Eli Lilly

This role focuses on ensuring the quality and compliance of regulatory affairs activities in China for a global healthcare company. Responsibilities include managing regulatory documentation, implementing company SOPs, coordinating local processes, managing RA systems, and providing training. The role also involves collaboration with internal teams and external vendors, supporting technology development, and conducting compliance monitoring and audits. It requires a bachelor's degree, 1-3 years of experience, strong computer skills, and excellent English communication.

Process Engineer role at Eli Lilly focused on ensuring reliable operation and qualified state of equipment and business processes in a pharmaceutical GMP manufacturing environment. Responsibilities include safety, engineering expertise, troubleshooting, problem-solving, and driving continuous improvement efforts. Requires a Bachelor's degree in Engineering or science discipline with experience in pharmaceutical GMP manufacturing.

MBA intern role focused on developing a launch plan for a new lung cancer drug, requiring financial and commercial acumen to assess readiness and create an action plan with cross-functional teams.

This role is for a Medical Science Liaison (MSL) in Norway, focusing on Incretins. The MSL will be a field-based scientific expert, engaging with clinical and scientific experts to share in-depth medical and scientific information, gather insights, and support research studies. The role requires advanced scientific knowledge, strong communication and interpersonal skills, and adherence to ethical and regulatory standards within the healthcare industry.

Automation Technician at Eli Lilly, a global healthcare leader, responsible for equipment performance, first-line production support, mechanical repairs, PMs, and troubleshooting in a GMP manufacturing environment. Requires expertise in production processes, commissioning, qualification, validation, and control system technologies, with experience in instrumentation, PLC/HMI programming, and business software.

This role is for a Maintenance Technician on the night shift at Eli Lilly, a global healthcare leader. The primary focus is to service, repair, and maintain process and utility pharmaceutical manufacturing equipment to improve uptime and efficiency. Responsibilities include troubleshooting, performing repairs, setting up equipment, and documenting actions in a CMMS. The role requires a high school diploma, minimum 2 years of maintenance experience, and the ability to work in a regulated manufacturing environment.

This role focuses on the design, development, and manufacturing of solid drug products within the pharmaceutical industry. It involves applying expertise in formulation, manufacturing processes, and technology platforms, including continuous manufacturing and process analytical technologies, to accelerate drug development and commercialization. The position requires collaboration with cross-functional teams and leadership in technical development and regulatory strategy.

This role is for a Sr. Principal Reliability Engineer in a new advanced manufacturing facility for API molecules. The engineer will be responsible for equipment reliability and maintenance strategy, developing reliability metrics, troubleshooting equipment issues, implementing improvements, and developing maintenance strategies to optimize operations, compliance, cost, and efficiency. The role requires collaboration with Process Engineering and expertise in Maximo CMMS, within a GMP/regulated environment.

The Advisor - Computational Modeling Engineer will provide diverse modeling expertise and develop computational models that drive decisions to design new manufacturing processes and improve existing ones across Lilly's global manufacturing network. This role applies modeling techniques across a broad range of domains — including physical properties, unit operations, scale-up, numerical and multiphysics simulation, discrete event simulation, and resource and operational logistics optimization — to support both continuous/batch process operations and discrete manufacturing operations. A core focus of the role is the development of Digital Twin computational models that provide online modeling capabilities to manufacturing facilities.

Pharmaceutical Sales Territory Manager for Eli Lilly's Dermatology Specialty division. Responsible for account-based selling to healthcare providers, building relationships, and driving adoption of therapies. Requires understanding of territory, reimbursement, and clinical information. Focuses on sales activity, partner collaboration, and achieving sales goals.

This role is for a Process Technician in a pharmaceutical manufacturing setting, focusing on the operation of automated filling equipment for syringes. The responsibilities include ensuring safe operation, maintaining quality standards (cGMP), supporting line leads, and performing area cleaning. It requires experience in a regulated industry and knowledge of manufacturing processes.

This role focuses on NMR spectroscopy and reaction characterization within the pharmaceutical industry, specifically for small molecule therapeutics, synthetic peptides, and oligonucleotides. The primary responsibilities include designing and interpreting NMR experiments, solving complex structure elucidation challenges, and applying quantitative NMR methods. While the role mentions familiarity with AI-enabled workflows as a preference, its core function is not AI/ML development.

This role focuses on developing and executing medical education initiatives for healthcare professionals within the pharmaceutical industry, specifically for Eli Lilly's immunology and cardiometabolic health therapies in Canada. It involves strategic planning, gap identification, program design, stakeholder management, and budget oversight, ensuring alignment with scientific, company, and regulatory standards.

