This Principal Engineer role in Parenteral Packaging R&D at Eli Lilly focuses on the selection, development, and qualification of container closure systems for drug products. The role involves collaborating with various teams, applying scientific principles to solve complex challenges, and driving technology innovation. While the role mentions collaborating with a data science SME to adopt AI technology, AI/ML is not the core craft, and the primary focus is on packaging engineering within the healthcare domain.

This is an internship position in Medical Affairs for Immunology 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.

Quality Assurance Engineer role at Eli Lilly's new API manufacturing facility, focusing on technical guidance for quality standards, regulatory compliance, and continuous improvement in manufacturing and laboratory operations.

Experienced patent attorney needed to provide solutions-oriented counseling for patent issues in the discovery, development, and commercialization of pharmaceutical products in the gene therapy and gene editing space. Responsibilities include drafting and prosecuting global patent applications, contributing to patent portfolio strategy, analyzing risks, and advising on exclusivity, freedom to operate, and litigation risks. Requires a scientific bachelor's degree, JD, and at least four years of post-JD experience as a patent attorney.

This role focuses on the automation aspects of plant engineering for HVAC, Utilities, and Facilities within pharmaceutical manufacturing. The engineer will develop, implement, and improve process automation solutions, ensuring systems are in-control, capable, and compliant. Responsibilities include defining user requirements, designing system architectures, developing and testing code, managing change control, and ensuring validation documentation is maintained. The role requires experience as a process automation engineer and ideally pharmaceutical and computer system validation experience.

Product Leader responsible for the entire commercialization lifecycle of a product, from post-Phase 2 through launch and beyond. Owns manufacturing CMC strategy, leads the Product Core Team, collaborates with development, and serves as the interface for senior executives. Requires deep pharma development/manufacturing knowledge and ability to drive alignment without direct authority.

QA Manager for Night Shift at a new pharmaceutical manufacturing site, focusing on device assembly and packaging. Responsibilities include technical oversight, document approvals, cross-functional collaboration, team management, and ensuring GMP compliance. The role transitions from commissioning and qualification to supporting routine manufacturing operations.

This role leads the cross-functional study team in the development and execution of clinical trials, accountable for delivering trials with quality, on time, and within scope and budget. It requires leveraging project management, regional operational knowledge, clinical trial process leadership, and scientific expertise.

Senior Director of Quality Assurance for a new pharmaceutical manufacturing facility in Katwijk, Netherlands. Accountable for setting and executing the site's QA strategy, ensuring cGMP compliance, regulatory readiness, and fostering a strong quality culture. This role involves executive quality leadership, governance, compliance, operational oversight, talent development, strategic planning, and EHS accountability within a highly regulated pharmaceutical manufacturing environment.

Associate Director for Reimbursement Analytics in Dermatology at Eli Lilly, focusing on developing data strategies, building scorecards, and analyzing product reimbursement services. This role involves leading data reporting, partnering with data enablement teams, and ensuring compliance with privacy and legal requirements within the healthcare domain.

Senior/Principal Manufacturing Scientist role at Eli Lilly focused on peptide API manufacturing. Responsibilities include providing technical support, executing experimental projects, modeling, data analysis to improve process control, yield, purity, and productivity within a cGMP environment. Requires experience in peptide synthesis or purification technologies.

This role is for a Specialist in Leak Detection and Repair (LDAR) Database Administration at a new Eli Lilly manufacturing facility. The primary focus is on building, maintaining, and optimizing the LDAR database to ensure data integrity, component tracking, and compliance with environmental regulations (EPA, IDEM, cGMP). The role involves reconciling drawings with database records, creating monitoring routes, providing technical support for the LDAR program, and assisting with training and audits. It is a greenfield site, so the role will evolve from initial setup to steady-state management.

