Eli Lilly

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.

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.

Oversees utility operations for a new advanced manufacturing and drug development center, ensuring safe and uninterrupted generation and distribution of utility services. Responsibilities include direct supervision of operators, troubleshooting, problem-solving, and implementing improvements within utility systems (water, air, steam, etc.). The role focuses on safety, quality, operational excellence, and people development within a regulated manufacturing environment.

Associate Director - Business Solutions IT Project Lead at Eli Lilly, responsible for deploying IT systems architecture for a new manufacturing site, managing major initiatives across Supply Chain, Logistics, Manufacturing, and Finance. Requires 7+ years of IT project leadership experience and a Bachelor's degree. Manufacturing IT systems knowledge and understanding of GMP/FDA regulations are preferred.

Junior Quality Assurance Engineer role at Eli Lilly, a global healthcare leader. The role focuses on monitoring GMP services, participating in qualification/validation projects for GMP equipment and systems, ensuring quality standards are met for facilities, services, equipment, and control systems (ISA 95 level 1). It also involves providing technical and quality advice for continuous improvement and ensuring systems remain validated throughout their lifecycle. No prior experience is required, but pharmaceutical sector internships are a plus. Fluency in English (C1) is mandatory. Key personal skills include teamwork, customer orientation, decision-making, strong communication, organization, attention to detail, knowledge of Good Manufacturing Practices (GMP), quality concepts in the pharmaceutical industry, and common IT tools.

Junior Data Administrator role focused on maintaining master data (GMP and business) for a manufacturing plant using SAP and other systems. Responsibilities include data entry, cleaning, verification, and supporting optimization and incident resolution. Requires technical training in administration/finance and user-level computer skills, with Excel/Office proficiency. SAP knowledge is desirable.

The Lead Maintenance Planner at Eli Lilly is responsible for improving equipment reliability and productivity by planning and scheduling maintenance activities. This role involves managing work orders, ensuring spare parts availability, coordinating with vendors, and utilizing a CMMS like Maximo. The position is in a manufacturing facility startup environment, with a transition from initial spare parts coordination to full-time planning and scheduling.

Maintenance Mechanic for pharmaceutical manufacturing equipment including UV curing, vision systems, laser marking stations, conveyors, and robotics. Responsibilities include machine maintenance, setup, condition monitoring, troubleshooting, developing repair part lists, and proactive reliability planning within a regulated industry.

Operator role focused on assembly and packaging of medical devices in a regulated manufacturing environment. Responsibilities include operating equipment, adhering to SOPs and cGMP, documenting processes, and ensuring product quality and safety. This is a fixed-duration employment role.

This role is for a Senior Manager of Process Control and Automation Engineering in a regulated GMP manufacturing environment. The individual will provide technical and people leadership for automation systems, ensure compliance with standards, and drive continuous improvement. Responsibilities include defining automation strategy, leading multi-disciplinary teams, and ensuring safe, compliant, and reliable automated systems.

This role is for a Process Control & Automation Engineer focused on Building Management and HVAC systems for a pharmaceutical manufacturing facility. It involves developing, implementing, and maintaining automation solutions within a Good Manufacturing Practices (GMP) environment. The role requires experience with control systems, computer system validation, and IT platform support, but is not directly involved in AI/ML model development.

Project Manager for Global Facilities Delivery at Eli Lilly, responsible for leading teams to deliver large capital asset programs ($50M+ or workstream of $200M+) in industrial/manufacturing facilities, focusing on safety, cost, schedule, and quality. Requires a Bachelor's in Engineering or Project Management and 5+ years of experience in capital project delivery, including greenfield projects.

Medical Monitor role at Eli Lilly focused on ophthalmology clinical trials. Responsibilities include providing medical input into trial design, reviewing study documents, assessing safety data, and training site staff. Requires an MD or DO, board eligible/certified in Ophthalmology, and at least 5 years of experience in medical monitoring, clinical development, or pharmacovigilance.

Process Technician role focused on the safe operation of highly automated equipment in formulation, filling, and material preparation within a pharmaceutical manufacturing environment. Requires adherence to Good Manufacturing Practices (GMP) and safety standards, with responsibilities including quality control, troubleshooting, and training support. The role operates on a night shift schedule and requires the ability to work in a cleanroom environment.

Associate Director for Quality Control (QC) Analytical Sciences at Eli Lilly, leading a team to support site operations, QC, and commercialization within IAPI. Responsibilities include developing technical capabilities, overseeing method development and transfers, driving improvements in analytical control strategy, identifying new technologies, prioritizing initiatives, and ensuring the technical soundness of the analytical control strategy from raw materials to drug substance. The role also involves troubleshooting analytical issues, collaborating on innovative solutions, supporting regulatory inspections, and developing technical coaching.

