Eli Lilly

Lead role in parenteral manufacturing operations at Eli Lilly, focusing on operating equipment, providing frontline leadership, technical troubleshooting, and operator development. The role involves supporting commissioning, qualification, and operational readiness in a new facility, ensuring compliance with safety and production procedures, and driving departmental objectives. Requires experience in pharmaceutical or medical device manufacturing and knowledge of cGMPs.

Supervisor for Parenteral Manufacturing Operations on the 3rd shift at Eli Lilly's Kenosha County facility. Responsibilities include direct line supervision of operators, ensuring safety and quality, driving operational improvements, supporting commissioning and qualification, and coaching employees. Requires a High School Diploma/GED and 2+ years of experience in pharmaceutical manufacturing operations with a strong understanding of FDA guidelines and cGMP requirements.

Supervisor for Parenteral Manufacturing Operations at Eli Lilly, focusing on direct line supervision of operators, ensuring safety and quality, and driving operational improvements in a pharmaceutical manufacturing setting. Requires experience in regulated environments and cGMP compliance.

Supervises parenteral manufacturing operations on the 1st shift, focusing on safety, quality, and operational improvements in a state-of-the-art facility. Responsibilities include direct line supervision, employee development, ensuring compliance with policies and procedures, participating in commissioning and qualification, and collaborating with cross-functional teams. The role requires a strong understanding of FDA guidelines and cGMP requirements, with experience in aseptic or sterile manufacturing environments preferred.

Associate Director for Capital Projects Procurement Leader at Eli Lilly, responsible for sourcing suppliers for automation, construction, engineering, and engineered equipment for manufacturing components, with a focus on the US and Puerto Rico. The role involves category management, leading sourcing strategies, contract negotiation, supplier due diligence, and managing supplier relationships to minimize costs and risks for major capital projects.

This role provides strategic, tactical, and operational regulatory CMC leadership for biologics, focusing on expediting development, supporting clinical trial applications, market registrations, and post-approval submissions. It requires deep technical knowledge of CMC development and manufacturing processes, coupled with a strong understanding of global regulations and guidelines.

Scientist role focused on assay validation, troubleshooting, and clinical testing for immunogenicity and biomarker studies in a healthcare setting. Involves developing and implementing laboratory protocols, ensuring regulatory compliance, and managing data. Requires a Bachelor's degree with industry experience and strong organizational and communication skills.

This role is for a Maintenance Technician in a pharmaceutical manufacturing environment. The primary responsibilities include servicing, repairing, and maintaining process and utility equipment to improve equipment uptime and efficiency. The role requires mechanical aptitude, troubleshooting skills, and adherence to safety procedures. Basic qualifications include a high school diploma and 2 years of automation experience.

Advisor - Computational Statistics role at Eli Lilly, focusing on statistical trial analysis, communication of results, and regulatory compliance within the healthcare domain. Requires a Master's degree in Statistics or Biostatistics and 6+ years of industry experience, with proficiency in SAS and R.

Supervisor for a QC Chemical Laboratory in a pharmaceutical setting, responsible for overseeing laboratory operations, ensuring compliance with GLPs and cGMPs, managing a team of analysts, and ensuring safety and adherence to regulations.

Associate Director of Quality Assurance responsible for ensuring operational readiness and GMP compliance for a healthcare site transitioning from project phase to operations. This role involves strategic quality leadership, cross-functional alignment, establishment of quality systems, risk management, and capability building within a regulated environment.

This role is for an Electrician C responsible for inspecting, repairing, and maintaining electrical equipment in process areas, labs, and utilities within a healthcare manufacturing facility. It requires knowledge of the National Electrical Code, electromechanical devices, troubleshooting electrical systems, and adhering to GMP procedures and safety protocols. The position involves hands-on maintenance of various electrical components and systems, documentation of work, and use of specialized test equipment.

