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.

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.

This role is for an Analytical Steward focused on Mass Spectrometry and related instrumentation for peptide and small molecule characterization within a pharmaceutical manufacturing and quality technical hub. The responsibilities include developing analytical methods, conducting experiments to optimize processes, and providing technical support for technology transfer. The role requires a Ph.D. in a relevant scientific discipline with 5-12 years of experience.

This role focuses on the process development and optimization of small molecule drug substance manufacturing within the pharmaceutical industry. It involves technical transfers, ensuring processes are robust and cost-effective, and collaborating with R&D and plant sites. The position requires a strong understanding of GMP, regulatory requirements, and the ability to lead technical projects and mentor junior staff. Experience with digitization and regulatory interactions is also highlighted.

This role manages and modernizes enterprise data integration platforms (Informatica, Denodo), focusing on installation, upgrades, performance, security, and migration to cloud-native solutions. It involves ensuring platform reliability, supporting data virtualization, and troubleshooting complex issues within a hybrid ecosystem.

This role focuses on leading and executing in vivo and PET imaging studies, including experimental design, advanced image analysis, and data interpretation within the healthcare domain. The scientist will integrate cutting-edge imaging technologies and novel agents into research pipelines, collaborate with global leaders, and disseminate findings through publications and presentations. The role requires a Bachelor's or Master's degree with at least 7 years of experience in molecular imaging and a strong publication record.

This role focuses on statistical trial design and analysis within clinical research and development in the healthcare domain. The primary responsibilities include developing protocol designs, writing protocols, selecting statistical methods, analyzing clinical study data, and communicating results. The role requires a Ph.D. in Statistics or Biostatistics with experience in clinical R&D and proficiency in statistical programming languages.

Lead Automation Technician role at Eli Lilly, a global healthcare leader, focusing on automated equipment performance, production support, and process improvements in a new state-of-the-art parenteral manufacturing site. Responsibilities include ensuring equipment is maintained, safe, and operated according to cGMPs, investigating production delays, and supporting engineering initiatives. Requires an Associate's Degree or equivalent experience, with preferences for GMP manufacturing, PLC/HMI programming (Studio 5000, FactoryTalk View SE, B&R), and experience with automated equipment and maintenance management systems.

This role is for a Utilities / Medium Voltage Electrician / Instrumentation at Eli Lilly, responsible for servicing, troubleshooting, and maintaining electrical and instrumentation equipment within utility systems. The position involves preventative and corrective maintenance on high and low voltage electrical equipment, process instrumentation, and ensuring compliance with safety and cGMP standards. It requires strong electrical and mechanical aptitude, with experience in utility systems and troubleshooting being preferred.

Internship opportunity for university students with a disability rate of 40% or above, registered with İŞ-KUR, to gain experience in various business functions within the pharmaceutical industry.

This role focuses on driving continuous improvement and operational excellence within a pharmaceutical manufacturing setting, primarily using Lean principles and digital tools. It involves facilitating the implementation of daily management systems, leading system design and governance, and partnering on improvement initiatives to enhance safety, quality, productivity, and cost.

This role is for a Sr. Scientist in Bioconjugation at Eli Lilly's new Medicine Foundry, focusing on transferring and optimizing chemical processes for bioconjugation (like ADCs) from development to clinical manufacturing. The role involves hands-on chemistry, process evaluation, analytical work, documentation, and troubleshooting within a regulated manufacturing environment.

Associate role focused on the end-to-end coordination, execution, and quality oversight of Recruitment & Retention (R&R) materials and appreciation item workflows in support of clinical trials. Responsibilities include managing vendors, overseeing documentation and approvals, and ensuring timely delivery of trial-ready materials.

This role focuses on regulatory affairs within the pharmaceutical industry, specifically managing Japan's regulatory policy and intelligence, ensuring compliance with drug and medical device laws, and driving operational excellence within the regulatory affairs department. It involves building relationships with regulatory bodies, contributing to policy strategy, managing submission processes, and enhancing compliance.

