Eli Lilly

The Principal Scientist - Process Translation and Execution at Eli Lilly will focus on translating chemical processes from development labs to pilot plant operations for clinical trial supply. This role involves operating and troubleshooting kilo-scale equipment, applying chemical engineering principles for scale-up, developing models for crystallization and filtration, and ensuring process safety and documentation. The position is part of the new Lilly Medicine Foundry, a center for advanced manufacturing and drug development.

This role focuses on configuring and developing applications on the Tulip platform for global manufacturing, aiming to eliminate paper-based processes. It involves the full delivery lifecycle from requirements to support, with a focus on quality, validation, and compliance. While the role mentions AI/automation use cases and AI-assisted development, its core function is application configuration and deployment within a regulated manufacturing environment, not direct AI/ML model development.

Senior Director role in Construction Capital Procurement for Eli Lilly, a global healthcare leader. The role focuses on leading procurement for major capital projects, including engineering, automation, equipment, and construction services, supporting multi-billion dollar expansion plans. Responsibilities include strategic sourcing, project leadership, client engagement, team development, and ensuring compliance within a regulated environment.

Supervisor for Biologics Operations in the Lilly Medicine Foundry, responsible for leading process operators, overseeing safety and quality, ensuring production schedules are met, and managing employee relations in a GMP manufacturing environment. Requires API supervisory experience and experience in biologics/biotechnology processing.

Associate Director of Engineering (Facilities) for a new API manufacturing facility in Houston, TX. This role will lead strategic planning, development, and execution of all facilities management aspects, including maintenance, reliability, and compliance with GMP operations. The position involves supervising engineers, managing external contracts, and ensuring site facilities meet business needs during the startup and operational phases.

Associate role in Parenteral Operations at Eli Lilly, focusing on implementing and monitoring manufacturing projects, driving process improvements, and ensuring a safe work environment. Requires a Bachelor's degree or equivalent experience in Parenteral Operations.

Senior Director role focused on leading embedded systems, manufacturing technologies, automated assembly processes, and global automation/control strategies for drug delivery systems and pharmaceutical devices within a healthcare company. The role involves functional and strategic leadership, defining and governing assembly solutions, and ensuring scalability, compliance, and robustness.

Perform solutions preparations, chemical tests, and analysis of samples in a QC laboratory setting, following analytical methods and SOPs. Requires knowledge of laboratory analysis, methods, practices, and specific chromatography and wet chemistry techniques.

The Kilo Lab Lead Technician at Eli Lilly supports the startup of a new advanced manufacturing and drug development center (Lilly Medicine Foundry). This role involves bringing manufacturing equipment into service, becoming an expert in assigned areas, and training other technicians. Upon project completion, the technician will provide on-the-floor leadership for API molecule production, ensuring safety and quality. Responsibilities include enforcing compliance, training junior technicians, operating equipment, conducting experiments, dispensing materials, maintaining equipment, leading troubleshooting, and promoting a strong safety culture. The role requires collaboration, creativity, and resilience during the transition from design to operations.

The Lilly Medicine Foundry Kilo Lab Technician supports the startup and operation of a new advanced manufacturing and drug development center. This role involves transferring chemical processes, operating equipment, conducting experiments, and ensuring compliance with safety and quality standards for clinical supply of various drug modalities. The technician will also support troubleshooting and process improvements.

Logistics Intern at Eli Lilly's Sesto Fiorentino manufacturing site, focusing on raw material management, process optimization, data analysis, and team collaboration within a regulated healthcare environment. Requires a Master's in Management Engineering and strong English skills.

Senior Application Support Engineer role focused on providing advanced technical support for a suite of products in the healthcare domain. Responsibilities include troubleshooting, diagnosing, and resolving incidents related to application functionality, integrations, performance, and security, acting as an escalation point for L2 support and customer queries. The role involves collaboration with development teams, monitoring application health, maintaining knowledge base articles, supporting deployment activities, and ensuring compliance with regulations like GDPR and HIPAA.

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.

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.