Associate Director of Process Engineering for Small Molecule API manufacturing, responsible for leading and developing a team of process engineers to ensure compliant and reliable operations in a new, advanced manufacturing facility. The role involves building the organization, implementing business systems, and supporting project delivery during the startup phase, transitioning to operational oversight and continuous improvement post-startup.

Senior Director of Engineering role focused on facilities and utilities for pharmaceutical manufacturing operations, ensuring infrastructure and leadership support site startup and long-term operations. Responsibilities include guiding GMP systems, building operational readiness, managing evolving responsibilities, and ensuring safety and quality standards.

Senior Director of Engineering at Eli Lilly, responsible for leading process engineering, automation, and maintenance for site startup and long-term manufacturing goals in a healthcare/pharmaceutical setting. Focuses on organizational development, functional strategy, safety leadership, and ensuring system readiness for GMP manufacturing.

This role supports the manufacturing process by operating, monitoring, maintaining, and shutting down clean utility systems and equipment within mechanical rooms. Responsibilities include improving equipment uptime, performing preventative and predictive maintenance, troubleshooting and repairing equipment, maintaining documentation, and collaborating with other departments, all while adhering to cGMPs and safety procedures.

This role is for a Production Worker in the Parenteral department at Eli Lilly's new high-tech manufacturing facility in Alzey, Germany. The position involves operating machinery, ensuring health and safety compliance, collaborating with team members, following SOPs, troubleshooting issues, and participating in training. The ideal candidate has relevant experience in the pharmaceutical/biotech industry, experience with aseptic filling and/or isolator technology, and knowledge of cGMPs.

The Cyber Intelligence Analyst role at Eli Lilly focuses on active defense within Global Cyber Defense Operations (GCDO). Responsibilities include monitoring, analyzing, investigating, and responding to cybersecurity events and incidents, managing the attack surface, producing threat intelligence, and ensuring readiness and detection capabilities. The role involves supporting various cybersecurity functions, developing capabilities, documenting analysis, identifying security issues, prioritizing threats, and recommending strategic changes. Rotational on-call availability is required.

This role is for a Network Manager in Oncology at Eli Lilly, focusing on building and maintaining relationships with healthcare professionals and institutions in a specific sales territory. It involves understanding customer needs, implementing sales and marketing strategies, and analyzing account structures. The role requires a background in pharmaceuticals or a related scientific field, strong sales and communication skills, and experience with CRM tools.

This role is for a Pharmaceutical Sales Representative specializing in Hematology, focusing on promoting an innovative substance in the hematology-oncology field. The position requires identifying key accounts, developing tailored solutions, conducting sales discussions, implementing sales and marketing strategies, and building access pathways to decision-makers. It emphasizes cross-functional teamwork and strategic analysis of customers.

Associate Director of Trade Compliance and Import-Export Services, focusing on Foreign-Trade Zone Operations within Lilly Research Laboratories. This role ensures compliance with U.S. Customs and Border Protection (CBP) and other Partner Government Agencies (PGAs) for global clinical supply operations, including managing FTZ protocols, advising on duty optimization, and supporting integration into enterprise systems.

Senior Director of Technical Services/Manufacturing Science (TS/MS) overseeing site operations, new product introduction, process development, and optimization within a pharmaceutical manufacturing context, ensuring compliance with cGMP and regulatory standards. This role involves strategic leadership, cross-functional engagement, and people development within a global healthcare company.

Senior Director of Operations for a new API manufacturing facility at Eli Lilly, responsible for leading manufacturing operations, building the organization, and ensuring compliance with GMP and regulatory requirements during startup and post-startup phases.

This role focuses on building and scaling business-to-business (B2B) and Disease State Education (DSE) partnerships within the Cardiometabolic Health (CMH) business unit in Switzerland. The lead will develop new business models, establish executive relationships, secure partnerships, and drive commercial and access outcomes in the private and digital healthcare ecosystem, ensuring compliance within a regulated environment.

