Eli Lilly

Senior Manager role in the pharmaceutical industry focused on developing and implementing pricing and reimbursement strategies for the China market. Responsibilities include new product strategy, payer engagement, health economic outcomes research, and cross-functional collaboration.

Quality Assurance Operations Representative for aseptic manufacturing at a pharmaceutical production site. Ensures compliance with Quality standards, proposes and implements Quality actions, approves relevant elements, coaches other functions on Quality topics, and drives continuous improvement of Quality processes and methods. Requires a PhD in Industrial Pharmacy (or in progress) with a Master's in Quality Assurance, Pharmaceutical Production, or Pharmaceutical Engineering, and prior experience in sterile drug production operations.

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 and market conditions, and requires a bachelor's degree in a pharmaceutical-related field, with preference for experience in endocrine products and new product launches.

This role focuses on the analytical development and technical transfer of small molecule synthesis processes within the pharmaceutical industry. It requires expertise in GMP, regulatory requirements, and laboratory work to optimize production processes, develop robust analytical methods, and ensure successful technology transfer globally. The position involves scientific and technical leadership, problem-solving, and collaboration across different teams and locations.

This role focuses on analytical development and process optimization for peptide synthesis within a pharmaceutical manufacturing and quality technical hub. The candidate will provide technical support, develop analytical methods, and ensure their transfer to production environments, requiring a strong understanding of GMP, regulatory requirements, and analytical instrumentation.

This role provides technical support and performs analytical development for small molecule synthesis and process development labs. It involves designing and executing experiments, developing analytical methods, and understanding analytical instrumentation. The role also includes people leadership for a team of process chemists and ensuring safety and lab management. The ideal candidate has a Ph.D. in Chemistry or Analytical Chemistry with 12+ years of experience.

Senior/Principal role in Materials Management QA for Device Assembly and Packaging, providing Quality Oversight for suppliers and materials. Responsibilities include managing the Approved Supplier List, conducting risk assessments, coordinating quality agreements, maintaining complaint databases, and supporting regulatory inspections within a GMP environment.

Principal Automation Engineer focused on Computer System Validation (CSV) for a new API manufacturing facility. The role involves supporting the design, delivery, and ongoing operations of process automation systems, ensuring compliance with cGMP standards and data integrity. Responsibilities include developing validation plans, leading validation efforts, and collaborating with quality, engineering, and external partners. Experience with automation platforms like Rockwell and DeltaV is preferred.

Principal Automation Engineer - Instrument & Controls role at Eli Lilly, focusing on the design, application, and troubleshooting of instrumentation within pharmaceutical manufacturing facilities. This role supports capital projects and GMP manufacturing operations, requiring expertise in process measurements, control theory, and automation platforms like Rockwell Automation and Emerson DeltaV. The position involves collaboration with A&E firms and system integrators, and contributes to site maintenance programs and process safety management.

This role focuses on the process development and manufacturing of RNA-lipid nanoparticles (LNPs) and other parenteral drug products for genetic medicines. The engineer will design and execute studies, lead process development, manage tech transfer, and collaborate across functions to advance these therapies from clinical to commercialization.

Senior Principal Process Engineer role at Eli Lilly focused on the startup and operation of a small molecule API manufacturing facility. The role involves technical leadership, mentoring, process optimization, and ensuring GMP compliance within a regulated healthcare environment.

This role is responsible for managing the cleaning program for process equipment and ancillary components in a pharmaceutical manufacturing facility, focusing on cleaning verification/validation activities, authoring documentation, coordinating investigations, and improving cleaning process efficiency. It requires knowledge of GMP, regulatory requirements, and pharmaceutical manufacturing.

Project Manager for Global Facilities Delivery at Eli Lilly, responsible for leading manufacturing capital projects from design to operational verification. Requires 10+ years of experience in capital project delivery in industrial or manufacturing facilities, with a focus on safety, quality, and compliance.