Director level role focused on clinical design for cardiometabolic health at Eli Lilly. Responsibilities include translating therapeutic area strategy into clinical development programs and trial optionality, developing study protocols, collaborating with cross-functional teams, and ensuring compliance with regulations. The role requires medical expertise and pharmaceutical industry experience in drug development and clinical trial design.

This role is for a Director in Discovery Immunology at Eli Lilly, focusing on developing biological strategy for new target validation, from target identification through mechanistic validation. The ideal candidate will have deep expertise in functional genomics, phenotypic and mechanistic discovery platforms, and primary human model systems. The role involves leading cross-functional discovery teams, driving scientific decision-making, and expanding functional genomics capabilities. This is a research-focused role within the healthcare domain, not directly related to AI/ML model development.

This role is for an Instrumentation Supervisor at Eli Lilly's Medicine Foundry, a new center for advanced manufacturing and drug development. The supervisor will oversee calibration activities to ensure equipment reliability and compliance with cGMP and other standards, leading a team of instrument technicians. The role involves managing people, ensuring quality and safety, and maintaining process, facility, and utility equipment. Experience in a regulated GMP manufacturing environment is required.

Research scientist role focused on developing and utilizing in vivo models to understand immunological mechanisms for drug discovery in autoimmune diseases. Responsibilities include leading research studies, hands-on laboratory work, data analysis, and mentoring junior scientists.

The Principal Automation Integration Engineer – API Network Integration role at Eli Lilly focuses on enabling data flow between various departments (Manufacturing Science, Quality, Engineering, Supply Chain, Operations) by integrating IT and Process Automation Technologies. The role supports innovation evaluation and application for Manufacturing Process Automation and IT Systems, with a focus on data historians, advanced analytics, cyber security, and process optimization. The primary responsibility is to integrate data for major capital projects within the API Network, working with systems like process automation platforms, HMI/SCADA, Data Historians, Alarm/Event management, and Manufacturing Execution systems. This role requires expertise in automation architecture, process automation, control systems, safety systems, and cyber security, acting as an "in-house system integrator".

This role focuses on integrating digital platforms with physical laboratory infrastructure in a healthcare setting. The engineer will design, develop, and validate software solutions, data pipelines, and APIs to connect laboratory systems, automation equipment, and enterprise platforms, ensuring secure, compliant, and scalable operations. The role involves hands-on engineering, business analysis, and collaboration with various teams and vendors to modernize laboratory workflows.

This role is for a Senior Engineer in Automation Engineering at Eli Lilly, focusing on Instrumentation and Control Hardware for pharmaceutical manufacturing. The engineer will provide automation support for operating areas and capital projects, collaborating with cross-functional teams to ensure robust control systems. Key responsibilities include design, development, commissioning, and troubleshooting of control systems using DeltaV DCS and Rockwell Allen Bradley PLC, with a strong emphasis on GMP regulated environments and validation.

This role is for a Sr. Principal Engineer in Automation Engineering, focusing on Instrumentation and Control Hardware for pharmaceutical manufacturing facilities. The engineer will provide automation support for operating areas and capital projects, lead project execution, commissioning, and qualification, and mentor other engineers. Key responsibilities include expertise in DeltaV DCS and Rockwell Allen Bradley PLCs, troubleshooting control loops, and ensuring compliance with GMP and regulatory requirements.

Lead Technician for Engineering (Night Shift) at Eli Lilly, responsible for device assembly and packaging equipment performance, providing technical support, and implementing process improvements in a GMP-regulated healthcare manufacturing environment.

Associate Director of Procurement for API External Manufacturing at Eli Lilly, responsible for managing contract manufacturing organizations (CMOs) for API production. The role involves developing category strategy, leading negotiations, managing contracts, and ensuring supply chain risks are addressed within the pharmaceutical industry.

