This role is an Engineering Subject Matter Expert (SME) for visual inspection of semi-finished products in parenteral manufacturing. It focuses on the evaluation, delivery, implementation, and support of automated, semi-automated, and manual inspection equipment. The position involves technical leadership, ensuring safety and compliance, global consultation, knowledge sharing, supporting major capital projects and external manufacturing, owning equipment platforms, and investigating emerging technologies. The core responsibilities are related to engineering support and optimization of inspection processes within a regulated healthcare manufacturing environment.

Executive Director role focused on early clinical development in neuroscience drug development, involving clinical pharmacology and mechanistic studies. Responsibilities include leading clinical trials, reporting adverse events, reviewing protocols, and ensuring compliance with regulations and GCPs. Requires an M.D. or D.O. with at least five years of relevant experience.

This role provides quality oversight of Quality Control activities at Contract Manufacturing organizations (CMs) for Active Pharmaceutical Ingredients (API) External Manufacturing. It involves ensuring compliance with cGMPs, supporting method validation/transfer, and managing quality-related issues with testing.

This role is for a Director in Analytical Development within the Bioproduct Research and Development organization at Eli Lilly. The position focuses on leading analytical efforts for pharmaceutical drug substance and drug product development, commercialization, clinical trials, and regulatory submissions. Responsibilities include developing analytical methods, designing stability studies, authoring regulatory documents, and providing technical guidance for external analytical activities. The role requires a strong foundation in analytical sciences and experience in the pharmaceutical industry, with a focus on ensuring the quality and control strategies for various therapeutic modalities.

This role focuses on leading PKPD project strategy for genetic medicines programs, developing and implementing modeling strategies to enhance decision-making in drug discovery and development. It involves designing, analyzing, and interpreting quantitative pharmacology studies, collaborating with cross-functional teams, and mentoring junior scientists. The role requires expertise in PK/PD and PBPK modeling, experience with relevant software, and a PhD in a related field.

This role is responsible for administering, maintaining, securing, and optimizing core data movement and integration platforms like IBM MQ, IBM App Connect Enterprise, Aspera, and Axway B2Bi. The individual will ensure high availability of messaging and file transfer services, automate operational tasks, and provide expert support for data exchange within the organization and with external partners. Key responsibilities include managing IBM MQ environments, supporting integration flows, administering file transfer solutions, configuring secure data exchange, developing automation scripts, implementing security configurations, and troubleshooting complex data flow issues.

Security Operations Engineer focused on Identity and Access Management (IAM) platforms, ensuring secure and timely access to enterprise resources. Responsibilities include day-to-day operations, incident management, change management, problem resolution, system monitoring, maintenance, documentation, and supporting audit/compliance requests for authentication systems like Entra ID, Active Directory, and Okta. Requires on-call rotation.

This role is a Technical Lead for SecOps Engineering focusing on Privileged Access Management (PAM), Encryption, and Identity Governance. It involves technical leadership, operational excellence, incident management, change management, and ensuring secure access to enterprise resources. The role requires managing and supporting 24/7 identity platforms and services, collaborating with cross-functional teams, and responding to audit and compliance requests. It is not directly related to AI/ML model development or deployment.

This role is responsible for assessing, establishing, and operationalizing the regulatory strategy and execution plan for assigned IVD performance studies and for clinical trials that use IVDs, ensuring compliance with EU IVDR and applicable national requirements. The role involves developing regulatory documents, supporting interactions with regulatory agencies, and providing expertise on IVD regulations for clinical trials.

This role is for an MSL Manager in the pharmaceutical industry, responsible for leading a team of Medical Science Liaisons, overseeing their performance, training, and strategic implementation within assigned therapeutic areas. The position requires a health science degree, experience in the pharmaceutical industry, and strong people management and communication skills.

This role is responsible for supporting the cleaning program for process equipment and ancillary components in a new Biotech Drug Substance Manufacturing Facility. Responsibilities include developing cleaning strategies, authoring validation plans and protocols, executing protocols, authoring procedures, and troubleshooting cleaning processes. The role requires a BSc in Engineering or Science with 2 years of experience in a pharmaceutical/biopharmaceutical manufacturing site.

Senior Manager for Quality Control Support in a pharmaceutical setting, focusing on team leadership, GMP compliance, and digital system management within QC operations.

