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.

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 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 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 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.

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.

This role focuses on ensuring the validation and data integrity of laboratory IT systems and computerized instruments within a pharmaceutical manufacturing environment. It involves implementing and maintaining systems according to regulatory requirements (cGMP, CSV) and collaborating with various quality and IT teams to ensure compliance and continuous improvement.

Associate Director - IT Systems Program Manager at Eli Lilly, focused on overseeing and aligning multiple programs for new API manufacturing sites. The role involves managing large-scale programs, release train engineering, GxP compliance, stakeholder management, risk management, and resource allocation. Requires a strong business understanding, analytical skills, and the ability to communicate complex technical information. Experience in Pharma and GMP Manufacturing is required.

The Instrument Technician role provides process instrumentation maintenance support for the Lilly Medicine Foundry, focusing on equipment availability, calibration, troubleshooting, and reliability in a cGMP-regulated environment. Responsibilities include performing preventative and corrective maintenance, troubleshooting instrumentation, operating test equipment, and supporting new equipment installations.

Senior Advisor/Director role in Small Molecule Process Development at Eli Lilly, focusing on leading teams, managing safety, and overseeing the scientific and technical aspects of chemical process development for drug substances and intermediates. The role involves planning, optimizing, troubleshooting, and transferring chemical processes, with a strong emphasis on scalability, robustness, safety, cost, and sustainability. Requires a Ph.D. in Chemistry or Chemical Engineering with 12+ years of experience.

This role is for an Analytical Steward focused on Mass Spectrometry and related instrumentation for peptide and small molecule characterization within a pharmaceutical manufacturing and quality technical hub. The responsibilities include developing analytical methods, conducting experiments to optimize processes, and providing technical support for technology transfer. The role requires a Ph.D. in a relevant scientific discipline with 5-12 years of experience.

This role focuses on the process development and optimization of small molecule drug substance manufacturing within the pharmaceutical industry. It involves technical transfers, ensuring processes are robust and cost-effective, and collaborating with R&D and plant sites. The position requires a strong understanding of GMP, regulatory requirements, and the ability to lead technical projects and mentor junior staff. Experience with digitization and regulatory interactions is also highlighted.

This role manages and modernizes enterprise data integration platforms (Informatica, Denodo), focusing on installation, upgrades, performance, security, and migration to cloud-native solutions. It involves ensuring platform reliability, supporting data virtualization, and troubleshooting complex issues within a hybrid ecosystem.

This role focuses on statistical trial design and analysis within clinical research and development in the healthcare domain. The primary responsibilities include developing protocol designs, writing protocols, selecting statistical methods, analyzing clinical study data, and communicating results. The role requires a Ph.D. in Statistics or Biostatistics with experience in clinical R&D and proficiency in statistical programming languages.

Lead Automation Technician role at Eli Lilly, a global healthcare leader, focusing on automated equipment performance, production support, and process improvements in a new state-of-the-art parenteral manufacturing site. Responsibilities include ensuring equipment is maintained, safe, and operated according to cGMPs, investigating production delays, and supporting engineering initiatives. Requires an Associate's Degree or equivalent experience, with preferences for GMP manufacturing, PLC/HMI programming (Studio 5000, FactoryTalk View SE, B&R), and experience with automated equipment and maintenance management systems.

This role is for a Utilities / Medium Voltage Electrician / Instrumentation at Eli Lilly, responsible for servicing, troubleshooting, and maintaining electrical and instrumentation equipment within utility systems. The position involves preventative and corrective maintenance on high and low voltage electrical equipment, process instrumentation, and ensuring compliance with safety and cGMP standards. It requires strong electrical and mechanical aptitude, with experience in utility systems and troubleshooting being preferred.

This role focuses on driving continuous improvement and operational excellence within a pharmaceutical manufacturing setting, primarily using Lean principles and digital tools. It involves facilitating the implementation of daily management systems, leading system design and governance, and partnering on improvement initiatives to enhance safety, quality, productivity, and cost.

This role is for a Sr. Scientist in Bioconjugation at Eli Lilly's new Medicine Foundry, focusing on transferring and optimizing chemical processes for bioconjugation (like ADCs) from development to clinical manufacturing. The role involves hands-on chemistry, process evaluation, analytical work, documentation, and troubleshooting within a regulated manufacturing environment.

This role is for an Instrumentation Supervisor at Eli Lilly's Medicine Foundry, a new center for advanced manufacturing and drug development. The supervisor will oversee calibration activities to ensure equipment reliability and compliance with cGMP and other standards, leading a team of instrument technicians. The role involves managing people, ensuring quality and safety, and maintaining process, facility, and utility equipment. Experience in a regulated GMP manufacturing environment is required.

