Eli Lilly

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.

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

The Sr. Specialist - Engineering role focuses on the operational monitoring and maintenance of automated warehouse systems (ASRS, conveyors, AGVs) within a pharmaceutical manufacturing environment. Responsibilities include first-line support, maintenance execution, commissioning, qualification, validation, and ensuring equipment operates safely and in compliance with cGMPs. The role also involves identifying and implementing process improvements and technical support for engineering teams.

The Sr Specialist- Warehouse - Engineering is responsible for on-shift monitoring and response for warehouse automation systems, including ASRS, conveyors, and AGVs, supporting manufacturing processes. The role involves first-line support, maintenance, commissioning, qualification, validation, and engineering initiatives focused on improving equipment reliability and operational effectiveness within a cGMP environment.

This role is for a Sr. Principal Engineer in Process (Critical Utilities) at Eli Lilly's new API manufacturing facility in Houston, TX. The position focuses on providing engineering support for facility start-up, design reviews, process safety, and operational readiness. Responsibilities include developing and implementing control strategies for utilities systems, supporting initial operations training, and continuous improvement of equipment and processes. The role requires a Bachelor's degree in engineering and 7+ years of experience in pharmaceutical manufacturing operations.

This role is for a Principal Automation Engineer focused on Building Management Systems (BMS) for a new API manufacturing facility. Responsibilities include system design, delivery strategy, testing, commissioning, and post-startup support for GMP manufacturing operations. The role requires collaboration with various internal and external teams and experience with automation platforms like Rockwell, JCI Metasys, or Siemens Desigo.

Senior Director of Analytical Development and Quality Control for diagnostic radiopharmaceutical products and associated precursors. Responsible for overseeing analytical development and quality control functions, driving strategies, ensuring business goals are met, and providing strategic leadership for the AD/QC organization. Focuses on scientific, operational, and compliance excellence, team leadership, cross-functional collaboration, and operational management. The role involves developing and validating analytical methods, managing QC activities, and authoring CMC documents for regulatory submissions.

This role at Eli Lilly focuses on designing, validating, and monitoring inspection, primary packaging, and secondary packaging processes within pharmaceutical manufacturing. It involves creating technical documents, identifying root causes for quality issues, developing CAPA, and ensuring compliance with internal and external standards and regulatory requirements. The role also includes leading projects for operational excellence, supporting contract manufacturers, and collaborating with global sites. While data analysis and team management are preferred, the core responsibilities are process engineering and quality assurance in a regulated healthcare environment.

This role focuses on computational chemistry and molecular design within the drug discovery process at Eli Lilly. While it mentions AI and machine learning as areas to stay updated on, the core responsibilities involve structure-based design, lead optimization, and collaboration with medicinal chemistry and structural biology, rather than building or deploying AI models directly. The role is primarily focused on the early stages of drug discovery (lead optimization).

Associate Vice President role at Eli Lilly focused on technical leadership for biopharmaceutical process and drug product development. Requires extensive experience in drug development, regulatory submissions, and collaboration with cross-functional teams in the healthcare sector.

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.

This role is a Process Safety Management technical resource within the Engineering Technology Center at Eli Lilly, providing expertise on mechanical integrity, pressure relief hazards, and process hazard reviews to support manufacturing and capital projects in the pharmaceutical industry.

Develop, optimize, and execute analytical methods for characterization of raw materials, RNA drug substances, and LNP products. Role involves testing non-GMP samples to support development studies and serving as a CMC representative on project teams. Requires hands-on experience with various analytical techniques and assay development for gRNA, mRNA, and LNPs, with familiarity of ICH regulations.

This role is for a Sr. Principal Site Molecule Steward at Eli Lilly's new manufacturing site in Alzey, Germany. The position focuses on providing scientific leadership and technical support for drug product manufacturing, acting as a subject matter expert for the site. Responsibilities include ownership of control strategy implementation, technical direction on deviations and change controls, and representing the TS/MS function in regulatory interactions. The role requires a minimum of a bachelor's degree in science or engineering and 5 years of experience supporting parenteral product manufacturing.

