Eli Lilly

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.

National Engagement Advisor for Oncology (Breast Cancer) at Eli Lilly Canada. This is a field-based marketing and customer-facing role focused on building relationships with thought leaders, developing engagement strategies, and supporting commercial objectives to improve patient outcomes. Requires extensive travel across Canada.

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.

This role is a Senior Associate in QA Materials Management within a pharmaceutical manufacturing facility. It focuses on overseeing quality assurance for material receipt, batch disposition, and related processes, ensuring compliance with GMP regulations. Responsibilities include managing change controls, deviations, CAPAs, documentation, and participating in audits, with a strong emphasis on quality systems and regulatory requirements in the pharmaceutical/biotechnology sector.

Data Engineer to accelerate the delivery of data solutions for analytics projects and business operations. Design, develop, and maintain data solutions to ensure availability and quality of data for business transactions. Design and implement efficient data storage, processing, and retrieval solutions. Build data pipelines and optimize database designs. Perform data integration, acquisition, cleansing, harmonization, and transformation.

This role is for a Program Manager in Global Facilities Delivery (GFD) at Eli Lilly, a healthcare company. The primary focus is on managing large capital asset projects (>$400M USD) from planning through operational qualification, ensuring safety, cost, schedule, and quality. The role requires experience in industrial or manufacturing facilities, particularly in pharma manufacturing (GMP), and involves leading cross-functional teams and managing stakeholders. It is not directly AI/ML related but operates within a regulated healthcare environment.

Associate Director, Joint Process Team (JPT) at Eli Lilly in Hyderabad, India. This role leads a cross-functional team of Lilly and API Contract Manufacturer representatives, managing the business relationship with the Contract Manufacturer. Responsibilities include overseeing technology transfer, process validation, regulatory approval, production, batch release, and supply chain management to ensure safety, quality, and operational excellence. The role requires strong leadership, interpersonal skills, and experience in API manufacturing and cGMP environments.

Associate Director for Capital Project Procurement at Eli Lilly, focusing on sourcing and managing contracts for manufacturing capital projects, including engineering, construction, and automation services. The role involves leading sourcing strategies, supplier due diligence, negotiation, and contract management to minimize costs and risks for major capital projects.

This role is for a Regulatory Affairs professional specializing in CMC (Chemistry, Manufacturing, and Controls) for pharmaceutical products at Eli Lilly in Kobe, Japan. The responsibilities include managing CMC-related regulatory tasks throughout the drug development lifecycle, from clinical trials to post-market maintenance, including preparing submission documents and liaising with regulatory authorities. The role requires experience in pharmaceutical regulatory affairs, particularly in CMC, and strong communication skills in Japanese and English.

Senior Executive Assistant to support Group Vice President and CEO, LillyDirect, providing communication, scheduling, office management, and other supportive duties. Requires strong organizational skills, attention to detail, and the ability to work independently in a dynamic environment.

Eli Lilly is seeking a Pharmaceutical Manufacturing Operator for a new, cutting-edge facility focused on advanced therapies like Gene Therapy. The role involves performing routine manufacturing activities in GMP areas, supporting equipment qualification, developing procedures, and setting up production areas during the startup phase. Once operational, the operator will execute production activities. The position requires adherence to strict quality and safety standards, documentation, and collaboration with various departments. Experience with pharmaceutical cleanrooms and manufacturing equipment is preferred.

Associate Director for Advanced Therapies Manufacturing at Eli Lilly, focusing on technical and people leadership for drug substance and drug product processes in a cGMP late-phase and commercial manufacturing facility. Responsibilities include technology transfer, process validation, control, and improvement, ensuring GMP compliance and partnering with cross-functional teams. Requires experience in gene therapy platforms and regulatory expectations.

Associate Director for Capital Project Procurement at Eli Lilly, focusing on sourcing and managing contracts for manufacturing capital projects, including automation, construction, and engineered equipment. The role involves developing sourcing strategies, negotiating agreements, managing supplier relationships, and identifying cost/risk reduction opportunities within the pharmaceutical manufacturing sector.

Senior Principal Application Support Engineering Lead responsible for end-to-end support operations in a highly regulated, high-availability healthcare environment. This role involves leading incident response, problem management, driving reliability strategy, and ensuring operational readiness and compliance. It is a strategic and hands-on position focused on organizational impact and scaling reliability through others.

Senior Principal Application Support Engineer & Shift Lead responsible for the health, stability, and operability of production systems in a regulated, high-availability healthcare environment. This role involves leading support operations end-to-end, incident command for major incidents, problem management, driving reliability strategy, and ensuring compliance.