This role is for an Operations Associate in Formulation and Material Preparation at a new high-tech manufacturing facility for injectable medicines. The role involves supporting commissioning, qualification, and validation during the project phase, and day-to-day performance management after site start-up. Key responsibilities include leading investigations, presenting to regulatory authorities, defining and procuring supplies, developing training materials, managing flows, and driving continuous improvement. The ideal candidate has a bachelor's degree, at least one year of pharmaceutical industry experience, strong organizational and project management skills, and excellent German and English.

This role is for an IAM SecOps Engineer focused on Public Key Infrastructure (PKI) and encryption services within a large enterprise. The engineer will be responsible for designing, implementing, and securing these technologies, managing certificate lifecycles, key management, and cryptographic standards. The role involves partnering with various stakeholders to ensure secure and compliant operations.

Engineering Associate Director responsible for leading the engineering group (process, automation, maintenance) supporting the delivery, commissioning, and startup of packaging lines and device assembly operations at a new pharmaceutical manufacturing site. The role involves managing teams, ensuring technical and maintenance support, driving continuous improvement, and supporting regulatory compliance.

Associate Director of Engineering for Packaging Operations at a new state-of-the-art manufacturing site. Responsible for leading a team of process, automation, and maintenance engineers to support asset delivery, process development, commissioning, qualification, validation, and startup of packaging lines. After startup, will support day-to-day engineering activities and future planning. Focus on safety, quality, engineering, optimization, and continuous improvement.

Principal Scientist role in pharmaceutical manufacturing, focusing on technical leadership, process improvements, compliance with cGMP and regulations, and technology transfer for dry product operations. Requires experience in pharmaceutical manufacturing and knowledge of process safety and regulatory expectations.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work as a Lilly employee while pursuing education at a local community college, with the opportunity for conversion to an Operator/Process Technician after completing apprenticeship requirements. Responsibilities include operating manufacturing equipment, adhering to safety and quality standards, documenting processes, and identifying operational improvements.

This role focuses on developing parenteral drug product clinical manufacturing processes and associated control strategies within the Biologics Research and Development organization. It involves collaborating with cross-functional teams, designing and executing manufacturing studies, leading tech transfer activities, authoring technical documents, and supporting process qualification and regulatory submissions. The position requires a B.S. or M.S. in Pharmaceutical Chemistry or Engineering with relevant industry experience and a working knowledge of parenteral product development.

This role is for a Senior Principal Process Engineering SME in Parenteral manufacturing at Eli Lilly. It involves providing global technical expertise in process engineering, aseptic processing, and parenteral technologies, including formulation, filling, freeze drying, and isolation systems. The role requires leadership in technical discipline, safety, compliance, consultation, knowledge sharing, capital project support, external manufacturing support, platform ownership, and innovation in manufacturing processes. A Bachelor's degree in engineering and over 10 years of cGMP manufacturing experience are required.

Director of Analytical Chemistry focused on peptide drug substance and drug product development and commercialization within a pharmaceutical company. Responsibilities include developing analytical methods, justifying specifications, designing stability studies, authoring regulatory submissions, and providing technical guidance for external analytical activities. Requires extensive experience in analytical chemistry and pharmaceutical development, with a focus on peptide therapeutics and regulatory compliance.

Principal Process Engineer for sterile drug product formulation and component preparation in parenteral (PFS/vial) manufacturing. Ensures safe, efficient, and compliant operations. Requires 8+ years of experience in sterile drug product manufacturing, strong knowledge of aseptic formulation and component preparation, and GMP requirements.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work with manufacturing equipment, adhere to safety and quality procedures, and pursue educational requirements. The role involves operating equipment in Material Prep, Formulation, or Filling teams, including robotics in the Filling area.

This is an Operations Apprentice role in pharmaceutical manufacturing at a highly automated facility. The apprentice will work with automated equipment in areas like Material Prep, Formulation, or Filling, including robotics, while pursuing education at a local community college. The role focuses on safe operation, quality, and adherence to Good Manufacturing Practices.

The Informatics Engineer will partner with Process Translation and Analytical Laboratories to implement and support digital laboratory solutions, focusing on key lab systems like LIMS, LES, ELN, and CDS. Responsibilities include system design, configuration, validation, and release, ensuring compliance with regulatory frameworks (21 CFR Part 11, EU Annex 11) and data integrity in a GMP-regulated environment.

