This role is for a Sr. Principal Associate for Analytical Quality Assurance at Eli Lilly, focusing on ensuring laboratory activities in the Lilly Medicine Foundry meet global quality standards and cGMP. The position involves quality oversight for GMP testing, analytical development, method verification, qualification, and validation, as well as managing quality systems and investigations for deviations and out-of-specification results. The role requires a strong understanding of analytical methods, quality management systems, and pharmaceutical industry experience.

This role supports laboratory and administrative operations for process development activities in advanced manufacturing for various drug modalities at the Lilly Medicine Foundry. Responsibilities include preparing equipment, running experiments, performing basic analyses, maintaining lab notebooks, and contributing to troubleshooting.

This role is for an Instrumentation/Medium Voltage Electrician responsible for servicing, troubleshooting, and maintaining equipment in utilities at Eli Lilly's manufacturing facilities. The position involves preventive and corrective maintenance on medium voltage electrical equipment, complex electrical equipment, and process instrumentation. It also includes performing modifications, new installations, and diagnosing electrical and instrumentation problems to minimize downtime. The role requires a strong electrical aptitude, compliance with safety and cGMP standards, and good documentation practices.

This role is for a Medical Science Liaison (MSL) in Neuroscience at Eli Lilly. The MSL will act as a scientific and clinical expert, engaging with healthcare professionals to provide in-depth information about therapeutic areas, Lilly compounds, and competitive landscapes. Responsibilities include continuous learning, customer engagement, territory ownership, and synthesizing customer insights for internal teams. The role requires an advanced degree in health sciences and clinical or therapeutic area experience, with a strong preference for Neuroscience experience. The position involves significant travel and requires strong communication, strategic thinking, and self-direction.

The Director, RWE, CMH role at Eli Lilly is responsible for developing and executing the Real-World Evidence strategy within Medical Affairs. This involves designing and overseeing observational studies, registries, and other real-world data analyses to inform clinical practice, regulatory decisions, and healthcare policy. The role requires collaboration with various internal and external stakeholders, including HEOR, Market Access, Regulatory, and KOLs, to generate and disseminate high-quality evidence across the product lifecycle.

Scientist responsible for the technical integrity, reliable supply, and compliance of reference standard manufacturing activities within a global healthcare company. This role involves influencing drug development phases by establishing and executing manufacturing strategies for reference standards, ensuring scientific soundness, integration with control strategies, and regulatory compliance. The Scientist collaborates with global teams and external partners, manages projects, and makes decisions regarding manufacturing strategies and technical issue resolution.

This role leads pharmacovigilance (PV) strategy with alliance partnerships for Global Patient Safety (GPS). It involves evaluating business deals for safety operational risks and planning for PV system integration of acquisitions/divestitures, defining strategy, performing due diligence, leading negotiations, and ensuring compliance with GVP regulations.

Process Technician for a Prefilled Syringe Line in a pharmaceutical manufacturing facility, focusing on safe operation of automated equipment, adherence to GMP, and supporting operational improvements.

Supervisor for a medical device assembly process team, responsible for daily operations including safety, compliance, operator development, scheduling, and issue resolution. This role involves shift leadership in a manufacturing environment with a focus on safety, quality, and productivity.

This is an apprenticeship role within the Utilities/HVAC team at Eli Lilly, focusing on energy efficiency and maintenance of production facilities. The role involves monitoring and improving the performance of energy installations, performing preventive and corrective maintenance, and ensuring safety. It also includes data logging and updating technical documentation. The role is aimed at developing skills in energy management and industrial processes within a healthcare manufacturing context.

Production Line Mechanic responsible for general maintenance support, equipment uptime, and reliability in a cleanroom manufacturing environment. This role involves troubleshooting, performing corrective and preventative maintenance on machinery, and supporting projects related to production and utility equipment, all while adhering to GMP standards and safety protocols.

This role is for a Synthetic Chemist/Peptide Therapeutics Advisor in Biotechnology Discovery Research. The individual will design, synthesize, optimize, and characterize therapeutic peptides and bioconjugates, leading hands-on research, driving SAR strategies, and generating data for project decisions. The role involves integrating knowledge across peptide chemistry, bioconjugation, and pharmaceutical developability, collaborating cross-functionally, and contributing to scientific productivity through publications and patents.

Senior Director of Process, Maintenance & Automation Engineering at Eli Lilly's new manufacturing facility in Katwijk, Netherlands. This role provides strategic and operational leadership for Process Engineering, Automation, and Maintenance functions, ensuring the reliability, compliance, and continuous performance of manufacturing equipment, control systems, and automated technologies. The position champions next-generation manufacturing capabilities and oversees a GMP-compliant maintenance program from site startup through steady-state operations.

Manager/Senior Manager Medical Science Liaison role at Eli Lilly, a global healthcare leader. The role focuses on engaging with scientific experts in oncology, providing deep scientific knowledge, and communicating clinical insights to inform Lilly's strategic direction. Requires advanced scientific expertise and strong communication and relationship-building skills.