Manager for Technical Platform Integrator role at Eli Lilly, focusing on developing and supporting applications for clinical trials. The role involves end-to-end delivery of software implementations, ensuring compliance with GxP, cybersecurity, and validation requirements. It also requires partnering with business stakeholders to define strategy and roadmap, translating business needs into technical requirements, and managing delivery risks. A key aspect is investigating and proposing the implementation of AI and automation solutions.

Process Engineer role at Eli Lilly's new Medicine Foundry, focusing on purification of biologics, peptides, oligonucleotides, and bioconjugates. Responsibilities include technical assessment, process knowledge development, optimization, and equipment management within a GMP manufacturing environment. Requires BS/MS in chemical engineering and 1-4 years of relevant experience.

The Engineer - Automation Engineering will provide automation support for manufacturing operations at Eli Lilly's new Medicine Foundry. This role involves technical leadership, mentoring, implementing automation projects, and ensuring compliant control applications and systems for GMP operations. The focus is on process automation, DCS/SCADA systems, and maintaining validated states of control systems.

Associate, Quality Assurance role supporting the startup of the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The role focuses on quality functions within a cGMP environment, ensuring compliance with regulations, and supporting cross-functional teams in optimizing manufacturing processes.

This role is within the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The Advisor will provide quality oversight of GMP operations for small molecule manufacturing, focusing on process quality, compliance, and operational readiness during the design and construction phase, with startup anticipated in 2027. The role involves developing early phase quality processes, ensuring compliance with regulations, and collaborating with cross-functional teams.

This role is for a Director of Process Engineering at Eli Lilly's new Lilly Medicine Foundry, focusing on advanced manufacturing and drug development for complex therapies. The position involves leading technical innovation in equipment design, developing predictive modeling capabilities, and establishing scalable manufacturing paradigms for novel therapeutic modalities, including small molecules, peptides, oligonucleotides, and bioconjugates. The role requires a PhD in Chemical Engineering and leadership of a small team.

Internship role focused on process automation, specifically analyzing spare parts, monitoring their lifecycle, and creating an inventory management application to anticipate supply needs and reduce production impact. Involves data collection, demand forecasting, and interdisciplinary collaboration within an industrial setting.

The role is for a Junior Technician in Quality Control Laboratory Equipment and Systems at Eli Lilly. The primary responsibilities include leading validation projects for laboratory equipment, evaluating new equipment, performing calibration and maintenance, resolving system incidents, creating instrumental methods, and maintaining the laboratory's quality system according to GMP standards. The role requires a university degree in Chemistry, Health Sciences, or Engineering, fluent English, and the ability to work in a regulated environment. Additional preferences include strong interpersonal, organizational, and technical skills related to GMP.

Senior Quality Control Laboratory Technician at Eli Lilly in Alcobendas, Spain. Responsibilities include leading validation projects for laboratory equipment, evaluating new equipment, performing calibration and maintenance, supervising chemical analyses, and collaborating on incident resolution and quality system maintenance. Requires a university degree in Chemistry, Health Sciences, or Chemical Engineering, minimum 3 years of GMP QC lab experience, and fluent English.

Associate Director - IT Systems Delivery Lead for a global healthcare leader in the pharmaceutical industry. This role will oversee and align multiple programs for new manufacturing sites, ensuring they meet objectives, timelines, and budgets. Responsibilities include program management, release train engineering, GxP compliance, stakeholder management, risk management, resource allocation, and reporting. Requires a strong business understanding, analytical skills, and the ability to manage large-scale, cross-functional projects. Experience in Pharma and GMP Manufacturing is required.

The Principal Scientist Visual Inspection Steward at Eli Lilly will serve as the technical subject matter expert and program owner for visual inspection processes in a new pharmaceutical manufacturing facility. This role involves developing and implementing control strategies, training personnel, troubleshooting issues, ensuring compliance with regulatory guidance (e.g., USP <1790>), and driving continuous improvement in visual inspection operations. The position requires strong technical writing, communication, and project management skills, with a focus on pharmaceutical manufacturing and quality.

This role is for a Senior/Principal Scientist in Technical Transfer at Eli Lilly, focusing on manufacturing processes for insulin products. The responsibilities include technical support for new product introductions, ensuring accurate documentation and control strategies, and executing validation activities. The role requires a degree in a relevant field, knowledge of GMP and parenteral manufacturing, and strong project management skills.

This role focuses on analytical development for protein synthesis and peptide chemistry within a pharmaceutical manufacturing and quality technical hub. It involves developing analytical methods, designing and analyzing experiments, and providing technical support for process development. The role requires a Ph.D. in Chemistry or Analytical Chemistry with 12+ years of experience and emphasizes safety, people leadership, and scientific/technical leadership in analytical and semi-preparative scale separation.