Associate Director - Quality Engineer at Eli Lilly, responsible for technical guidance and leadership in quality standards for API/Fill finish Operations and Facilities Management, focusing on utilities and materials. Key responsibilities include quality oversight of production, engineering, automation, and laboratory operations, document review and approval, providing quality guidance, participating in investigations, data review, material disposition, and maintaining/improving quality systems. Requires BS in Engineering or science, 8 years of experience, and hands-on experience with ADC processes.

Director of Analytical Chemistry focused on Antibody-Drug Conjugates (ADCs), specifically the linker payload intermediate. Responsibilities include leading analytical method development, qualification, characterization, and control strategies, collaborating with cross-functional teams, authoring regulatory submissions, and mentoring staff. Requires PhD or MS/BS with extensive experience in pharmaceutical analytical development and regulatory affairs.

The Digital Plant Scientist will develop, implement, and maintain digital solutions, including models and data systems, to support continuous manufacturing operations in a cGMP environment. This role involves process monitoring, data analysis, integration of batch data, and collaboration with cross-functional teams to build and validate digital tools for a robust control strategy.

This role focuses on analytical chemistry for antibody-drug conjugates (ADCs) within a pharmaceutical company. It involves leading the development, qualification, and characterization of analytical methods for linker-payload intermediates, supporting regulatory submissions, and collaborating with cross-functional teams. The role requires expertise in CMC analytical development and understanding of regulatory requirements in the pharmaceutical industry.

Senior Principal Engineer for Automation Engineering at Eli Lilly's new Medicine Foundry, focusing on advanced manufacturing and drug development. The role involves leading capital project execution, providing automation support for manufacturing operations, mentoring peers, and ensuring compliant control applications and systems. Key responsibilities include technical leadership in design, development, commissioning, and qualification of control systems, promoting digital innovation, and maintaining validated states. Requires deep expertise in DeltaV DCS, Rockwell PLCs, and GMP processes, with a strong understanding of regulatory compliance.

The Engineering Automation Technician provides high-level automation and controls support for OEM filling equipment and associated systems in a cGMP pharmaceutical manufacturing environment. This role focuses on troubleshooting, maintenance, and ensuring automated lines operate safely and reliably, partnering with Operations, Engineering, and Quality.

Operator role in pharmaceutical manufacturing, focusing on operating equipment, troubleshooting, ensuring safety and quality, and training new staff. Requires a high school diploma and basic computer proficiency, with preferences for CGMP knowledge and lean manufacturing principles.

This role is for a Principal/Sr. Principal Scientist in pharmaceutical manufacturing, focusing on process understanding, technical support, and continuous improvement for API molecules. It requires a deep understanding of chemistry, experimental design, data analysis, and collaboration with cross-functional teams to ensure safe, compliant, and efficient manufacturing operations in a cGMP environment.

The Automation Engineer role focuses on enabling data flow between various manufacturing and operations departments by leveraging IT and Process Automation Technologies. This includes supporting innovation, data historians (OSI PI), OT data integration, advanced analytics, data integrity, and process optimization. The role involves leading design, development, and deployment of technical solutions, providing frontline support for PI and LogMate users, managing system health checks, performing emergency response, and acting as a subject matter expert on the OSI PI Data Historian platform. Key responsibilities include data integration for manufacturing improvements, implementing technology governance, incident response, PI tag governance, patch/reboot coordination, change control, DeltaV integration support, service account management, vendor engagement, user support, training, documentation, and audit trail review.

This role is for a Process Engineer in Device Contract Manufacturing at Eli Lilly, focusing on providing technical engineering oversight for production processes to ensure stable supply of devices, subassemblies, and components. Responsibilities include leading prioritization of process changes, coordinating engineering project teams, resolving manufacturing issues, and completing engineering activities for process/product improvements. The role requires a Bachelor's in Engineering and a minimum of 2 years of manufacturing engineering experience, with a preference for pharmaceutical/medical device experience.