This role is for a Senior Director of Corporate Health Safety and Environment (HSE) at Eli Lilly, a global healthcare leader. The position involves providing leadership and oversight for global HSE programs, including compliance, risk management, auditing, business development processes, performance monitoring, and integration strategies. The director will manage the global HSE staff, oversee the annual business plan, and lead corporate governance teams. Key responsibilities include maintaining HSE standards, overseeing auditing functions, assessing HSE aspects for business development, driving integration into new sites, promoting HSE in business continuity, managing enterprise-wide HSE aspects, developing IT system strategy, and coordinating HSE considerations across the value chain. The role also involves establishing and tracking HSE goals, reporting performance, monitoring external trends and best practices, and influencing leadership on regulatory matters. People management includes leading and developing the HSE team, providing direction, coaching, and performance management.

This role is for a Pharmaceutical Sales Representative in the Cardiovascular Metabolic Health business unit. The primary responsibilities include promoting company products in clinical settings within a designated territory, achieving sales targets, building and maintaining customer relationships (especially with hospitals), providing information about drug characteristics and efficacy, gathering market intelligence, and collaborating with internal teams. The role requires a Bachelor's degree, preferably in a pharmaceutical-related field, and experience in pharmaceutical promotion, new product launches, academic promotion, and key account management.

This role is for a pharmaceutical sales representative focused on promoting company products within a specific territory, managing customer relationships, and achieving sales targets. It involves understanding drug features and market conditions, and collaborating with internal teams.

This role is a Finance Analyst position at Eli Lilly's Suzhou manufacturing plant. Responsibilities include cost accounting, financial reporting, budgeting, internal controls, and financial analysis. Requires a Bachelor's degree in Finance/Accounting, 3+ years of experience, and familiarity with SAP and Power BI.

This role provides Extended Warehouse Management (EWM) business support and expertise for warehouse and logistics operations. Responsibilities include troubleshooting issues, driving continuous improvement, training teams, assessing system/process changes, and managing EWM master data. The role requires SAP EWM experience and comfort with automated warehouse technologies.

Reliability Technician role at Eli Lilly's new Medicine Foundry, focusing on ensuring equipment availability and performance through predictive maintenance, data analysis, and continuous improvement in a cGMP-regulated manufacturing environment.

This is an administrative support role within the Communication and Public Affairs department of Eli Lilly France. The responsibilities include managing schedules, purchase orders, event planning, updating communication channels, and taking meeting minutes. The role requires strong organizational and communication skills, proficiency in office software, and a willingness to learn.

This role manages laboratory, device, imaging, and other diagnostic support for clinical trials, coordinating vendor activities, partnering with medical staff on protocol development, and ensuring high-quality data. It focuses on clinical trial initiation and execution within the healthcare domain.

This role supports Lilly's people strategy through talent acquisition, talent development, and the creation of a safe environment with HSE plans. It partners with business leaders to identify, attract, and retain a diverse workforce within a safe environment. Responsibilities include managing talent acquisition strategy, partnering with leaders on talent management, developing and implementing HSE programs, and designing/delivering learning initiatives.

This role is for a Senior Warehouse Manager in the pharmaceutical industry, responsible for overseeing all aspects of warehouse operations, including material receipt, storage, dispensing, shipping, inventory control, and compliance with quality, safety, and regulatory requirements (GMP, AEO). The role also involves project management for warehousing initiatives, team leadership, and ensuring a safe work environment. Experience with SAP/PMX and GMP regulations is required.

The Automation Technician is responsible for the performance of automated equipment, providing first-line support to production processes, and supporting area engineering initiatives, process improvements, and project implementation within a pharmaceutical manufacturing environment. This role requires expertise in production processes, commissioning, qualification, and validation requirements, as well as equipment-specific code and control system technologies.

This role is for an Advisor, Project Controls at Eli Lilly, focusing on managing project controls for large capital programs (>$500MM USD) in global facilities delivery. The responsibilities include leading project controls teams, establishing cost and schedule baselines, managing resources, change control, risk management, and ensuring compliance with finance policies. It requires significant experience in project controls on major industrial or manufacturing projects.

Associate Director for Project Controls in Global Facilities Delivery (GFD) at Eli Lilly, focusing on manufacturing network projects. Responsibilities include budgeting, cost control, earned value management, change and risk management, forecasting, and planning. The role involves process improvement, governance, mentoring, and ensuring compliance with finance policies for capital projects.