Sr. Principal Associate in Microbiology at Eli Lilly, focusing on QC laboratory operations, GMP compliance, method validation, investigations, and regulatory inspections within the pharmaceutical industry.

Associate Director, TS/MS Manufacturing CMC Project Management role at Eli Lilly, focused on integrating Manufacturing CMC elements for molecule commercialization and managing the development and implementation of technical plans for commercially manufactured molecules. The role leads cross-functional teams to ensure integrated CMC plans, accelerate medicine delivery, and coordinate Global Product Assessments. It requires strong project management, leadership, and communication skills within the pharmaceutical manufacturing context.

This role is an IT Analyst focused on supporting manufacturing operations at Eli Lilly. Responsibilities include managing IT systems, troubleshooting issues, ensuring compliance with GMP and data integrity standards, and leading IT projects. The role requires knowledge of IT infrastructure, business processes, and computer system validation (CSV) within a regulated healthcare environment.

Lead role in parenteral manufacturing operations at Eli Lilly, focusing on operating equipment, providing frontline leadership, technical troubleshooting, and operator development. The role involves supporting commissioning, qualification, and operational readiness in a new facility, ensuring compliance with safety and production procedures, and driving departmental objectives. Requires experience in pharmaceutical or medical device manufacturing and knowledge of cGMPs.

Supervisor for Parenteral Manufacturing Operations on the 3rd shift at Eli Lilly's Kenosha County facility. Responsibilities include direct line supervision of operators, ensuring safety and quality, driving operational improvements, supporting commissioning and qualification, and coaching employees. Requires a High School Diploma/GED and 2+ years of experience in pharmaceutical manufacturing operations with a strong understanding of FDA guidelines and cGMP requirements.

Supervisor for Parenteral Manufacturing Operations at Eli Lilly, focusing on direct line supervision of operators, ensuring safety and quality, and driving operational improvements in a pharmaceutical manufacturing setting. Requires experience in regulated environments and cGMP compliance.

Supervises parenteral manufacturing operations on the 1st shift, focusing on safety, quality, and operational improvements in a state-of-the-art facility. Responsibilities include direct line supervision, employee development, ensuring compliance with policies and procedures, participating in commissioning and qualification, and collaborating with cross-functional teams. The role requires a strong understanding of FDA guidelines and cGMP requirements, with experience in aseptic or sterile manufacturing environments preferred.

Associate Director for Capital Projects Procurement Leader at Eli Lilly, responsible for sourcing suppliers for automation, construction, engineering, and engineered equipment for manufacturing components, with a focus on the US and Puerto Rico. The role involves category management, leading sourcing strategies, contract negotiation, supplier due diligence, and managing supplier relationships to minimize costs and risks for major capital projects.

This role provides strategic, tactical, and operational regulatory CMC leadership for biologics, focusing on expediting development, supporting clinical trial applications, market registrations, and post-approval submissions. It requires deep technical knowledge of CMC development and manufacturing processes, coupled with a strong understanding of global regulations and guidelines.

Scientist role focused on assay validation, troubleshooting, and clinical testing for immunogenicity and biomarker studies in a healthcare setting. Involves developing and implementing laboratory protocols, ensuring regulatory compliance, and managing data. Requires a Bachelor's degree with industry experience and strong organizational and communication skills.

The Associate Director - Medical Science Liaison (Cardiometabolic) role at Eli Lilly is responsible for engaging with scientific and clinical experts in a specific therapeutic area to provide in-depth scientific and clinical information. This role involves synthesizing research, responding to medical information needs, and communicating insights to inform Lilly's strategic direction. It requires deep content knowledge, strategic thinking, and field execution.

This role is for a Maintenance Technician in a pharmaceutical manufacturing environment. The primary responsibilities include servicing, repairing, and maintaining process and utility equipment to improve equipment uptime and efficiency. The role requires mechanical aptitude, troubleshooting skills, and adherence to safety procedures. Basic qualifications include a high school diploma and 2 years of automation experience.

Advisor - Computational Statistics role at Eli Lilly, focusing on statistical trial analysis, communication of results, and regulatory compliance within the healthcare domain. Requires a Master's degree in Statistics or Biostatistics and 6+ years of industry experience, with proficiency in SAS and R.

Supervisor for a QC Chemical Laboratory in a pharmaceutical setting, responsible for overseeing laboratory operations, ensuring compliance with GLPs and cGMPs, managing a team of analysts, and ensuring safety and adherence to regulations.

Associate Director of Quality Assurance responsible for ensuring operational readiness and GMP compliance for a healthcare site transitioning from project phase to operations. This role involves strategic quality leadership, cross-functional alignment, establishment of quality systems, risk management, and capability building within a regulated environment.

This role is for an Electrician C responsible for inspecting, repairing, and maintaining electrical equipment in process areas, labs, and utilities within a healthcare manufacturing facility. It requires knowledge of the National Electrical Code, electromechanical devices, troubleshooting electrical systems, and adhering to GMP procedures and safety protocols. The position involves hands-on maintenance of various electrical components and systems, documentation of work, and use of specialized test equipment.

