Eli Lilly

Associate, Supply Chain Master Data Steward for the Lilly Medicine Foundry, responsible for maintaining master data in SAP and Manufacturing Execution Systems (MES) for materials, BOMs, recipes, and warehousing. Focuses on data quality, integrity, documentation, and continuous improvement within a regulated pharmaceutical manufacturing environment.

This role provides technical and scientific expertise in external manufacturing for small molecule pharmaceutical products, focusing on technical transfers, process validations, and optimization. It requires knowledge of pharmaceutical manufacturing, GMP, and regulatory requirements to ensure processes are compliant, capable, and in a validated state.

Associate Director of CMC Development Program Management for radiopharmaceutical programs within Lilly Avid, focusing on leading cross-functional teams to execute development and manufacturing programs, manage risks, and ensure delivery of CMC milestones for clinical development.

Director level role in oligonucleotide analytical chemistry at Eli Lilly, focusing on technical leadership, method development, and team management within the biopharmaceutical sector. This role involves ensuring the integrity and compliance of analytical characterization for novel drug modalities.

This role focuses on the process development and engineering of genetic medicines, specifically RNA-lipid nanoparticles (LNPs) and oligonucleotide drug products, for parenteral formulations. The position involves building process capabilities, assessing and mitigating scale-up risks, collaborating across functions, and supporting regulatory filings within the pharmaceutical industry.

Associate Director for MES Architecture & Technical Lead role at Eli Lilly, focusing on designing, implementing, and optimizing Manufacturing Execution Systems (MES) for new state-of-the-art pharmaceutical manufacturing sites. The role involves architectural guidance, technical oversight, setting strategic roadmaps, and collaborating with various teams to ensure MES solutions align with business objectives and industry best practices. Requires deep technical knowledge, experience with Pharma and GMP manufacturing, and leadership skills.

This role is for a Quality Assurance Technician in Device Assembly and Packaging at Eli Lilly's new production facility in Alzey, Germany. The technician will support the startup of the facility, ensure processes and products meet quality standards, monitor production on-site, assist with deviations and investigations, and support batch release. The role requires a technical education or bachelor's degree, knowledge of cGMP practices, and at least 2 years of experience in the pharmaceutical industry with a focus on shopfloor quality assurance.

This role is for a Production Shift Leader in parenteral manufacturing at Eli Lilly's new facility in Alzey, Germany. The position involves leading a team, ensuring safety and quality in sterile filling and inspection processes, and supporting the startup of the facility. It requires experience in sterile filling, production, and leadership, with knowledge of cGMP and FDA guidelines.

This role is for a Site Master Planning and Project Engineer in the pharmaceutical industry, focusing on strategic site master plans and capital projects to support manufacturing growth, ensuring compliance with global and local regulations. The role involves project management, engineering design, stakeholder collaboration, cost control, and continuous improvement within a regulated manufacturing environment.

This role is for a Fitter responsible for the servicing, troubleshooting, and maintenance of production equipment in a manufacturing facility. It requires mechanical aptitude, adherence to safety and cGMP standards, and prompt response to downtime events. The position involves night shifts and may require working on holidays. It is not AI-related and focuses on industrial maintenance.

This role focuses on leading the oligonucleotide synthesis scale-up team within Lilly Genetic Medicines to accelerate RNAi Therapeutics from pre-clinical to clinical development. It involves expertise in oligonucleotide synthesis methodologies, collaborating with chemistry teams, and supporting the discovery of lead drug candidates by providing essential materials for key studies. The role requires a PhD or MS in a relevant scientific discipline with significant experience in oligonucleotide synthesis and solid-phase synthesis.

Associate Director for Process Control & Automation Engineering at a new advanced manufacturing facility for ATMPs. Responsibilities include supervising engineers, ensuring reliable control applications, and supporting the technical agenda and business plan. The role involves leadership during project delivery and startup phases, focusing on building processes, systems, and culture for GMP manufacturing.

Senior Principal/Principal Bioprocess Engineer role at Eli Lilly in Limerick, Ireland, supporting the expansion of a Next Generation Biotech Drug Substance Manufacturing Facility. The role involves providing engineering subject matter expertise for design, construction, and startup, focusing on process engineering fundamentals, continuous improvement, and root cause analysis.

Associate Director-Engineering role focused on managing and optimizing Computerized Maintenance Management Systems (CMMS), specifically the Maximo platform, within pharmaceutical operations. Responsibilities include leading platform consolidation, developing analytics dashboards, ensuring data integrity and regulatory compliance (GMP/GLP), and providing technical support for global maintenance teams.

Production operator for packaging area at a pharmaceutical company, responsible for operating and cleaning machinery, following packaging orders, and ensuring quality and safety standards are met.

This role is for an Engineering Senior Director focused on leading site expansion projects within a pharmaceutical manufacturing environment. It involves project delivery, operational excellence, and effective communication to ensure seamless integration of new facilities into existing operations. The role requires strong engineering and project management experience, particularly in parenteral manufacturing.

This role is in quality assurance within a pharmaceutical company, focusing on the management of lab equipment and systems used for quality control and analytical testing of pharmaceutical products. It involves qualification, maintenance, and retirement of equipment, as well as documentation and process improvement. The role is not directly involved in AI/ML development.