This role is for a Chemist Laboratory position at Eli Lilly in Puerto Rico. The primary responsibilities include ensuring laboratory compliance with regulations, reviewing analytical results, generating and reviewing laboratory documents, and providing analytical and technical support. Requirements include a Bachelor's or Master's degree in Chemistry, a chemist license, and at least three years of experience in a manufacturing environment. The role emphasizes leadership, customer focus, continuous improvement, computer literacy, teamwork, and strong communication skills. Bilingualism is also required.

Lead Analyst for Cyber Threat Intelligence (CTI) at Eli Lilly, focusing on strategy, operations, and team development. This player/coach role involves hands-on technical leadership in threat analysis and attribution, while also shaping the function's strategy, developing analysts, and representing the team in various forums. Responsibilities include threat actor tracking, brand and executive protection, partner collaboration, intelligence sharing, team leadership, and enhancing tooling for automated enrichment and response workflows.

Supervisor providing leadership and direct management to process operators in the Medicine Foundry operations group, overseeing the production of API molecules with a safety-first, quality-always approach. Responsibilities include enforcing compliance, overseeing operations, leading safety culture, troubleshooting process upsets, reporting safety and quality events, managing shift communications, and ensuring personnel follow cGMP practices.

Associate Director, Clinical Development Trial Lead (CDTL) at Eli Lilly, responsible for leading cross-functional teams in the development and execution of complex clinical trials. This role involves project management, risk assessment, budget management, and ensuring trial quality, timeliness, and adherence to scope and budget. The position requires deep understanding of clinical drug development processes and regulatory requirements to ensure inspection readiness and drive continuous improvement.

Operator role in biotechnology manufacturing, responsible for performing production tasks, following GMP, and ensuring safety and quality. Requires an Associate's degree and experience in fermentation or isolation.

This role is for a Visual Inspection Operator in a pharmaceutical manufacturing site. The primary responsibilities include safely inspecting high-quality pharmaceutical products using Lilly standards, operating automated and semi-automated equipment, and adhering to Good Manufacturing Practices (GMPs). The role requires strong attention to detail, basic math and computer skills, and the ability to work in a manufacturing environment. Experience with GMPs and pharmaceutical manufacturing is preferred.

Associate Director for Biotech Operations at Eli Lilly, leading manufacturing operations and cross-functional process teams in a new, advanced biotech facility. Focuses on daily operations, people management, site leadership, and startup priorities, ensuring safety, quality, and productivity.

Senior/Principal Process Engineer at Eli Lilly focused on API External Manufacturing for Peptides. The role involves providing technical leadership and expertise to contract manufacturers, ensuring reliable supply and commercialization of medicines. Key responsibilities include developing and sustaining process knowledge, coaching team members, leading tech transfers and scale-up, supporting process optimization, ensuring equipment capability, and overseeing health, safety, and environmental (HSE) and process safety management (PSM) elements at contract manufacturing sites. The role requires a strong understanding of chemical engineering principles and experience in a regulated manufacturing environment.

This entry-level role supports the development, configuration, and localization of global manufacturing applications on the Tulip platform, aiming to eliminate paper-based processes. The associate will contribute across the full delivery lifecycle, including requirements, configuration, validation, deployment, and support, while adhering to GxP and data integrity principles. The role also involves exploring AI-assisted development and AI/automation use cases to advance paperless manufacturing goals.

This role is responsible for the overall execution, management, and oversight of assigned clinical trials, ensuring adherence to regulatory requirements, Good Clinical Practice (GCP), and company standard operating procedures. It involves leading cross-functional teams to deliver high-quality clinical trial data on time and within budget.

Automation Technician at Eli Lilly, a global healthcare leader, responsible for equipment performance, first-line production support, mechanical repairs, PMs, and troubleshooting in a GMP manufacturing environment. Requires expertise in production processes, commissioning, qualification, validation, and control system technologies, with experience in instrumentation, PLC/HMI programming, and business software.

