Associate Director of Trade Compliance and Import-Export Services, focusing on Foreign-Trade Zone Operations within Lilly Research Laboratories. This role ensures compliance with U.S. Customs and Border Protection (CBP) and other Partner Government Agencies (PGAs) for global clinical supply operations, including managing FTZ protocols, advising on duty optimization, and supporting integration into enterprise systems.

Senior Director of Technical Services/Manufacturing Science (TS/MS) overseeing site operations, new product introduction, process development, and optimization within a pharmaceutical manufacturing context, ensuring compliance with cGMP and regulatory standards. This role involves strategic leadership, cross-functional engagement, and people development within a global healthcare company.

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

Clinical Research Physician specializing in Ophthalmology Gene Therapy Development at Eli Lilly. This role involves the development, conduct, and reporting of global clinical trials for ophthalmologic products, including protocol review, patient safety monitoring, adverse event reporting, and scientific data dissemination. The physician will serve as a medical resource for study teams and external healthcare professionals, collaborating on clinical strategy, trial execution, and regulatory support.

The Equipment Support Group Lead at the Lilly Medicine Foundry is responsible for the commissioning, qualification, compliance, maintenance, calibration, reliability, and lifecycle management of general equipment and analytical instrumentation supporting LMF laboratories. This role ensures equipment is fit for use, properly installed, qualified, and compliant, acting as a technical bridge between scientists and support teams.

This role provides Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for products manufactured by third-party partners. Responsibilities include leading quality aspects of external sites, conducting audits, reviewing documents, collaborating cross-functionally, providing QA guidance, developing quality agreements, investigating incidents, and representing Lilly during regulatory inspections.

Associate Director of Engineering (Automation) at Eli Lilly's new API manufacturing facility in Houston, TX. Responsible for leading and developing the Process Control Engineering team, ensuring reliable and compliant control applications and systems for GMP manufacturing. Role involves hiring, process development, and collaboration during the facility startup and ongoing operations, with a focus on safety, quality, and operational excellence.

Lead Maintenance Mechanic role at Eli Lilly's new API manufacturing facility in Lebanon, IN. Responsibilities include overseeing maintenance and repair of manufacturing equipment, ensuring optimal performance and compliance with GMP and safety regulations. Requires expertise in mechanical, electrical, and instrumentation disciplines, troubleshooting, documentation, and leading a team of mechanics. Focus on startup operations for a greenfield manufacturing site.

Senior Engineer role focused on technical project management and delivery oversight for intralogistics system deployments in manufacturing. This involves integrating various systems like SAP/EWM, MES, and automation hardware (AGVs, ASRS) to enable autonomous material flow. The role requires developing integrated schedules, coordinating dependencies, and ensuring system requirements are met.

This role provides technical stewardship for an advanced manufacturing facility for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing. It requires expertise in bioconjugate manufacturing processes, including conjugation chemistry, purification, filtration, and analytical/process controls. The role involves data-driven decision-making, process improvements, and leveraging digital plant technologies. It also requires experience with regulatory guidance and cGMP requirements.

Associate Director for Technical Services/Manufacturing Science (TS/MS) at Eli Lilly, responsible for leading a team that provides technical oversight for biological and bioconjugate manufacturing processes. The role involves building and developing the TS/MS organization, ensuring process reliability, supporting regulatory compliance, and managing documentation within a new advanced manufacturing facility.

Associate Director of Operational Readiness for a new API manufacturing facility in the pharmaceutical industry. This role involves developing and managing an integrated project plan for facility startup, leading a cross-functional team, and establishing Lean principles for operational excellence. The position requires experience in GMP operations and project leadership within the pharmaceutical sector.

Scientist role focused on developing and maintaining operations for sample preparation, organization, and tracking within a drug discovery environment. Involves managing compound libraries, designing plate preparation, collaborating with global sample management networks, and troubleshooting lab automation systems. The role emphasizes process improvement, data integrity, and safety in a laboratory setting.

