This role focuses on the development and analysis of immunoassay-based biomarker methods for neurodegenerative diseases within a healthcare/pharmaceutical context. It involves laboratory work, method validation, and sample analysis for preclinical and clinical studies.

This role focuses on developing technical solutions for spray drying in pharmaceutical particle manufacturing. It involves operating pilot scale equipment, designing and executing experiments to understand the impact of parameters on particle size and morphology, developing analytical techniques for measurement, and refining models for atomization and drying. The goal is to identify and solve manufacturing needs, present findings, and publish research.

Instrumentation Technician responsible for maintenance, calibration, troubleshooting, and installation of instrumentation systems in a new API manufacturing facility. The role ensures equipment availability and compliance with cGMP standards during pre-startup, startup, and post-startup phases.

Process Engineer role at Eli Lilly's new manufacturing site in Concord, NC, focusing on supporting and managing state-of-the-art production lines for parenteral medications and device assembly. Responsibilities include ensuring safe design and operation, providing engineering expertise, optimizing equipment performance, leading troubleshooting, managing system/component classification, and participating in IQ/OQ/PQ activities. Requires a Bachelor's degree in Engineering and 1-3 years of experience in automation or process control, with pharmaceutical manufacturing experience being a plus.

The Scientist - TS/MS Parenteral role at Eli Lilly focuses on technical transfer, process validation, and maintaining the validated state of parenteral operations, specifically in visual inspection. This role involves establishing and monitoring metrics, harmonizing control strategies, evaluating process improvements, and serving as an escalation point for operational issues. It requires authoring and executing protocols, conducting root cause investigations, and providing technical leadership for the Parenteral Process Team. The role also involves supporting manufacturing components, equipment, and operations, representing the team in communications, leading risk management activities, and providing technical support for investigations and quality/stability issues. Key deliverables include preparing technical documents, developing and reacting to statistically based metrics, identifying opportunities for process improvement, driving stability strategy, and providing audit support.

This role is for a Lead Operator in Utilities at a new Eli Lilly manufacturing facility. The primary responsibility is to ensure the uninterrupted generation and distribution of utility services (water systems, boilers, chillers, etc.) to support GMP manufacturing. The role involves daily monitoring, testing, cleaning, troubleshooting, and ensuring compliance with regulatory requirements in a regulated environment. Experience in facility/area start-up and understanding of cGMP are preferred.

This role is for a Sr. Manager of Regulatory Affairs CMC at Eli Lilly, focusing on new product registrations and life-cycle maintenance from a Chemistry, Manufacturing, and Controls (CMC) perspective. The individual will drive CMC strategy, prepare dossiers, oversee testing, manage queries, and shape the regulatory environment in China. It requires deep technical expertise in CMC drug development and compliance, with a strong understanding of China's regulations and ICH guidelines.

This role focuses on securing market access for Lilly products by demonstrating their value throughout the reimbursement lifecycle. Responsibilities include implementing access strategies, developing submission dossiers, owning the value proposition for payers, and managing HEOR planning and pharmaco-economic models to support product reimbursement.

This role leads the design and delivery of automation for major capital projects in pharmaceutical manufacturing, specifically for Active Pharmaceutical Ingredient (API) production. It involves managing workstreams, suppliers, and ensuring compliance and qualification within a global engineering team.

This role focuses on clinical pharmacology and translational modeling for gene editing therapeutics in the cardiovascular space. It involves leading the development and execution of strategies across preclinical and clinical development, including dose selection and regulatory filings. The role utilizes advanced modeling techniques like PBPK, population PK/PD, QSP, and exposure-response analysis to inform drug development decisions and regulatory submissions.

Operator for a logistics center in a biopharmaceutical manufacturing environment, responsible for materials management, inventory control, and shipping compliance within a regulated setting. Requires experience with SAP/MES systems and adherence to GMP/GDP standards.

This role is for a Senior Advisor, Clinical Research in Oncology at Eli Lilly, focusing on providing medical expertise for clinical strategy and execution in China. The responsibilities include collaborating on clinical development strategy, interacting with health authorities, developing evidence generation plans, supporting brand commercialization, contributing to payer partnerships, leading medical meetings, and establishing external collaborations. The role requires a Medical Doctor with experience in clinical research or medical advising in the pharmaceutical industry.

