This role focuses on operating, maintaining, and advancing lab automation equipment and robotic systems in a biopharmaceutical discovery setting. The goal is to support early-stage discovery and screening of protein therapeutics by improving laboratory workflows and digitalization, with a vision towards autonomous discovery systems.

This role is a Senior Associate in QA Materials Management within a pharmaceutical manufacturing facility. It focuses on overseeing quality assurance for material receipt, batch disposition, and related processes, ensuring compliance with GMP regulations. Responsibilities include managing change controls, deviations, CAPAs, documentation, and participating in audits, with a strong emphasis on quality systems and regulatory requirements in the pharmaceutical/biotechnology sector.

This role is for a Program Manager in Global Facilities Delivery (GFD) at Eli Lilly, a healthcare company. The primary focus is on managing large capital asset projects (>$400M USD) from planning through operational qualification, ensuring safety, cost, schedule, and quality. The role requires experience in industrial or manufacturing facilities, particularly in pharma manufacturing (GMP), and involves leading cross-functional teams and managing stakeholders. It is not directly AI/ML related but operates within a regulated healthcare environment.

Associate Director, Joint Process Team (JPT) at Eli Lilly in Hyderabad, India. This role leads a cross-functional team of Lilly and API Contract Manufacturer representatives, managing the business relationship with the Contract Manufacturer. Responsibilities include overseeing technology transfer, process validation, regulatory approval, production, batch release, and supply chain management to ensure safety, quality, and operational excellence. The role requires strong leadership, interpersonal skills, and experience in API manufacturing and cGMP environments.

Associate Director for Capital Project Procurement at Eli Lilly, focusing on sourcing and managing contracts for manufacturing capital projects, including engineering, construction, and automation services. The role involves leading sourcing strategies, supplier due diligence, negotiation, and contract management to minimize costs and risks for major capital projects.

This role is for a Regulatory Affairs professional specializing in CMC (Chemistry, Manufacturing, and Controls) for pharmaceutical products at Eli Lilly in Kobe, Japan. The responsibilities include managing CMC-related regulatory tasks throughout the drug development lifecycle, from clinical trials to post-market maintenance, including preparing submission documents and liaising with regulatory authorities. The role requires experience in pharmaceutical regulatory affairs, particularly in CMC, and strong communication skills in Japanese and English.

Eli Lilly is seeking a Pharmaceutical Manufacturing Operator for a new, cutting-edge facility focused on advanced therapies like Gene Therapy. The role involves performing routine manufacturing activities in GMP areas, supporting equipment qualification, developing procedures, and setting up production areas during the startup phase. Once operational, the operator will execute production activities. The position requires adherence to strict quality and safety standards, documentation, and collaboration with various departments. Experience with pharmaceutical cleanrooms and manufacturing equipment is preferred.

Associate Director for Advanced Therapies Manufacturing at Eli Lilly, focusing on technical and people leadership for drug substance and drug product processes in a cGMP late-phase and commercial manufacturing facility. Responsibilities include technology transfer, process validation, control, and improvement, ensuring GMP compliance and partnering with cross-functional teams. Requires experience in gene therapy platforms and regulatory expectations.

Associate Director for Capital Project Procurement at Eli Lilly, focusing on sourcing and managing contracts for manufacturing capital projects, including automation, construction, and engineered equipment. The role involves developing sourcing strategies, negotiating agreements, managing supplier relationships, and identifying cost/risk reduction opportunities within the pharmaceutical manufacturing sector.

Senior Principal Application Support Engineer & Shift Lead responsible for the health, stability, and operability of production systems in a regulated, high-availability healthcare environment. This role involves leading support operations end-to-end, incident command for major incidents, problem management, driving reliability strategy, and ensuring compliance.

This role is for a Principal Engineer focused on Automation for Utility Systems in a GMP pharmaceutical manufacturing facility. Responsibilities include system design, hardware/software selection, delivery strategy, testing, and supporting manufacturing operations. Experience with Rockwell Automation or Emerson DeltaV platforms is preferred.

Senior Director role leading global network for Primary Packaging Components, Container Closure Systems, Process Contact Materials, and Excipients in a pharmaceutical manufacturing setting. Focus on standardization, compliance, and operational excellence.

