Eli Lilly

Manufacturing Operator role at Eli Lilly in Puerto Rico, responsible for following manufacturing procedures, preparing and inspecting equipment, reporting discrepancies, and ensuring safety and environmental compliance. Requires an Associate's degree, knowledge of manufacturing operations and cGMP, and bilingual skills.

Director of Analytical Chemistry focused on peptide drug substance and drug product development and commercialization within a pharmaceutical company. Responsibilities include developing analytical methods, justifying specifications, designing stability studies, authoring regulatory submissions, and providing technical guidance for external analytical activities. Requires extensive experience in analytical chemistry and pharmaceutical development, with a focus on peptide therapeutics and regulatory compliance.

This role focuses on Identity and Access Management (IAM) Security Operations (SecOps) with an emphasis on Identity Governance (IGA). The engineer will be responsible for delivering and securing IGA technologies, partnering with various teams to ensure secure design and deployment of IGA solutions. Key responsibilities include developing technical specifications, optimizing identity lifecycle management, access certifications, role engineering, and continuous improvement of IGA technologies. The role requires evaluating, architecting, and implementing IGA solutions, designing integrations, ensuring operational excellence, and understanding the threat landscape related to identity governance. Collaboration with cross-functional teams and staying current on IGA technologies and regulatory requirements are also crucial.

Principal Process Engineer for sterile drug product formulation and component preparation in parenteral (PFS/vial) manufacturing. Ensures safe, efficient, and compliant operations. Requires 8+ years of experience in sterile drug product manufacturing, strong knowledge of aseptic formulation and component preparation, and GMP requirements.

Associate Vice President, Ethics and Compliance - Consumer, Digital Lilly Direct. This role provides embedded E&C partnership for Lilly’s Consumer Digital Experience portfolio, including LillyDirect, digital pharmacy operations, third-party platform partnerships, and direct-to-consumer programs. The AVP will shape compliance architecture, design frameworks, manage risks, and lead a team, ensuring adherence to pharmaceutical regulations, healthcare fraud and abuse laws, consumer protection, and ecommerce regulations within a digital health context. Collaboration with Legal, Regulatory, Privacy, and AI governance teams is key.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work with manufacturing equipment, adhere to safety and quality procedures, and pursue educational requirements. The role involves operating equipment in Material Prep, Formulation, or Filling teams, including robotics in the Filling area.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work with automated equipment in areas like Material Prep, Formulation, or Filling, including robotics, while pursuing education at a local community college. The role focuses on safe operation, quality, and adherence to Good Manufacturing Practices.

Director of Medical Affairs for Cardiometabolic Health in Primary Care, focusing on strategic planning, medical education, and scientific exchange within the German healthcare system.

Student role in Medical Affairs Neuroscience focusing on researching scientific trends in dementia, analyzing preclinical and clinical study data, conducting literature reviews, and supporting the creation of medical materials and scientific events.

The Informatics Engineer will partner with Process Translation and Analytical Laboratories to implement and support digital laboratory solutions, focusing on key lab systems like LIMS, LES, ELN, and CDS. Responsibilities include system design, configuration, validation, and release, ensuring compliance with regulatory frameworks (21 CFR Part 11, EU Annex 11) and data integrity in a GMP-regulated environment.

Associate Process Engineer for Dry External Manufacturing at Eli Lilly, focusing on technical leadership and support for contract manufacturers to ensure reliable supply and commercialization of medicines. Responsibilities include developing and sustaining process knowledge, assessing risks, participating in equipment specification and qualification, establishing process monitoring, and overseeing HSE and PSM elements. The role requires a BS in Engineering and 5 years of manufacturing/process engineering experience, with technical knowledge of dry manufacturing equipment and unit operations.

Operator role in a pharmaceutical manufacturing setting, focusing on running processes, troubleshooting, ensuring quality and safety, and training team members. The role involves operating equipment, managing production schedules, and collaborating with cross-functional teams to ensure the continuous supply of medicines.

Associate Director - Quality Engineer at Eli Lilly, responsible for technical guidance and leadership in quality standards for API/Fill finish Operations and Facilities Management, focusing on utilities and materials. Key responsibilities include quality oversight of production, engineering, automation, and laboratory operations, document review and approval, providing quality guidance, participating in investigations, data review, material disposition, and maintaining/improving quality systems. Requires BS in Engineering or science, 8 years of experience, and hands-on experience with ADC processes.

