Engineering leader for the ChatNow program, responsible for managing development and support teams, implementing AI Service Desk strategy, and driving engineering excellence in a healthcare setting. Requires strong leadership, GenAI concepts knowledge, and experience with ITIL, Agile, and DevOps.

Lead Consultant for Quality Engineering at Eli Lilly, focusing on digital health and patient-facing applications. This role involves leading a team of Quality Engineers, defining and executing test strategies, and developing engineering talent. The position requires hands-on technical contributions to test automation frameworks, CI/CD integration, cloud-based testing (AWS, Kubernetes, Docker), and specifically includes contributions to AI-based application testing, LLM evaluation, and validation using frameworks like RAGAS. The role also involves people leadership, stakeholder management, and process improvement within an Agile environment.

The Sr. Manager in Tech@Lilly Business Capabilities and Operations team serves as the technology business partner to the CMO teams. This role is accountable for shaping and executing the HCP engagement technology strategy to enable broader reach, elevating the digital experience for HCPs, and driving scalable and high impact tech solutions. The role combines business partnership, tech leadership, solution integration, and innovation driver to empower and elevate HCP education impact.

Principal Quality Engineer/Test Architect responsible for defining and driving the overall test architecture strategy across enterprise platforms, microservices, and cloud-native applications. This role involves designing scalable quality engineering frameworks, embedding testing into the SDLC, and partnering with engineering leadership to establish best practices for automation, performance, security, accessibility, and resilience testing. The role also includes evaluating and introducing AI-assisted testing tools and mentoring quality engineers. The company is a global healthcare leader, and experience in regulated industries is required.

This role leads a data and analytics team focused on the Source to Pay (S2P) value chain within a healthcare company. The responsibilities include delivering actionable insights, building scalable data products, enabling self-service analytics, and evolving the S2P data strategy using Microsoft Fabric. The role involves applying advanced analytical methods, developing predictive and prescriptive capabilities, and leading a team of data professionals. While AI is mentioned as an area to explore for future capabilities, the core focus is on data strategy, architecture, and analytics delivery for procurement, P2P, and TPRM processes.

This role focuses on developing and executing comprehensive strategies for acquiring, building, and utilizing real-world data (RWD) throughout the pharmaceutical lifecycle to enhance evidence generation. It involves leading RWD acquisition and development strategies, maximizing RWD utilization, ensuring quality assurance and dataset creation for analysis, and innovating data platforms with IT solutions. The role requires a Master's degree in Data Science, Medical Informatics, or Health Informatics, with at least 3 years of experience in data management and statistical analysis using RWD in clinical trials or observational studies. Strong communication skills in Japanese and English, and logical, scientific, and strategic thinking are essential.

Seeking an experienced drug hunter as a Discovery ADME Project Leader for Antibody Drug Conjugates (ADCs). The role requires deep mechanistic understanding of drug disposition, PK, and translational science, integrating biology, chemistry, and modeling. Responsibilities include developing integrated preclinical ADME strategies, driving ADME strategy by aligning pharmacokinetics, metabolism, and safety data, and guiding compound design. The role involves serving as the ADME single-point-of-accountability on cross-functional program teams, collaborating with various discovery functions, and contributing to candidate selection decisions. The position also requires implementing best practices, mentoring junior scientists, and leveraging AI/agentic tools where possible. A PhD in a related field and 6+ years of industry experience in drug discovery are required.

This role focuses on the biological aspects of an in vivo CAR-T platform, involving molecule SAR, screening, and characterization. It integrates emerging technologies including AI tools for analysis and design, but the core function is biological research in drug discovery, not AI model development.

The Associate Director of Pharmacovigilance (PV) Systems Strategy and Implementation at Eli Lilly is responsible for developing, implementing, and maintaining compliant systems for the PV organization. This role involves analyzing business processes, identifying improvements, and driving the PV technology and analytics strategy. Key responsibilities include leading analytics and automation solutions, managing PV systems, ensuring compliance with regulations, and partnering with IT and business teams to build and deploy applications and analytics models. While the role mentions AI and analytics models, its core focus is on system implementation and compliance within a regulated healthcare environment, rather than core AI/ML development.