Develops and optimizes analytical methods for RNA drug substances and LNP products in a healthcare setting, partnering with cross-functional teams and ensuring compliance with regulations.

Internship role focused on maintenance and reliability in a pharmaceutical manufacturing environment, involving data collection, technical analysis, and optimization of preventive maintenance strategies. Collaborates with cross-functional teams in a GMP-regulated setting.

Seeking an Advisor/Senior Advisor, Engineering for Biologics Drug Product Development at Eli Lilly. This role focuses on defining and developing clinical manufacturing processes for parenteral drug products, establishing control strategies, and collaborating with cross-functional teams. The position also involves leading process design, tech transfer, authoring regulatory documents, and evaluating new technologies in drug product development. Requires a PhD/MS/BS in a relevant field with significant industry experience in pharmaceutical development or manufacturing, and a strong understanding of cGMP and regulatory guidelines.

Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innovation - Small Molecules role at Eli Lilly. This position provides strategic, tactical, and operational regulatory CMC leadership for the small molecule portfolio, supporting clinical trial applications, market registrations, and post-approval submissions. Requires deep technical knowledge of CMC development and manufacturing processes, and global regulatory requirements. The role involves leading the preparation, review, and approval of CMC documents for global regulatory submissions and providing regulatory guidance to development teams. Requires a B.S. degree in a science, engineering, or STEM related field with 10+ years of Regulatory CMC or technical CMC experience supporting synthetic molecules.

Director, Global Regulatory Affairs - Chemistry, Manufacturing and Controls (CMC), Platform Innovation - Small Molecules at Eli Lilly. This role provides strategic, tactical and operational regulatory CMC leadership across therapeutic modalities and manufacturing technologies to expedite development of the small molecule portfolio and to support clinical trial applications, market registrations, and post approval submissions. Requires deep technical knowledge of small molecule CMC drug development and manufacturing sciences, and knowledge of global CMC regulatory requirements and guidelines. Requires 10+ years of Regulatory CMC or technical CMC experience.

Process Engineer at Eli Lilly's Medicine Foundry, focusing on the development, scale-up, and manufacturing support for small molecule drug substances. The role involves technical authority for equipment design, engineering calculations, process simulation, and ensuring compliance with GMP and regulatory standards.

This role is for an Automation Engineer with expertise in Data Historian systems (OSI PI) and Data Architecture within a pharmaceutical manufacturing environment. The engineer will provide automation support for operating areas, manage data contextualization, and ensure compliance with GMP standards. Responsibilities include collaborating with cross-functional teams, troubleshooting system issues, maintaining system health, developing documentation, and ensuring the validated state of control systems.

This role is for a Senior Principal Engineer in Automation Engineering within the Lilly Medicine Foundry. The primary focus is on providing automation support for laboratory and analytical equipment in a pharmaceutical manufacturing setting, ensuring reliable and compliant control applications and systems. Responsibilities include technical leadership, mentoring, project plan development, overseeing system integrators, DCS software design, troubleshooting control loops, and maintaining validated states of control systems in line with GMP and quality standards. Experience with SCADA, DCS, MES, LIMS, and Site Historian systems is preferred.

Senior Principal Engineer for Automation Engineering at Eli Lilly's Medicine Foundry, focusing on automation support for advanced manufacturing and drug development. The role involves technical leadership, mentorship, and implementation of control applications and systems within a GMP environment, ensuring reliable and compliant operations. This includes developing automation plans, overseeing system integration, designing and configuring DCS software, and supporting capital projects and new product introductions.

This role is for an MES System Engineer in the pharmaceutical industry, focusing on designing, developing, implementing, and maintaining Manufacturing Execution Systems (MES) to optimize production processes, ensure data accuracy, and maintain compliance with GMP regulations. The role involves integrating production operations with business systems and collaborating with cross-functional teams.

This role focuses on the technical aspects of drug substance manufacturing, including process optimization, technical transfers, and developing the technical agenda within the pharmaceutical industry. It requires comprehensive knowledge of GMP, regulatory requirements, and external influence in the peptide space. The position involves leading a team of process chemists, resolving technical issues, and ensuring processes are compliant and well-documented.

Senior Scientist role at Eli Lilly in Germany focused on technical leadership and stewardship for aseptic filling processes in a new high-tech production facility. Responsibilities include supporting validation, lifecycle management, process issues, continuous improvement, and ensuring compliance with GMP and regulatory expectations. Requires a degree in a relevant field, professional experience in the industry, and knowledge of GMP operations.

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.