This role is for a Pharmaceutical Sales Representative specializing in Cardiometabolic Health. The responsibilities include conducting sales calls, implementing sales and marketing strategies, developing action plans, and organizing educational events. The ideal candidate has a scientific background, at least 2 years of experience as a pharmaceutical representative with knowledge in diabetes, strong sales skills, and digital literacy.

Director of Analytical Chemistry focused on Antibody-Drug Conjugates (ADCs), specifically the linker payload intermediate. Responsibilities include leading analytical method development, qualification, characterization, and control strategies, collaborating with cross-functional teams, authoring regulatory submissions, and mentoring staff. Requires PhD or MS/BS with extensive experience in pharmaceutical analytical development and regulatory affairs.

The Digital Plant Scientist will develop, implement, and maintain digital solutions, including models and data systems, to support continuous manufacturing operations in a cGMP environment. This role involves process monitoring, data analysis, integration of batch data, and collaboration with cross-functional teams to build and validate digital tools for a robust control strategy.

This role focuses on analytical chemistry for antibody-drug conjugates (ADCs) within a pharmaceutical company. It involves leading the development, qualification, and characterization of analytical methods for linker-payload intermediates, supporting regulatory submissions, and collaborating with cross-functional teams. The role requires expertise in CMC analytical development and understanding of regulatory requirements in the pharmaceutical industry.

Market Access Manager responsible for strategic planning and operational implementation of market access for innovative therapies within the Lilly portfolio in Austria. The role focuses on ensuring sustainable, timely, and broad patient access and actively shaping the health policy environment. It acts as a central interface between internal departments, the international Lilly organization, and external healthcare system partners. Key responsibilities include developing and executing market access strategies, managing reimbursement and financing mechanisms, analyzing regulatory and health policy frameworks, building relationships with stakeholders (insurers, associations, hospitals, medical societies), collaborating cross-functionally, coordinating reimbursement dossiers and value stories, translating evidence into access narratives, identifying market access barriers, and monitoring market/policy developments.

Operator for Plant Utilities at a pharmaceutical company, responsible for operating and monitoring various equipment like boilers, cooling towers, and generators. Requires an Associate degree in science or engineering, with a desirable wastewater or potable water license. Experience in pharmaceutical utilities is preferred. Must be available for 24/7 operations.

Associate Director PRA role at Eli Lilly in the Czech Republic, responsible for developing and implementing pricing and access strategies for Lilly's medicines, managing hospital business operations, and building external stakeholder relationships to ensure market access and support business priorities.

Sales Representative for Eli Lilly's Alzheimer Team in Portugal, focusing on driving sales and strategic territory management by engaging with healthcare providers and leveraging digital tools. The role requires deep knowledge of the Alzheimer's therapeutic area, strong selling skills, and the ability to manage accounts and report sales activities.

This role is for a Senior Associate Regional Trainer focused on coaching and capabilities for sales representatives in the pharmaceutical industry. The primary responsibilities include field and remote coaching to enhance sales and territory management skills, analyzing coaching success, and developing training concepts. It requires experience in sales, training, and coaching within the pharmaceutical sector, with a focus on diabetes, obesity, or CMH. Strong communication, analytical, and organizational skills are essential, along with fluency in German and English.

Marketing Lead for Cardiometabolic Health (Obesity & Diabetes) at Eli Lilly, responsible for developing and executing integrated brand and customer strategies, leading a marketing team, and driving commercialization efforts. Requires strong consumer marketing, digital channel, and media strategy expertise, with a focus on product launches and omnichannel campaigns.

Brand Manager for Obesity portfolio, responsible for developing and implementing brand and customer engagement strategies, managing omnichannel campaigns, and driving market positioning and growth in the pharmaceutical sector.

This is an internship position for a Communications Officer at Eli Lilly in France. The role involves contributing to communication strategy, creating external and internal communication materials, organizing events, and updating institutional information. The ideal candidate is a student in communication with a strong interest in the healthcare field, social media savvy, and good organizational and writing skills.