The Sr. Principal Scientist, MES Data and Integration Lead will support the design, deployment, and operation of the Manufacturing Execution System (MES)/Electronic Batch Record (EBR) for a new API manufacturing facility. This role focuses on translating manufacturing requirements into MES solutions, ensuring data governance, and integrating MES with other enterprise systems to support compliant and efficient GMP operations. The role involves working with process data for continuous improvement and performance analytics.

This role focuses on the Manufacturing Execution System (MES) and Electronic Batch Record (EBR) for a new, digitally native API manufacturing facility. The Sr. Principal Scientist will lead the MES technical agenda, translate manufacturing requirements into MES solutions, and ensure compliant, data-driven production. The role involves system ownership, support, risk assessment, and developing best practices for MES-enabled operations within a GMP environment.

This role supports the design, deployment, and operation of a contamination control strategy in a new pharmaceutical manufacturing facility. It involves ensuring strategies align with technical, quality, and regulatory guidance, applying data-driven decision-making, and improving contamination control performance through innovative technologies. Responsibilities include authoring technical documents, monitoring environmental conditions, investigating contamination events, analyzing trending data, and training staff.

This role focuses on managing printed packaging materials (PPMs) for contract manufacturers in the pharmaceutical space, ensuring they meet technical and company standards. Responsibilities include managing layouts, metadata, artwork development, and technical changes, as well as participating in testing, investigations, and projects, including digital transformation initiatives within packaging.

This role focuses on operational readiness and continuous improvement in pharmaceutical manufacturing, specifically within the new Lilly Medicine Foundry. It involves analyzing processes, implementing Lean and OpEx principles, managing projects, and ensuring safety and quality in a regulated environment. The role requires strong leadership and cross-functional collaboration to optimize manufacturing processes and support the startup and production phases of the facility.

This role provides technical oversight of raw materials and consumables for gene therapy manufacturing, focusing on ensuring reliable supply, safety, and quality. Responsibilities include qualifying, implementing, and improving materials management processes, establishing an Extractables and Leachables (E&L) program, assessing supplier risk, and collaborating with various internal and external groups. The position is crucial for the startup of a new, advanced manufacturing facility.

Executive Director role focused on early clinical development in neuroscience drug development, involving clinical pharmacology and mechanistic studies. Responsibilities include leading clinical trials, reporting adverse events, reviewing protocols, and ensuring compliance with regulations and GCPs. Requires an M.D. or D.O. with at least five years of relevant experience.

This role provides quality oversight of Quality Control activities at Contract Manufacturing organizations (CMs) for Active Pharmaceutical Ingredients (API) External Manufacturing. It involves ensuring compliance with cGMPs, supporting method validation/transfer, and managing quality-related issues with testing.

This role is for a Director in Analytical Development within the Bioproduct Research and Development organization at Eli Lilly. The position focuses on leading analytical efforts for pharmaceutical drug substance and drug product development, commercialization, clinical trials, and regulatory submissions. Responsibilities include developing analytical methods, designing stability studies, authoring regulatory documents, and providing technical guidance for external analytical activities. The role requires a strong foundation in analytical sciences and experience in the pharmaceutical industry, with a focus on ensuring the quality and control strategies for various therapeutic modalities.

This role focuses on leading PKPD project strategy for genetic medicines programs, developing and implementing modeling strategies to enhance decision-making in drug discovery and development. It involves designing, analyzing, and interpreting quantitative pharmacology studies, collaborating with cross-functional teams, and mentoring junior scientists. The role requires expertise in PK/PD and PBPK modeling, experience with relevant software, and a PhD in a related field.

This role is responsible for administering, maintaining, securing, and optimizing core data movement and integration platforms like IBM MQ, IBM App Connect Enterprise, Aspera, and Axway B2Bi. The individual will ensure high availability of messaging and file transfer services, automate operational tasks, and provide expert support for data exchange within the organization and with external partners. Key responsibilities include managing IBM MQ environments, supporting integration flows, administering file transfer solutions, configuring secure data exchange, developing automation scripts, implementing security configurations, and troubleshooting complex data flow issues.

