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.

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.

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.

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.

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.

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.

Associate Director - Legal Counsel for the Neuroscience business unit and Suzhou Plant, providing expert legal advice, managing risks, and ensuring compliance with laws and company policies. Responsibilities include advising on corporate, commercial, regulatory, and litigation matters, drafting agreements, supporting compliance programs, and training business teams.

This role supports Eli Lilly's Health Safety and Environmental (HSE) External Partner Program by managing HSE risks associated with external partners in their research labs. The position involves operational support for partner assessments, data management, and program administration, ensuring alignment with regulatory requirements and company expectations. Key responsibilities include screening and qualifying external partners, conducting onsite and virtual assessments of their HSE capabilities, preparing risk assessment reports, tracking corrective actions, and providing technical HSE consultation. The role also contributes to program development, process improvement, and strategic collaboration.

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 is for a Senior Director of Legal Counsel for the Iberia Hub at Eli Lilly, focusing on managing legal risk, providing expert guidance on pharmaceutical regulations, and supporting business strategies and daily operations across Spain, Portugal, and Greece. The position requires a Law Degree, Bar Admission in Spain, 10+ years of legal experience, and fluency in Spanish and English, with a strong preference for in-house experience in the pharmaceutical industry.

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 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.

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.

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 Health Keeper at Eli Lilly's Kobe office in Japan, focusing on employee health and wellness through services like massage and acupuncture, as well as conducting wellness webinars. It requires a licensed massage therapist with at least one year of experience and a disability certificate. The role is contract-based with a maximum term of five years.

This role is for a Director of Ethics and Compliance Internal Investigations in China, responsible for leading complex compliance investigations within the pharmaceutical industry. It requires experience in legal, compliance, or regulatory environments, with a strong emphasis on analytical skills, judgment, and discretion. The role involves developing investigation strategies, analyzing evidence, preparing reports, and collaborating with various departments.

This role is for a Regulatory Affairs Associate Director at Eli Lilly in China, focusing on developing and implementing regulatory strategies to accelerate drug submissions, approvals, and launches. It involves close collaboration with global and local teams, interaction with regulatory authorities, and ensuring compliance with regulations and Lilly's policies. The position requires deep knowledge of drug development, risk management in a regulated environment, and strong negotiation and communication skills in both Chinese and English.

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.

Executive Medical Director for Early Clinical Development in Immunology at Eli Lilly, focusing on developing transformational medicines for autoimmune and inflammatory diseases. This role bridges discovery science and clinical application, requiring strong matrix leadership and strategic portfolio management.

Internship role supporting communication team with internal and external communication activities, event organization, content creation, vendor communication, and reporting. Requires basic awareness of AI tools in communication or analysis.

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 is for a Sr. Principal Process Safety Management Engineer at Eli Lilly, focusing on supporting the startup and ramp-up of new manufacturing sites for the API/Dry Product Network. The engineer will provide process safety expertise, support operational readiness, manage change, conduct hazard analyses, and train staff to ensure a strong process safety culture. The role requires a Bachelor's degree in chemical engineering or related field, at least 10 years of experience in chemical/pharmaceutical manufacturing, and knowledge of OSHA PSM regulations.

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).

This role focuses on building and maintaining clinical study databases and associated systems for clinical trials, ensuring data quality and compliance with regulatory requirements. It involves collaborating with clinical teams, developing EDC systems, implementing data checks, and managing timelines. The role also includes team management responsibilities.

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.

The Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is responsible for developing and implementing innovative global regulatory strategies for products in the neuroscience and immunology therapeutic areas. This role acts as the accountable decision-maker for global regulatory strategies from portfolio entry to end-of-life, ensuring alignment with business objectives and regional requirements. The GRL leads the Global Regulatory Team, creates and maintains the Regulatory Strategy Document (RSD), and serves as the primary interface with the Global Brand Development (GBD)/global program team, representing regulatory affairs and managing risks. For early-stage programs, the GRL leads US and Canada submissions and agency interactions for IND, IDE, and CTA.

This role is a Senior Director position focused on Quality Management Systems (QMS) Core Quality Governance within a global healthcare company. The primary responsibility is to lead a team in overseeing and evolving core quality processes, ensuring compliance, scalability, and alignment with regulatory expectations. The role involves embedding strong governance, standardized reporting, and continuous improvement across the QMS, collaborating with various departments and external partners to integrate enterprise-level processes.

Clinical Research Physician role focused on late-phase and marketed compounds in Neuroscience at Eli Lilly. Responsibilities include clinical trial monitoring, patient safety oversight, protocol development, scientific data dissemination, and ensuring compliance with regulations and company policies. This role acts as a scientific resource for study teams and external healthcare professionals.

Postdoctoral Research Scientist position focused on translational research in Alzheimer's disease, investigating mechanisms of amyloid immunotherapy-related microhemorrhage using in vivo two-photon imaging. Requires PhD, experience in in vivo dosing, stereotactic surgery, two-photon imaging, and image analysis. Background in neurodegeneration or neurovascular biology is preferred.

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.

This role is for a Clinical Research Physician (CRP) in Medical Affairs at Eli Lilly, focusing on strategic planning for launch and commercialization activities to meet patient needs. The CRP will contribute to global and regional clinical/medical plans, oversee local clinical trials, report adverse events, review protocols and publications, and support pricing, reimbursement, and access (PRA) initiatives. The role also involves engaging with external clinical customers and thought leaders, and ensuring compliance with regulations and company standards. The CRP acts as a scientific resource and provides expert medical support for marketed products and new drug submissions.

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.