HR Manager for Compensation & Benefits at Eli Lilly in Germany, responsible for developing and implementing compensation strategies, managing C&B processes, and advising on benefits. The role involves using AI-assisted analyses and tools for process optimization.

Senior Director of Ethics & Compliance for Eli Lilly in the Gulf region, responsible for implementing the global E&C program, cultivating a speak-up culture, and providing expert guidance on affiliate strategies and activities. This role involves risk assessment, policy implementation, training, monitoring, and ensuring business processes align with global standards. It also requires influencing leadership, collaborating cross-functionally, and representing Lilly with external stakeholders and regulators.

Senior Director of Ethics & Compliance for Eli Lilly in Saudi Arabia, responsible for integrating high performance with high integrity, implementing the Global E&C Program, and cultivating a Speak up Culture. The role involves providing expert guidance on strategies, decisions, and activities, conducting risk assessments, developing and implementing training, monitoring, and ensuring alignment with ethics and compliance objectives. It requires collaboration with leadership, business partners, and regulators, and involves managing E&C program elements, influencing business practices, and driving compliance communications.

This role is a Pharmaceutical Sales Territory Manager focused on Neuroscience Specialty, specifically Alzheimer's disease. The primary responsibilities include driving brand strategies, managing accounts, educating healthcare providers and stakeholders on treatments, and building relationships within the healthcare ecosystem to ensure patient access to medication. The role emphasizes account management, sales experience, and a data-driven approach to business results.

Seeking an experienced discovery biologist to provide scientific leadership and hands-on expertise to shape early research strategy and advance novel therapeutic concepts for osteoporosis at Eli Lilly. This role involves driving mechanism-based discovery, maintaining a laboratory presence, designing and conducting experiments, and contributing to cross-functional project teams.

Senior Principal Engineer for Automation Engineering at Eli Lilly's new Medicine Foundry, focusing on advanced manufacturing and drug development. The role involves leading capital project execution, providing automation support for manufacturing operations, mentoring peers, and ensuring compliant control applications and systems. Key responsibilities include technical leadership in design, development, commissioning, and qualification of control systems, promoting digital innovation, and maintaining validated states. Requires deep expertise in DeltaV DCS, Rockwell PLCs, and GMP processes, with a strong understanding of regulatory compliance.

Associate - QA Master Data Steward role at Eli Lilly, focusing on managing master data in SAP and LIMS for specifications in a new pharmaceutical manufacturing facility. The role involves developing programs in accordance with GQS guidelines and participating in regulatory inspections.

Executive Assistant and Chief of Staff supporting the head of diabetes at Lilly, who is also the VP and site head of Lilly’s Protomer site in Los Angeles. This role provides critical administrative support, manages site initiatives, tracks projects, schedules meetings, and supports visitor arrangements. Requires strong organizational and communication skills.

The Engineering Automation Technician provides high-level automation and controls support for OEM filling equipment and associated systems in a cGMP pharmaceutical manufacturing environment. This role focuses on troubleshooting, maintenance, and ensuring automated lines operate safely and reliably, partnering with Operations, Engineering, and Quality.

Operator role in pharmaceutical manufacturing, focusing on operating equipment, troubleshooting, ensuring safety and quality, and training new staff. Requires a high school diploma and basic computer proficiency, with preferences for CGMP knowledge and lean manufacturing principles.

Physician role focused on designing Phase II to Phase IV clinical programs and studies within the neuroscience therapeutic area at Eli Lilly. Responsibilities include translating strategy into clear objectives, representing design optionality, informing protocol design, contributing to asset strategy, and collaborating with cross-functional teams. The role also involves scientific data dissemination, evaluating medical literature, and contributing to organizational learning on clinical design best practices.

This is an apprenticeship role in pharmaceutical manufacturing, specifically in the packaging area of a highly automated facility. The apprentice will work as a Lilly employee while pursuing education at a local community college, with the goal of converting to an Operator/Process Technician upon completion of the apprenticeship requirements. Responsibilities include operating automated equipment, adhering to safety and quality standards, and documenting processes.

