Eli Lilly

Associate Director of Regulatory Affairs for China at Eli Lilly, focusing on developing and implementing regulatory strategies to accelerate drug submissions, approvals, and launches in the Chinese market. This role involves close collaboration with global and local teams, interaction with regulatory authorities, and ensuring compliance with local laws and Lilly's policies. The position requires expertise in drug development, risk assessment in a regulated environment, and strong communication and negotiation skills in both Chinese and English.

Associate Director, Product Quality & Quality Information (PQQI) at Eli Lilly Japan, responsible for setting strategy and leading teams focused on product quality and quality information management throughout the product lifecycle, ensuring compliance with GQP and Japanese regulatory requirements, driving operational excellence, and supporting product launches.

Senior Application Support Engineer role focused on providing advanced technical support for a suite of products in the healthcare domain. Responsibilities include troubleshooting, diagnosing, and resolving incidents related to application functionality, integrations, performance, and security, acting as an escalation point for L2 support and customer queries. The role involves collaboration with development teams, monitoring application health, maintaining knowledge base articles, supporting deployment activities, and ensuring compliance with regulations like GDPR and HIPAA.

Apprenticeship role focused on electrical instrumentation maintenance within a regulated GMP environment at a pharmaceutical manufacturing site. Responsibilities include supporting repair, replacement, installation, and maintenance of equipment, working with industrial control systems, interpreting schematics, and analyzing system faults.

Apprenticeship role focused on mechanical automation and maintenance fitting within a regulated GMP environment to support production activities. Responsibilities include installation, repair, and maintenance of plant and machinery, working with various machine tools, and understanding technical drawings.

This role is for a Chemist Laboratory position at Eli Lilly in Puerto Rico. The primary responsibilities include ensuring laboratory compliance with regulations, reviewing analytical results, generating and reviewing laboratory documents, and providing analytical and technical support. Requirements include a Bachelor's or Master's degree in Chemistry, a chemist license, and at least three years of experience in a manufacturing environment. The role emphasizes leadership, customer focus, continuous improvement, computer literacy, teamwork, and strong communication skills. Bilingualism is also required.

Lead Analyst for Cyber Threat Intelligence (CTI) at Eli Lilly, focusing on strategy, operations, and team development. This player/coach role involves hands-on technical leadership in threat analysis and attribution, while also shaping the function's strategy, developing analysts, and representing the team in various forums. Responsibilities include threat actor tracking, brand and executive protection, partner collaboration, intelligence sharing, team leadership, and enhancing tooling for automated enrichment and response workflows.

Supervisor providing leadership and direct management to process operators in the Medicine Foundry operations group, overseeing the production of API molecules with a safety-first, quality-always approach. Responsibilities include enforcing compliance, overseeing operations, leading safety culture, troubleshooting process upsets, reporting safety and quality events, managing shift communications, and ensuring personnel follow cGMP practices.

This role is a senior operational and strategic leader accountable for the end-to-end process and systems architecture applied by Exploratory Medicine and Pharmacology (EMP). It ensures EMP can deliver its clinical portfolio compliantly and efficiently through external vendors and CRO partners, while remaining aligned to Lilly's internal quality and regulatory frameworks. The role involves process and systems integration, compliant outsourcing process design, and acquisition/program integration.

Associate Director, Clinical Development Trial Lead (CDTL) at Eli Lilly, responsible for leading cross-functional teams in the development and execution of complex clinical trials. This role involves project management, risk assessment, budget management, and ensuring trial quality, timeliness, and adherence to scope and budget. The position requires deep understanding of clinical drug development processes and regulatory requirements to ensure inspection readiness and drive continuous improvement.

Operator role in biotechnology manufacturing, responsible for performing production tasks, following GMP, and ensuring safety and quality. Requires an Associate's degree and experience in fermentation or isolation.

