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 |
|---|---|---|
| Post-Doctoral Scientist or Engineer - TSMS This role focuses on developing technical solutions for spray drying in pharmaceutical particle manufacturing. It involves operating pilot scale equipment, designing and executing experiments to understand the impact of parameters on particle size and morphology, developing analytical techniques for measurement, and refining models for atomization and drying. The goal is to identify and solve manufacturing needs, present findings, and publish research. | — | 0 |
| Instrumentation Technician Instrumentation Technician responsible for maintenance, calibration, troubleshooting, and installation of instrumentation systems in a new API manufacturing facility. The role ensures equipment availability and compliance with cGMP standards during pre-startup, startup, and post-startup phases. | — | 0 |
| Scientist - TS/MS Parenteral - Visual Inspection The Scientist - TS/MS Parenteral role at Eli Lilly focuses on technical transfer, process validation, and maintaining the validated state of parenteral operations, specifically in visual inspection. This role involves establishing and monitoring metrics, harmonizing control strategies, evaluating process improvements, and serving as an escalation point for operational issues. It requires authoring and executing protocols, conducting root cause investigations, and providing technical leadership for the Parenteral Process Team. The role also involves supporting manufacturing components, equipment, and operations, representing the team in communications, leading risk management activities, and providing technical support for investigations and quality/stability issues. Key deliverables include preparing technical documents, developing and reacting to statistically based metrics, identifying opportunities for process improvement, driving stability strategy, and providing audit support. |
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| Lead Operator - Utilities This role is for a Lead Operator in Utilities at a new Eli Lilly manufacturing facility. The primary responsibility is to ensure the uninterrupted generation and distribution of utility services (water systems, boilers, chillers, etc.) to support GMP manufacturing. The role involves daily monitoring, testing, cleaning, troubleshooting, and ensuring compliance with regulatory requirements in a regulated environment. Experience in facility/area start-up and understanding of cGMP are preferred. | — | 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 |
| Sr. Associate – Value & Access This role focuses on securing market access for Lilly products by demonstrating their value throughout the reimbursement lifecycle. Responsibilities include implementing access strategies, developing submission dossiers, owning the value proposition for payers, and managing HEOR planning and pharmaco-economic models to support product reimbursement. | — | 0 |
| Corporate Automation Program Lead – API Drug Substance This role leads the design and delivery of automation for major capital projects in pharmaceutical manufacturing, specifically for Active Pharmaceutical Ingredient (API) production. It involves managing workstreams, suppliers, and ensuring compliance and qualification within a global engineering team. | — | 0 |
| Director, Clinical Pharmacology and Translational Modeling This role focuses on clinical pharmacology and translational modeling for gene editing therapeutics in the cardiovascular space. It involves leading the development and execution of strategies across preclinical and clinical development, including dose selection and regulatory filings. The role utilizes advanced modeling techniques like PBPK, population PK/PD, QSP, and exposure-response analysis to inform drug development decisions and regulatory submissions. | — | 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 |
| Senior Advisor, Clinical Research, Oncology This role is for a Senior Advisor, Clinical Research in Oncology at Eli Lilly, focusing on providing medical expertise for clinical strategy and execution in China. The responsibilities include collaborating on clinical development strategy, interacting with health authorities, developing evidence generation plans, supporting brand commercialization, contributing to payer partnerships, leading medical meetings, and establishing external collaborations. The role requires a Medical Doctor with experience in clinical research or medical advising in the pharmaceutical industry. | — | 0 |
