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.

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.

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.

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.

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.

This role leads discovery toxicology project strategy and execution for new pharmaceutical products at Eli Lilly. It involves designing toxicology plans, overseeing studies, analyzing data, and collaborating with cross-functional teams to identify and address toxicity risks for compounds moving into development. The role requires a PhD in Toxicology or related field with relevant experience, strong project management, communication, and data analysis skills, and knowledge of drug discovery, development, and regulatory guidelines.

This role focuses on Health Technology Assessment (HTA) strategy management within the pharmaceutical industry, specifically for the German and Austrian markets. The primary responsibilities involve developing strategies to translate evidence from clinical studies into added benefit for drug evaluations, managing the creation of dossiers according to regulatory requirements (AMNOG, EU-HTA), and coordinating with internal and external stakeholders. While the role mentions 'Digitalization/AI' as an area for process improvement, AI/ML is not the core craft of this position.

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.

Duales Studium (dual study program) in Wirtschaftsinformatik (Business Informatics) at Eli Lilly, a global healthcare leader. The program offers insights into the pharmaceutical industry, IT, and digital marketing, with opportunities to participate in system planning, adaptation, and introduction projects. It combines theoretical studies with practical experience.

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.

Senior Quality Scientist role in pharmaceutical device assembly and packaging, focusing on GMP compliance, quality systems, and regulatory adherence. This role involves overseeing manufacturing processes, investigating non-conformances, managing change controls, and ensuring readiness for inspections. It requires experience in the pharmaceutical industry and a strong understanding of cGMP regulations.

The Engineer - Automation Engineering will provide automation support for manufacturing operations and capital projects at Eli Lilly's new Medicine Foundry. This role involves technical leadership, mentoring, and implementing control applications and systems to ensure reliable and compliant manufacturing. The engineer will work on design, development, commissioning, and validation of automation systems, collaborating with various teams to optimize processes and maintain validated states in a GMP environment.

Associate, Supply Chain Master Data Steward for the Lilly Medicine Foundry, responsible for maintaining master data in SAP and Manufacturing Execution Systems (MES) for materials, BOMs, recipes, and warehousing. Focuses on data quality, integrity, documentation, and continuous improvement within a regulated pharmaceutical manufacturing environment.

This role provides technical and scientific expertise in external manufacturing for small molecule pharmaceutical products, focusing on technical transfers, process validations, and optimization. It requires knowledge of pharmaceutical manufacturing, GMP, and regulatory requirements to ensure processes are compliant, capable, and in a validated state.

Associate Director of CMC Development Program Management for radiopharmaceutical programs within Lilly Avid, focusing on leading cross-functional teams to execute development and manufacturing programs, manage risks, and ensure delivery of CMC milestones for clinical development.

Director level role in oligonucleotide analytical chemistry at Eli Lilly, focusing on technical leadership, method development, and team management within the biopharmaceutical sector. This role involves ensuring the integrity and compliance of analytical characterization for novel drug modalities.

This role is for a Director-level Project Statistician at Eli Lilly, focusing on providing statistical leadership for the Verve Gene-editing program and Lilly Research Laboratory. The role involves leading the assessment and introduction of new statistical technologies and methodologies, developing clinical plans, protocol designs, and statistical analysis plans, and providing statistical direction on clinical projects. The position requires a Ph.D. in Statistics or Biostatistics and at least 7 years of experience in clinical research and development.

This role focuses on the process development and engineering of genetic medicines, specifically RNA-lipid nanoparticles (LNPs) and oligonucleotide drug products, for parenteral formulations. The position involves building process capabilities, assessing and mitigating scale-up risks, collaborating across functions, and supporting regulatory filings within the pharmaceutical industry.

Associate Director for MES Architecture & Technical Lead role at Eli Lilly, focusing on designing, implementing, and optimizing Manufacturing Execution Systems (MES) for new state-of-the-art pharmaceutical manufacturing sites. The role involves architectural guidance, technical oversight, setting strategic roadmaps, and collaborating with various teams to ensure MES solutions align with business objectives and industry best practices. Requires deep technical knowledge, experience with Pharma and GMP manufacturing, and leadership skills.

Senior Manager for Quality Assurance in Device Assembly and Packaging at a new high-tech pharmaceutical production facility. Responsibilities include leading the operational QA organization, supporting startup and routine operations, technical oversight, developing quality culture, and managing QA teams. Requires a Bachelor's degree or equivalent experience, over 5 years in a leadership role in a highly regulated industry with a focus on QA, and strong knowledge of GMP regulations and quality management systems. Fluency in German and English is essential.

This role is for a Quality Assurance Technician in Device Assembly and Packaging at Eli Lilly's new production facility in Alzey, Germany. The technician will support the startup of the facility, ensure processes and products meet quality standards, monitor production on-site, assist with deviations and investigations, and support batch release. The role requires a technical education or bachelor's degree, knowledge of cGMP practices, and at least 2 years of experience in the pharmaceutical industry with a focus on shopfloor quality assurance.

This role is for a Production Shift Leader in parenteral manufacturing at Eli Lilly's new facility in Alzey, Germany. The position involves leading a team, ensuring safety and quality in sterile filling and inspection processes, and supporting the startup of the facility. It requires experience in sterile filling, production, and leadership, with knowledge of cGMP and FDA guidelines.

This role is for a Site Master Planning and Project Engineer in the pharmaceutical industry, focusing on strategic site master plans and capital projects to support manufacturing growth, ensuring compliance with global and local regulations. The role involves project management, engineering design, stakeholder collaboration, cost control, and continuous improvement within a regulated manufacturing environment.

This role is for a Fitter responsible for the servicing, troubleshooting, and maintenance of production equipment in a manufacturing facility. It requires mechanical aptitude, adherence to safety and cGMP standards, and prompt response to downtime events. The position involves night shifts and may require working on holidays. It is not AI-related and focuses on industrial maintenance.

This role focuses on leading the oligonucleotide synthesis scale-up team within Lilly Genetic Medicines to accelerate RNAi Therapeutics from pre-clinical to clinical development. It involves expertise in oligonucleotide synthesis methodologies, collaborating with chemistry teams, and supporting the discovery of lead drug candidates by providing essential materials for key studies. The role requires a PhD or MS in a relevant scientific discipline with significant experience in oligonucleotide synthesis and solid-phase synthesis.

Associate Director for Process Control & Automation Engineering at a new advanced manufacturing facility for ATMPs. Responsibilities include supervising engineers, ensuring reliable control applications, and supporting the technical agenda and business plan. The role involves leadership during project delivery and startup phases, focusing on building processes, systems, and culture for GMP manufacturing.

This role is for a Manufacturing Finance and Procurement professional at Eli Lilly's Seishin plant in Kobe, Japan. The position involves financial planning, analysis, OPEX/CAPEX management, and procurement strategy development. It requires strong finance and procurement experience, fluency in Japanese and English, and proficiency in SAP. The role focuses on supporting the manufacturing business through financial insights and strategic procurement, aiming to gain competitive advantage and serve patients better. It does not involve AI/ML development.

Senior Principal/Principal Bioprocess Engineer role at Eli Lilly in Limerick, Ireland, supporting the expansion of a Next Generation Biotech Drug Substance Manufacturing Facility. The role involves providing engineering subject matter expertise for design, construction, and startup, focusing on process engineering fundamentals, continuous improvement, and root cause analysis.