Director level role in Eli Lilly's Medicine Foundry, focused on advanced manufacturing and drug development for biologics and other modalities. The role involves leading a team of scientists and engineers to drive scientific excellence, accelerate manufacturing advancements, oversee technology transfer, implement control strategies, and ensure right-first-time clinical manufacturing. It requires technical oversight, documentation, risk mitigation, process stewardship, deviation investigations, and collaboration with cross-functional teams and external partners. The role also involves defining and leading the site's technical innovation strategy for manufacturing capabilities.

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

Seeking a Sr. Principal Bioprocess Engineer to support a new monoclonal antibody manufacturing facility. Responsibilities include facility start-up (design reviews, process safety, C&Q support, SOP development, tech transfer) and post-start-up support (continuous improvement, root cause analysis, equipment performance monitoring, control strategy development).

Responsible Scientist role in a Quality Control Microbiology Lab at Eli Lilly, focusing on in-depth problem solving, investigation of aberrant data, technical review, and mentoring lab staff within a GMP manufacturing environment. The role involves ensuring the quality of raw materials, in-process, and finished products.

Brand Manager for pharmaceutical brands in Taiwan, responsible for developing and executing strategic marketing plans to drive brand growth and achieve commercial objectives. This role involves market analysis, product lifecycle management, cross-functional collaboration, budget management, and ensuring compliance with regulations.

This is a Brand Manager role in the Neuroscience division at Eli Lilly Taiwan. The role focuses on understanding market landscapes, developing and executing commercialization strategies, leading cross-functional teams, and managing product launches and ongoing commercialization. It requires strategic planning, marketing experience, and strong leadership and analytical skills. AI/ML is not a core component of this role.

This role serves as a scientific and clinical expert in a specific therapeutic area, facilitating scientific exchange between Lilly and healthcare professionals. The MSL provides in-depth, cutting-edge scientific and clinical information, synthesizes research, and communicates insights to inform Lilly's strategic direction. Responsibilities include supporting researchers and practitioners, acting as a primary interface between Lilly Medical and external experts, partnering with clinical development for studies, managing territory, and synthesizing actionable insights.

Clinical Research Physician/Scientist role at Eli Lilly focused on immunology, responsible for owning the medical strategy, driving data generation, late-phase development, and supporting access and Real World Evidence (RWE). The role involves developing strategic medical plans, providing medical expertise for regulatory affairs, leading local scientific data generation and dissemination, and acting as a scientific expert externally. Responsibilities include clinical planning, developing medical strategies to close clinical care and scientific gaps, contributing to promotional material review, and providing scientific training. It also involves managing medical symposia, advisory boards, integrated evidence generation, and collaborating with external scientific experts and thought leaders. The role requires collaboration in the design, conduct, and reporting of local clinical trials, and participation in investigator identification and selection.

This role is for an Operations Supervisor in the filling area at Eli Lilly's Suzhou manufacturing plant. The supervisor is responsible for leading and managing frontline staff, ensuring safe and quality production of pharmaceutical products, adhering to GMP and environmental standards, managing shift performance, and facilitating communication between teams. The role involves direct supervision, training, coaching, troubleshooting, and ensuring compliance with all company policies and procedures.

The role is for a Quality Assurance Technician in a new parenteral manufacturing facility. Responsibilities include on-site quality monitoring during production shifts, material/equipment preparation, formulation and aseptic filling, visual inspection, supporting batch release, GMP documentation, and investigating deviations. The role requires a science/technical background, knowledge of cGMP, and experience in pharmaceutical QA/QC.

Visionary Director, Software Product Management to lead strategy, development, and execution of digital product portfolios for LillyDirect in Silicon Valley. This role is pivotal in shaping the future of Lilly's digital products—driving transformational outcomes through customer-centric design, modular architecture, and operational scalability. As a senior product leader, you will define and own the strategies and roadmaps for digital product portfolios designed to meet user needs while delivering innovative technology solutions that advance the company’s mission.

Director level physician role focused on clinical study design for cardiometabolic health within a biopharmaceutical company. Responsibilities include translating strategy into study designs, developing protocols, collaborating with cross-functional teams, and disseminating scientific data. The role requires deep understanding of drug development, clinical research, and specific disease states.