This role is for an Engineer focused on Manufacturing Execution Systems (MES) in a pharmaceutical manufacturing setting. The primary responsibility is to design, develop, deliver, and qualify the MES solution for a new drug substance manufacturing site. The role involves partnering with automation and operations teams, ensuring operational readiness, adapting project roadmaps, and maintaining system validation. A key requirement is the ability to incorporate AI tools into daily workflows to improve MES recipes and activities, alongside a strong understanding of GMP and regulatory requirements.

Warehouse Technician responsible for receiving, storage, and shipping of raw materials and packaging components in a cGMP manufacturing environment. Ensures material availability for production and accurate inventory quantities, adhering to all safety and regulatory requirements.

This role is for a Sr. Director of Business Solutions MQ IT at Eli Lilly, focusing on defining and deploying the digital strategy for a new manufacturing facility. It involves integrating various systems like SAP, MES, and Data Historian, ensuring cGMP compliance, and managing the IT/OT footprint. The role requires strong leadership in Pharma IT, with a focus on manufacturing operations and technology.

This role is for a Production Operator at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The operator will support the startup phase of the facility, bringing manufacturing equipment into service, and then oversee the production of API molecules. The role emphasizes safety, quality, and adherence to GMP practices in a pharmaceutical manufacturing environment.

The Sterility Assurance Advisor role at Eli Lilly is responsible for maintaining a safe work environment and understanding the scientific principles required for manufacturing parenteral drug products. This includes using sterility assurance risk management to evaluate manufacturing processes and controls, leading projects associated with sterility assurance programs, and developing/executing process and facility monitoring strategies. The role also involves leading deviations, staying updated on regulatory requirements, influencing corporate guidance, identifying continuous improvements, providing design input for new processes, defending sterility assurance programs during audits, assisting with regulatory submissions, and providing training and technical mentorship.

This role is in Quality Assurance for Material/Supplier Management at a new gene therapy manufacturing facility. It focuses on ensuring compliance with quality standards, overseeing incoming materials, and managing supplier relationships in a regulated pharmaceutical environment.

This is a financial planning and analysis role within a pharmaceutical company. The responsibilities include assisting operational teams with results tracking and analysis, participating in sales and expense forecasting, assisting with financial closing processes, developing and disseminating activity reports, and responding to financial study requests. The role requires a Master's degree in Business or University, strong analytical and synthesis skills, teamwork, rigor, organization, autonomy, flexibility, and business acumen. Proficiency in Excel is required, and knowledge of Power BI is a plus. English proficiency is essential.

This role focuses on process engineering for drug substance and drug product manufacturing, involving laboratory-scale process development, optimization, and technology transfer. It requires collaboration with scientists and cross-functional engineering groups, hands-on experimentation, data analysis, and ensuring safe and compliant laboratory operations. The position emphasizes applying engineering fundamentals to improve process understanding and robustness, with a focus on pharmaceutical and biotechnology industries.

Principal Automation Engineer - Data & Platforms integration role at Eli Lilly, focusing on designing, delivering, and managing data historian and integration platforms for a new API manufacturing facility. Requires expertise in Aveva PI Data Historian, system integration, validation practices (cGMP, data integrity), and server administration within a pharmaceutical manufacturing context.

This role is for a Principal Automation Engineer specializing in DeltaV System Administration within a pharmaceutical manufacturing facility. It involves supporting the design, delivery, validation, and ongoing management of DeltaV DCS platforms, ensuring compliance with cGMP standards and data integrity. The position requires a deep understanding of process automation systems and Lilly's computer system validation practices, with responsibilities including hardware design, administrative procedures, and collaboration with various internal and external stakeholders. The role transitions from project delivery to site-based support for GMP manufacturing operations.

Pharmaceutical Sales Territory Manager for Eli Lilly's Gastroenterology specialty, responsible for account-based selling to healthcare providers to drive adoption of therapies. Requires understanding of territory, reimbursement, and clinical information to build relationships and achieve sales goals.