Principal Process Engineer role at Eli Lilly focused on API External Manufacturing for small molecules. Responsibilities include providing technical leadership to contract manufacturers, developing process knowledge, assessing equipment suitability, ensuring reliable supply, and managing HSE/PSM elements. The role involves scale-up, tech transfer, process optimization, and continuous improvement, with a strong emphasis on safety and quality.

Senior Director of Health, Safety & Environmental (HSE) for a new state-of-the-art oral solid dosage manufacturing facility in Katwijk, Netherlands. This role leads the EHS function, ensuring compliance with Dutch and EU regulations, developing safety strategies, and integrating EHS into all aspects of the site's operations, from design to start-up and ongoing manufacturing. The position requires strong leadership, strategic planning, and experience in pharmaceutical manufacturing environments.

Senior/Principal Scientist in Quality Operations at Eli Lilly, responsible for QA oversight and final disposition of radioligand drug product manufacturing. The role involves ensuring GMP compliance, supporting manufacturing processes, reviewing batch records, managing deviations, and driving operational excellence through data analysis. Requires experience in pharmaceutical QA/QC and regulatory requirements.

This role is for a Computational Statistician at Eli Lilly, focusing on statistical analysis and programming for clinical trials. It involves collaborating with statisticians and study personnel, selecting and applying statistical methods, writing reports, responding to regulatory queries, and ensuring data quality. The role requires proficiency in statistical programming languages like SAS and R, and understanding of relevant disease states and regulatory compliance. It is a senior-level position with a focus on applying statistical expertise to healthcare research and development.

Supervisor for Peptide Manufacturing Operations at Eli Lilly, responsible for managing day-to-day production activities in a new advanced manufacturing facility. The role focuses on safety, quality, regulatory compliance, and team supervision within API synthesis and purification.

Process Technician role at Eli Lilly focused on operating highly automated equipment for material preparation, formulation, and filling in a night shift capacity. Requires adherence to Good Manufacturing Practices and safety standards, with opportunities for cross-training and supporting leadership in troubleshooting and training.

This role focuses on the development and optimization of purification processes for bioproduct active pharmaceutical ingredients. It involves experimental design, process transfers, and authoring regulatory documents within a healthcare/pharmaceutical context. The role requires a background in chemical engineering or biochemistry and experience in purification development.

This role is for a Process Controls and Instrumentation Technician at Eli Lilly's new Gene Therapy manufacturing facility. The technician will be responsible for the maintenance, calibration, troubleshooting, and installation of process instrumentation (Temperature, Pressure, Flow, Control Valves) to ensure equipment compliance with cGMP and operational readiness for clinical and commercial supply. The role involves supporting startup activities, preventive and corrective maintenance, documentation, and collaboration with various site teams.

Associate Director of Process Engineering for a new Small Molecule API manufacturing facility. Responsibilities include hiring and developing a team of process engineers, establishing business systems and processes for GMP operations, and overseeing engineering deliverables for facility startup and ongoing production. Requires a BS in Chemical Engineering or related field with extensive API/chemical manufacturing experience.

This role is for an Expert Maintenance Technician at Eli Lilly's new Medicine Foundry, a center for advanced manufacturing and drug development. The technician will be responsible for maintaining and repairing manufacturing and facilities equipment, ensuring optimal performance and compliance with GMP and safety regulations. The role involves multi-craft expertise in mechanical, electrical, and instrumentation, troubleshooting, documentation, and potentially leading a team. It is a critical role in ensuring the efficient and compliant operation of a state-of-the-art pharmaceutical manufacturing facility.

This role oversees maintenance activities for a new advanced manufacturing and drug development center, ensuring equipment availability, reliability, and optimal performance in compliance with cGMP and other standards. The Maintenance Supervisor leads and develops the maintenance team, fostering a culture of safety, technical expertise, and innovation, while aligning maintenance programs with organizational goals for safety, quality, and efficiency.

This role leads discovery toxicology projects for pharmaceutical small molecule products, involving the design, execution, and interpretation of toxicology studies. The position requires a PhD or MS/BS with extensive experience in toxicology and a strong understanding of the drug discovery and development process, including regulatory guidelines.