Eli Lilly

This role is for a Medical Science Liaison in the Cardiometabolic Health field. The primary responsibilities include engaging with healthcare professionals to provide and gather scientific and clinical information, acting as a liaison between Lilly and the scientific community, and contributing to Lilly's strategic direction. The role requires advanced scientific knowledge, strong communication and presentation skills, and the ability to manage a territory effectively.

Junior Quality Assurance Engineer role at Eli Lilly, a global healthcare leader. The role focuses on monitoring GMP services, participating in qualification/validation projects for GMP equipment and systems, ensuring quality standards are met for facilities, services, equipment, and control systems (ISA 95 level 1). It also involves providing technical and quality advice for continuous improvement and ensuring systems remain validated throughout their lifecycle. No prior experience is required, but pharmaceutical sector internships are a plus. Fluency in English (C1) is mandatory. Key personal skills include teamwork, customer orientation, decision-making, strong communication, organization, attention to detail, knowledge of Good Manufacturing Practices (GMP), quality concepts in the pharmaceutical industry, and common IT tools.

Junior Data Administrator role focused on maintaining master data (GMP and business) for a manufacturing plant using SAP and other systems. Responsibilities include data entry, cleaning, verification, and supporting optimization and incident resolution. Requires technical training in administration/finance and user-level computer skills, with Excel/Office proficiency. SAP knowledge is desirable.

Post-doctoral Biologist role at Eli Lilly focused on discovering and advancing peptide and antibody drugs. Responsibilities include developing rodent models, executing in vivo studies, performing cell culture and assays, analyzing data, and collaborating with internal and external teams. Requires a Ph.D. in Biology, proficiency in in vivo studies, and experience with small animal surgery and cell-based assays.

The Lead Maintenance Planner at Eli Lilly is responsible for improving equipment reliability and productivity by planning and scheduling maintenance activities. This role involves managing work orders, ensuring spare parts availability, coordinating with vendors, and utilizing a CMMS like Maximo. The position is in a manufacturing facility startup environment, with a transition from initial spare parts coordination to full-time planning and scheduling.

Maintenance Mechanic for pharmaceutical manufacturing equipment including UV curing, vision systems, laser marking stations, conveyors, and robotics. Responsibilities include machine maintenance, setup, condition monitoring, troubleshooting, developing repair part lists, and proactive reliability planning within a regulated industry.

Operator role focused on assembly and packaging of medical devices in a regulated manufacturing environment. Responsibilities include operating equipment, adhering to SOPs and cGMP, documenting processes, and ensuring product quality and safety. This is a fixed-duration employment role.

This role is for a Senior Manager of Process Control and Automation Engineering in a regulated GMP manufacturing environment. The individual will provide technical and people leadership for automation systems, ensure compliance with standards, and drive continuous improvement. Responsibilities include defining automation strategy, leading multi-disciplinary teams, and ensuring safe, compliant, and reliable automated systems.

This role is for a Process Control & Automation Engineer focused on Building Management and HVAC systems for a pharmaceutical manufacturing facility. It involves developing, implementing, and maintaining automation solutions within a Good Manufacturing Practices (GMP) environment. The role requires experience with control systems, computer system validation, and IT platform support, but is not directly involved in AI/ML model development.

This is an apprenticeship role in Medical Affairs Oncology at Eli Lilly, focusing on supporting medico-marketing activities, scientific literature analysis, and participation in medical unit activities. The role requires a scientific background, autonomy, organizational skills, and proficiency in English and Microsoft Office.

Project Manager for Global Facilities Delivery at Eli Lilly, responsible for leading teams to deliver large capital asset programs ($50M+ or workstream of $200M+) in industrial/manufacturing facilities, focusing on safety, cost, schedule, and quality. Requires a Bachelor's in Engineering or Project Management and 5+ years of experience in capital project delivery, including greenfield projects.

Director of Regenerative Biology at Eli Lilly, leading preclinical inner ear regeneration programs. Focuses on scientific strategy, study design, execution, and external collaborations for gene therapy and regenerative approaches. Requires PhD and extensive experience in inner ear biology or related fields, with a track record of advancing programs through preclinical development.