Executive Director role in Medical Affairs for Cardiometabolic Health at Eli Lilly, focusing on executing medical strategy, evidence generation, scientific communication, and external engagement within the US healthcare system. Requires an MD or DO with significant experience in Medical Affairs or clinical research, preferably in cardiometabolic therapeutic areas.

This role focuses on preclinical drug discovery, specifically ADME (Absorption, Distribution, Metabolism, Excretion) and PK/PD (Pharmacokinetics/Pharmacodynamics). The Senior Advisor will develop integrated preclinical ADME strategies, integrate ADME and pharmacology for translational simulations, guide compound design based on data-driven principles, and serve as the ADME single-point-of-accountability on cross-functional program teams. The role also involves mentoring junior scientists and implementing procedures, assay innovation, and automation, with a stated interest in leveraging AI and agentic tools where possible.

This role is for a Technical Lead Scientist in Advanced Therapies Manufacturing at Eli Lilly, focusing on gene therapy product commercialization. It involves technical leadership for clinical and commercial activities, including technology transfer, validation, production, and regulatory submissions. The position requires understanding manufacturing principles, identifying new technologies, leading risk management, and ensuring process documentation and validation strategies are in place. The role supports the construction and startup of a state-of-the-art manufacturing facility.

This role focuses on programming and testing clinical trial data collection databases, including mapping, testing, and normalizing data into a clinical data warehouse. It requires expertise in data technology, data flow, data standards, database programming, normalization, and testing within the healthcare domain.

Senior/Principal Scientist role focused on Quality Control of incoming raw materials for a new GMP manufacturing facility. Responsibilities include managing raw material lifecycle, reviewing data, supporting validation, leading investigations, authoring GMP documentation, and mentoring staff within a regulated healthcare environment.

Associate Director of Process Engineering for Peptides API at Eli Lilly, responsible for leading and directing process engineers in a new advanced manufacturing facility. The role involves building the engineering team and organization, developing business systems, supporting project delivery, and ensuring compliant GMP manufacturing operations for peptide products. Key responsibilities include hiring, coaching, setting standards, managing operational expenses, and collaborating with R&D and project teams.

This role is for a Director in Quality Control for Advanced Therapies at Eli Lilly, focusing on the startup and operation of a new, highly advanced manufacturing facility for gene therapy. The position involves leading a laboratory team, ensuring compliance with cGMP, managing daily operations, personnel, and external partnerships, and contributing to the design, commissioning, and testing of new products. The role requires a strong understanding of regulatory requirements and laboratory processes within the healthcare/pharmaceutical domain.

This role focuses on synthetic chemistry and process development for highly potent small molecule APIs within a new advanced manufacturing and drug development center (Lilly Medicine Foundry). The chemist will evaluate and facilitate the transfer of chemical processes from development labs to pilot plant operations, ensuring readiness for early-phase cGMP manufacturing. Responsibilities include performing synthetic chemistry, assessing routes, evaluating safety, ordering materials, setting up analytical methods, analyzing data, summarizing findings, performing familiarization reactions, conducting use-tests, maintaining lab notebooks, authoring technical documents, and contributing to process improvement and troubleshooting.

Scientist/Principal Scientist role focused on parenteral operations, technical transfer, and process validation within a cGMP manufacturing environment in the pharmaceutical industry. Responsibilities include supporting formulation, filling, or visual inspection, maintaining validated states, establishing process metrics, leading improvement projects, and authoring/executing technical documents.

Operator role in pharmaceutical manufacturing, focusing on running processes, troubleshooting, and ensuring quality and safety in medicine production. This is a hands-on role in a regulated environment.