Eli Lilly is seeking a Utilities Operator for their new Gene Therapy manufacturing facility in Lebanon, Indiana. This role is responsible for ensuring the uninterrupted generation and distribution of utility services (gray, clean, and plant utilities) to support manufacturing operations. The position involves operating and maintaining various utility systems, adhering to SOPs and regulatory requirements (cGMP), and collaborating with other teams during startup and post-startup phases. The role requires mechanical aptitude, basic computer skills, and the ability to work in a regulated environment.

Eli Lilly is seeking a High Voltage Electrician - Instrument Technician for their new API manufacturing facility in Lebanon, IN. The role involves servicing, troubleshooting, and maintaining electrical equipment (4160V, 480V) and process instrumentation, ensuring cGMP compliance and safety. This is a hands-on role critical to the startup and operation of a greenfield manufacturing site.

Lead Technician - HVAC role at Eli Lilly, a global healthcare leader, focused on maintaining and repairing HVAC systems in a new, advanced pharmaceutical manufacturing facility in Lebanon, IN. Responsibilities include leading a team, ensuring compliance with GMP and safety regulations, troubleshooting, preventive maintenance, and documentation for critical equipment like chillers and air handling units. Requires strong mechanical and electrical knowledge, leadership experience, and EPA certification, with a preference for experience in regulated environments.

Lead Operator for a new pharmaceutical manufacturing facility (Lilly Medicine Foundry), focusing on bringing equipment into service, training teams, and providing on-the-floor leadership for API production. Ensures adherence to safety, quality, and environmental compliance, operates processes according to batch records, and troubleshoots production issues.

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.

This role focuses on automation engineering for laboratory and analytical equipment within a pharmaceutical manufacturing setting. The engineer will provide automation support, mentor a team, and ensure reliable and compliant control applications and systems. Responsibilities include technical leadership, overseeing design and implementation of control systems (DCS, SCADA, MES, LIMS), commissioning, validation, and troubleshooting. The role emphasizes operational excellence, organizational capability, and adherence to GMP and regulatory requirements.

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.

Senior Bioanalytical Scientist to lead a broad portfolio spanning small molecules, biologics, ADCs, and cell & gene therapy modalities. Responsibilities include establishing bioanalytical strategy, guiding method development and validation, leading scientific teams, managing study execution, and collaborating with cross-functional teams. Requires PhD, 10+ years of industry experience in bio-analysis, and experience with analytical platforms like LC-MS and ligand-binding assays. Experience with CRO partnerships and regulated bioanalytical programs is preferred.

This role is for a Senior/Principal Process Engineer at Eli Lilly, focusing on the startup and operation of an advanced manufacturing facility for ATMPs. The responsibilities include supporting facility start-up, defining operational readiness plans, developing control strategies, leading tech transfer, and providing process engineering support for API production. The role also involves integrating modeling and simulation into processes and identifying continuous improvement opportunities. It requires a Bachelor's degree in a relevant engineering field and 3+ years of manufacturing experience, preferably in pharmaceuticals.

This role provides QA oversight to GMP operations, supporting the start-up and qualification of a manufacturing site, and escalating issues from manufacturing to the site-based process team. Responsibilities include on-the-floor manufacturing support, GMP documentation review, SOP creation support, troubleshooting quality systems, and evaluating product quality impact.

Engineering Technician role focused on supporting Parenteral Operations by ensuring efficient setup, operation, maintenance, troubleshooting, and repair of Pre-Filled Syringe and Isolator Equipment in a manufacturing setting. Requires hands-on mechanical aptitude and adherence to GMP and quality standards.

This role is for a Warehouse Technician at Eli Lilly, responsible for receiving, storing, and shipping raw materials and packaging components to support manufacturing operations. The position requires adherence to cGMP and regulatory requirements, accurate inventory management, and safe handling of materials. It is not directly related to AI/ML development.