| Director - Biologics Process Translation & Execution Lilly Medicine Foundry Director level role in Eli Lilly's Medicine Foundry, focused on advanced manufacturing and drug development for biologics and other modalities. The role involves leading a team of scientists and engineers to drive scientific excellence, accelerate manufacturing advancements, oversee technology transfer, implement control strategies, and ensure right-first-time clinical manufacturing. It requires technical oversight, documentation, risk mitigation, process stewardship, deviation investigations, and collaboration with cross-functional teams and external partners. The role also involves defining and leading the site's technical innovation strategy for manufacturing capabilities. | — | 0 |
| Senior Director - API Operations Senior Director of Operations for a new API manufacturing facility, responsible for leading manufacturing operations, building the organization, developing GMP systems, and ensuring compliance with regulatory requirements during the startup and post-startup phases. | — | 0 |
| Sr. Principal Engineer - Bioprocess Seeking a Sr. Principal Bioprocess Engineer to support a new monoclonal antibody manufacturing facility. Responsibilities include facility start-up (design reviews, process safety, C&Q support, SOP development, tech transfer) and post-start-up support (continuous improvement, root cause analysis, equipment performance monitoring, control strategy development). | — | 0 |
| Responsible Scientist – Quality Control Microbiology Lab (m/w/d) Responsible Scientist role in a Quality Control Microbiology Lab at Eli Lilly, focusing on in-depth problem solving, investigation of aberrant data, technical review, and mentoring lab staff within a GMP manufacturing environment. The role involves ensuring the quality of raw materials, in-process, and finished products. | — | 0 |
| (Sr.) Medical Science Liaison This role serves as a scientific and clinical expert in a specific therapeutic area, facilitating scientific exchange between Lilly and healthcare professionals. The MSL provides in-depth, cutting-edge scientific and clinical information, synthesizes research, and communicates insights to inform Lilly's strategic direction. Responsibilities include supporting researchers and practitioners, acting as a primary interface between Lilly Medical and external experts, partnering with clinical development for studies, managing territory, and synthesizing actionable insights. | — | 0 |
| Technician - Quality Assurance - Parenteral (m/w/d) The role is for a Quality Assurance Technician in a new parenteral manufacturing facility. Responsibilities include on-site quality monitoring during production shifts, material/equipment preparation, formulation and aseptic filling, visual inspection, supporting batch release, GMP documentation, and investigating deviations. The role requires a science/technical background, knowledge of cGMP, and experience in pharmaceutical QA/QC. | — | 0 |
| Director - Software Product Management, LillyDirect - Silicon Valley Hub Visionary Director, Software Product Management to lead strategy, development, and execution of digital product portfolios for LillyDirect in Silicon Valley. This role is pivotal in shaping the future of Lilly's digital products—driving transformational outcomes through customer-centric design, modular architecture, and operational scalability. As a senior product leader, you will define and own the strategies and roadmaps for digital product portfolios designed to meet user needs while delivering innovative technology solutions that advance the company’s mission. | — | 0 |
| Director Engineering - Synthetic Molecule Design and Development Director of Engineering role focused on synthetic molecule design and development for pharmaceutical drug substances and products. Responsibilities include leading teams in unit operation development, process optimization, scale-up, and technology transfer, with a focus on clinical trials, regulatory submission, and commercialization. Requires strong chemical engineering background and experience in process development from mid-cycle to commercialization. | — | 0 |
| Engineer - Automation Engineering – Control System Data Analyst- Lilly Medicine Foundry This role is for an Engineer - Automation Engineering – Control System Data Analyst at Eli Lilly's Medicine Foundry. The individual will provide data engineering and analytics solutions for the Automation Engineering organization, focusing on maintaining, configuring, and troubleshooting automation control systems and interfaces. Responsibilities include developing analytics strategies, creating visualizations and dashboards, supporting system qualification, ensuring compliance with regulatory requirements (GAMP, 21 CFR Part 11, Data Integrity), and collaborating with various teams to optimize manufacturing processes. | — | 0 |
| Engineer - Project Engineer-Design Lead Project Engineer-Design Lead role at Eli Lilly, focusing on leading the design delivery for capital projects within the Global Facilities Delivery organization. Responsibilities include ensuring designs meet standards, coordinating with A/E firms, managing design schedules, and resolving design-related issues in pharmaceutical manufacturing environments. | — | 0 |