Senior Manager of Engineering responsible for supporting asset delivery, process development, commissioning, qualification, validation, and startup of the Parenteral/DAP area and other engineering systems. The role involves leading a team of 5-10 individuals and ensuring business plan goals related to safety, quality, and efficiency are met. Requires a Bachelor's degree in Engineering, at least 5 years of engineering experience, and pharmaceutical experience. Experience with regulatory agencies (FDA, EMEA), automated equipment, combination products, and facility startups is preferred.

Lead Chemical Operator for API manufacturing operations at a new Eli Lilly facility, responsible for production, safety, quality, and compliance in a regulated pharmaceutical environment.

This role is for a Manufacturing Chemical Operator at a new pharmaceutical API manufacturing facility. The operator will be responsible for the production of API molecules, maintaining compliance with regulatory requirements, and ensuring equipment is in good operating condition. The role involves monitoring, testing, cleaning, and responding to production issues, with a strong emphasis on safety and quality within a GMP environment. Experience in facility startups and pharmaceutical manufacturing is preferred.

Manager for Financial Planning in Mexico at Eli Lilly, focusing on business partnership, financial planning (OPEX cycle, projections, business cases), and driving innovation through process automation and AI tools. Requires 5+ years of FP&A experience, advanced Excel, and familiarity with AI tools like Claude and Copilot.

Associate Director of Operations for Device, Assembly, and Packaging in the pharmaceutical industry. Responsibilities include leading operations teams, ensuring production goals, managing cross-functional teams, and presenting to regulatory agencies. Requires experience in pharmaceutical manufacturing, leadership, and understanding of regulatory requirements.

This role is for a Sr. Program Director in Global Facilities Delivery at Eli Lilly, focusing on managing large capital projects (>$1BN USD) in pharmaceutical manufacturing. The role requires extensive experience in project management, interface management, compliance, and safety/environmental execution within regulated facilities. It involves leading cross-functional teams and ensuring projects meet safety, cost, schedule, and quality objectives from planning through operational qualification.

This role focuses on the design and development of drug products for synthetic molecules within the pharmaceutical industry. It involves applying fundamental pharmaceutical sciences, predicting in vivo performance using molecular properties and preclinical data, and leveraging modeling to guide formulation development. The position also requires collaboration with partners, influencing scientific communities, and authoring technical reports and regulatory documentation. While it involves modeling and data analytics, the core function is not AI/ML model development but rather drug product research and development in a healthcare context.

This role focuses on designing, developing, and supporting electronic laboratory notebook (ELN) templates and other laboratory informatics platforms within the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The position requires collaboration with scientists and IT teams to ensure data integrity, system reliability, and compliant scientific operations in a regulated environment.

The Laboratory Informatics Scientist will deploy and support laboratory informatics platforms, primarily the MODA environmental monitoring system, within the Lilly Medicine Foundry. This role involves configuring systems, managing data, ensuring compliance with cGMP/GLP, and collaborating with IT and lab scientists to optimize digital workflows in a regulated healthcare environment.

Internship role focused on continuous improvement in a pharmaceutical manufacturing setting, involving data collection, process analysis, Lean optimization, KPI management, and SOP updates. Requires a Master's degree in a relevant field and strong analytical skills.

Manager, Regulatory Delivery Excellence, China Regulatory Affairs at Eli Lilly is responsible for managing regulatory registration processes and submission preparation support, covering clinical trial permit applications through to marketing applications. This role involves developing submission plans, collaborating with cross-functional teams and vendors, managing RIM-related activities, and ensuring compliance with regulations and internal quality systems. The position also requires serving as a Subject Matter Expert for regulatory business processes and the Veeva Vault RIM system, and maintaining data in IT systems.

The Bioinformatics Platform Engineer will operate, improve, and scale scientific computing infrastructure for production bioinformatics workflows in AWS. This role involves supporting and troubleshooting NGS workflows, managing Linux environments, and contributing to infrastructure automation and platform reliability. The engineer will collaborate with scientists to translate workflow needs into scalable solutions and participate in architecture decisions.