This role is for a Pharmaceutical Sales Representative specializing in Hematology, focusing on marketing a new substance in a new market for Eli Lilly. The position requires identifying key accounts, developing tailored solutions, conducting professional sales discussions, implementing sales and marketing strategies, and building access pathways. It emphasizes strong cross-functional collaboration and strategic analysis.

Director of Engineering role focused on synthetic molecule design and development for pharmaceutical drug substances and products. Responsibilities include leading teams in unit operation development, process optimization, scale-up, and technology transfer, with a focus on clinical trials, regulatory submission, and commercialization. Requires strong chemical engineering background and experience in process development from mid-cycle to commercialization.

This role is for a Medical Representative in the Cardiovascular Metabolism Health business unit, responsible for promoting company products within a designated territory in China. Key responsibilities include achieving sales plans, building and maintaining customer relationships, providing product information, gathering market intelligence, and collaborating with internal teams.

This role is for an Engineer - Automation Engineering – Control System Data Analyst at Eli Lilly's Medicine Foundry. The individual will provide data engineering and analytics solutions for the Automation Engineering organization, focusing on maintaining, configuring, and troubleshooting automation control systems and interfaces. Responsibilities include developing analytics strategies, creating visualizations and dashboards, supporting system qualification, ensuring compliance with regulatory requirements (GAMP, 21 CFR Part 11, Data Integrity), and collaborating with various teams to optimize manufacturing processes.

Project Engineer-Design Lead role at Eli Lilly, focusing on leading the design delivery for capital projects within the Global Facilities Delivery organization. Responsibilities include ensuring designs meet standards, coordinating with A/E firms, managing design schedules, and resolving design-related issues in pharmaceutical manufacturing environments.

Alternating contract for an "Ingénieur Génie des Procédés" (Process Engineering Engineer) at Eli Lilly, focusing on supporting injectable product manufacturing and managing technology transfer projects. The role involves analyzing production events, identifying corrective actions, coordinating project activities, and conducting studies.

This role is for a Sr. Director of Medical Affairs in Neuroscience at Eli Lilly, focusing on leading the Therapeutic Area (TA) strategy, partnering with cross-functional groups for product commercialization, and driving the execution of TA strategic initiatives. It involves medical and scientific leadership, defining and executing strategic integration, managing cross-functional partnerships, fostering a culture of inclusion and innovation, and leading the generation of Real-World Evidence (RWE) and local data.

Associate Vice President - Global Facilities Delivery Projects at Eli Lilly, responsible for leading and managing multibillion-dollar capital projects in the healthcare sector, from planning through operational verification. The role involves managing staff, ensuring safety and environmental compliance, and representing Lilly to external partners.

This role focuses on statistical analysis for clinical trials within the healthcare domain, requiring expertise in statistical methods, programming (SAS, R), and collaboration with study personnel and regulatory bodies. It is not directly involved in building AI/ML models but uses statistical tools for data analysis and reporting.

This role is a Junior Quality Control Laboratory Technician at Eli Lilly, a global healthcare leader. The position requires a university degree in Chemical Sciences and fluent English. Key responsibilities include performing analytical investigations, reviewing technical documentation, managing internal QC documents, collaborating on data review for product release, identifying improvements, and ensuring compliance with Good Manufacturing Practices (GMP) and safety regulations in a highly regulated environment. No prior experience is required.

This role focuses on overseeing and harmonizing technical programs for contamination control strategies in pharmaceutical API manufacturing. It involves direct network oversight, influencing peers and external manufacturers, and ensuring control strategies align with technical, quality, and regulatory guidance. The position also supports building technical capability, engaging with R&D, and providing technical support for new product introductions and external manufacturing transfers. Key responsibilities include understanding contamination control requirements across diverse platforms, influencing industry and regulatory expectations, providing technical support during design and start-up, and supporting regulatory applications.

This role is for a Pharmaceutical Sales Representative specializing in Cardiometabolic Health (Diabetes) in the Brandenburg region of Germany. The responsibilities include conducting sales calls to healthcare professionals, implementing sales and marketing strategies, developing action plans, organizing educational events, and utilizing digital communication channels. The ideal candidate has a scientific education or is a certified pharmaceutical representative, with at least 2 years of experience in diabetes, strong sales skills, and digital proficiency.