| Alternance 24 mois - Double diplôme Ingénieur Pharmacien, PHARMAPLUS - F/H Alternating contract for an "Ingénieur Génie des Procédés" (Process Engineering Engineer) at Eli Lilly, focusing on supporting injectable product manufacturing and managing technology transfer projects. The role involves analyzing production events, identifying corrective actions, coordinating project activities, and conducting studies. | — | 0 |
| Sr. Director, Medical Affairs - Neuroscience This role is for a Sr. Director of Medical Affairs in Neuroscience at Eli Lilly, focusing on leading the Therapeutic Area (TA) strategy, partnering with cross-functional groups for product commercialization, and driving the execution of TA strategic initiatives. It involves medical and scientific leadership, defining and executing strategic integration, managing cross-functional partnerships, fostering a culture of inclusion and innovation, and leading the generation of Real-World Evidence (RWE) and local data. | — | 0 |
| Associate Vice President - Global Facilities Delivery Projects Associate Vice President - Global Facilities Delivery Projects at Eli Lilly, responsible for leading and managing multibillion-dollar capital projects in the healthcare sector, from planning through operational verification. The role involves managing staff, ensuring safety and environmental compliance, and representing Lilly to external partners. | — | 0 |
| Sr. Computational Statistician This role focuses on statistical analysis for clinical trials within the healthcare domain, requiring expertise in statistical methods, programming (SAS, R), and collaboration with study personnel and regulatory bodies. It is not directly involved in building AI/ML models but uses statistical tools for data analysis and reporting. | — | 0 |
| Advisor– API/DS Network Contamination & Bioburden Control Strategy This role focuses on overseeing and harmonizing technical programs for contamination control strategies in pharmaceutical API manufacturing. It involves direct network oversight, influencing peers and external manufacturers, and ensuring control strategies align with technical, quality, and regulatory guidance. The position also supports building technical capability, engaging with R&D, and providing technical support for new product introductions and external manufacturing transfers. Key responsibilities include understanding contamination control requirements across diverse platforms, influencing industry and regulatory expectations, providing technical support during design and start-up, and supporting regulatory applications. | — | 0 |
| ExploR&D Clinical Program Lead-China This role is a Clinical Program Lead in the ExploR&D organization at Eli Lilly, focusing on managing external collaboration projects in drug discovery and development. The role involves leading cross-functional teams, defining project strategy, managing timelines and budgets, and serving as the primary liaison between Lilly and external biotech collaborators. While the company mentions 'AI/ML tools' as part of its Catalyze360 initiative, the core responsibilities of this specific role are in traditional drug development program management, not in building or directly applying AI/ML models. | — | 0 |
| ＜製造本部＞Proces Engineer/担当-担当課長/P1-P3/西神工場 Process Engineer role focused on establishing, maintaining, and improving manufacturing processes and equipment in a pharmaceutical manufacturing environment. Responsibilities include ensuring safety, technical expertise, troubleshooting, data analysis for optimization, process improvement initiatives, and collaboration with cross-functional teams. Requires engineering degree, strong communication skills, and adherence to safety and quality standards (cGMP). | — | 0 |
| Packaging Expert - Engineer/ Scientist This role is for a Packaging Expert - Engineer/Scientist at Eli Lilly in Germany, focusing on device assembly and packaging operations. Responsibilities include technical transfer, process validation, maintaining validated states, establishing metrics, harmonizing control strategies, evaluating process improvements, and providing technical leadership. The role also involves mentoring, floor-level support, risk management, technical documentation, and supporting investigations and audits. Requires a Bachelor's degree in engineering or packaging science with 4+ years of manufacturing experience, preferably in pharmaceutical/medical device packaging. | — | 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 |