Head of Medical Affairs / CRP in Austria, providing medical and scientific leadership, overseeing the medical team, driving innovation, ensuring scientific excellence, regulatory compliance, and cross-functional collaboration for pre- and post-launch activities. Responsibilities include leadership, talent development, medical strategy, clinical oversight, scientific expertise, external engagement, and cross-functional collaboration.

This role is within Bioproduct Research and Development (BR&D) at Eli Lilly, focusing on developing and optimizing biologically derived products. The Principal Engineer will design and execute experiments for cell culture processes, analyze data, author technical reports, and support scale-up and technology transfer. The role also involves evaluating emerging technologies and implementing automation, with a preference for candidates comfortable using AI tools for analysis and design.

This role is for a Maintenance Technician in pharmaceutical manufacturing, focusing on servicing, repairing, and maintaining process and utility equipment to improve uptime, efficiency, and overall equipment effectiveness. Responsibilities include troubleshooting mechanical issues, performing repairs, setting up equipment, documenting actions in CMMS, and working with safety protocols. Requires a high school diploma, minimum 2 years of automation experience, and mechanical skills.

This role is for an Advisor Parenteral Global Product Steward in Genetic Medicines at Eli Lilly. The individual will provide technical stewardship for parenteral drug products and genetic medicines, collaborating with cross-functional teams to support global manufacturing sites for new product commercialization, process improvements, and technology transfers. The role involves shepherding new pipeline products from development into manufacturing, integrating cross-functional information for data-driven decisions, and driving advancements in technical capabilities. It requires a PhD with 5+ years, Master's with 10+ years, or Bachelor's with 15+ years of experience in parenteral product manufacturing, with proficiency in biomolecule and genetic medicine characterization and GMP manufacturing.

This role is for a Business Process Architect focused on Global Supply Chain (Logistics) technology platforms at Eli Lilly. The responsibilities include platform ownership, governance, continuous improvement, vendor management, and project delivery for logistics, transportation visibility, and supply chain intelligence applications. The role requires experience in supply chain technology, IT product ownership, and managing logistics/transportation platforms, with a focus on ensuring operational value and adherence to IT policies.

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 oncology therapeutic area. This role acts as the accountable decision-maker for the execution of global regulatory strategies from portfolio entry to end of life cycle, ensuring alignment with business objectives and regional requirements. The GRL leads the Global Regulatory Team, develops and maintains the Regulatory Strategy Document (RSD), and serves as the primary interface with the Global Brand Development (GBD)/global program team. For early development programs, the GRL leads US submissions and agency interactions, including IND and IDE.

Laboratory Analyst role in a Next Generation Biotech Drug Substance Manufacturing Facility, focusing on cell-based assay quality control. Responsibilities include executing analytical procedures, maintaining cell cultures, managing digital systems, reporting results, instrument qualification, methodology development/validation, deviation investigations, and inventory management. Requires expertise in GMP/GLP, cell culture, virology, bioassays, and instrument platforms.

This role focuses on developing and implementing analytical and separation methodologies for the characterization and quality control of oligonucleotides and their conjugates in a healthcare setting. It involves lab-based work, method development, instrumentation maintenance, and collaboration with IT for informatics systems.

This role focuses on leading the strategic development and maturity of a global process owner network within a Quality Management System (QMS) in the pharmaceutical industry. It involves defining capability maturity models, identifying competencies, designing training, establishing governance, and leveraging analytics for continuous improvement. The role requires extensive experience in process excellence and quality systems within the pharmaceutical sector.

This role provides technical support for GMP manufacturing of API intermediates and bulk drug substances, utilizing peptide synthesis and purification platforms. It involves understanding scientific principles for scale-up, process improvements, and technical innovation within a cross-functional team. The position requires a Bachelor's degree in scientific disciplines and strong teamwork, technical knowledge, and problem-solving skills.