Sales & Marketing Lead for the Oncology portfolio in Turkey, responsible for achieving business objectives, developing brand strategies, enhancing customer experience, and leading the sales team. Requires 5+ years of pharmaceutical sales and marketing experience, with a strong understanding of therapeutic areas and market dynamics. Oncology/Hematology experience is preferred.

This role is a Clinical Program Lead in the ExploR&D organization at Eli Lilly, focusing on managing external collaboration projects in drug discovery and development. The role involves leading cross-functional teams, defining project strategy, managing timelines and budgets, and serving as the primary liaison between Lilly and external biotech collaborators. While the company mentions 'AI/ML tools' as part of its Catalyze360 initiative, the core responsibilities of this specific role are in traditional drug development program management, not in building or directly applying AI/ML models.

This role is for a Pharmaceutical Sales Representative specializing in obesity treatments. The responsibilities include consulting with doctors, implementing sales and marketing strategies, building networks, and organizing educational events. The ideal candidate has a background in life sciences or business, is a certified pharmaceutical representative, has at least 2 years of sales experience in the pharmaceutical field, and possesses strong sales and relationship-building skills. Experience with digital communication tools and CRM systems is also required.

This role is for a Pharmaceutical Sales Representative (Pharmareferent) focused on the Adipositas (obesity) indication in Germany. The responsibilities include consulting with doctors, implementing sales and marketing strategies, building networks, and organizing educational events. The ideal candidate has a background in science or business, is a certified pharmaceutical representative, has at least 2 years of experience in pharmaceutical sales, and possesses strong sales and digital skills.

Process Engineer role focused on establishing, maintaining, and improving manufacturing processes and equipment in a pharmaceutical manufacturing environment. Responsibilities include ensuring safety, technical expertise, troubleshooting, data analysis for optimization, process improvement initiatives, and collaboration with cross-functional teams. Requires engineering degree, strong communication skills, and adherence to safety and quality standards (cGMP).

This role is for a Packaging Expert - Engineer/Scientist at Eli Lilly in Germany, focusing on device assembly and packaging operations. Responsibilities include technical transfer, process validation, maintaining validated states, establishing metrics, harmonizing control strategies, evaluating process improvements, and providing technical leadership. The role also involves mentoring, floor-level support, risk management, technical documentation, and supporting investigations and audits. Requires a Bachelor's degree in engineering or packaging science with 4+ years of manufacturing experience, preferably in pharmaceutical/medical device packaging.

This role is a Senior Manager/Manager in Corporate Communications with a digital focus at Eli Lilly, a global healthcare leader. The position is responsible for leading digital-focused corporate communications, managing the corporate website and social media channels, and developing digital content to enhance the company's reputation and brand. It requires strong experience in digital communications, website management, and social media, with a preference for experience in the pharmaceutical or regulated healthcare industry. The role also emphasizes collaboration, agility, and innovation.

Associate QA Representative responsible for GMP compliance in the design, verification, and startup of manufacturing areas at a new pharmaceutical manufacturing site. Role transitions to site-based process support.

This role at Eli Lilly is for an Advisor - Technical Steward in their TSMS function, focusing on the stewardship and site transfer of commercial molecules for API manufacturing. The position requires extensive experience in cGMP small molecule, peptide, or oligonucleotide API commercial-scale manufacturing, with responsibilities including technical oversight, process troubleshooting, authoring technical reports, and ensuring compliance with GMP and regulatory requirements. The role supports the startup and validation of new facilities and drives continuous improvement in manufacturing processes.

This is an HR role focused on recruitment, internal communication, and training within a pharmaceutical company.

Manager Regional Field Market Access for Diabetes & Obesity at Eli Lilly, focusing on shaping regional market access, ensuring prescription security, and developing solutions to improve patient care by engaging with health insurance funds, physician associations, and regional health policy stakeholders.

This role is for a Sr. Director of Quality Assurance in API manufacturing at Eli Lilly. The primary focus is on ensuring compliance with cGMP standards, managing the QA team, overseeing quality systems, and preparing for regulatory inspections in a pharmaceutical manufacturing environment. It does not involve AI/ML development or research.