Eli Lilly

The Informatics Engineer will partner with Process Translation and Analytical Laboratories to implement and support digital laboratory solutions, focusing on key lab systems like LIMS, LES, ELN, and CDS. Responsibilities include system design, configuration, validation, and release, ensuring compliance with regulatory frameworks (21 CFR Part 11, EU Annex 11) and data integrity in a GMP-regulated environment.

Associate Director - Quality Engineer at Eli Lilly, responsible for technical guidance and leadership in quality standards for API/Fill finish Operations and Facilities Management, focusing on utilities and materials. Key responsibilities include quality oversight of production, engineering, automation, and laboratory operations, document review and approval, providing quality guidance, participating in investigations, data review, material disposition, and maintaining/improving quality systems. Requires BS in Engineering or science, 8 years of experience, and hands-on experience with ADC processes.

Director of Analytical Chemistry focused on Antibody-Drug Conjugates (ADCs), specifically the linker payload intermediate. Responsibilities include leading analytical method development, qualification, characterization, and control strategies, collaborating with cross-functional teams, authoring regulatory submissions, and mentoring staff. Requires PhD or MS/BS with extensive experience in pharmaceutical analytical development and regulatory affairs.

The Digital Plant Scientist will develop, implement, and maintain digital solutions, including models and data systems, to support continuous manufacturing operations in a cGMP environment. This role involves process monitoring, data analysis, integration of batch data, and collaboration with cross-functional teams to build and validate digital tools for a robust control strategy.

This role focuses on analytical chemistry for antibody-drug conjugates (ADCs) within a pharmaceutical company. It involves leading the development, qualification, and characterization of analytical methods for linker-payload intermediates, supporting regulatory submissions, and collaborating with cross-functional teams. The role requires expertise in CMC analytical development and understanding of regulatory requirements in the pharmaceutical industry.

Market Access Manager responsible for strategic planning and operational implementation of market access for innovative therapies within the Lilly portfolio in Austria. The role focuses on ensuring sustainable, timely, and broad patient access and actively shaping the health policy environment. It acts as a central interface between internal departments, the international Lilly organization, and external healthcare system partners. Key responsibilities include developing and executing market access strategies, managing reimbursement and financing mechanisms, analyzing regulatory and health policy frameworks, building relationships with stakeholders (insurers, associations, hospitals, medical societies), collaborating cross-functionally, coordinating reimbursement dossiers and value stories, translating evidence into access narratives, identifying market access barriers, and monitoring market/policy developments.

Associate Director PRA role at Eli Lilly in the Czech Republic, responsible for developing and implementing pricing and access strategies for Lilly's medicines, managing hospital business operations, and building external stakeholder relationships to ensure market access and support business priorities.

This is an internship position for a Communications Officer at Eli Lilly in France. The role involves contributing to communication strategy, creating external and internal communication materials, organizing events, and updating institutional information. The ideal candidate is a student in communication with a strong interest in the healthcare field, social media savvy, and good organizational and writing skills.

Seeking an experienced discovery biologist to provide scientific leadership and hands-on expertise to shape early research strategy and advance novel therapeutic concepts for osteoporosis at Eli Lilly. This role involves driving mechanism-based discovery, maintaining a laboratory presence, designing and conducting experiments, and contributing to cross-functional project teams.

Senior Principal Engineer for Automation Engineering at Eli Lilly's new Medicine Foundry, focusing on advanced manufacturing and drug development. The role involves leading capital project execution, providing automation support for manufacturing operations, mentoring peers, and ensuring compliant control applications and systems. Key responsibilities include technical leadership in design, development, commissioning, and qualification of control systems, promoting digital innovation, and maintaining validated states. Requires deep expertise in DeltaV DCS, Rockwell PLCs, and GMP processes, with a strong understanding of regulatory compliance.

Associate - QA Master Data Steward role at Eli Lilly, focusing on managing master data in SAP and LIMS for specifications in a new pharmaceutical manufacturing facility. The role involves developing programs in accordance with GQS guidelines and participating in regulatory inspections.

Executive Assistant and Chief of Staff supporting the head of diabetes at Lilly, who is also the VP and site head of Lilly’s Protomer site in Los Angeles. This role provides critical administrative support, manages site initiatives, tracks projects, schedules meetings, and supports visitor arrangements. Requires strong organizational and communication skills.