This role provides statistical support for drug development in a healthcare setting, focusing on experimental design, analysis, and the development of novel methods. It involves collaboration with scientists and engineers across various disciplines, including chemistry and biology, and requires expertise in statistical software and methodologies. The role also involves communicating results, contributing to regulatory submissions, and potentially developing training materials.

Associate Director for Clinical Research in Oncology, responsible for driving clinical trial execution through investigator engagement and site performance management. This role requires deep therapeutic and scientific knowledge to influence investigators, ensure protocol understanding, and develop enrollment strategies. The CRL acts as a trusted partner to investigators, collaborating with internal teams to shape development strategies and ensure operational excellence. Responsibilities include investigator management, clinical trial management, business management, and country/regulatory engagement.

The Environmental Scientist will be responsible for overseeing all environmental permits and programs at the RTP site, ensuring compliance with federal, state, and local environmental regulations, and serving as the primary interface with regulatory agencies. This role requires a Bachelor's degree in Environmental Science or a related field and experience managing environmental compliance programs in a regulated manufacturing or pharmaceutical environment.

This role supports Parenteral Operations by performing environmental monitoring of manufacturing areas and utility sampling/analysis in a QC laboratory. It involves adherence to cGMP, training other technicians, and participating in continuous improvement projects. Requires a High School Diploma, 2+ years of relevant experience in GMP Pharmaceutical Manufacturing, and experience with Laboratory IT systems.

Reliability Engineer responsible for establishing and executing maintenance and reliability strategies to ensure equipment and process uptime in a regulated healthcare manufacturing environment. This role involves data analysis of key metrics (MTTR, MTBF, OEE), root cause analysis of failures, implementing reliability improvements, and supporting cross-functional teams. Experience with vision systems, CMMS, and regulatory compliance (cGMP, FDA) is preferred.

This role involves performing environmental monitoring and utility sampling in a pharmaceutical manufacturing facility to ensure product safety and efficacy. It requires adherence to cGMP procedures and quality systems, with a focus on aseptic production. The technician will also provide training and support to other team members and participate in continuous improvement projects.

Senior Director of Corporate Development at Eli Lilly, focusing on identifying and executing complex transactions for white space opportunities outside core therapeutic areas. Requires strong corporate development, transactional experience, and market agility to assess new markets and structure deals.

Associate Director, Project Management Office (PMO) responsible for staffing, training, and leading the PMO to manage the site project portfolio, including implementation of project governance tools. Coaches and develops project management fundamentals, establishes project management guidelines and processes, and ensures projects align with manufacturing and quality goals. Ensures projects adhere to industry regulations (FDA, EMA, GxP).

Associate Director - Medical Science Liaison for Cardiometabolic Health at Eli Lilly. This role focuses on providing in-depth scientific and clinical information to healthcare professionals and researchers within a specific therapeutic area. The MSL acts as a key interface, facilitating scientific exchange, sharing insights, and supporting clinical development and research opportunities. Requires advanced scientific/clinical acumen and experience in a relevant health science field.

This role is for a Sr. Director of COO Strategy & Operations within the Global Patient Safety (GPS) Capabilities function at Eli Lilly. The primary focus is on driving strategic execution, financial stewardship, and organizational effectiveness, with a key near-term objective of orchestrating the PV Affiliate Centralization initiative. The role also involves supporting broader GPS Capabilities pillars through cross-functional alignment, resource planning, stakeholder communications, and leadership meeting governance. It requires a blend of strategic thinking, operational rigor, change management, and executive communication skills within a healthcare context.

This role provides technical and project administrative support for clinical trial execution at Eli Lilly. Responsibilities include managing study budgets, ordering and tracking supplies, tracking enrollment data, maintaining study files and documentation for regulatory inspections and submissions, and managing clinical trial systems by inputting and updating study timelines and generating reports. The role requires a two-year degree or equivalent experience and proficiency in various software packages.

Senior Director of Health, Safety, and Environment (HSE) responsible for developing, implementing, and maintaining HSE programs and systems at a new API manufacturing facility. This role leads the site HSE team, ensures compliance with global and regulatory standards, and contributes to strategic planning during the project delivery and startup phase, focusing on building HSE systems, processes, and culture for GMP operations. Post-startup, the role owns the HSE Management System and ensures ongoing compliance.

Process Technician role at Eli Lilly focused on operating automated equipment for formulation, filling, and material preparation in a healthcare manufacturing setting. Requires adherence to safety and quality standards (cGMP), with opportunities for training and troubleshooting. Basic requirements include a high school diploma and ability to work specific shifts and overtime. Preferred skills include knowledge of cGMP, manufacturing systems, and lean principles.

Reliability Engineer for Eli Lilly's new Medicine Foundry, focusing on optimizing manufacturing processes and ensuring equipment reliability for drug development and clinical trials. This role supports advanced manufacturing research by maintaining optimal equipment performance and implementing reliability monitoring programs.