This role is for a (Sr./Principal) TS/MS Engineer focused on commercialization of pharmaceutical products within a regulated healthcare manufacturing environment. Responsibilities include technology transfer, process improvements, post-approval changes, deviation investigation, and supporting regulatory registration. The role requires experience in sterile formulation manufacturing within a cGMP environment.

Senior Director of Process Engineering & Automation responsible for leading site's process-facing engineering functions, including process engineering, automation, and process controls, to support startup and long-term manufacturing goals for monoclonal antibodies, bioconjugates, and aseptic drug product manufacturing. Role involves organizational development, functional strategy, safety leadership, project support, and ensuring system readiness for GMP operations.

Senior Director of Engineering responsible for leading facilities, utilities, and maintenance operations for a new advanced manufacturing facility. This role involves building the organization, defining strategies for site startup and long-term GMP manufacturing, ensuring system readiness, and driving operational excellence, asset reliability, and compliance with cGMP standards. The position requires leadership in developing and implementing maintenance strategies, managing capital projects, and ensuring a safe and qualified operational environment.

Process Engineer (R3-R4) at Eli Lilly responsible for ensuring a safe working environment and improving the safety culture within pharmaceutical manufacturing. The role involves technical expertise in equipment and process, leading troubleshooting efforts using formal problem-solving techniques like Root Cause Analysis, and providing oversight to support staff. Requires a Bachelor's degree in a related STEM field and significant experience with validated systems, safety improvements, testing, and equipment problem resolution in the pharmaceutical industry.

Director, Engineering, Parenteral (M2-M3) to lead a team of professionals in delivering the full scope of parenteral/DAP systems—from user requirements through design, build, commissioning, qualification, validation, and operation—while supporting site leadership in building a diverse, engineering-driven organization.

Systems Engineer to design, develop, and maintain Manufacturing Execution System (MES) software applications, integrating production processes with business systems to optimize manufacturing efficiency, quality, and safety. Responsibilities include testing, troubleshooting, ongoing maintenance, ensuring system reliability and data accuracy, and ensuring compliance with FDA guidelines and GMP requirements.

This role focuses on operational excellence in a warehouse and logistics setting, centered on training, continuous improvement initiatives (Lean, Six Sigma), and standard work documentation. It requires expertise in SAP Extended Warehouse Management (EWM) and adherence to GMP and regulatory requirements. The role involves process analysis, problem-solving, and implementing improvements to enhance warehouse safety, compliance, and efficiency. It also touches on warehouse automation like ASRS and AGVs.

This role provides technical guidance for visual inspection operations and projects for parenteral drug products. It involves teaching, mentoring, and coaching personnel on visual inspection processes, defect classification, and ensuring scientific understanding. The role also participates in troubleshooting, continuous improvement, and technical project support, interacting with peers and regulatory guidance.

Associate Director for a highly automated manufacturing facility focused on device assembly, vial packaging, and dry products packaging. The role is responsible for supervision, safety, performance, and development of direct-reporting employees, strategic direction for the automation team, productivity improvement, automation infrastructure, integration with cybersecurity, data integrity, regulatory requirements, data analytics, MES integration, life cycle management, and asset delivery. It also involves providing technical leadership, mentoring, and collaboration with global automation organizations and external communities.

This role is a Quality Assurance Operator at Eli Lilly's Seishin plant in Japan. The primary responsibilities involve ensuring data integrity in manufacturing records, managing status changes for intermediate products and materials, problem-solving in warehouse and manufacturing areas, and preparing documentation for meetings and annual surveys. The role supports shipment decisions and quality assurance operations by reviewing records and inputting data into electronic systems. It requires attention to detail, accuracy, and the ability to follow Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).

This role is for a Sr. Specialist-Engineering at Eli Lilly, focusing on the reliable, cost-effective, and compliant operation and maintenance of utility systems. Responsibilities include project management for contractors, change control management, daily support to operations, reliability engineering (BOMs, job plans, RCA), HSE participation, and process monitoring/technical support. The role requires experience with maintenance, CMMS, GMP, QMS, and strong communication skills. It involves responding to off-hour emergencies and requires a high school diploma or equivalent.