The Engineering Automation Technician provides high-level automation and controls support for OEM filling equipment and associated systems in a cGMP pharmaceutical manufacturing environment. This role focuses on troubleshooting, maintenance, and ensuring automated lines operate safely and reliably, partnering with Operations, Engineering, and Quality.

Operator role in pharmaceutical manufacturing, focusing on operating equipment, troubleshooting, ensuring safety and quality, and training new staff. Requires a high school diploma and basic computer proficiency, with preferences for CGMP knowledge and lean manufacturing principles.

Physician role focused on designing Phase II to Phase IV clinical programs and studies within the neuroscience therapeutic area at Eli Lilly. Responsibilities include translating strategy into clear objectives, representing design optionality, informing protocol design, contributing to asset strategy, and collaborating with cross-functional teams. The role also involves scientific data dissemination, evaluating medical literature, and contributing to organizational learning on clinical design best practices.

This role is for a Principal/Sr. Principal Scientist in pharmaceutical manufacturing, focusing on process understanding, technical support, and continuous improvement for API molecules. It requires a deep understanding of chemistry, experimental design, data analysis, and collaboration with cross-functional teams to ensure safe, compliant, and efficient manufacturing operations in a cGMP environment.

Seeking a Senior Director Operational Leader with strong project management, portfolio operations, and budget governance experience to transform how the DMPK/ADME organization plans, forecasts, tracks, and delivers its book of work. This role involves leading a team, optimizing operational workflows, ensuring accurate forecasting, tracking results, managing budgets, and collaborating cross-functionally.

The Automation Engineer role focuses on enabling data flow between various manufacturing and operations departments by leveraging IT and Process Automation Technologies. This includes supporting innovation, data historians (OSI PI), OT data integration, advanced analytics, data integrity, and process optimization. The role involves leading design, development, and deployment of technical solutions, providing frontline support for PI and LogMate users, managing system health checks, performing emergency response, and acting as a subject matter expert on the OSI PI Data Historian platform. Key responsibilities include data integration for manufacturing improvements, implementing technology governance, incident response, PI tag governance, patch/reboot coordination, change control, DeltaV integration support, service account management, vendor engagement, user support, training, documentation, and audit trail review.

This role is for a Process Engineer in Device Contract Manufacturing at Eli Lilly, focusing on providing technical engineering oversight for production processes to ensure stable supply of devices, subassemblies, and components. Responsibilities include leading prioritization of process changes, coordinating engineering project teams, resolving manufacturing issues, and completing engineering activities for process/product improvements. The role requires a Bachelor's in Engineering and a minimum of 2 years of manufacturing engineering experience, with a preference for pharmaceutical/medical device experience.

Principal Process Engineer role at Eli Lilly focused on API External Manufacturing for small molecules. Responsibilities include providing technical leadership to contract manufacturers, developing process knowledge, assessing equipment suitability, ensuring reliable supply, and managing HSE/PSM elements. The role involves scale-up, tech transfer, process optimization, and continuous improvement, with a strong emphasis on safety and quality.

Senior Director of Health, Safety & Environmental (HSE) for a new state-of-the-art oral solid dosage manufacturing facility in Katwijk, Netherlands. This role leads the EHS function, ensuring compliance with Dutch and EU regulations, developing safety strategies, and integrating EHS into all aspects of the site's operations, from design to start-up and ongoing manufacturing. The position requires strong leadership, strategic planning, and experience in pharmaceutical manufacturing environments.

Senior/Principal Scientist in Quality Operations at Eli Lilly, responsible for QA oversight and final disposition of radioligand drug product manufacturing. The role involves ensuring GMP compliance, supporting manufacturing processes, reviewing batch records, managing deviations, and driving operational excellence through data analysis. Requires experience in pharmaceutical QA/QC and regulatory requirements.

This role is a Senior Associate/Manager for Clinical Trial Project Management within Exploratory Medicine at Eli Lilly. The primary focus is on leading cross-functional teams to develop and execute clinical trials, ensuring quality, timeliness, and adherence to budget and scope. Responsibilities include project planning, timeline and risk management, budget oversight, investigator training coordination, enrollment strategy, vendor management, and ensuring the Trial Master File is up-to-date. The role requires a strong understanding of the drug development process and clinical trial operations.

