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.

Principal Automation Engineer - Instrument & Controls role at Eli Lilly, focusing on the design, application, and troubleshooting of instrumentation within pharmaceutical manufacturing facilities. This role supports capital projects and GMP manufacturing operations, requiring expertise in process measurements, control theory, and automation platforms like Rockwell Automation and Emerson DeltaV. The position involves collaboration with A&E firms and system integrators, and contributes to site maintenance programs and process safety management.

This role focuses on the process development and manufacturing of RNA-lipid nanoparticles (LNPs) and other parenteral drug products for genetic medicines. The engineer will design and execute studies, lead process development, manage tech transfer, and collaborate across functions to advance these therapies from clinical to commercialization.

Senior Principal Process Engineer role at Eli Lilly focused on the startup and operation of a small molecule API manufacturing facility. The role involves technical leadership, mentoring, process optimization, and ensuring GMP compliance within a regulated healthcare environment.

This role is responsible for managing the cleaning program for process equipment and ancillary components in a pharmaceutical manufacturing facility, focusing on cleaning verification/validation activities, authoring documentation, coordinating investigations, and improving cleaning process efficiency. It requires knowledge of GMP, regulatory requirements, and pharmaceutical manufacturing.

Project Manager for Global Facilities Delivery at Eli Lilly, responsible for leading manufacturing capital projects from design to operational verification. Requires 10+ years of experience in capital project delivery in industrial or manufacturing facilities, with a focus on safety, quality, and compliance.

This role is for an Engineer focused on Manufacturing Execution Systems (MES) in a pharmaceutical manufacturing setting. The primary responsibility is to design, develop, deliver, and qualify the MES solution for a new drug substance manufacturing site. The role involves partnering with automation and operations teams, ensuring operational readiness, adapting project roadmaps, and maintaining system validation. A key requirement is the ability to incorporate AI tools into daily workflows to improve MES recipes and activities, alongside a strong understanding of GMP and regulatory requirements.

Warehouse Technician responsible for receiving, storage, and shipping of raw materials and packaging components in a cGMP manufacturing environment. Ensures material availability for production and accurate inventory quantities, adhering to all safety and regulatory requirements.

This role is for a Sr. Director of Business Solutions MQ IT at Eli Lilly, focusing on defining and deploying the digital strategy for a new manufacturing facility. It involves integrating various systems like SAP, MES, and Data Historian, ensuring cGMP compliance, and managing the IT/OT footprint. The role requires strong leadership in Pharma IT, with a focus on manufacturing operations and technology.

This role is for a Production Operator at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The operator will support the startup phase of the facility, bringing manufacturing equipment into service, and then oversee the production of API molecules. The role emphasizes safety, quality, and adherence to GMP practices in a pharmaceutical manufacturing environment.

The Sterility Assurance Advisor role at Eli Lilly is responsible for maintaining a safe work environment and understanding the scientific principles required for manufacturing parenteral drug products. This includes using sterility assurance risk management to evaluate manufacturing processes and controls, leading projects associated with sterility assurance programs, and developing/executing process and facility monitoring strategies. The role also involves leading deviations, staying updated on regulatory requirements, influencing corporate guidance, identifying continuous improvements, providing design input for new processes, defending sterility assurance programs during audits, assisting with regulatory submissions, and providing training and technical mentorship.

This role focuses on process engineering for drug substance and drug product manufacturing, involving laboratory-scale process development, optimization, and technology transfer. It requires collaboration with scientists and cross-functional engineering groups, hands-on experimentation, data analysis, and ensuring safe and compliant laboratory operations. The position emphasizes applying engineering fundamentals to improve process understanding and robustness, with a focus on pharmaceutical and biotechnology industries.

Principal Automation Engineer - Data & Platforms integration role at Eli Lilly, focusing on designing, delivering, and managing data historian and integration platforms for a new API manufacturing facility. Requires expertise in Aveva PI Data Historian, system integration, validation practices (cGMP, data integrity), and server administration within a pharmaceutical manufacturing context.

This role is for a Principal Automation Engineer specializing in DeltaV System Administration within a pharmaceutical manufacturing facility. It involves supporting the design, delivery, validation, and ongoing management of DeltaV DCS platforms, ensuring compliance with cGMP standards and data integrity. The position requires a deep understanding of process automation systems and Lilly's computer system validation practices, with responsibilities including hardware design, administrative procedures, and collaboration with various internal and external stakeholders. The role transitions from project delivery to site-based support for GMP manufacturing operations.

Senior Manager of Engineering responsible for supporting asset delivery, process development, commissioning, qualification, validation, and startup of the Parenteral/DAP area and other engineering systems. The role involves leading a team of 5-10 individuals and ensuring business plan goals related to safety, quality, and efficiency are met. Requires a Bachelor's degree in Engineering, at least 5 years of engineering experience, and pharmaceutical experience. Experience with regulatory agencies (FDA, EMEA), automated equipment, combination products, and facility startups is preferred.