Associate Director of Learning & Development for a new API manufacturing facility, responsible for leading the L&D team, developing learning strategies, and ensuring compliance and operational effectiveness in a regulated environment. The role involves driving a modern learning culture, leveraging learning technologies, and partnering cross-functionally.

Lead Specialist for Radiation Safety at Eli Lilly's radioligand therapy facility. This role involves technical expertise and operational support for radiation safety programs, including contamination surveys, sample analysis, instrument testing, and compliance activities. The position requires collaboration with operations, maintenance, and engineering teams to ensure safe and compliant GMP manufacturing. The role also involves incident prevention, response, and internal audits. Requires a Bachelor's degree in a related science or equivalent experience, and familiarity with unsealed radioactive materials and radiation detection instrumentation. Experience in a GMP environment and knowledge of NRC/Agreement State regulations are preferred.

This role is for a Senior Director in Oncology and Peripheral Imaging Clinical Development at Eli Lilly. The primary focus is on leading the clinical development of imaging strategies for oncology, immunology, and cardiometabolic diseases, spanning early to late-phase trials. While the role involves evaluating AI in imaging, its core function is in clinical research and development within the healthcare domain, not in building or shipping AI models.

Senior/Principal Upstream Bioprocess Scientist at Eli Lilly in Limerick, Ireland, focusing on technical support for manufacturing processes, data-driven decision-making, and continuous process improvement in upstream bioprocessing. Requires expertise in cell culture, process monitoring, statistical methodologies, and regulatory compliance within the biopharmaceutical industry.

Associate Director for a Technical Services & Manufacturing Sciences (TSMS) Laboratory focused on small molecule and oligonucleotide API process troubleshooting and continuous improvement. Responsibilities include leading laboratory staff, designing and executing experiments, managing a safe work environment, hiring and developing staff, and collaborating with cross-functional teams for technology transfer, process validation, and manufacturing operations. The role also involves commissioning new equipment and defining the technical agenda for process capability and yield improvement.

Associate Director of Utilities Operations for a new API manufacturing facility, responsible for managing day-to-day utility operations, ensuring safety, quality, and regulatory compliance, and leading a team to support the startup and ongoing operations.

This role is for an Automation Engineer at Eli Lilly's new manufacturing site in Concord, NC. The engineer will be responsible for automation design, managing system integrators, supporting corporate initiatives like lifecycle management and cybersecurity, and driving automation governance. The role involves evaluating new technologies and innovation trends for application within Lilly.

Associate Director of Process Engineering for Oligonucleotides manufacturing, responsible for leading and developing a team of process engineers. This role involves building a new manufacturing facility from the ground up, establishing operational processes, ensuring compliance with GMP standards, and overseeing engineering deliverables for both startup and ongoing operations. The position requires strong leadership, talent acquisition, and a focus on safety, quality, and operational excellence in a regulated pharmaceutical environment.

This role is a commercial leadership position focused on shaping and executing strategies to penetrate and scale the market through partnerships with private ecosystem players (telehealth, private hospitals, employers, insurers) for obesity care adoption in Turkey. The leader will develop go-to-market strategies, build C-level relationships, drive strategic alliances, and deliver commercial results by accelerating private-market adoption of obesity treatments.

Director of Engineering role focused on purification and conjugation technologies within Bioproduct Research and Development (BRD) at Eli Lilly. Responsibilities include providing technical expertise for GMP manufacturing of drug substance, focusing on chromatography, filtration, and bulk unit operations. The role involves developing control systems, performing risk assessments, collaborating with development scientists and manufacturing, evaluating new technologies, supporting tech transfers, mentoring engineers, and ensuring compliance with quality systems and cGMP requirements. Requires a Ph.D. or MS/BS in Chemical Engineering with significant experience in biopharmaceutical downstream processing and equipment design/qualification.

Seeking a Sr. Director for Employee Health Services at Eli Lilly, a Primary Care Physician to deliver comprehensive, patient-centered care in an onsite clinic. The role focuses on prevention, early intervention, chronic disease management, and longitudinal health planning within a direct primary care model, emphasizing unhurried visits and shared decision-making.

Associate Director for Technical Services and Manufacturing Support (TSMS) in a small molecule API manufacturing facility. Responsibilities include leading a team of scientists, managing technical transfer, process validation, manufacturing operations, continuous improvement, and ensuring GMP compliance. Requires experience in cGMP API manufacturing and technical leadership.