This role is for a Computational Statistician at Eli Lilly, focusing on statistical analysis and programming for clinical trials. It involves collaborating with statisticians and study personnel, selecting and applying statistical methods, writing reports, responding to regulatory queries, and ensuring data quality. The role requires proficiency in statistical programming languages like SAS and R, and understanding of relevant disease states and regulatory compliance. It is a senior-level position with a focus on applying statistical expertise to healthcare research and development.

Supervisor for Peptide Manufacturing Operations at Eli Lilly, responsible for managing day-to-day production activities in a new advanced manufacturing facility. The role focuses on safety, quality, regulatory compliance, and team supervision within API synthesis and purification.

Process Technician role at Eli Lilly focused on operating highly automated equipment for material preparation, formulation, and filling in a night shift capacity. Requires adherence to Good Manufacturing Practices and safety standards, with opportunities for cross-training and supporting leadership in troubleshooting and training.

Senior Director of Regulatory Strategy at Eli Lilly, focusing on gene-editing programs in early development. Responsibilities include planning, developing, and implementing regulatory strategy, submissions, and compliance activities to support regulatory approvals. The role involves leading regulatory affairs for assigned programs, interacting with global health authorities, and ensuring compliance with regulatory standards.

This role focuses on the development and optimization of purification processes for bioproduct active pharmaceutical ingredients. It involves experimental design, process transfers, and authoring regulatory documents within a healthcare/pharmaceutical context. The role requires a background in chemical engineering or biochemistry and experience in purification development.

This role is for a Process Controls and Instrumentation Technician at Eli Lilly's new Gene Therapy manufacturing facility. The technician will be responsible for the maintenance, calibration, troubleshooting, and installation of process instrumentation (Temperature, Pressure, Flow, Control Valves) to ensure equipment compliance with cGMP and operational readiness for clinical and commercial supply. The role involves supporting startup activities, preventive and corrective maintenance, documentation, and collaboration with various site teams.

This role focuses on applying mass spectrometry techniques to characterize the pharmacokinetic, biotransformation, and biodistribution properties of therapeutic proteins and genetic medicine modalities in preclinical animal models within the Bioanalytical Research Group at Eli Lilly. It involves developing and implementing LC/MS approaches and collaborating with project teams. The role requires a Master's or Bachelor's degree in a relevant scientific field with significant work experience in protein and oligonucleotide mass spectrometry and bioanalysis.

The Qualified Person (QP) is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility, ensuring compliance with GMP, marketing authorization, and current regulations. This role involves continuous quality and regulatory monitoring, analysis of corporate standards, participation in regulatory updates, and oversight of imported products.

This role is for a Sr. Director/Executive Director of E&C Core Capabilities at Eli Lilly in Shanghai, China. The primary function is to serve as a senior Ethics and Compliance (E&C) Business Partner, providing expert leadership in managing E&C risks and advising on program design, process controls, and risk management. The role involves leading Centers of Excellence for Monitoring & Data Intelligence and Third-Party Organization (TPO) Management, and partnering with business leaders to strengthen controls through risk-based oversight and data-driven insights. The ideal candidate will have over 10 years of experience in ethics and compliance within highly regulated industries, strong analytical capabilities, and the ability to influence senior leaders. Fluency in Mandarin and English is required.

This role focuses on discovery research in preclinical women's health, specifically preeclampsia, involving target identification, hypothesis development, and advancing preclinical biology. It requires a PhD in a related field and hands-on laboratory experience with in vitro, ex vivo, and in vivo models.

Associate Director of Process Engineering for a new Small Molecule API manufacturing facility. Responsibilities include hiring and developing a team of process engineers, establishing business systems and processes for GMP operations, and overseeing engineering deliverables for facility startup and ongoing production. Requires a BS in Chemical Engineering or related field with extensive API/chemical manufacturing experience.