| Advisor - Technical Steward - TSMS This role at Eli Lilly is for an Advisor - Technical Steward in their TSMS function, focusing on the stewardship and site transfer of commercial molecules for API manufacturing. The position requires extensive experience in cGMP small molecule, peptide, or oligonucleotide API commercial-scale manufacturing, with responsibilities including technical oversight, process troubleshooting, authoring technical reports, and ensuring compliance with GMP and regulatory requirements. The role supports the startup and validation of new facilities and drives continuous improvement in manufacturing processes. | — | 0 |
| Sr. Director - API Manufacturing Quality Assurance This role is for a Sr. Director of Quality Assurance in API manufacturing at Eli Lilly. The primary focus is on ensuring compliance with cGMP standards, managing the QA team, overseeing quality systems, and preparing for regulatory inspections in a pharmaceutical manufacturing environment. It does not involve AI/ML development or research. | — | 0 |
| < コーポレートアフェアーズ本部 > Sr. Director – Government Affairs (P5), Tokyo, Japan Sr. Director of Government Affairs in Japan responsible for national policy and advocacy strategies, stakeholder relationships, and influencing regulatory/legislative outcomes to support business objectives. Also oversees Innovation Readiness programs, identifying and addressing policy barriers and opportunities in the healthcare/pharmaceutical sector. | — | 0 |
| Sr. Principal Process Engineer - Oligonucleotides This role is for a Senior Principal Process Engineer in API manufacturing for oligonucleotides at Eli Lilly. The position involves technical leadership, mentoring, process optimization, and supporting the startup of a new advanced manufacturing facility. The focus is on building the organization, systems, and culture for GMP manufacturing operations. | — | 0 |
| Sr. Director- Packaging This role is for a Sr. Director of Packaging at Eli Lilly, responsible for operational leadership in device packaging at the Research Triangle Park site. It involves ensuring effective delivery, supporting site leadership, partnering with various departments, developing processes, and interacting with regulatory agencies. The role requires significant engineering and management experience in manufacturing, particularly in device assembly and packaging operations. | — | 0 |
| Associate Director – Ethics and Compliance Internal Investigations – Asia Pacific Associate Director for Ethics and Compliance Internal Investigations in the Asia Pacific region, responsible for conducting investigations into potential violations of company policies, developing investigative plans, preparing reports, and collaborating with other departments. Requires experience in compliance, investigations, HR, audit, or litigation, preferably in the pharmaceutical or biotech industry. | — | 0 |
| Alternance 12 mois - Ingénieur/Pharmacien gestion de projet - H/F Alternating contract for an engineer/pharmacist in project management within the Packaging & Devices department at Eli Lilly's Fegersheim production site. Responsibilities include contributing to machine impact analyses, participating in new format qualification, coordinating cross-functional teams, updating documentation, managing project timelines, identifying process improvements, and standardizing operating procedures. | — | 0 |
| ALTERNANCE 2 ou 3 ans - BUT en Génie électrique et Informatique Industrielle, Option Electricité et Maîtrise de l'Energie (F/H) Apprenticeship for electrical engineering and industrial IT, focusing on electrical network maintenance and energy equipment for an industrial site. Develops skills in electrical safety, industrial maintenance, electrical design, and energy consumption management. | — | 0 |
| Sr. Director - Quality Control Laboratories This role is for a Sr. Director of Quality Control Laboratories at a new Eli Lilly manufacturing facility. The position involves administrative leadership for quality laboratories, ensuring appropriate capabilities and business processes are developed, and leading an organization that supports quality control and analytical laboratories. The facility will utilize automation for analytical capabilities, including in-process testing, stability, and process monitoring. The role requires expertise in analytical operations, quality systems, and leadership experience. | — | 0 |
| Alternance 24 mois - M1 M2 Supply Chain F/H This is an apprenticeship role (24 months) in Supply Chain Management at Eli Lilly's Fegersheim production site. The role involves learning product line planning, analyzing customer needs, developing optimized production schedules in SAP, communicating with internal teams, and participating in continuous improvement projects for planning processes and tools. The position is for Master's level students (M1/M2) and requires proficiency in Office Suite and SAP, strong organizational and analytical skills, and good communication abilities in French and English. | — | 0 |