Student internship role focused on digital marketing, omnichannel strategy, and AI within the Specialty Business Unit (Oncology, Immunology, Neuroscience) at Eli Lilly. The role involves supporting digital engagement, campaign execution, expanding reach, contributing to omnichannel strategy, and collaborating cross-functionally. Familiarity with AI and digital tools is a plus.

Executive Medical Director role in Early Clinical Development for the Immunology team at Eli Lilly, focusing on developing transformational medicines for autoimmune and inflammatory diseases. The role involves strategic leadership, designing and executing early clinical studies, integrating translational endpoints, and collaborating with cross-functional teams, regulatory affairs, and external experts. Requires a physician scientist with strong clinical translational experience and leadership skills.

This role is for a Visual Inspection Operator in a pharmaceutical manufacturing site. The primary responsibilities include safely inspecting high-quality pharmaceutical products using Lilly standards, operating automated and semi-automated equipment, and adhering to Good Manufacturing Practices (GMPs). The role requires strong attention to detail, basic math and computer skills, and the ability to work in a manufacturing environment. Experience with GMPs and pharmaceutical manufacturing is preferred.

Associate Director for Biotech Operations at Eli Lilly, leading manufacturing operations and cross-functional process teams in a new, advanced biotech facility. Focuses on daily operations, people management, site leadership, and startup priorities, ensuring safety, quality, and productivity.

Associate Vice President for Health Economics and Outcomes Research (HEOR) in the Oncology Business Unit, responsible for global HEOR strategy and execution. This leadership role involves partnering with cross-functional teams to build a strong evidence base supporting the clinical and economic value of oncology medicines, managing the HEOR program end-to-end, and ensuring alignment with asset milestones and payer access needs.

Senior/Principal Process Engineer at Eli Lilly focused on API External Manufacturing for Peptides. The role involves providing technical leadership and expertise to contract manufacturers, ensuring reliable supply and commercialization of medicines. Key responsibilities include developing and sustaining process knowledge, coaching team members, leading tech transfers and scale-up, supporting process optimization, ensuring equipment capability, and overseeing health, safety, and environmental (HSE) and process safety management (PSM) elements at contract manufacturing sites. The role requires a strong understanding of chemical engineering principles and experience in a regulated manufacturing environment.

Internship role supporting the Human Resources team at Eli Lilly, focusing on core HR operations, employee lifecycle processes, recruitment support, HR metrics tracking, and contributing to HR process improvement, AI, and automation projects.

Associate Director - Digital & Data Lead at Eli Lilly, responsible for overseeing and aligning digital programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. The role involves championing digital plant strategy, influencing senior leadership on technology direction, providing input to business and strategic financial plans, and ensuring GxP compliance for all digital solutions. This position requires a deep understanding of manufacturing, lab, and quality processes, and the ability to translate business needs into actionable digital strategies.

This entry-level role supports the development, configuration, and localization of global manufacturing applications on the Tulip platform, aiming to eliminate paper-based processes. The associate will contribute across the full delivery lifecycle, including requirements, configuration, validation, deployment, and support, while adhering to GxP and data integrity principles. The role also involves exploring AI-assisted development and AI/automation use cases to advance paperless manufacturing goals.

The Sr. Principal Scientist, Advisor role in Global Regulatory Affairs (GRA) at Eli Lilly focuses on providing strategic and operational direction for Chemistry, Manufacturing, and Controls (CMC) development and regulatory strategies for market registrations and lifecycle maintenance in the EMEA region. This involves deep knowledge of global and regional regulations, manufacturing processes, and collaboration with various internal and external stakeholders to ensure timely and successful product registrations.

This role is responsible for the overall execution, management, and oversight of assigned clinical trials, ensuring adherence to regulatory requirements, Good Clinical Practice (GCP), and company standard operating procedures. It involves leading cross-functional teams to deliver high-quality clinical trial data on time and within budget.

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.

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.

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.

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.

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.

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.

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 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 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.

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.