The Principal Automation Integration Engineer – API Network Integration role at Eli Lilly focuses on enabling data flow between various departments (Manufacturing Science, Quality, Engineering, Supply Chain, Operations) by integrating IT and Process Automation Technologies. The role supports innovation evaluation and application for Manufacturing Process Automation and IT Systems, with a focus on data historians, advanced analytics, cyber security, and process optimization. The primary responsibility is to integrate data for major capital projects within the API Network, working with systems like process automation platforms, HMI/SCADA, Data Historians, Alarm/Event management, and Manufacturing Execution systems. This role requires expertise in automation architecture, process automation, control systems, safety systems, and cyber security, acting as an "in-house system integrator".

This role focuses on integrating digital platforms with physical laboratory infrastructure in a healthcare setting. The engineer will design, develop, and validate software solutions, data pipelines, and APIs to connect laboratory systems, automation equipment, and enterprise platforms, ensuring secure, compliant, and scalable operations. The role involves hands-on engineering, business analysis, and collaboration with various teams and vendors to modernize laboratory workflows.

This role is for a Senior Engineer in Automation Engineering at Eli Lilly, focusing on Instrumentation and Control Hardware for pharmaceutical manufacturing. The engineer will provide automation support for operating areas and capital projects, collaborating with cross-functional teams to ensure robust control systems. Key responsibilities include design, development, commissioning, and troubleshooting of control systems using DeltaV DCS and Rockwell Allen Bradley PLC, with a strong emphasis on GMP regulated environments and validation.

This role is for a Sr. Principal Engineer in Automation Engineering, focusing on Instrumentation and Control Hardware for pharmaceutical manufacturing facilities. The engineer will provide automation support for operating areas and capital projects, lead project execution, commissioning, and qualification, and mentor other engineers. Key responsibilities include expertise in DeltaV DCS and Rockwell Allen Bradley PLCs, troubleshooting control loops, and ensuring compliance with GMP and regulatory requirements.

Lead Technician for Engineering (Night Shift) at Eli Lilly, responsible for device assembly and packaging equipment performance, providing technical support, and implementing process improvements in a GMP-regulated healthcare manufacturing environment.

This role is for a Sr. Director of Project Management within Global Facilities Delivery at Eli Lilly, focusing on delivering large capital assets for medical innovation and medicine supply chains. The position requires leading cross-functional teams to manage projects from conceptual design through operational qualification, ensuring safety, cost, schedule, and quality. Key responsibilities include stakeholder communication, compliance with company policies, and developing safety/environmental execution plans. The role is based in various locations including the Netherlands and US, with travel flexibility required.

Senior Application Security Engineer responsible for integrating security testing tools into the SDLC, partnering with engineering teams on secure coding, and coordinating vulnerability remediation. The role involves developing and implementing application security strategies, performing threat analysis, and ensuring secure configurations for containers.

Principal Computational Statistician at Eli Lilly, responsible for statistical analysis in clinical trials, including selecting methods, conducting analysis, writing reports, and responding to regulatory queries. Requires a Master's degree in Statistics or Biostatistics and 2+ years of experience with SAS/R programming.

Associate VP for Dry Products/Spray Dried Dispersions at Eli Lilly, responsible for scientific and organizational leadership, technical product stewardship, and ensuring the organization provides rigorous support to dry product sites. This role involves managing talent, overseeing control strategy, commercialization, and the technical agenda, fostering functional excellence at manufacturing sites, and ensuring a culture of safety and compliance within a regulated healthcare environment.

This role focuses on the process design, development, and optimization of purification processes, specifically chromatography, for synthetic active pharmaceutical ingredients (APIs) within the pharmaceutical sector. The Director will lead teams, collaborate with scientists and project teams, and ensure the delivery of GMP clinical material while developing control strategies for regulatory submissions and commercialization. The position requires expertise in chromatography, scale-up methodologies, and a strong understanding of the pharmaceutical development lifecycle.

This role is for a Sr. Director of Process Chemistry at Eli Lilly, focusing on synthetic molecule route commercialization, process optimization, and unit operation definition for drug candidates. The position involves leading cross-disciplinary teams, providing technical leadership in scale-up, and collaborating with internal CMC networks and external regulatory bodies. The role requires deep expertise in synthetic organic and process chemistry, with a focus on developing and optimizing manufacturing processes for APIs. Experience with modern synthetic technologies, process modeling, scale-up methodologies, and regulatory requirements is essential.

Associate Distribution Quality Assurance role focused on ensuring compliant and efficient distribution of medicinal products in the APAC region, maintaining oversight of GMP/GDP activities, evaluating risks, and ensuring external logistics providers adhere to regulatory requirements and quality agreements. Responsibilities include managing product quality during storage and transport, assessing deviations, overseeing logistics partners, making decisions on product usability, and managing goods releases.

This role is for a Senior Operator at Eli Lilly's Suzhou manufacturing facility. The primary responsibilities include supporting production, adhering to GMP and SOPs, performing manual and automatic packaging operations, and ensuring HSE compliance. The role requires a high school education, adaptability to shift work, and good vision.