| Director/Sr. Director—Immunology Research Cutaneous Biology This role is for a Director/Sr. Director in Immunology Research focused on Cutaneous Biology within the healthcare domain. The primary responsibilities involve providing scientific guidance, leading research projects for skin and hair disorders, contributing to external innovation and business development due diligence, identifying and validating novel targets, guiding the design and implementation of preclinical models, and managing a research team. The role requires a PhD with 10+ years of experience in biotech or pharma, with preferred qualifications including experience leading discovery programs, knowledge of the dermatology therapeutic landscape, and expertise in cutaneous biology. | — | 0 |
| Engineer - Design Lead Lead the design delivery for capital projects in pharmaceutical manufacturing, ensuring compliance with engineering standards, regulatory requirements, and project specifications. Coordinate with A/E firms, manage design schedules, and resolve design-related issues. | — | 0 |
| Advisor - Corporate Architect This role is for an Advisor - Corporate Architect at Eli Lilly, focusing on managing the architectural process for global facility delivery. The responsibilities include integrating with engineering teams, developing facility assessments, programming, and designs, contributing to site master planning, and representing Lilly as the lead architect in design phases. The role also involves developing workplace strategies, ensuring architectural design consistency and compliance, coordinating information flow, leading architectural design governance, and supporting value engineering. The position requires a Registered Architect with a minimum of 10 years of experience in architecture and construction project management within pharmaceutical processes. | — | 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 |
| Lab Analytical Automation Scientist This role focuses on designing, developing, and integrating high-throughput analytical automation modules (e.g., PCR, LC, LC/MS) to support chemistry and biology automation workcells. The scientist will partner with external vendors and internal teams to ensure robust data quality, operational reliability, and seamless integration with other systems, ultimately accelerating data generation for drug discovery. | — | 0 |
| RNA synthetic automation specialist The role focuses on designing, optimizing, and operating automation platforms for RNA therapeutics research, bridging wet-lab biology and automation engineering to create efficient systems for RNA synthesis, purification, quality control, and functional assays within a healthcare setting. | — | 0 |
| Director - Analytical Chemistry Director of Analytical Chemistry at Eli Lilly, focusing on the development of synthetic drug substances and drug products from pre-clinical to commercialization. This role involves leading analytical efforts within multidisciplinary teams, managing a small team of analytical scientists, developing analytical methods, justifying specifications, designing stability studies, and ensuring compliance with regulatory requirements. The position requires strong technical expertise in analytical chemistry and pharmaceutical sciences, along with people leadership and collaboration skills. | — | 0 |
| Senior Manager - Qualitätssicherung – Parenteral (m/w/d) Senior Manager of Quality Assurance for Parenteral production at a new high-tech pharmaceutical manufacturing site in Alzey, Germany. The role involves leading the operational QA organization, supporting the startup and routine operation of the facility, overseeing quality aspects, and developing a strong quality culture. Responsibilities include managing a team, ensuring compliance with cGMP regulations, and collaborating with cross-functional teams. | — | 0 |
| (Sr.) Manager-Country Study Management The Country Study Manager (CSM) provides clinical operational expertise for country-level study operations, driving initiation, enrollment targets, quality oversight, and timely delivery of study deliverables. The role also involves contributing to process improvements and change management within ongoing business objectives. | — | 0 |
| Director/Sr. Director/ Executive Director - Medicinal Chemistry This role is for a leader in Medicinal Chemistry at Eli Lilly, focused on optimizing molecules into drug candidates. The position involves scientific and people leadership, overseeing a portfolio of small molecule programs, mentoring teams, and making strategic decisions. While the role mentions utilizing AI/ML for data analysis and compound prioritization, its core function is in drug discovery and development within the healthcare domain, not in building or advancing AI/ML models themselves. | — | 0 |