Security Operations Engineer focused on Identity and Access Management (IAM) platforms, ensuring secure and timely access to enterprise resources. Responsibilities include day-to-day operations, incident management, change management, problem resolution, system monitoring, maintenance, documentation, and supporting audit/compliance requests for authentication systems like Entra ID, Active Directory, and Okta. Requires on-call rotation.

This role is a Technical Lead for SecOps Engineering focusing on Privileged Access Management (PAM), Encryption, and Identity Governance. It involves technical leadership, operational excellence, incident management, change management, and ensuring secure access to enterprise resources. The role requires managing and supporting 24/7 identity platforms and services, collaborating with cross-functional teams, and responding to audit and compliance requests. It is not directly related to AI/ML model development or deployment.

This role is responsible for assessing, establishing, and operationalizing the regulatory strategy and execution plan for assigned IVD performance studies and for clinical trials that use IVDs, ensuring compliance with EU IVDR and applicable national requirements. The role involves developing regulatory documents, supporting interactions with regulatory agencies, and providing expertise on IVD regulations for clinical trials.

This role is for an MSL Manager in the pharmaceutical industry, responsible for leading a team of Medical Science Liaisons, overseeing their performance, training, and strategic implementation within assigned therapeutic areas. The position requires a health science degree, experience in the pharmaceutical industry, and strong people management and communication skills.

This role is responsible for supporting the cleaning program for process equipment and ancillary components in a new Biotech Drug Substance Manufacturing Facility. Responsibilities include developing cleaning strategies, authoring validation plans and protocols, executing protocols, authoring procedures, and troubleshooting cleaning processes. The role requires a BSc in Engineering or Science with 2 years of experience in a pharmaceutical/biopharmaceutical manufacturing site.

Senior Manager for Quality Control Support in a pharmaceutical setting, focusing on team leadership, GMP compliance, and digital system management within QC operations.

This role provides Extended Warehouse Management (EWM) business support and expertise for warehouse and logistics operations. Responsibilities include troubleshooting issues, driving continuous improvement, training teams, assessing system/process changes, and managing EWM master data. The role requires SAP EWM experience and comfort with automated warehouse technologies.

Reliability Technician role at Eli Lilly's new Medicine Foundry, focusing on ensuring equipment availability and performance through predictive maintenance, data analysis, and continuous improvement in a cGMP-regulated manufacturing environment.

This is an administrative support role within the Communication and Public Affairs department of Eli Lilly France. The responsibilities include managing schedules, purchase orders, event planning, updating communication channels, and taking meeting minutes. The role requires strong organizational and communication skills, proficiency in office software, and a willingness to learn.

This role manages laboratory, device, imaging, and other diagnostic support for clinical trials, coordinating vendor activities, partnering with medical staff on protocol development, and ensuring high-quality data. It focuses on clinical trial initiation and execution within the healthcare domain.

This role is for a Senior Warehouse Manager in the pharmaceutical industry, responsible for overseeing all aspects of warehouse operations, including material receipt, storage, dispensing, shipping, inventory control, and compliance with quality, safety, and regulatory requirements (GMP, AEO). The role also involves project management for warehousing initiatives, team leadership, and ensuring a safe work environment. Experience with SAP/PMX and GMP regulations is required.

The Automation Technician is responsible for the performance of automated equipment, providing first-line support to production processes, and supporting area engineering initiatives, process improvements, and project implementation within a pharmaceutical manufacturing environment. This role requires expertise in production processes, commissioning, qualification, and validation requirements, as well as equipment-specific code and control system technologies.

This role is for an Advisor, Project Controls at Eli Lilly, focusing on managing project controls for large capital programs (>$500MM USD) in global facilities delivery. The responsibilities include leading project controls teams, establishing cost and schedule baselines, managing resources, change control, risk management, and ensuring compliance with finance policies. It requires significant experience in project controls on major industrial or manufacturing projects.