This role is for an MBA intern candidate at Eli Lilly, focused on leading the design and modeling of a virtual program for Alzheimer's Disease within the Neuroscience division. The position requires strong financial and commercial acumen to develop a scalable and sustainable operating model, drawing on best practices from established care ecosystems. The role is part of a global strategy to grow international business and offers a foundational platform to learn the industry and understand customers.

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 (hospitals), providing product information, gathering market intelligence, and contributing to team efforts.

This role is for a (Senior) Advisor-Medical Affairs CMH in Primary Care at Eli Lilly, focusing on the CardioMetabolic Health portfolio. The individual will act as a medical expert, translate clinical insights into strategies, manage relationships with healthcare professionals, and contribute to medical strategy development and execution within the primary care setting. The role requires a medical degree (BIG registration) and experience in CMH-related care, preferably in primary care or the pharmaceutical industry.

Senior Director role responsible for the technical strategy and process excellence of drug product manufacturing at an Oral Solid Dosage manufacturing site. This includes technical oversight for drug product intermediates control strategy from spray dried dispersion through tablet and capsule manufacturing. Serves as the site’s authority on technology transfer, scale-up, and manufacturing science for oral solid dose forms (tablets, capsules).

Manager for Regulatory Delivery Excellence in China, focusing on managing regulatory registration processes, submission preparation, and ensuring compliance with regulations and internal quality systems for pharmaceutical products. The role involves developing submission plans, supporting regulatory teams, acting as a Subject Matter Expert for regulatory business processes and the Veeva Vault RIM system, and maintaining data in IT systems.

This role is for a Medical Representative in the Cardiovascular Metabolic Health business unit at Eli Lilly in Zibo, China. The primary responsibilities include promoting company products in clinical settings, achieving business objectives, building and maintaining client relationships, providing drug information, and reporting market information. Qualifications include a bachelor's degree in a relevant field, and experience in pharmaceutical promotion and client development is preferred. Strong execution, communication, coordination, problem-solving, and resilience are required.

This apprenticeship role in aseptic production at Eli Lilly focuses on supporting routine production activities, proposing and implementing process improvements, managing continuous improvement projects, and ensuring compliance with quality systems. The role involves collaboration with various teams and understanding of manufacturing processes like material preparation, formulation, and filling.

Pharmaceutical Sales Representative for Eli Lilly's GI Specialty division, responsible for account-based selling to healthcare providers to drive adoption of therapies. Requires understanding of territory, reimbursement, and clinical information, with a focus on building relationships and achieving sales goals.

Lead Calibration Technician responsible for performing and documenting routine and non-routine instrument calibrations, including maintenance, testing, troubleshooting, and repairs on manufacturing equipment in a GMP/regulated environment.

Associate Scientist role in drug target identification and validation for CNS diseases, focusing on psychiatric disorders. Responsibilities include designing and executing rodent in vivo studies, stereotaxic surgeries, tissue collection, and quantitative immunohistochemistry (IHC) and immunofluorescence (IF) workflows. The role also involves molecular and biochemical assays, collaboration with multidisciplinary teams, and presenting experimental results. Requires an MS in Neuroscience, Biology, or Pharmacology with 2-5 years of lab experience in in vivo rodent work and IHC.

This role is for a Sr. Principal Engineer focused on Manufacturing Execution Systems (MES) within a pharmaceutical manufacturing facility. The primary responsibilities involve developing and integrating MES components, supporting site startups, and ensuring compliance with cGMP regulations. The role requires extensive experience with MES systems and data integration in a regulated environment.

Associate Director for Clinical Trial Foundations (CTF) at Eli Lilly, focusing on eSource technologies for clinical development. This role involves defining and executing implementation plans for systems that capture direct patient data from investigator sites, including electronic medical records. The position requires expertise in clinical systems, project management, and partnerships with internal teams, IT, and external vendors to optimize clinical development processes and technologies.