Clinical Research Physician specializing in Ophthalmology Gene Therapy Development at Eli Lilly. This role involves the development, conduct, and reporting of global clinical trials for ophthalmologic products, including protocol review, patient safety monitoring, adverse event reporting, and scientific data dissemination. The physician will serve as a medical resource for study teams and external healthcare professionals, collaborating on clinical strategy, trial execution, and regulatory support.

Lead Operator for Eli Lilly's new Medicine Foundry, focusing on advanced manufacturing and drug development for small molecules. This role supports the startup phase of a new facility, ensuring operational readiness, training teams, and eventually providing on-the-floor leadership for API production. Responsibilities include adhering to safety and quality compliance, operating equipment, troubleshooting process upsets, and promoting a strong safety culture within a GMP environment.

The Equipment Support Group Lead at the Lilly Medicine Foundry is responsible for the commissioning, qualification, compliance, maintenance, calibration, reliability, and lifecycle management of general equipment and analytical instrumentation supporting LMF laboratories. This role ensures equipment is fit for use, properly installed, qualified, and compliant, acting as a technical bridge between scientists and support teams.

This role provides Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for products manufactured by third-party partners. Responsibilities include leading quality aspects of external sites, conducting audits, reviewing documents, collaborating cross-functionally, providing QA guidance, developing quality agreements, investigating incidents, and representing Lilly during regulatory inspections.

Associate Director of Engineering (Automation) at Eli Lilly's new API manufacturing facility in Houston, TX. Responsible for leading and developing the Process Control Engineering team, ensuring reliable and compliant control applications and systems for GMP manufacturing. Role involves hiring, process development, and collaboration during the facility startup and ongoing operations, with a focus on safety, quality, and operational excellence.

Lead Maintenance Mechanic role at Eli Lilly's new API manufacturing facility in Lebanon, IN. Responsibilities include overseeing maintenance and repair of manufacturing equipment, ensuring optimal performance and compliance with GMP and safety regulations. Requires expertise in mechanical, electrical, and instrumentation disciplines, troubleshooting, documentation, and leading a team of mechanics. Focus on startup operations for a greenfield manufacturing site.

Senior Engineer role focused on technical project management and delivery oversight for intralogistics system deployments in manufacturing. This involves integrating various systems like SAP/EWM, MES, and automation hardware (AGVs, ASRS) to enable autonomous material flow. The role requires developing integrated schedules, coordinating dependencies, and ensuring system requirements are met.

This role provides technical stewardship for an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing. It requires expertise in bioconjugate manufacturing processes, including conjugation chemistry, purification, filtration, and analytical/process controls. The role involves data-driven decision-making, process improvements, and leveraging digital plant technologies. It also requires experience with regulatory guidance and cGMP requirements.

Associate Director for Technical Services/Manufacturing Science (TS/MS) at Eli Lilly, responsible for leading a team that provides technical oversight for biological and bioconjugate manufacturing processes. The role involves building and developing the TS/MS organization, ensuring process reliability, supporting regulatory compliance, and managing documentation within a new advanced manufacturing facility.

Associate Director of Operational Readiness for a new API manufacturing facility in the pharmaceutical industry. This role involves developing and managing an integrated project plan for facility startup, leading a cross-functional team, and establishing Lean principles for operational excellence. The position requires experience in GMP operations and project leadership within the pharmaceutical sector.

Scientist role focused on developing and maintaining operations for sample preparation, organization, and tracking within a drug discovery environment. Involves managing compound libraries, designing plate preparation, collaborating with global sample management networks, and troubleshooting lab automation systems. The role emphasizes process improvement, data integrity, and safety in a laboratory setting.

HSE Engineer role at Eli Lilly's new high-tech production facility in Alzey, Germany. Responsibilities include technical leadership in HSE programs, environmental permits, compliance, process hazard reviews, incident investigations, and supporting facility design for environmental compliance. Requires a degree in a relevant field, experience in HSE/PSM, and knowledge of regulations. Authorization to work in Germany is mandatory.