This is an Operations Apprentice role in pharmaceutical manufacturing at Eli Lilly. The apprentice will work in a highly automated facility, operating equipment in areas like Material Prep, Formulation, or Filling, including robotics. The role involves adhering to safety and quality standards, documenting processes, and completing educational requirements as part of a one-year apprenticeship with potential for conversion to an Operator/Process Technician.

This role is for a Principal/Sr. Principal Scientist in pharmaceutical manufacturing, focusing on process understanding, technical support, and continuous improvement for API molecules. It requires a deep understanding of chemistry, experimental design, data analysis, and collaboration with cross-functional teams to ensure safe, compliant, and efficient manufacturing operations in a cGMP environment.

Seeking a Senior Director Operational Leader with strong project management, portfolio operations, and budget governance experience to transform how the DMPK/ADME organization plans, forecasts, tracks, and delivers its book of work. This role involves leading a team, optimizing operational workflows, ensuring accurate forecasting, tracking results, managing budgets, and collaborating cross-functionally.

The Automation Engineer role focuses on enabling data flow between various manufacturing and operations departments by leveraging IT and Process Automation Technologies. This includes supporting innovation, data historians (OSI PI), OT data integration, advanced analytics, data integrity, and process optimization. The role involves leading design, development, and deployment of technical solutions, providing frontline support for PI and LogMate users, managing system health checks, performing emergency response, and acting as a subject matter expert on the OSI PI Data Historian platform. Key responsibilities include data integration for manufacturing improvements, implementing technology governance, incident response, PI tag governance, patch/reboot coordination, change control, DeltaV integration support, service account management, vendor engagement, user support, training, documentation, and audit trail review.

This role is for a Process Engineer in Device Contract Manufacturing at Eli Lilly, focusing on providing technical engineering oversight for production processes to ensure stable supply of devices, subassemblies, and components. Responsibilities include leading prioritization of process changes, coordinating engineering project teams, resolving manufacturing issues, and completing engineering activities for process/product improvements. The role requires a Bachelor's in Engineering and a minimum of 2 years of manufacturing engineering experience, with a preference for pharmaceutical/medical device experience.

Principal Process Engineer role at Eli Lilly focused on API External Manufacturing for small molecules. Responsibilities include providing technical leadership to contract manufacturers, developing process knowledge, assessing equipment suitability, ensuring reliable supply, and managing HSE/PSM elements. The role involves scale-up, tech transfer, process optimization, and continuous improvement, with a strong emphasis on safety and quality.

Senior Director of Health, Safety & Environmental (HSE) for a new state-of-the-art oral solid dosage manufacturing facility in Katwijk, Netherlands. This role leads the EHS function, ensuring compliance with Dutch and EU regulations, developing safety strategies, and integrating EHS into all aspects of the site's operations, from design to start-up and ongoing manufacturing. The position requires strong leadership, strategic planning, and experience in pharmaceutical manufacturing environments.

Senior/Principal Scientist in Quality Operations at Eli Lilly, responsible for QA oversight and final disposition of radioligand drug product manufacturing. The role involves ensuring GMP compliance, supporting manufacturing processes, reviewing batch records, managing deviations, and driving operational excellence through data analysis. Requires experience in pharmaceutical QA/QC and regulatory requirements.

This role is a Senior Associate/Manager for Clinical Trial Project Management within Exploratory Medicine at Eli Lilly. The primary focus is on leading cross-functional teams to develop and execute clinical trials, ensuring quality, timeliness, and adherence to budget and scope. Responsibilities include project planning, timeline and risk management, budget oversight, investigator training coordination, enrollment strategy, vendor management, and ensuring the Trial Master File is up-to-date. The role requires a strong understanding of the drug development process and clinical trial operations.

Sales Representative role focused on promoting pharmaceutical products, managing business strategy, and utilizing multi-channel resources. Requires strong analytical, communication, and problem-solving skills, along with a driver's license and experience with technology platforms for information analysis and virtual communication.

This role is for a Computational Statistician at Eli Lilly, focusing on statistical analysis and programming for clinical trials. It involves collaborating with statisticians and study personnel, selecting and applying statistical methods, writing reports, responding to regulatory queries, and ensuring data quality. The role requires proficiency in statistical programming languages like SAS and R, and understanding of relevant disease states and regulatory compliance. It is a senior-level position with a focus on applying statistical expertise to healthcare research and development.