Associate Director for Project Controls in Global Facilities Delivery (GFD) at Eli Lilly, focusing on manufacturing network projects. Responsibilities include budgeting, cost control, earned value management, change and risk management, forecasting, and planning. The role involves process improvement, governance, mentoring, and ensuring compliance with finance policies for capital projects.

This role is for a Senior Director in Oncology and Peripheral Imaging Clinical Development at Eli Lilly. The primary focus is on leading the clinical development of imaging strategies for oncology, immunology, and cardiometabolic diseases, spanning early to late-phase trials. While the role involves evaluating AI in imaging, its core function is in clinical research and development within the healthcare domain, not in building or shipping AI models.

Senior/Principal Upstream Bioprocess Scientist at Eli Lilly in Limerick, Ireland, focusing on technical support for manufacturing processes, data-driven decision-making, and continuous process improvement in upstream bioprocessing. Requires expertise in cell culture, process monitoring, statistical methodologies, and regulatory compliance within the biopharmaceutical industry.

Associate Director for a Technical Services & Manufacturing Sciences (TSMS) Laboratory focused on small molecule and oligonucleotide API process troubleshooting and continuous improvement. Responsibilities include leading laboratory staff, designing and executing experiments, managing a safe work environment, hiring and developing staff, and collaborating with cross-functional teams for technology transfer, process validation, and manufacturing operations. The role also involves commissioning new equipment and defining the technical agenda for process capability and yield improvement.

Associate Director of Utilities Operations for a new API manufacturing facility, responsible for managing day-to-day utility operations, ensuring safety, quality, and regulatory compliance, and leading a team to support the startup and ongoing operations.

This role is for an Automation Engineer at Eli Lilly's new manufacturing site in Concord, NC. The engineer will be responsible for automation design, managing system integrators, supporting corporate initiatives like lifecycle management and cybersecurity, and driving automation governance. The role involves evaluating new technologies and innovation trends for application within Lilly.

Associate Director of Process Engineering for Oligonucleotides manufacturing, responsible for leading and developing a team of process engineers. This role involves building a new manufacturing facility from the ground up, establishing operational processes, ensuring compliance with GMP standards, and overseeing engineering deliverables for both startup and ongoing operations. The position requires strong leadership, talent acquisition, and a focus on safety, quality, and operational excellence in a regulated pharmaceutical environment.

Director of Engineering role focused on purification and conjugation technologies within Bioproduct Research and Development (BRD) at Eli Lilly. Responsibilities include providing technical expertise for GMP manufacturing of drug substance, focusing on chromatography, filtration, and bulk unit operations. The role involves developing control systems, performing risk assessments, collaborating with development scientists and manufacturing, evaluating new technologies, supporting tech transfers, mentoring engineers, and ensuring compliance with quality systems and cGMP requirements. Requires a Ph.D. or MS/BS in Chemical Engineering with significant experience in biopharmaceutical downstream processing and equipment design/qualification.

Associate Director for Technical Services and Manufacturing Support (TSMS) in a small molecule API manufacturing facility. Responsibilities include leading a team of scientists, managing technical transfer, process validation, manufacturing operations, continuous improvement, and ensuring GMP compliance. Requires experience in cGMP API manufacturing and technical leadership.

Associate Director for Technical Services/Manufacturing Support (TSMS) in an oligonucleotide API manufacturing facility. Responsibilities include leading a team, managing production support, implementing technical projects, process optimization, technical transfer, validation, and ensuring GMP compliance. Requires a Bachelor's or Master's in a science field and 5+ years of cGMP commercial API manufacturing experience.

Associate Director TSMS - API role at Eli Lilly responsible for technical and people leadership in API manufacturing processes. Focuses on technology transfer, process validation, manufacturing support, process optimization, and lifecycle management. Emphasizes leveraging data analytics and digitalization strategies for process improvement and site capabilities, requiring collaboration across multiple functions.