Medical Monitor role at Eli Lilly focused on ophthalmology clinical trials. Responsibilities include providing medical input into trial design, reviewing study documents, assessing safety data, and training site staff. Requires an MD or DO, board eligible/certified in Ophthalmology, and at least 5 years of experience in medical monitoring, clinical development, or pharmacovigilance.

Associate role focused on supply chain project planning within a pharmaceutical company, involving data gathering, solution development, and change management in a regulated environment.

Process Technician role focused on the safe operation of highly automated equipment in formulation, filling, and material preparation within a pharmaceutical manufacturing environment. Requires adherence to Good Manufacturing Practices (GMP) and safety standards, with responsibilities including quality control, troubleshooting, and training support. The role operates on a night shift schedule and requires the ability to work in a cleanroom environment.

Associate Director for Quality Control (QC) Analytical Sciences at Eli Lilly, leading a team to support site operations, QC, and commercialization within IAPI. Responsibilities include developing technical capabilities, overseeing method development and transfers, driving improvements in analytical control strategy, identifying new technologies, prioritizing initiatives, and ensuring the technical soundness of the analytical control strategy from raw materials to drug substance. The role also involves troubleshooting analytical issues, collaborating on innovative solutions, supporting regulatory inspections, and developing technical coaching.

Associate Director for Clinical Development Neuroscience at Eli Lilly, responsible for leading and directing teams involved in clinical trials. The role focuses on operational oversight, resource management, and ensuring compliance with regulations and best practices in drug development.

Manager for Technical Platform Integrator role at Eli Lilly, focusing on developing and supporting applications for clinical trials. The role involves end-to-end delivery of software implementations, ensuring compliance with GxP, cybersecurity, and validation requirements. It also requires partnering with business stakeholders to define strategy and roadmap, translating business needs into technical requirements, and managing delivery risks. A key aspect is investigating and proposing the implementation of AI and automation solutions.

This role is for a Quality Assurance System Manager at Eli Lilly's Fegersheim production site. The primary focus is on managing a team, ensuring adherence to quality and safety procedures, managing documentation and quality systems, and resolving operational and technical issues within a pharmaceutical manufacturing environment. It involves leadership, team management, and ensuring compliance with regulations.

Process Engineer role at Eli Lilly's new Medicine Foundry, focusing on purification of biologics, peptides, oligonucleotides, and bioconjugates. Responsibilities include technical assessment, process knowledge development, optimization, and equipment management within a GMP manufacturing environment. Requires BS/MS in chemical engineering and 1-4 years of relevant experience.

The Engineer - Automation Engineering will provide automation support for manufacturing operations at Eli Lilly's new Medicine Foundry. This role involves technical leadership, mentoring, implementing automation projects, and ensuring compliant control applications and systems for GMP operations. The focus is on process automation, DCS/SCADA systems, and maintaining validated states of control systems.

Associate, Quality Assurance role supporting the startup of the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The role focuses on quality functions within a cGMP environment, ensuring compliance with regulations, and supporting cross-functional teams in optimizing manufacturing processes.

This role is within the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The Advisor will provide quality oversight of GMP operations for small molecule manufacturing, focusing on process quality, compliance, and operational readiness during the design and construction phase, with startup anticipated in 2027. The role involves developing early phase quality processes, ensuring compliance with regulations, and collaborating with cross-functional teams.

This role is for a Director of Process Engineering at Eli Lilly's new Lilly Medicine Foundry, focusing on advanced manufacturing and drug development for complex therapies. The position involves leading technical innovation in equipment design, developing predictive modeling capabilities, and establishing scalable manufacturing paradigms for novel therapeutic modalities, including small molecules, peptides, oligonucleotides, and bioconjugates. The role requires a PhD in Chemical Engineering and leadership of a small team.

Internship role focused on process automation, specifically analyzing spare parts, monitoring their lifecycle, and creating an inventory management application to anticipate supply needs and reduce production impact. Involves data collection, demand forecasting, and interdisciplinary collaboration within an industrial setting.