This role is for a Sr. Specialist-Utilities Maintenance Technician at Eli Lilly, a healthcare company. The position involves leading skilled trades personnel, developing work plans, scheduling assignments, and coordinating electrical outages. Responsibilities include servicing, diagnosing, and maintaining various utility systems such as electrical, high purity water, steam, and chilled water. The role requires adherence to HSE standards, performing preventive and corrective maintenance on electrical gear and process instrumentation, and updating CMMS data. Basic requirements include at least three years of experience in utilities electrical aptitude, experience with various utility systems, and a willingness to respond to call-ins and work overtime. Preferences include an Associate's degree or Technical Certificate in an electrical discipline and experience in an FDA-regulated manufacturing environment.

Operations Lead Technician for visual inspection in a new pharmaceutical manufacturing facility. Responsibilities include supporting commissioning and qualification of automated vision systems during the project phase, and then leading daily operations, training operators, and ensuring compliance post-project. This is a hands-on "working leader" role.

This role is for a Senior/Principal Scientist Validation at Eli Lilly's new production facility in Alzey, Germany. The primary focus is on instructing and supporting the validation of production equipment and systems, including sterilization, cleaning, filter, shipping, and process validation. The role involves preparing and reviewing technical documents, participating in process functional teams, and ensuring compliance with GMP and quality objectives. It is an onsite position requiring a degree in engineering or pharmacy with at least 5 years of industry experience and knowledge of GMP operations.

This role is for a Process Permitting role at a new biotech manufacturing facility. The primary responsibility is to provide safety leadership and expertise for the permit to work program, including drafting, reviewing, and authorizing various types of permits. The role also involves reviewing hazards and controls, ensuring personnel competence, and supporting emergency response and maintenance activities. Basic requirements include a trade qualification and experience in GMP manufacturing and operations/engineering.

This role leads cross-functional study teams in the development and execution of clinical trials, focusing on quality, timeliness, and budget adherence. It requires strong project management, operational knowledge, and scientific expertise within the drug development process.

This role leads cross-functional study teams in the development and execution of clinical trials, ensuring quality, timeliness, and adherence to scope and budget. It requires strong project management, regional operational knowledge, and scientific expertise within the drug development process.

Associate Director for Technical Services/Manufacturing Science (TS/MS) group responsible for PAR (formulation, filling, visual inspection) or DAP (device assembly, packaging) operations for commercially manufactured products. The role involves leading a team, providing technical guidance, ensuring safety and quality, managing technology transfer, process validation, and supporting regulatory inspections within a cGMP environment.

Warehouse Supervisor role at a new Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. Responsibilities include leading Warehouse Operators, ensuring safe and efficient daily operations, optimizing workflows, supporting continuous improvement, and developing the team. The role involves direct supervision, oversight of inbound/outbound activities, inventory management, and ensuring compliance with GMP, safety, and environmental standards.

Engineering Technician role focused on supporting Parenteral Operations by ensuring efficient setup and operation of Pre-Filled Syringe and Isolator Equipment, including hands-on maintenance, troubleshooting, and repairs in a healthcare manufacturing setting.

This role is for a Director-level Project Statistician in the pharmaceutical industry, focusing on leading the statistical aspects of clinical trial design, analysis, and interpretation of results. The role requires a Ph.D. in Statistics or Biostatistics with at least 7 years of experience in clinical research and development. Responsibilities include developing clinical plans, designing studies, performing statistical analysis, communicating results to regulatory bodies and stakeholders, and applying innovative statistical methodology. The role emphasizes collaboration, influencing teams, and ensuring regulatory compliance within a healthcare setting.

Production Technician role at Eli Lilly, focusing on filling and packaging sterile syringes in a manufacturing environment. Responsibilities include adhering to safety policies, preparing equipment, following standard operating procedures and Good Manufacturing Practices (GMP), and documenting process steps. Requires attention to detail, basic math and computer skills, and strong documentation abilities. This is a manufacturing role within the healthcare industry.

Scientist role focused on providing technical support for Active Pharmaceutical Ingredient (API) manufacturing processes, including process control, yield, purity, and productivity improvements through experimental projects, modeling, and data analysis within a cGMP environment.