This role is for an Advisor in Technical Services and Manufacturing Science (TSMS) within a pharmaceutical API manufacturing facility. The focus is on laboratory operations, process development, analytical expertise, and ensuring compliance with cGMP regulations. It involves experimental design, data analysis, troubleshooting, and mentoring. The role requires expertise in small molecule and peptide manufacturing, advanced analytical techniques, and regulatory knowledge.

This role focuses on the development and engineering of linker-payload (L-P) chemistry and bioconjugation processes for Antibody-Drug Conjugates (ADCs) and Antibody-Oligonucleotide/siRNA conjugates (AOCs) within a pharmaceutical R&D organization. It involves laboratory experimentation, process design, and collaboration with cross-functional teams to support drug development from early stages through manufacturing.

This role is in Quality Assurance for a pharmaceutical company, focusing on product quality testing, including chemical and microbial analysis, procedure verification, deviation investigation, and change management. It involves collaboration with global teams and potentially team management for higher positions. The role requires experience in QC/analytical testing within the pharmaceutical, medical device, cosmetics, or chemical industries.

This role focuses on the implementation and integration of Manufacturing Execution Systems (MES) and other production IT systems within a pharmaceutical manufacturing environment. The primary responsibilities include bridging business needs with technology, developing and integrating MES components, supporting system startups, ensuring compliance with validation requirements, and evaluating new technologies. The role requires experience with MES platforms and understanding of GMP regulations and Computer System Validation (CSV).

Scientist/Sr Scientist role focused on large-scale oligonucleotide synthesis for RNAi-based therapeutic modalities in healthcare. Responsibilities include leading the synthesis scale-up team, developing internal capabilities, collaborating with chemistry teams, and supporting drug candidate discovery. Requires expertise in synthetic organic and nucleic acid chemistry.

This role is for a Technician in Quality Assurance for parenteral manufacturing at a new Eli Lilly production facility in Germany. The primary focus is on ensuring compliance with cGMP standards during the setup and operation of the facility, including material preparation, aseptic filling, and visual inspection. The role involves on-site quality monitoring, deviation management, batch release support, and GMP documentation.

Associate Director for Technical Services/Manufacturing Science (TSMS) at a new API manufacturing facility. Responsibilities include managing technical staff, overseeing technical projects, process optimizations, ensuring cGMP compliance, and collaborating cross-functionally. The role involves building the organization and systems for a greenfield startup into GMP operations.

This role is for a Sr. Director of Quality Control in API manufacturing at Eli Lilly. It involves strategic leadership for quality control and analytical sciences laboratories, ensuring GMP compliance, and building a high-performing team for a new manufacturing site. The role focuses on operational excellence, regulatory compliance, and personnel development within a healthcare manufacturing context.

Senior Director of Engineering role focused on leading process engineering, automation, and maintenance for a new API manufacturing facility at Eli Lilly. The role involves building the organization, facility, and culture for startup and long-term manufacturing goals, ensuring safety, quality, and operational excellence within a regulated pharmaceutical environment.

Senior Principal Engineer role focused on automation engineering within Biologics manufacturing at Eli Lilly. The role involves providing automation support for operating areas and capital projects, ensuring reliable and compliant control applications and systems. Responsibilities include technical leadership, mentoring, overseeing system integrators, designing and implementing DCS/SCADA software, troubleshooting control loops, supporting electronic systems for data capture, maintaining validated systems, and supporting capital projects. The role requires experience in biopharma engineering, SCADA, DCS, PLC, and MES systems, with a strong emphasis on GMP and computer system validation.

Eli Lilly is seeking an Associate Director for Biotech Operations in Limerick, Ireland, to lead a new, advanced manufacturing facility. This role involves providing technical leadership, managing daily operations, ensuring safety and quality, and building and developing a team. The position requires strong GMP manufacturing experience, leadership skills, and the ability to collaborate with cross-functional teams during the facility's startup phase, focusing on implementing new technologies and processes.

The Senior Director – Quality Control will provide administrative and technical leadership for the Quality Control Labs during the startup, implementation, and operation of a new API manufacturing facility. This role involves managing technical staff, ensuring GMP compliance, overseeing technical projects, and collaborating cross-functionally to meet quality and business objectives in a regulated pharmaceutical manufacturing environment.

This role is for a Solution Delivery Lead/Manager at Eli Lilly Japan, responsible for leading the execution of IT projects, ensuring alignment between business needs and technical requirements, managing vendors, and overseeing project delivery within budget and on time. The role requires experience in IT project management, system design, development, and implementation, with a strong emphasis on cloud technologies and global communication skills.

This role is for a Supply Chain Planning Associate/Senior Associate at Eli Lilly's Seishin laboratories in Kobe, Japan. The primary responsibilities include planning raw material and intermediate product requirements, purchase timing, and production schedules based on the S&OP process. The role involves ownership as a product leader within the manufacturing division, coordinating with various departments to ensure stable supply of Lilly products. Key tasks include inventory planning, standard production planning, coordinating with international manufacturing sites and global supply chains, risk identification and mitigation, and maintaining/operating production planning systems like SAP and APO. Required experience includes at least 3 years in production planning/execution or procurement/delivery management in a manufacturing company (preferably chemical industry), and strong English and Japanese language skills.