Senior Director, Medical Affairs – Oncology (solid tumor and hematology) is a senior scientific and strategic leader responsible for setting the medical vision and driving cross-functional execution across the oncology therapeutic area (TA). This individual serves as the primary medical authority for the oncology business unit, leading a team of Medical Affairs professionals to deliver evidence-based, patient-centric medical strategies that support peri-launch and lifecycle commercialization of oncology assets. This role combines deep oncology expertise with organizational leadership, requiring the ability to influence at the executive level, partner effectively with Commercial, Regulatory, Clinical Development, Market Access, and external stakeholders, and shape a high-performance culture grounded in scientific rigor, inclusion, and continuous learning.

This role is for an Operations Associate in Formulation and Material Preparation at a new high-tech manufacturing facility for injectable medicines. The role involves supporting commissioning, qualification, and validation during the project phase, and day-to-day performance management after site start-up. Key responsibilities include leading investigations, presenting to regulatory authorities, defining and procuring supplies, developing training materials, managing flows, and driving continuous improvement. The ideal candidate has a bachelor's degree, at least one year of pharmaceutical industry experience, strong organizational and project management skills, and excellent German and English.

This role is for a Supply Chain Associate in the External Manufacturing organization, focusing on ensuring reliable supply of medicines through effective supply chain processes. Responsibilities include forecasting, supply planning, purchase order generation, inventory management, and data stewardship within a GMP regulated environment, primarily using SAP.

Senior Director role responsible for medical review of Individual Case Safety Reports (ICSRs) in a global healthcare company. This role ensures accuracy, integrity, and compliance of global regulatory reports, provides technical leadership within Case Management and Global Patient Safety (GPS), and collaborates cross-functionally. Responsibilities include conducting comprehensive ICSR medical reviews, escalating significant cases, providing medical and regulatory guidance, training, and ensuring audit readiness. Requires a Medical Doctor or Doctor of Osteopathy.

This role is for a Lead Chemist in RNAi drug discovery at Eli Lilly. The primary focus is on evaluating scientific opportunities, designing and executing RNAi therapeutic projects, and managing partnerships. While the role mentions AI/ML tools as part of a broader ecosystem, the core responsibilities are in traditional drug discovery and chemistry, not in building or researching AI/ML models.

This role is for an IAM SecOps Engineer focused on Public Key Infrastructure (PKI) and encryption services within a large enterprise. The engineer will be responsible for designing, implementing, and securing these technologies, managing certificate lifecycles, key management, and cryptographic standards. The role involves partnering with various stakeholders to ensure secure and compliant operations.

Engineering Associate Director responsible for leading the engineering group (process, automation, maintenance) supporting the delivery, commissioning, and startup of packaging lines and device assembly operations at a new pharmaceutical manufacturing site. The role involves managing teams, ensuring technical and maintenance support, driving continuous improvement, and supporting regulatory compliance.

Associate Director of Engineering for Packaging Operations at a new state-of-the-art manufacturing site. Responsible for leading a team of process, automation, and maintenance engineers to support asset delivery, process development, commissioning, qualification, validation, and startup of packaging lines. After startup, will support day-to-day engineering activities and future planning. Focus on safety, quality, engineering, optimization, and continuous improvement.

Scientist role focused on developing and optimizing analytical methods for small molecule drug substances and synthetic intermediates, leveraging techniques like HPLC, GC, NMR, and MS to support drug candidate development from early stages through manufacturing readiness. This role involves close collaboration with synthetic chemists and process engineers in a laboratory setting.

Principal Scientist role in pharmaceutical manufacturing, focusing on technical leadership, process improvements, compliance with cGMP and regulations, and technology transfer for dry product operations. Requires experience in pharmaceutical manufacturing and knowledge of process safety and regulatory expectations.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work as a Lilly employee while pursuing education at a local community college, with the opportunity for conversion to an Operator/Process Technician after completing apprenticeship requirements. Responsibilities include operating manufacturing equipment, adhering to safety and quality standards, documenting processes, and identifying operational improvements.

The Quality Intern will support the Quality Department by performing administrative tasks related to product complaints, sample management, and documentation. This role involves translation, sample handling, cargo arrangements, permit drafting, and reconciliation of complaint data. The intern will also assist with archiving and ensuring compliance with global policies and local procedures.

This role focuses on developing parenteral drug product clinical manufacturing processes and associated control strategies within the Biologics Research and Development organization. It involves collaborating with cross-functional teams, designing and executing manufacturing studies, leading tech transfer activities, authoring technical documents, and supporting process qualification and regulatory submissions. The position requires a B.S. or M.S. in Pharmaceutical Chemistry or Engineering with relevant industry experience and a working knowledge of parenteral product development.

This role is for a Senior Principal Process Engineering SME in Parenteral manufacturing at Eli Lilly. It involves providing global technical expertise in process engineering, aseptic processing, and parenteral technologies, including formulation, filling, freeze drying, and isolation systems. The role requires leadership in technical discipline, safety, compliance, consultation, knowledge sharing, capital project support, external manufacturing support, platform ownership, and innovation in manufacturing processes. A Bachelor's degree in engineering and over 10 years of cGMP manufacturing experience are required.

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.

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.