This role is for a Medical Science Liaison in Cardiometabolic Health at Eli Lilly. The primary responsibilities include scientific engagement and education with healthcare professionals, managing relationships with Key Opinion Leaders (KOLs), generating insights from therapeutic trends, collaborating cross-functionally, and ensuring compliance with regulations. The role requires a strong scientific background, excellent communication skills, and the ability to travel.

This role is for a Principal / Sr. Principal - In Vivo Biologist in Cardiometabolic Research at Eli Lilly. The primary focus is on conducting experiments using animal models of cardiorenal and cardiometabolic diseases, including developing and validating models, performing in vivo studies, executing laboratory procedures, preparing formulations, administering test articles, performing surgical techniques, and analyzing/interpreting data. The role also involves mentoring staff and ensuring compliance with policies and safety guidelines.

This role is for a Principal Engineer focused on Automation for Utility Systems in a GMP pharmaceutical manufacturing facility. Responsibilities include system design, hardware/software selection, delivery strategy, testing, and supporting manufacturing operations. Experience with Rockwell Automation or Emerson DeltaV platforms is preferred.

Senior Director role leading global network for Primary Packaging Components, Container Closure Systems, Process Contact Materials, and Excipients in a pharmaceutical manufacturing setting. Focus on standardization, compliance, and operational excellence.

Eli Lilly is seeking a TS/MS Primary Loop (R4) to act as a process expert for external manufacturing, focusing on pre-filled syringes, autoinjectors, and packaging. The role involves owning the process control strategy, ensuring validated states, managing deviations, and driving continuous improvement. Requires a Bachelor's degree in a relevant field and 5 years of experience in pharmaceutical manufacturing, cGMPs, validation, deviation resolution, device assembly/packaging, and technology transfer.

This role is for a (Sr./Principal) TS/MS Engineer focused on commercialization of pharmaceutical products within a regulated healthcare manufacturing environment. Responsibilities include technology transfer, process improvements, post-approval changes, deviation investigation, and supporting regulatory registration. The role requires experience in sterile formulation manufacturing within a cGMP environment.

Associate Director - Clinical Research Lead for Oncology, responsible for driving the execution of clinical trials through investigator engagement and site performance management. This role requires deep therapeutic and scientific knowledge to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies. The CRL serves as a trusted partner to investigators, building strong relationships to improve enrollment and position Lilly as the sponsor of choice. The role also involves partnering with internal teams to ensure field insights shape development strategies and that strategies are delivered with operational excellence and scientific clarity. Where applicable, the CRL may represent Investigator Engagement with Regulatory and External Bodies.

This role is for a Pharmaceutical Sales Representative focused on promoting immune products within a specific territory in China. Responsibilities include achieving sales targets, developing and maintaining customer relationships (hospitals), providing product information, gathering market intelligence, and contributing to team efforts. The role requires a bachelor's degree in a pharmaceutical-related field and prior experience in pharmaceutical promotion or new product launches is preferred.

This role is for a pharmaceutical sales representative focused on promoting company products within a specific territory in Xi'an, China. The responsibilities include achieving sales targets, building and maintaining customer relationships (hospitals), providing product information, 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 or new product launches is preferred.

Associate Director role focused on Quality Management System (QMS) Lifecycle Management within R&D at a pharmaceutical company. The role involves partnering with Global Process Owners to support the integrity and evolution of QMS processes, monitor health, report on metrics, identify improvements, and ensure alignment with global regulatory standards and internal requirements for R&D processes.

Senior Director of Process Engineering & Automation responsible for leading site's process-facing engineering functions, including process engineering, automation, and process controls, to support startup and long-term manufacturing goals for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing. Role involves organizational development, functional strategy, safety leadership, project support, and ensuring system readiness for GMP operations.

Senior Director of Engineering responsible for leading facilities, utilities, and maintenance operations for a new advanced manufacturing facility. This role involves building the organization, defining strategies for site startup and long-term GMP manufacturing, ensuring system readiness, and driving operational excellence, asset reliability, and compliance with cGMP standards. The position requires leadership in developing and implementing maintenance strategies, managing capital projects, and ensuring a safe and qualified operational environment.