Associate Director for Technical Services/Manufacturing Support (TSMS) in an oligonucleotide API manufacturing facility. Responsibilities include leading a team, managing production support, implementing technical projects, process optimization, technical transfer, validation, and ensuring GMP compliance. Requires a Bachelor's or Master's in a science field and 5+ years of cGMP commercial API manufacturing experience.

Associate Director TSMS - API role at Eli Lilly responsible for technical and people leadership in API manufacturing processes. Focuses on technology transfer, process validation, manufacturing support, process optimization, and lifecycle management. Emphasizes leveraging data analytics and digitalization strategies for process improvement and site capabilities, requiring collaboration across multiple functions.

This role focuses on ensuring the validation and data integrity of laboratory IT systems and computerized instruments within a pharmaceutical manufacturing environment. It involves implementing and maintaining systems according to regulatory requirements (cGMP, CSV) and collaborating with various quality and IT teams to ensure compliance and continuous improvement.

Associate Director - IT Systems Program Manager at Eli Lilly, focused on overseeing and aligning multiple programs for new API manufacturing sites. The role involves managing large-scale programs, release train engineering, GxP compliance, stakeholder management, risk management, and resource allocation. Requires a strong business understanding, analytical skills, and the ability to communicate complex technical information. Experience in Pharma and GMP Manufacturing is required.

Director of Medical Affairs for Cardiometabolic Health in Turkey, responsible for providing clinical and scientific input to brand teams, supporting medical launch activities, developing promotional materials, and engaging with healthcare professionals. The role involves responding to customer inquiries, managing thought leader engagement, and contributing to the medical affairs plan. Requires an advanced degree in health sciences with relevant experience, strong communication and interpersonal skills, and fluency in English. Experience in Cardiometabolic Health is preferred.

This is an apprenticeship role for Market Research at Eli Lilly, a global healthcare leader. The role involves participating in market studies, analyzing customer needs, identifying external partners, and tracking studies. The intern will provide analytical elements for marketing strategy development, conduct analyses and syntheses of studies, and present recommendations to sales and marketing partners. A key aspect is contributing to the use of new technologies and AI tools. The role requires a Master's degree in marketing, management, or market research, with strong analytical skills, autonomy, rigor, initiative, dynamism, reactivity, teamwork, creativity, curiosity, adaptability, and a good command of digital tools and innovation. Fluency in English is also required.

This is a Brand Manager apprenticeship role in the Oncology/Hematology division at Eli Lilly, focusing on marketing campaigns, competitive analysis, and contributing to tactical/strategic product development. While the role mentions an "appetite for new technologies and artificial intelligence," AI/ML is not the core craft or deliverable.

This role is for a Director/Senior Director/Executive Director in AAV R&D at Eli Lilly, focusing on inventing, characterizing, and advancing novel genetic reagents for clinical applications. The responsibilities include developing AAV therapies, driving data-based decisions, implementing strategic vision, leading screening of AAV technologies, ensuring best practices in model development and validation, and leading a team. The role requires a PhD with 10+ years of industry experience, with a mastery of ophthalmology gene therapy and proven experience in leading gene therapy programs.

The Instrument Technician role provides process instrumentation maintenance support for the Lilly Medicine Foundry, focusing on equipment availability, calibration, troubleshooting, and reliability in a cGMP-regulated environment. Responsibilities include performing preventative and corrective maintenance, troubleshooting instrumentation, operating test equipment, and supporting new equipment installations.

This role is for a Sr. Technician in a QC Chemical Laboratory at Eli Lilly in Italy. Responsibilities include performing analytical tests on raw materials and finished products, operating and calibrating laboratory instrumentation, managing data and results using specific software (Empower, SmartLab, Darwin LIMS), ensuring GMP compliance, and collaborating with HSE. Requires a Master's degree in Chemistry or CTF and knowledge of laboratory instrumentation like HPLC and spectrophotometers, with good English proficiency.

Senior Advisor/Director role in Small Molecule Process Development at Eli Lilly, focusing on leading teams, managing safety, and overseeing the scientific and technical aspects of chemical process development for drug substances and intermediates. The role involves planning, optimizing, troubleshooting, and transferring chemical processes, with a strong emphasis on scalability, robustness, safety, cost, and sustainability. Requires a Ph.D. in Chemistry or Chemical Engineering with 12+ years of experience.