This role is for a Maintenance Technician on the night shift at Eli Lilly, a global healthcare leader. The primary focus is to service, repair, and maintain process and utility pharmaceutical manufacturing equipment to improve uptime and efficiency. Responsibilities include troubleshooting, performing repairs, setting up equipment, and documenting actions in a CMMS. The role requires a high school diploma, minimum 2 years of maintenance experience, and the ability to work in a regulated manufacturing environment.

This role focuses on the design, development, and manufacturing of solid drug products within the pharmaceutical industry. It involves applying expertise in formulation, manufacturing processes, and technology platforms, including continuous manufacturing and process analytical technologies, to accelerate drug development and commercialization. The position requires collaboration with cross-functional teams and leadership in technical development and regulatory strategy.

This role is for a Sr. Principal Reliability Engineer in a new advanced manufacturing facility for API molecules. The engineer will be responsible for equipment reliability and maintenance strategy, developing reliability metrics, troubleshooting equipment issues, implementing improvements, and developing maintenance strategies to optimize operations, compliance, cost, and efficiency. The role requires collaboration with Process Engineering and expertise in Maximo CMMS, within a GMP/regulated environment.

The Advisor - Computational Modeling Engineer will provide diverse modeling expertise and develop computational models that drive decisions to design new manufacturing processes and improve existing ones across Lilly's global manufacturing network. This role applies modeling techniques across a broad range of domains — including physical properties, unit operations, scale-up, numerical and multiphysics simulation, discrete event simulation, and resource and operational logistics optimization — to support both continuous/batch process operations and discrete manufacturing operations. A core focus of the role is the development of Digital Twin computational models that provide online modeling capabilities to manufacturing facilities.

This role is for a Process Technician in a pharmaceutical manufacturing setting, focusing on the operation of automated filling equipment for syringes. The responsibilities include ensuring safe operation, maintaining quality standards (cGMP), supporting line leads, and performing area cleaning. It requires experience in a regulated industry and knowledge of manufacturing processes.

This role provides statistical support for drug development in a healthcare setting, focusing on experimental design, analysis, and the development of novel methods. It involves collaboration with scientists and engineers across various disciplines, including chemistry and biology, and requires expertise in statistical software and methodologies. The role also involves communicating results, contributing to regulatory submissions, and potentially developing training materials.

This role supports Parenteral Operations by performing environmental monitoring of manufacturing areas and utility sampling/analysis in a QC laboratory. It involves adherence to cGMP, training other technicians, and participating in continuous improvement projects. Requires a High School Diploma, 2+ years of relevant experience in GMP Pharmaceutical Manufacturing, and experience with Laboratory IT systems.

Reliability Engineer responsible for establishing and executing maintenance and reliability strategies to ensure equipment and process uptime in a regulated healthcare manufacturing environment. This role involves data analysis of key metrics (MTTR, MTBF, OEE), root cause analysis of failures, implementing reliability improvements, and supporting cross-functional teams. Experience with vision systems, CMMS, and regulatory compliance (cGMP, FDA) is preferred.

This role involves performing environmental monitoring and utility sampling in a pharmaceutical manufacturing facility to ensure product safety and efficacy. It requires adherence to cGMP procedures and quality systems, with a focus on aseptic production. The technician will also provide training and support to other team members and participate in continuous improvement projects.

Senior Director of Health, Safety, and Environment (HSE) responsible for developing, implementing, and maintaining HSE programs and systems at a new API manufacturing facility. This role leads the site HSE team, ensures compliance with global and regulatory standards, and contributes to strategic planning during the project delivery and startup phase, focusing on building HSE systems, processes, and culture for GMP operations. Post-startup, the role owns the HSE Management System and ensures ongoing compliance.

Reliability Engineer for Eli Lilly's new Medicine Foundry, focusing on optimizing manufacturing processes and ensuring equipment reliability for drug development and clinical trials. This role supports advanced manufacturing research by maintaining optimal equipment performance and implementing reliability monitoring programs.

This role is for a Quality Assurance professional in the pharmaceutical industry, focusing on product quality testing, documentation, deviation investigation, and process improvement. It involves chemical and microbiological testing, method transfer, and potentially team management for higher-level positions. The role is not directly related to AI/ML development.