The role is for a Junior Technician in Quality Control Laboratory Equipment and Systems at Eli Lilly. The primary responsibilities include leading validation projects for laboratory equipment, evaluating new equipment, performing calibration and maintenance, resolving system incidents, creating instrumental methods, and maintaining the laboratory's quality system according to GMP standards. The role requires a university degree in Chemistry, Health Sciences, or Engineering, fluent English, and the ability to work in a regulated environment. Additional preferences include strong interpersonal, organizational, and technical skills related to GMP.

Senior Quality Control Laboratory Technician at Eli Lilly in Alcobendas, Spain. Responsibilities include leading validation projects for laboratory equipment, evaluating new equipment, performing calibration and maintenance, supervising chemical analyses, and collaborating on incident resolution and quality system maintenance. Requires a university degree in Chemistry, Health Sciences, or Chemical Engineering, minimum 3 years of GMP QC lab experience, and fluent English.

Associate Director - IT Systems Delivery Lead for a global healthcare leader in the pharmaceutical industry. This role will oversee and align multiple programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. Responsibilities include program management, release train engineering, GxP compliance, stakeholder management, risk management, resource allocation, and reporting. Requires a strong business understanding, analytical skills, and the ability to manage large-scale, cross-functional projects. Experience in Pharma and GMP Manufacturing is required.

The Principal Scientist Visual Inspection Steward at Eli Lilly will serve as the technical subject matter expert and program owner for visual inspection processes in a new pharmaceutical manufacturing facility. This role involves developing and implementing control strategies, training personnel, troubleshooting issues, ensuring compliance with regulatory guidance (e.g., USP <1790>), and driving continuous improvement in visual inspection operations. The position requires strong technical writing, communication, and project management skills, with a focus on pharmaceutical manufacturing and quality.

This role is for a Senior/Principal Scientist in Technical Transfer at Eli Lilly, focusing on manufacturing processes for insulin products. The responsibilities include technical support for new product introductions, ensuring accurate documentation and control strategies, and executing validation activities. The role requires a degree in a relevant field, knowledge of GMP and parenteral manufacturing, and strong project management skills.

This is an Associate Quality Assurance role within a pharmaceutical company, focusing on maintaining compliance with pharmaceutical regulations, managing product complaints, and contributing to the quality management system. It involves preparing for inspections and audits, and managing documentation. The role requires a background in pharmacy or quality management and proficiency in MS Office and English.

This role focuses on analytical development for protein synthesis and peptide chemistry within a pharmaceutical manufacturing and quality technical hub. It involves developing analytical methods, designing and analyzing experiments, and providing technical support for process development. The role requires a Ph.D. in Chemistry or Analytical Chemistry with 12+ years of experience and emphasizes safety, people leadership, and scientific/technical leadership in analytical and semi-preparative scale separation.

Develops and optimizes analytical methods for RNA drug substances and LNP products in a healthcare setting, partnering with cross-functional teams and ensuring compliance with regulations.

Internship role focused on maintenance and reliability in a pharmaceutical manufacturing environment, involving data collection, technical analysis, and optimization of preventive maintenance strategies. Collaborates with cross-functional teams in a GMP-regulated setting.

Associate Director/Director, Global Intake and Triage Leader at Eli Lilly, responsible for operational leadership of end-to-end intake and triage processes for Individual Case Safety Reports (ICSRs) globally. This role ensures timely, accurate, and compliant receipt, acknowledgment, and initial assessment of adverse event information from all sources, managing global operations, triage, acknowledgment, invalid case assessment, literature screening, and escalation pathways. It requires collaboration with various internal teams and technology partners, people management of manager-level leaders, and support for regulatory inspections. The role demands a strong understanding of global pharmacovigilance regulations and experience with safety databases.

Seeking an Advisor/Senior Advisor, Engineering for Biologics Drug Product Development at Eli Lilly. This role focuses on defining and developing clinical manufacturing processes for parenteral drug products, establishing control strategies, and collaborating with cross-functional teams. The position also involves leading process design, tech transfer, authoring regulatory documents, and evaluating new technologies in drug product development. Requires a PhD/MS/BS in a relevant field with significant industry experience in pharmaceutical development or manufacturing, and a strong understanding of cGMP and regulatory guidelines.

Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innovation - Small Molecules role at Eli Lilly. This position provides strategic, tactical, and operational regulatory CMC leadership for the small molecule portfolio, supporting clinical trial applications, market registrations, and post-approval submissions. Requires deep technical knowledge of CMC development and manufacturing processes, and global regulatory requirements. The role involves leading the preparation, review, and approval of CMC documents for global regulatory submissions and providing regulatory guidance to development teams. Requires a B.S. degree in a science, engineering, or STEM related field with 10+ years of Regulatory CMC or technical CMC experience supporting synthetic molecules.

Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innovation - Small Molecules at Eli Lilly. This role provides strategic, tactical and operational regulatory CMC leadership across therapeutic modalities and manufacturing technologies to expedite development of the small molecule portfolio and to support clinical trial applications, market registrations, and post approval submissions. Requires deep technical knowledge of small molecule CMC drug development and manufacturing sciences, and knowledge of global CMC regulatory requirements and guidelines. Requires 10+ years of Regulatory CMC or technical CMC experience.

Senior/Executive Director Clinical Research Physician focused on Breast Cancer and PI3K pathway drugs within Eli Lilly's Global Medical Affairs organization. This role involves strategic planning, drug development support, commercialization activities, engaging with external stakeholders (KOLs, investigators), and leading a team of medical affairs professionals. The primary focus is on improving patient outcomes through scientific and medical expertise, particularly for tersolisib, a PI3Ki in late-phase development.

Process Engineer at Eli Lilly's Medicine Foundry, focusing on the development, scale-up, and manufacturing support for small molecule drug substances. The role involves technical authority for equipment design, engineering calculations, process simulation, and ensuring compliance with GMP and regulatory standards.

This role is for an Automation Engineer with expertise in Data Historian systems (OSI PI) and Data Architecture within a pharmaceutical manufacturing environment. The engineer will provide automation support for operating areas, manage data contextualization, and ensure compliance with GMP standards. Responsibilities include collaborating with cross-functional teams, troubleshooting system issues, maintaining system health, developing documentation, and ensuring the validated state of control systems.

This role is for a Senior Principal Engineer in Automation Engineering within the Lilly Medicine Foundry. The primary focus is on providing automation support for laboratory and analytical equipment in a pharmaceutical manufacturing setting, ensuring reliable and compliant control applications and systems. Responsibilities include technical leadership, mentoring, project plan development, overseeing system integrators, DCS software design, troubleshooting control loops, and maintaining validated states of control systems in line with GMP and quality standards. Experience with SCADA, DCS, MES, LIMS, and Site Historian systems is preferred.

Senior Principal Engineer for Automation Engineering at Eli Lilly's Medicine Foundry, focusing on automation support for advanced manufacturing and drug development. The role involves technical leadership, mentorship, and implementation of control applications and systems within a GMP environment, ensuring reliable and compliant operations. This includes developing automation plans, overseeing system integration, designing and configuring DCS software, and supporting capital projects and new product introductions.

This role is for an MES System Engineer in the pharmaceutical industry, focusing on designing, developing, implementing, and maintaining Manufacturing Execution Systems (MES) to optimize production processes, ensure data accuracy, and maintain compliance with GMP regulations. The role involves integrating production operations with business systems and collaborating with cross-functional teams.

This role focuses on the technical aspects of drug substance manufacturing, including process optimization, technical transfers, and developing the technical agenda within the pharmaceutical industry. It requires comprehensive knowledge of GMP, regulatory requirements, and external influence in the peptide space. The position involves leading a team of process chemists, resolving technical issues, and ensuring processes are compliant and well-documented.

Senior Scientist role at Eli Lilly in Germany focused on technical leadership and stewardship for aseptic filling processes in a new high-tech production facility. Responsibilities include supporting validation, lifecycle management, process issues, continuous improvement, and ensuring compliance with GMP and regulatory expectations. Requires a degree in a relevant field, professional experience in the industry, and knowledge of GMP operations.

Senior Manager role in the pharmaceutical industry focused on developing and implementing pricing and reimbursement strategies for the China market. Responsibilities include new product strategy, payer engagement, health economic outcomes research, and cross-functional collaboration.