This role focuses on Health, Safety, and Environment (HSE) within a pharmaceutical manufacturing facility. The Associate HSE / Sr. Associate HSE will assist in developing and implementing HSE programs, ensuring compliance with regulations, supporting project teams, conducting audits, and investigating incidents. The role requires a Bachelor's degree in a related science or engineering field and several years of experience in manufacturing operations, preferably in pharmaceuticals or chemicals. Authorization to work in Germany is mandatory.

The Sr. Principal Scientist, MES Data and Integration Lead will support the design, deployment, and operation of the Manufacturing Execution System (MES)/Electronic Batch Record (EBR) for a new API manufacturing facility. This role focuses on translating manufacturing requirements into MES solutions, ensuring data governance, and integrating MES with other enterprise systems to support compliant and efficient GMP operations. The role involves working with process data for continuous improvement and performance analytics.

This role focuses on the Manufacturing Execution System (MES) and Electronic Batch Record (EBR) for a new, digitally native API manufacturing facility. The Sr. Principal Scientist will lead the MES technical agenda, translate manufacturing requirements into MES solutions, and ensure compliant, data-driven production. The role involves system ownership, support, risk assessment, and developing best practices for MES-enabled operations within a GMP environment.

This role supports the design, deployment, and operation of a contamination control strategy in a new pharmaceutical manufacturing facility. It involves ensuring strategies align with technical, quality, and regulatory guidance, applying data-driven decision-making, and improving contamination control performance through innovative technologies. Responsibilities include authoring technical documents, monitoring environmental conditions, investigating contamination events, analyzing trending data, and training staff.

This role focuses on managing printed packaging materials (PPMs) for contract manufacturers in the pharmaceutical space, ensuring they meet technical and company standards. Responsibilities include managing layouts, metadata, artwork development, and technical changes, as well as participating in testing, investigations, and projects, including digital transformation initiatives within packaging.

This is a Project Manager - Operational Marketing role in the pharmaceutical industry. The responsibilities include managing and coordinating marketing projects, overseeing the operational follow-up of deliverables, managing relationships with external providers and agencies, supporting continuous improvement of processes, and internal communication and coordination. The ideal candidate has a marketing background, preferably with experience in the pharmaceutical industry, and possesses strong organizational, relational, and adaptability skills. A good command of English and an interest in new technologies and artificial intelligence are also mentioned.

This is a Brand Manager apprenticeship role in Oncology at Eli Lilly, focusing on marketing campaigns, data dashboards, competitive analysis, and strategic product development. While the role mentions an interest in new technologies and AI, it is not core to the job's responsibilities.

This role is for a pharmaceutical sales representative focused on promoting neuroscience products within a specific territory in Chang Chun, China. The responsibilities include achieving sales targets, building and maintaining relationships with healthcare professionals and hospitals, providing product information, and gathering market intelligence. The role requires a bachelor's degree, preferably in a pharmaceutical-related field, and 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, managing customer relationships, and achieving sales targets. It involves understanding drug characteristics and market conditions, with a preference for candidates with relevant experience in pharmaceutical promotion and new product launches.

This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory, managing customer relationships, and achieving sales targets. It involves understanding drug features, market conditions, and building professional relationships with healthcare providers.

This role is for a pharmaceutical sales representative focused on promoting and selling company products within a specific territory in the cardiovascular and metabolic health division. Responsibilities include achieving sales targets, building and maintaining customer relationships, providing product information, and gathering market intelligence. The role requires a bachelor's degree, preferably in a pharmaceutical-related field, and experience in product promotion and client management.

QC Technician responsible for release testing of raw materials, excipients, and packaging components in a chemistry laboratory. Duties include method verification, SOP drafting and revision, management of consumables and standards, document control, 5S management, and assisting with GLIMS system implementation and quality system improvement.