This role is for an Expert Maintenance Technician at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The technician will be responsible for maintaining and repairing manufacturing and facilities equipment, ensuring optimal performance and compliance with GMP and safety regulations. The role involves multi-craft expertise in mechanical, electrical, and instrumentation, troubleshooting, documentation, and potentially leading a team. It is a critical role in ensuring the efficient and compliant operation of a state-of-the-art pharmaceutical manufacturing facility.

This role oversees maintenance activities for a new advanced manufacturing and drug development center, ensuring equipment availability, reliability, and optimal performance in compliance with cGMP and other standards. The Maintenance Supervisor leads and develops the maintenance team, fostering a culture of safety, technical expertise, and innovation, while aligning maintenance programs with organizational goals for safety, quality, and efficiency.

This role leads discovery toxicology projects for pharmaceutical small molecule products, involving the design, execution, and interpretation of toxicology studies. The position requires a PhD or MS/BS with extensive experience in toxicology and a strong understanding of the drug discovery and development process, including regulatory guidelines.

This role is for a Sr. Principal Architect-Data at Eli Lilly, focusing on defining, designing, building, and maintaining the data architecture vision and strategy for a manufacturing site. Responsibilities include setting data standards, data modeling, data warehousing, data integration, data governance, and ensuring data security and cloud architecture principles. The role requires extensive experience in data modeling, statistical methods, ontology development, and working with various database technologies and cloud platforms.

Seeking a scientist to develop and apply advanced in vitro models (co-culture systems, iPS-derived cells, spheroids, organoids, organ-on-a-chip) or new approach methodologies (NAMs) to address mechanistic/investigative toxicology questions in drug discovery. The role involves qualifying novel assays, investigating mechanisms of compound-induced toxicity, and collaborating with external partners.

Associate Director role focused on leading cross-functional teams for contract manufacturing of new modalities (Gene Therapy) in a pharmaceutical setting. Responsibilities include developing and implementing quality and supply plans, managing production schedules, resolving supply chain issues, ensuring regulatory compliance, and serving as a liaison between Eli Lilly and contract manufacturers. Requires experience in pharmaceutical manufacturing, technical support, quality assurance, and managing external relationships.

This role is for a Senior / Principal Associate QA API External Manufacturing at Eli Lilly, focusing on ensuring the quality and compliance of externally manufactured Active Pharmaceutical Ingredients (APIs) according to cGMP regulations and company standards. Responsibilities include serving as a QA point of contact for external sites, reviewing manufacturing documentation, leading audits, overseeing quality events, and collaborating with internal teams.

This role focuses on the analytical testing of peptides and oligonucleotides in a pharmaceutical manufacturing setting. Responsibilities include reviewing and releasing data from contract manufacturers, investigating out-of-specification results, performing method validation, and ensuring compliance with regulatory expectations. The role requires a strong background in GMP laboratory practices and analytical techniques.

Senior Principal Chemist role in Pharmaceutical Investigations Team, focusing on analytical testing of drug substances, drug products, and other materials. Responsibilities include foreign/unknown material analysis, counterfeit/tampering investigations, and supporting legal initiatives using various analytical techniques and IT tools. Requires expertise in physical and chemical analytical techniques, good documentation practices, and strong communication skills.

This role is for a Production Technician at Eli Lilly's Parenteral Manufacturing site, responsible for preparing equipment and formulating products for sterile filling. It requires adherence to safety policies, SOPs, and GMPs, with basic math and computer skills. Experience in GMPs, formulation, and/or equipment prep is preferred.

Quality Assurance Floor Support Specialist role at Eli Lilly, focusing on GMP operations in pharmaceutical manufacturing. Responsibilities include QA oversight, documentation review, sample collection, and system support in a night shift environment.

This role is a Master Planner responsible for creating and managing production plans, inventory, and material requirements within SAP for a pharmaceutical manufacturing facility. It involves close collaboration with regulatory, production, and quality departments to ensure compliance and optimize capacity, with a focus on meeting demand while minimizing inventory costs. The role also includes managing change control and reporting on key supply chain metrics.

Process Engineer role focused on supporting and improving manufacturing processes, equipment, and facilities in a pharmaceutical (healthcare) setting. Responsibilities include troubleshooting, cross-functional collaboration, process support, equipment monitoring, safety basis development, and utilizing modeling/simulation for process understanding. Requires a BS in Engineering and experience in chemical manufacturing.