This role is for a Laboratory Technician at Eli Lilly in France, focusing on physico-chemical analysis of pharmaceutical products, APIs, excipients, and ACPs. The technician will perform routine and non-routine analyses using various laboratory techniques, manage equipment, prepare reagents and samples, interpret results, and ensure data integrity according to Good Laboratory Practices (GLP) and ALCOA+ principles. Responsibilities also include evaluating quality deviations, revising procedural documents, and proposing solutions for method and equipment optimization. The role requires a Bac +2 or +3 in chemistry or physico-chemistry and significant analytical experience in the pharmaceutical industry.

Associate Analytical Technical Steward in Dry External Manufacturing Quality Control at Eli Lilly. This role involves technical review, interpretation, and release of analytical data from contract manufacturers, stability studies, and process validation. Responsibilities include leading investigations for out-of-specification results, performing root cause analysis, developing investigational testing protocols, and representing quality laboratories on cross-functional teams. The role also supports method validation, transfer, and improvement for marketed products, ensuring compliance with regulatory expectations and quality standards.

This role is for a Process Visual Inspection Technician in a new pharmaceutical manufacturing facility. Responsibilities include supporting commissioning and qualification of automated inspection lines, operating automated and manual inspection equipment, ensuring compliance with Good Manufacturing Practices (CGMPs) and safety standards, and supporting leadership in troubleshooting and operator development. The role requires experience in a regulated industry and familiarity with automated inspection equipment.

This role is for a Sr. Principal Associate for Analytical Quality Assurance at Eli Lilly, focusing on ensuring laboratory activities in the Lilly Medicine Foundry meet global quality standards and cGMP. The position involves quality oversight for GMP testing, analytical development, method verification, qualification, and validation, as well as managing quality systems and investigations for deviations and out-of-specification results. The role requires a strong understanding of analytical methods, quality management systems, and pharmaceutical industry experience.

This role supports laboratory and administrative operations for process development activities in advanced manufacturing for various drug modalities at the Lilly Medicine Foundry. Responsibilities include preparing equipment, running experiments, performing basic analyses, maintaining lab notebooks, and contributing to troubleshooting.

This role is for an Instrumentation/Medium Voltage Electrician responsible for servicing, troubleshooting, and maintaining equipment in utilities at Eli Lilly's manufacturing facilities. The position involves preventive and corrective maintenance on medium voltage electrical equipment, complex electrical equipment, and process instrumentation. It also includes performing modifications, new installations, and diagnosing electrical and instrumentation problems to minimize downtime. The role requires a strong electrical aptitude, compliance with safety and cGMP standards, and good documentation practices.

Scientist responsible for the technical integrity, reliable supply, and compliance of reference standard manufacturing activities within a global healthcare company. This role involves influencing drug development phases by establishing and executing manufacturing strategies for reference standards, ensuring scientific soundness, integration with control strategies, and regulatory compliance. The Scientist collaborates with global teams and external partners, manages projects, and makes decisions regarding manufacturing strategies and technical issue resolution.

Process Technician for a Prefilled Syringe Line in a pharmaceutical manufacturing facility, focusing on safe operation of automated equipment, adherence to GMP, and supporting operational improvements.

Supervisor for a medical device assembly process team, responsible for daily operations including safety, compliance, operator development, scheduling, and issue resolution. This role involves shift leadership in a manufacturing environment with a focus on safety, quality, and productivity.

This is an apprenticeship role within the Utilities/HVAC team at Eli Lilly, focusing on energy efficiency and maintenance of production facilities. The role involves monitoring and improving the performance of energy installations, performing preventive and corrective maintenance, and ensuring safety. It also includes data logging and updating technical documentation. The role is aimed at developing skills in energy management and industrial processes within a healthcare manufacturing context.

Production Line Mechanic responsible for general maintenance support, equipment uptime, and reliability in a cleanroom manufacturing environment. This role involves troubleshooting, performing corrective and preventative maintenance on machinery, and supporting projects related to production and utility equipment, all while adhering to GMP standards and safety protocols.