This role focuses on bioconjugation process development for new bioconjugate medicines, including ADCs, APCs, and AOCs. The scientist will establish laboratory programs, design and execute research plans, analyze results, and propose next steps. Responsibilities include learning and applying bioconjugation techniques, purification screening, experimental design, and analytical sample analysis. The role involves collaboration across disciplines, performing fundamental studies of process steps, scale-up demonstrations, and proposing new methods. Documentation, report authoring, and contributing to commercial manufacturing strategy are also key. The role requires a BS or MS in a relevant scientific field with several years of experience in synthetic organic chemistry or biochemistry.

This role is for a Sr. Director of Project Management within Global Facilities Delivery at Eli Lilly, focusing on delivering large capital assets for medical innovation and medicine supply chains. The position requires leading cross-functional teams to manage projects from conceptual design through operational qualification, ensuring safety, cost, schedule, and quality. Key responsibilities include stakeholder communication, compliance with company policies, and developing safety/environmental execution plans. The role is based in various locations including the Netherlands and US, with travel flexibility required.

This role focuses on developing and executing health outcomes and real-world evidence (HEOR/RWE) strategies for pharmaceutical products in Japan. It involves scientific leadership in evidence generation, study design, analysis, and dissemination to support drug development, market access, and product value demonstration. The role requires collaboration with cross-functional teams and external stakeholders, and an understanding of healthcare systems and relevant regulations.

Senior Application Security Engineer responsible for integrating security testing tools into the SDLC, partnering with engineering teams on secure coding, and coordinating vulnerability remediation. The role involves developing and implementing application security strategies, performing threat analysis, and ensuring secure configurations for containers.

This role is for a Medical Science Liaison (MSL) in Oncology at Eli Lilly. The MSL is a field-based medical professional responsible for maintaining deep scientific knowledge in oncology, engaging with scientific experts to understand and communicate their medical and scientific information needs, and synthesizing complex data and insights to inform Lilly's strategic direction. The role requires strategic thinking, territory ownership, and strong communication and interpersonal skills.

Principal Computational Statistician at Eli Lilly, responsible for statistical analysis in clinical trials, including selecting methods, conducting analysis, writing reports, and responding to regulatory queries. Requires a Master's degree in Statistics or Biostatistics and 2+ years of experience with SAS/R programming.

This role is for a Sr. Director (Medical) Oral Therapies at Eli Lilly, focusing on medical affairs and clinical research. The position involves strategic planning for launch and commercialization activities, supporting local clinical trials, managing adverse event reporting, reviewing protocols and publications, and interacting with regulatory and reimbursement agencies. The role requires scientific and medical expertise to support marketed products and potentially early-phase trials, ensuring all activities comply with regulations and company standards.

Program Manager for Global Facilities Delivery (GFD) at Eli Lilly, responsible for managing large capital asset programs (>$500MM USD) from planning through operational qualification. Focuses on safety, cost, schedule, and quality assurance in pharmaceutical manufacturing facilities, requiring strong project management, communication, and compliance skills.

Associate VP for Dry Products/Spray Dried Dispersions at Eli Lilly, responsible for scientific and organizational leadership, technical product stewardship, and ensuring the organization provides rigorous support to dry product sites. This role involves managing talent, overseeing control strategy, commercialization, and the technical agenda, fostering functional excellence at manufacturing sites, and ensuring a culture of safety and compliance within a regulated healthcare environment.

This role focuses on the process design, development, and optimization of purification processes, specifically chromatography, for synthetic active pharmaceutical ingredients (APIs) within the pharmaceutical sector. The Director will lead teams, collaborate with scientists and project teams, and ensure the delivery of GMP clinical material while developing control strategies for regulatory submissions and commercialization. The position requires expertise in chromatography, scale-up methodologies, and a strong understanding of the pharmaceutical development lifecycle.

This role is for a Sr. Director of Process Chemistry at Eli Lilly, focusing on synthetic molecule route commercialization, process optimization, and unit operation definition for drug candidates. The position involves leading cross-disciplinary teams, providing technical leadership in scale-up, and collaborating with internal CMC networks and external regulatory bodies. The role requires deep expertise in synthetic organic and process chemistry, with a focus on developing and optimizing manufacturing processes for APIs. Experience with modern synthetic technologies, process modeling, scale-up methodologies, and regulatory requirements is essential.