This role is for a Manager of Access in Qatar for Eli Lilly, a global healthcare leader. The primary responsibility is to gain and maintain formulary access and reimbursement for Lilly's product portfolio within the public sector by working with payer customers, government affairs, and sales teams. The role requires strong market access, business case development, contract negotiation, and local market knowledge.

This role is for a Quality Assurance professional in the pharmaceutical industry, focusing on product quality testing, documentation, deviation investigation, and process improvement. It involves chemical and microbiological testing, method transfer, and potentially team management for higher-level positions. The role is not directly related to AI/ML development.

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 plans, 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 customer management.

Sales role for a Therapeutic Advisor in Cardiometabolic Health, responsible for managing and expanding the customer base in a specific region of the Netherlands. This involves building relationships with healthcare professionals, managing accounts, and providing scientific information about medications.

Pharmaceutical Sales - Associate Territory Manager for Cardiometabolic Health in Manhattan, NY. This role involves account-based selling to healthcare providers, promoting Lilly's portfolio, understanding the market, and utilizing data and analytics. It also mentions integrating AI company-approved tools to streamline customer interactions.

This role is for a Laboratory Technician at Eli Lilly in France, focusing on physico-chemical analysis of pharmaceutical products, APIs, excipients, and ACPs. The technician will perform routine and non-routine analyses using various laboratory techniques, manage equipment, prepare reagents and samples, interpret results, and ensure data integrity according to Good Laboratory Practices (GLP) and ALCOA+ principles. Responsibilities also include evaluating quality deviations, revising procedural documents, and proposing solutions for method and equipment optimization. The role requires a Bac +2 or +3 in chemistry or physico-chemistry and significant analytical experience in the pharmaceutical industry.

Pharmaceutical sales role focused on account-based selling of cardiometabolic health medicines to healthcare providers. The role requires understanding the market, tailoring territory strategy, and utilizing business insights and data. It also mentions embracing new technologies, including AI-approved tools, to streamline customer interactions, but this is not the core function of the role.

Associate Analytical Technical Steward in Dry External Manufacturing Quality Control at Eli Lilly. This role involves technical review, interpretation, and release of analytical data from contract manufacturers, stability studies, and process validation. Responsibilities include leading investigations for out-of-specification results, performing root cause analysis, developing investigational testing protocols, and representing quality laboratories on cross-functional teams. The role also supports method validation, transfer, and improvement for marketed products, ensuring compliance with regulatory expectations and quality standards.

Medical Affairs Director for Switzerland, responsible for providing medical and scientific leadership, strategic direction, and oversight for Medical Affairs activities. This role involves leading and developing the medical team, driving innovation, ensuring scientific excellence, regulatory compliance, and cross-functional collaboration to support pre- and post-launch activities. The position requires an MD with clinical research and/or Medical Affairs experience, leadership skills, and fluency in English.

Medical Science Liaison (MSL) role focused on Oncology in Türkiye, requiring deep scientific knowledge of disease states and Lilly/competitor compounds. The role involves engaging with scientific experts to facilitate scientific exchange, gather insights, and inform Lilly's research and commercialization strategies. Responsibilities include maintaining scientific expertise, supporting medical/scientific information needs, strategic planning, and territory ownership, all while adhering to compliance and company policies.

This role is for a pharmaceutical sales representative focused on promoting neuroscience products within a specific territory in Beijing, China. Responsibilities include achieving sales targets, building and maintaining customer relationships with healthcare providers, 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.

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 with healthcare providers, 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 customer management.

This role is for a Medical Representative in the Cardiovascular Metabolic Health business unit, responsible for promoting company products within a designated territory in Tai Yuan, China. The primary focus is on achieving sales targets, building and maintaining customer relationships, providing product information, and gathering market intelligence. Experience in pharmaceutical promotion and new product launches is preferred.

The Associate Director – Patient Data Engineering Lead will own the data engineering foundation for Lilly's direct-to-patient pharmacy platform (LillyDirect). This role is responsible for designing and delivering patient analytics data products, integrating data flows, and ensuring HIPAA and SPI consent governance. The role involves building scalable ingestion pipelines, implementing tokenization and identity resolution, and delivering semantic layers for downstream BI, reporting, and agentic AI use cases. The ideal candidate has deep data engineering expertise, a strong command of healthcare privacy regulations, and experience enabling trusted patient analytics.

This role is for a Process Visual Inspection Technician in a new pharmaceutical manufacturing facility. Responsibilities include supporting commissioning and qualification of automated inspection lines, operating automated and manual inspection equipment, ensuring compliance with Good Manufacturing Practices (CGMPs) and safety standards, and supporting leadership in troubleshooting and operator development. The role requires experience in a regulated industry and familiarity with automated inspection equipment.

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.