The position involves technical leadership, team development, operational excellence, incident management, and ensuring secure access to enterprise resources. It requires participation in an on-call rotation to support a follow-the-sun model and maintain 24/7 operational resilience for identity platforms and services. The role is not directly related to AI/ML model development or research. | — | 0 |
| SecOps Engineer - Identity Governance and Administration This role is for a SecOps Engineer focused on Identity Governance and Administration (IGA) within a global healthcare company. The engineer will be responsible for the day-to-day operations, incident management, change management, and problem resolution of IAM platforms and services, ensuring secure and timely access to enterprise resources. Key responsibilities include monitoring system performance, responding to alerts, maintaining system documentation, collaborating with IT teams, and supporting audit and compliance requests. The role also involves on-call rotation and weekend shifts. | — | 0 |
| Senior/Principal Bioprocess Engineer - Single Use (Consumables) This role supports the design, procurement, and ongoing support of Single Use Technology for a new biopharmaceutical manufacturing facility. It involves developing strategies, flow diagrams, specifications, and managing vendor relationships to ensure efficient and high-quality manufacturing processes. The role also supports commissioning, qualification, and operational activities, including extractables and leachables assessments. | — | 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 |
| Cloud Security Engineer Cloud Security Engineer responsible for managing cloud security tools, conducting security reviews, developing IaC/policy as code, and implementing security controls in a multi-cloud environment (AWS/Azure). The role involves creating integrations and automations for security detection and response, and collaborating with various stakeholders to ensure secure cloud adoption. | — | 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 |
| Associate Director - Biotech Operations Eli Lilly is seeking an Associate Director for Biotech Operations in Limerick, Ireland, to lead a new, advanced manufacturing facility. This role involves providing technical leadership, managing daily operations, ensuring safety and quality, and building and developing a team. The position requires strong GMP manufacturing experience, leadership skills, and the ability to collaborate with cross-functional teams during the facility's startup phase, focusing on implementing new technologies and processes. | — | 0 |