This role focuses on developing and executing post-approval CMC regulatory strategies for Eli Lilly's global commercial portfolio, ensuring compliance with global CMC regulatory requirements for pharmaceutical manufacturing and product registrations. It involves strategic planning, submission preparation, and providing technical and regulatory expertise to manufacturing and quality teams.

The (Sr.) Medical Education Manager-Onco role at Eli Lilly in Shanghai is responsible for implementing the medical education plan for oncology. This involves identifying educational needs, developing agendas and content, managing speakers, ensuring compliance with policies, and tracking event success. The role also involves engaging with medical societies and TPOs, and ensuring all programs adhere to corporate standards. A Master's degree or above in Medicine with at least 5 years of clinical or industrial experience in Medical Affairs is required. Experience in medical affairs launch and knowledge of adult education principles are preferred.

This role focuses on developing and executing pricing, reimbursement, and market access strategies for pharmaceutical products within the healthcare domain. It involves analyzing market landscapes, preparing reimbursement dossiers, conducting financial modeling, and engaging with stakeholders and payers to ensure product success and achieve business goals. The role requires in-depth knowledge of the healthcare regulatory environment, including HTA/PE, RWE, and NHI pricing rules, and involves negotiation with payers.

Associate/Senior Associate role focused on clinical trial site initiation and management, requiring regulatory document submission, budget negotiation, contract management, and ensuring site compliance. The role involves communication with sites, regulatory authorities, and internal teams, with a strong emphasis on compliance with regulatory, data privacy, financial, and legal requirements. Fluency in both English and Spanish is required.

Associate Distribution Quality Assurance role focused on ensuring compliant and efficient distribution of medicinal products in the APAC region, maintaining oversight of GMP/GDP activities, evaluating risks, and ensuring external logistics providers adhere to regulatory requirements and quality agreements. Responsibilities include managing product quality during storage and transport, assessing deviations, overseeing logistics partners, making decisions on product usability, and managing goods releases.

This role is for a Senior Operator at Eli Lilly's Suzhou manufacturing facility. The primary responsibilities include supporting production, adhering to GMP and SOPs, performing manual and automatic packaging operations, and ensuring HSE compliance. The role requires a high school education, adaptability to shift work, and good vision.

This is a high school internship program focused on skilled trades at Eli Lilly, aimed at identifying future talent. Interns will participate in hands-on activities, learn safety and work practices, and assist with basic maintenance tasks under strict supervision. The role emphasizes adherence to safety and environmental regulations, self-management, and good communication.

Executive Medical Director role at Eli Lilly focused on clinical development leadership for cardiometabolic and renal disease portfolio. Responsibilities include developing clinical strategies and trials, overseeing global clinical trials, ensuring compliance with regulations, and interacting with regulatory bodies and external experts. Requires broad scientific expertise in renal diseases, with additional experience in cardiovascular and/or metabolic disease being a bonus.

This role is for a Utilities Engineer at Eli Lilly's new manufacturing site, focusing on the startup and ongoing support of plant utility systems like steam, chilled water, and compressed air. The position requires experience in regulated manufacturing environments and involves commissioning, qualification, validation, and continuous improvement of these critical systems to support pharmaceutical operations.

Senior/Advisor role in Peptide Process Development at Eli Lilly's Manufacturing and Quality technical hub in Hyderabad. Focuses on technical oversight, process optimization, technical transfers, and development of the technical agenda for drug substance manufacturing, with a strong emphasis on peptide chemistry and manufacturing processes. Requires comprehensive knowledge of GMP, regulatory requirements, and pharmaceutical industry practices.

This role focuses on operating, maintaining, and advancing lab automation equipment and robotic systems in a biopharmaceutical discovery setting. The goal is to support early-stage discovery and screening of protein therapeutics by improving laboratory workflows and digitalization, with a vision towards autonomous discovery systems.