Scientist/Sr. Scientist role focused on protein engineering, specifically antibody optimization and phage display-based discovery within a healthcare/biotechnology research division. Involves molecular biology, biochemistry, and developing/optimizing assays.

Senior Laboratory Analyst role at Eli Lilly focused on executing analytical procedures, maintaining digital systems, reporting results, and validating methodologies in a pharmaceutical manufacturing environment. Requires a BSc in Analytical Sciences with pharmaceutical experience and knowledge of various analytical techniques and instrument platforms.

The Technician – QC – IAPI performs routine laboratory testing in a quality control setting, adhering to GMP and safety guidelines. Responsibilities include sample handling, microbiological testing, data recording, deviation identification, and supporting audits. This role is crucial for ensuring product quality and compliance in a regulated healthcare environment.

This role is for a Lead Engineering Technician in Plant Engineering at Eli Lilly, focusing on maintaining and ensuring the reliable operation of facility infrastructure and utility systems within a parenteral manufacturing plant. Responsibilities include system ownership, troubleshooting, supporting capital projects, coordinating maintenance, and ensuring compliance and safety. The role requires technical understanding of utilities and mechanical equipment, strong problem-solving skills, and effective communication within a cross-functional environment. It is not directly involved in AI/ML development.

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.

Associate Director of Clinical Development in the Immunology therapeutic area, responsible for executing integrated clinical development plans and clinical trial packages, leading clinical teams, managing submission strategies, ensuring clinical execution, managing risks and budgets, and overseeing cross-functional communication and partner expectations. The role also involves people management, including recruiting, developing, and retaining staff, and fostering an inclusive organizational culture. Requires a Bachelor's degree, significant experience in pharmaceutical/clinical development and project management, and team management experience.

This is an apprenticeship role for a Pharmacovigilance Officer at Eli Lilly, focusing on managing and processing pharmacovigilance case information according to company procedures. The role involves data collection, translation, coding, data entry, and quality control of safety data. It requires a Master's degree in Pharmacovigilance, strong English skills, and proficiency in IT tools.

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 of Communications for Eli Lilly Japan, responsible for guiding and leading all product and environmental shaping communications efforts. This role involves developing disease state and consumer communications, supporting data and regulatory milestones, coordinating with global teams, and managing relationships with internal and external partners. The position also includes leading, coaching, and developing a team of communicators, providing media training, and managing issues preparedness.

The Associate Director - Medical Science Liaison (MSL) for Cardiometabolic Health at Eli Lilly is responsible for engaging with scientific and clinical experts to provide in-depth scientific and clinical information about specific disease states and Lilly's compounds. This role involves synthesizing the latest research, responding to medical information needs, facilitating scientific exchange, and communicating insights to internal teams. The MSL acts as a key interface between Lilly Medical and healthcare professionals, supporting clinical care gaps and potentially facilitating collaborative research. The role also involves territory management, strategic planning, and ensuring compliant partnerships.

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.

This role is responsible for executing and maintaining global regulatory submissions throughout the product lifecycle, coordinating the creation and legalization of submission documents, and ensuring adherence to regulatory agency electronic common technical document (eCTD) specifications. The role requires technical proficiency in publishing tools like RIM, Adobe Acrobat, Lorenz, and ISIToolbox, and involves collaboration with various internal and external stakeholders to ensure timely and compliant submissions.

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 Sr. Director-Medical role at Eli Lilly provides leadership, supervision, coordination, coaching, career development, and performance management for staff within a specified therapeutic or product subgroup of Development. This role involves administrative and technical responsibilities, strategic planning for clinical research and medical support, interaction with external consultants and regulatory agencies, and ensuring compliance with all relevant regulations and company policies. The position plays a significant role in submission, registration, and product launch, and maintains contact with relevant local and global clinical research management, marketing management, and corporate teams. The Sr. Director-Medical also maintains ongoing responsibilities as a Clinical Research Physician.

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.