Eli Lilly

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.

Associate role in Global Manufacturing & Quality Learning and Development at Eli Lilly, focusing on implementing, maintaining, and optimizing learning interventions and administrative tasks within a GxP-regulated environment. Responsibilities include managing learning plans, analyzing training effectiveness, automating processes, and serving as a liaison between business partners and the Learning Operations team. The role also involves instructor management, GMP compliance, and leveraging digital tools for learning enhancement.

Associate role in Enterprise Meeting Services at Eli Lilly, focusing on project management, operational coordination, compliance, and stakeholder management for global business services supporting the company's mission in healthcare. The role involves transforming services, ensuring adherence to global standards, and managing external partners.

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.

This role is for a Sr. Director of Health, Safety, and Environment (HSE) at a new Eli Lilly manufacturing facility for monoclonal antibodies and bioconjugates. The position involves developing and implementing HSE programs, leading the site HSE team, ensuring compliance with global and regulatory standards, and contributing to strategic planning. The role focuses on building HSE systems and culture during the project delivery and startup phase for GMP operations, and then owning the HSE Management System post-startup.

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.

This role is for a Territory Manager in institutional sales for a pharmaceutical company, focusing on driving business growth by enabling access to biopharmaceutical products within government and large healthcare institutions. Responsibilities include account planning, reimbursement navigation, scientific engagement, product promotion, customer calls, stockist management, and sales reporting, all while adhering to compliance and ethical standards.

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.

Senior Product Specialist / Territory Manager for Oncology in the UAE, responsible for promoting Lilly's products to healthcare professionals and pharmacies, achieving business objectives, and enhancing customer experience through education and solutions. Requires a qualified pharmacist with pharmaceutical sales experience, preferably in Oncology.

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.

Process Engineer responsible for ensuring reliable operation and qualified state of packaging process equipment, driving continuous improvement, troubleshooting mechanical issues, and collaborating with internal customers and cross-functional teams in a GMP-regulated healthcare manufacturing 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.

The Associate Vice President/Vice President and CFO LillyDirect will support and report directly to the Group Vice President and CEO, LillyDirect. LillyDirect’s mission is to expand patient access to Lilly’s innovative medicines and digital health solutions through an end-to-end consumer health platform. This role will build, scale, and lead the finance organization needed to execute on that mission — providing the Finance capabilities required for a high-growth digital health platform operating within a Fortune 100 pharmaceutical company. This is a high-impact role, and the ideal candidate brings deep strategic finance experience and is comfortable operating in an ambiguous and fast-moving environment while maintaining financial controls. The goals of the role are to drive financial discipline and insight, enable smart capital allocation and partnership decisions, and ensure LillyDirect operates with a mission-focused, innovative, and high-performing culture.

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 focuses on developing and executing customer expansion strategies within the healthcare sector, specifically for obesity treatment. It involves defining strategic priorities, leading engagement approaches for primary care, collaborating with cross-functional teams, and optimizing customer journeys. The role requires experience in brand management, marketing, or strategy, with a strong understanding of healthcare market dynamics and analytical skills.

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.

Full stack developer for scientific workflow management applications in a healthcare/discovery setting, focusing on lab processes like assay requests, plate definitions, and sample tracking. Requires Django, Python, PostgreSQL, CI/CD, and API development. Familiarity with AWS and cheminformatics is a plus.

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.

Werkstudent (m/f/d) in Marketing - Neurology / Alzheimer. Supports daily business in a new, innovative, and competitive business field regarding national and international marketing activities, e.g., creation of (digital) advertising materials and campaigns, PR, congresses, and events. Independently handles projects and manages marketing channels. Works closely with the Brand Team to create marketing campaigns from planning to success control for online and offline channels. Collaborates with agencies and manages measures. Develops new concepts and projects with the cross-functional team.

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 provides legal counsel for clinical development programs, focusing on regulatory and Good Clinical Practice (GCP) expertise. It supports AI and automation initiatives within clinical trials, advising on legal and regulatory considerations to enable innovation while managing risk.

This is a field-based commercial role responsible for driving business growth through the promotion of an Oncology portfolio. The role involves building relationships with healthcare professionals, engaging customers, and executing brand strategies while adhering to compliance standards and local regulations. Key responsibilities include customer engagement, territory management, business execution, cross-functional collaboration, and ensuring compliance.

Sales Representative for Eli Lilly's diabetes products in Taipei, responsible for managing a territory, meeting sales targets, promoting products, and implementing corporate strategies.