Lead Chemical Operator for API manufacturing operations at a new Eli Lilly facility, responsible for production, safety, quality, and compliance in a regulated pharmaceutical environment.

This role is for a Manufacturing Chemical Operator at a new pharmaceutical API manufacturing facility. The operator will be responsible for the production of API molecules, maintaining compliance with regulatory requirements, and ensuring equipment is in good operating condition. The role involves monitoring, testing, cleaning, and responding to production issues, with a strong emphasis on safety and quality within a GMP environment. Experience in facility startups and pharmaceutical manufacturing is preferred.

Associate Director of Operations for Device, Assembly, and Packaging in the pharmaceutical industry. Responsibilities include leading operations teams, ensuring production goals, managing cross-functional teams, and presenting to regulatory agencies. Requires experience in pharmaceutical manufacturing, leadership, and understanding of regulatory requirements.

This role is for a Sr. Program Director in Global Facilities Delivery at Eli Lilly, focusing on managing large capital projects (>$1BN USD) in pharmaceutical manufacturing. The role requires extensive experience in project management, interface management, compliance, and safety/environmental execution within regulated facilities. It involves leading cross-functional teams and ensuring projects meet safety, cost, schedule, and quality objectives from planning through operational qualification.

This role focuses on the design and development of drug products for synthetic molecules within the pharmaceutical industry. It involves applying fundamental pharmaceutical sciences, predicting in vivo performance using molecular properties and preclinical data, and leveraging modeling to guide formulation development. The position also requires collaboration with partners, influencing scientific communities, and authoring technical reports and regulatory documentation. While it involves modeling and data analytics, the core function is not AI/ML model development but rather drug product research and development in a healthcare context.

This role focuses on designing, developing, and supporting electronic laboratory notebook (ELN) templates and other laboratory informatics platforms within the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The position requires collaboration with scientists and IT teams to ensure data integrity, system reliability, and compliant scientific operations in a regulated environment.

The Laboratory Informatics Scientist will deploy and support laboratory informatics platforms, primarily the MODA environmental monitoring system, within the Lilly Medicine Foundry. This role involves configuring systems, managing data, ensuring compliance with cGMP/GLP, and collaborating with IT and lab scientists to optimize digital workflows in a regulated healthcare environment.

Manager, Regulatory Delivery Excellence, China Regulatory Affairs at Eli Lilly is responsible for managing regulatory registration processes and submission preparation support, covering clinical trial permit applications through to marketing applications. This role involves developing submission plans, collaborating with cross-functional teams and vendors, managing RIM-related activities, and ensuring compliance with regulations and internal quality systems. The position also requires serving as a Subject Matter Expert for regulatory business processes and the Veeva Vault RIM system, and maintaining data in IT systems.

The Bioinformatics Platform Engineer will operate, improve, and scale scientific computing infrastructure for production bioinformatics workflows in AWS. This role involves supporting and troubleshooting NGS workflows, managing Linux environments, and contributing to infrastructure automation and platform reliability. The engineer will collaborate with scientists to translate workflow needs into scalable solutions and participate in architecture decisions.

This role is for a (Senior) Advisor-Medical Affairs CMH in Primary Care at Eli Lilly, focusing on the CardioMetabolic Health portfolio. The individual will act as a medical expert, translate clinical insights into strategies, manage relationships with healthcare professionals, and contribute to medical strategy development and execution within the primary care setting. The role requires a medical degree (BIG registration) and experience in CMH-related care, preferably in primary care or the pharmaceutical industry.

Senior Director role responsible for the technical strategy and process excellence of drug product manufacturing at an Oral Solid Dosage manufacturing site. This includes technical oversight for drug product intermediates control strategy from spray dried dispersion through tablet and capsule manufacturing. Serves as the site’s authority on technology transfer, scale-up, and manufacturing science for oral solid dose forms (tablets, capsules).

This apprenticeship role in aseptic production at Eli Lilly focuses on supporting routine production activities, proposing and implementing process improvements, managing continuous improvement projects, and ensuring compliance with quality systems. The role involves collaboration with various teams and understanding of manufacturing processes like material preparation, formulation, and filling.

Lead Calibration Technician responsible for performing and documenting routine and non-routine instrument calibrations, including maintenance, testing, troubleshooting, and repairs on manufacturing equipment in a GMP/regulated environment.

Associate Scientist role in drug target identification and validation for CNS diseases, focusing on psychiatric disorders. Responsibilities include designing and executing rodent in vivo studies, stereotaxic surgeries, tissue collection, and quantitative immunohistochemistry (IHC) and immunofluorescence (IF) workflows. The role also involves molecular and biochemical assays, collaboration with multidisciplinary teams, and presenting experimental results. Requires an MS in Neuroscience, Biology, or Pharmacology with 2-5 years of lab experience in in vivo rodent work and IHC.