This role is for a Sr. Principal Engineer focused on Automation for Small Molecule API manufacturing at Eli Lilly. The primary responsibility is to lead the design, delivery, and qualification of the DeltaV platform and associated software integration teams for a new greenfield manufacturing facility. The role involves collaborating with various stakeholders, managing system integrators, and ensuring the automation systems meet GMP standards. Post-project delivery, the role will support ongoing manufacturing operations.

This role provides quality oversight for medical devices and combination products during technical transfer to contract manufacturing operations, ensuring design meets critical requirements and risks are identified and addressed. It also verifies equipment fitness for use and manufacturing readiness for contract manufacturers and suppliers.

Principal Statistician - Computation (R3) at Eli Lilly to collaborate on statistical analysis plans, select statistical methods, perform data analysis, and apply SAS programming and statistical methodology. Requires a Master's degree in Statistics or related field, experience with SAS and R, clinical trial data standards (CDISC SDTM/ADaM), regulatory guidelines (ICH E9/E3), version control (Git/GitHub), and reporting tools (Pinnacle 21, Spotfire, SAS ODS Graphics, R Markdown).

This role is for a SAP Transportation Management Systems Architect at Eli Lilly, focusing on implementing and designing SAP EWM and TM solutions for manufacturing and distribution operations. It involves partnering with various IT and business teams to design future state landscapes and integrate warehouse automation technologies.

Quality Control Associate at Eli Lilly responsible for technical support in pharmaceutical device testing, including design verifications, process validations, stability testing, and batch release testing. The role involves investigating quality deviations, supporting change management, reviewing GMP laboratory data, and participating in regulatory inspections. Requires a Bachelor's degree and experience in quality control operations for parenteral or pharmaceutical products, documentation systems, and regulatory requirements like CGMP and ISO13485.

Process Engineer (R3-R4) at Eli Lilly responsible for ensuring a safe working environment and improving the safety culture within pharmaceutical manufacturing. The role involves technical expertise in equipment and process, leading troubleshooting efforts using formal problem-solving techniques like Root Cause Analysis, and providing oversight to support staff. Requires a Bachelor's degree in a related STEM field and significant experience with validated systems, safety improvements, testing, and equipment problem resolution in the pharmaceutical industry.

Manager for the Maximo System, responsible for delivering, maintaining, and supporting products and solutions. This role involves identifying system architecture requirements, designing integration solutions with third-party applications (like SAP, Oracle, OSI PI), and driving agile delivery. Requires extensive experience with IBM Maximo, integrations, business intelligence, data analytics, and Computer System Validation within GxP environments.

Director, Engineering, Parenteral (M2-M3) to lead a team of professionals in delivering the full scope of parenteral/DAP systems—from user requirements through design, build, commissioning, qualification, validation, and operation—while supporting site leadership in building a diverse, engineering-driven organization.

Principal Software Engineer at Eli Lilly to design, develop, and maintain software solutions for pharmaceutical operations, focusing on CI/CD, automation, database optimization, and ensuring performance, security, scalability, reliability, and cost-efficiency. Requires a Bachelor's degree and 4 years of full-stack development experience with specific technologies like Javascript, C#, .NET, and API development.

Clinical Research Physician role at Eli Lilly focused on providing medical leadership and guidance on the safety of pharmaceutical compounds, supporting surveillance programs, conducting risk management planning, and reviewing safety signal data within a regulated healthcare industry setting.

This role focuses on data integration and analytics within a manufacturing context, involving data pipeline development, data transformation, and stakeholder management to provide data-driven solutions. It requires experience in creating data pipelines, developing stored procedures, analyzing survey data, data cleaning, and implementing automation solutions.

Develops product and process improvements for a regulated manufacturing environment, focusing on design control, validation, verification, and manufacturing control strategy. Responsibilities include developing specifications, protocols, and technical reports, supporting product lifecycle management, leading FMEA and root cause investigations, and participating in design reviews. Requires experience in technical services/manufacturing sciences within a regulated setting, CAD software, continuous improvement, analytical evaluations, device platforms, and drug product/medical device regulatory requirements.

This role is for a Principal Engineer focused on designing and developing system-to-system interfaces within the SAP environment. It involves configuring, monitoring, tuning, and troubleshooting the SAP technical environment, analyzing user needs, and modifying existing software. The position requires experience with enterprise integration solutions, API management tools, and various SAP modules, as well as standard data formats and API standards.

Global Marketing Director role at Eli Lilly, a healthcare company. Responsibilities include developing brand strategy, product positioning, and executing marketing campaigns. Requires a Bachelor's degree and experience in pharmaceutical marketing, budget management, international collaboration, product launches, and cross-functional team leadership.