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 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.

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.

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.

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.

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.

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.

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.

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.

This role is for a Production Worker in the Parenteral department at Eli Lilly's new high-tech manufacturing facility in Alzey, Germany. The position involves operating machinery, ensuring health and safety compliance, collaborating with team members, following SOPs, troubleshooting issues, and participating in training. The ideal candidate has relevant experience in the pharmaceutical/biotech industry, experience with aseptic filling and/or isolator technology, and knowledge of cGMPs.

The Cyber Intelligence Analyst role at Eli Lilly focuses on active defense within Global Cyber Defense Operations (GCDO). Responsibilities include monitoring, analyzing, investigating, and responding to cybersecurity events and incidents, managing the attack surface, producing threat intelligence, and ensuring readiness and detection capabilities. The role involves supporting various cybersecurity functions, developing capabilities, documenting analysis, identifying security issues, prioritizing threats, and recommending strategic changes. Rotational on-call availability is required.

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.

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.