This role leads cross-functional study teams in the development and execution of clinical trials, ensuring quality, timeliness, and adherence to scope and budget. It requires project management, regional operational knowledge, and scientific expertise to drive trial deliverables and manage risks.

Associate Director in Software Product Engineering (SPE) leading a high-performing engineering team to design, build, and optimize enterprise-grade platforms and applications for Lilly's mission-critical operations in a regulated healthcare environment. The role involves strategic leadership, technical direction, fostering innovation, and ensuring scalability and security of solutions, with a focus on modern engineering principles and Agile methodologies.

Operations Supervisor for a pharmaceutical filling line, responsible for shift leadership, staff development, ensuring adherence to safety and quality standards, and managing direct reports. Requires experience in pharmaceutical manufacturing, understanding of FDA guidelines and CGMP, and strong leadership skills.

This role is for an Engineer - Facilities and Site Services Lead at Eli Lilly, a global healthcare company. The position is based in Concord, NC, and focuses on managing facility operations, campus security, utilities, and site services for a 24x7 manufacturing facility. Responsibilities include developing and sustaining technical systems, managing third-party contractors, ensuring site compliance with corporate standards and regulations, and leading emergency response for facilities and infrastructure. The role requires a BS in Engineering or equivalent experience with at least 5 years in facilities or site services, and experience with GMP, CAPA, and managing service providers is preferred.

Instrumentation Technician responsible for maintenance, calibration, troubleshooting, and installation of instrumentation systems in a new API manufacturing facility. The role ensures equipment availability and compliance with cGMP standards during pre-startup, startup, and post-startup phases.

The Scientist - TS/MS Parenteral role at Eli Lilly focuses on technical transfer, process validation, and maintaining the validated state of parenteral operations, specifically in visual inspection. This role involves establishing and monitoring metrics, harmonizing control strategies, evaluating process improvements, and serving as an escalation point for operational issues. It requires authoring and executing protocols, conducting root cause investigations, and providing technical leadership for the Parenteral Process Team. The role also involves supporting manufacturing components, equipment, and operations, representing the team in communications, leading risk management activities, and providing technical support for investigations and quality/stability issues. Key deliverables include preparing technical documents, developing and reacting to statistically based metrics, identifying opportunities for process improvement, driving stability strategy, and providing audit support.

This role is for a Lead Operator in Utilities at a new Eli Lilly manufacturing facility. The primary responsibility is to ensure the uninterrupted generation and distribution of utility services (water systems, boilers, chillers, etc.) to support GMP manufacturing. The role involves daily monitoring, testing, cleaning, troubleshooting, and ensuring compliance with regulatory requirements in a regulated environment. Experience in facility/area start-up and understanding of cGMP are preferred.

This role leads the design and delivery of automation for major capital projects in pharmaceutical manufacturing, specifically for Active Pharmaceutical Ingredient (API) production. It involves managing workstreams, suppliers, and ensuring compliance and qualification within a global engineering team.

Operator for a logistics center in a biopharmaceutical manufacturing environment, responsible for materials management, inventory control, and shipping compliance within a regulated setting. Requires experience with SAP/MES systems and adherence to GMP/GDP standards.

Director level role in Eli Lilly's Medicine Foundry, focused on advanced manufacturing and drug development for biologics and other modalities. The role involves leading a team of scientists and engineers to drive scientific excellence, accelerate manufacturing advancements, oversee technology transfer, implement control strategies, and ensure right-first-time clinical manufacturing. It requires technical oversight, documentation, risk mitigation, process stewardship, deviation investigations, and collaboration with cross-functional teams and external partners. The role also involves defining and leading the site's technical innovation strategy for manufacturing capabilities.

Senior Director of Operations for a new API manufacturing facility, responsible for leading manufacturing operations, building the organization, developing GMP systems, and ensuring compliance with regulatory requirements during the startup and post-startup phases.

Seeking a Sr. Principal Bioprocess Engineer to support a new monoclonal antibody manufacturing facility. Responsibilities include facility start-up (design reviews, process safety, C&Q support, SOP development, tech transfer) and post-start-up support (continuous improvement, root cause analysis, equipment performance monitoring, control strategy development).