This role is for a Sr. Principal Engineer focused on Manufacturing Execution Systems (MES) within a pharmaceutical manufacturing facility. The primary responsibilities involve developing and integrating MES components, supporting site startups, and ensuring compliance with cGMP regulations. The role requires extensive experience with MES systems and data integration in a regulated environment.

Associate Director for Clinical Trial Foundations (CTF) at Eli Lilly, focusing on eSource technologies for clinical development. This role involves defining and executing implementation plans for systems that capture direct patient data from investigator sites, including electronic medical records. The position requires expertise in clinical systems, project management, and partnerships with internal teams, IT, and external vendors to optimize clinical development processes and technologies.

This role focuses on developing and implementing Real-World Evidence (RWE) strategies within the healthcare domain, specifically at Eli Lilly. The Advisor will plan, conduct, and communicate results from Real-World and Health Outcomes studies, such as database studies and chart reviews. Responsibilities include managing RWE projects, collaborating with internal teams and external partners, and ensuring adherence to research principles and regulatory guidelines. The ideal candidate has a strong academic background (PhD or Master's) in a relevant field and prior experience in Real-World Research.

This is an internship position in Medical Affairs for Immunology at Eli Lilly, focusing on supporting medico-marketing activities, scientific literature analysis, and participation in medical unit activities. The role requires a scientific background, autonomy, organizational skills, and proficiency in English and Microsoft Office.

Quality Assurance Engineer role at Eli Lilly's new API manufacturing facility, focusing on technical guidance for quality standards, regulatory compliance, and continuous improvement in manufacturing and laboratory operations.

This role focuses on the automation aspects of plant engineering for HVAC, Utilities, and Facilities within pharmaceutical manufacturing. The engineer will develop, implement, and improve process automation solutions, ensuring systems are in-control, capable, and compliant. Responsibilities include defining user requirements, designing system architectures, developing and testing code, managing change control, and ensuring validation documentation is maintained. The role requires experience as a process automation engineer and ideally pharmaceutical and computer system validation experience.

Product Leader responsible for the entire commercialization lifecycle of a product, from post-Phase 2 through launch and beyond. Owns manufacturing CMC strategy, leads the Product Core Team, collaborates with development, and serves as the interface for senior executives. Requires deep pharma development/manufacturing knowledge and ability to drive alignment without direct authority.

QA Manager for Night Shift at a new pharmaceutical manufacturing site, focusing on device assembly and packaging. Responsibilities include technical oversight, document approvals, cross-functional collaboration, team management, and ensuring GMP compliance. The role transitions from commissioning and qualification to supporting routine manufacturing operations.

This role leads the cross-functional study team in the development and execution of clinical trials, accountable for delivering trials with quality, on time, and within scope and budget. It requires leveraging project management, regional operational knowledge, clinical trial process leadership, and scientific expertise.

Senior Director of Quality Assurance for a new pharmaceutical manufacturing facility in Katwijk, Netherlands. Accountable for setting and executing the site's QA strategy, ensuring cGMP compliance, regulatory readiness, and fostering a strong quality culture. This role involves executive quality leadership, governance, compliance, operational oversight, talent development, strategic planning, and EHS accountability within a highly regulated pharmaceutical manufacturing environment.

Associate Director for Reimbursement Analytics in Dermatology at Eli Lilly, focusing on developing data strategies, building scorecards, and analyzing product reimbursement services. This role involves leading data reporting, partnering with data enablement teams, and ensuring compliance with privacy and legal requirements within the healthcare domain.

Senior/Principal Manufacturing Scientist role at Eli Lilly focused on peptide API manufacturing. Responsibilities include providing technical support, executing experimental projects, modeling, data analysis to improve process control, yield, purity, and productivity within a cGMP environment. Requires experience in peptide synthesis or purification technologies.

Associate Director of Process Engineering for Small Molecule API manufacturing, responsible for leading and developing a team of process engineers to ensure compliant and reliable operations in a new, advanced manufacturing facility. The role involves building the organization, implementing business systems, and supporting project delivery during the startup phase, transitioning to operational oversight and continuous improvement post-startup.

Senior Director of Engineering role focused on facilities and utilities for pharmaceutical manufacturing operations, ensuring infrastructure and leadership support site startup and long-term operations. Responsibilities include guiding GMP systems, building operational readiness, managing evolving responsibilities, and ensuring safety and quality standards.

Senior Director of Engineering at Eli Lilly, responsible for leading process engineering, automation, and maintenance for site startup and long-term manufacturing goals in a healthcare/pharmaceutical setting. Focuses on organizational development, functional strategy, safety leadership, and ensuring system readiness for GMP manufacturing.

This role supports the manufacturing process by operating, monitoring, maintaining, and shutting down clean utility systems and equipment within mechanical rooms. Responsibilities include improving equipment uptime, performing preventative and predictive maintenance, troubleshooting and repairing equipment, maintaining documentation, and collaborating with other departments, all while adhering to cGMPs and safety procedures.