Senior Principal Scientist role at Eli Lilly focused on planning and implementing experiments using in vitro assays and technologies to support drug discovery. Requires experience with biochemical assays, cell culture, assay development, liquid handling systems, automation, data analysis software, and protein interaction technologies. The role supports small molecule discovery and SAR for multiple projects within a multidisciplinary team.

Manager role focused on designing, developing, and configuring Veeva Vault software applications within the R&D space for a global healthcare company. Responsibilities include gathering requirements, implementing configuration changes, and ensuring adherence to standards and best practices.

Senior Principal Scientist to execute experiments on the cutting edge of pharmaceutical sciences, supporting research programs for identified targets. This role involves overseeing portfolio programs independently, demonstrating laboratory expertise with biologic assays for drug development (mAb, ADC, and CD3 platforms), performing assay development, functional mAb screening and profiling, and evaluating in vitro and ex vivo assays. Requires a Master's degree and experience with phenotypic screens, cellular assays, multi-color flow cytometry, NanoString nCounter, RASL sequencing, and developing/optimizing flow cytometry, ELISA, and Luminex based functional assays in specific model systems.

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.

Project Manager for Medical Affairs at Eli Lilly, responsible for creating integrated operational plans, managing project budgets, and driving process improvements in medical affairs deliverables. Requires a Bachelor's degree and significant experience in project management, cross-functional team leadership, change management, stakeholder management, and financial/business planning.

This role focuses on designing, executing, and analyzing in vitro screening assays for oligonucleotide therapeutics in early-phase drug discovery. It involves developing and troubleshooting assays, applying bioinformatics and statistical methods for data analysis, and potentially implementing semi-automated workflows. The position requires a Bachelor's degree and experience in pharmaceutical research, including cell culture, assay development, data analysis, and documentation.

This role focuses on integrating technology and applications within a healthcare company, requiring experience in IT solution delivery, project management, IT platform management, and ITIL/Agile frameworks. The primary focus is on enabling effective information flows and implementing innovative approaches for business transformation, rather than direct AI/ML development.

Biologist role focused on implementing high throughput molecular biology protocols and assays for biotherapeutic discovery projects, including cloning, protein binding assays, and data analysis using tools like Benchling.

Principal Engineer – Materials role at Eli Lilly focused on materials engineering and selection for drug product packaging and devices. Responsibilities include failure analysis, molding recommendations, process control, design reviews, risk assessment, and root cause analysis for medical device components. Requires a Bachelor's degree in a relevant engineering field and 3 years of experience in medical device materials engineering, polymer selection/processing, product development, failure analysis, process control, and risk assessment.

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).

Scientist in Histology Discovery Technologies at Eli Lilly, focusing on end-to-end histopathology workflows for non-clinical specimens in cancer research. Responsibilities include tissue processing, staining, quality control, and applying quantitative image analysis techniques. Requires expertise in IHC/IF and whole-slide imaging.

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.

This role is an Analyst in Purchase to Pay (P2P) for Global Disbursements, focusing on managing payment processes, bank relations, and accounting for rejected/returned payments. It requires fluency in English and Spanish or Portuguese, with experience in SSC/GBS P2P (Treasury & payments). The role involves supporting team members, owning processes like Cash In Transit, liaising with global project teams, and ensuring compliance with SOx and other regulations.

This role is for a Purchase to Pay (P2P) Analyst specializing in invoicing, responsible for processing third-party invoices, resolving vendor issues, and ensuring compliance with company policies and KPIs. The role requires fluency in English and Spanish or Portuguese, and experience in accounts payable or a similar operations environment. Desirable skills include SAP, ARIBA, and e-invoicing experience.

This is an Associate Human Resources Generalist role at Eli Lilly, focusing on supporting daily HR operations, managing employee relations, coordinating with payroll, administering HR data, and contributing to HR projects and policy development. The role requires experience in generalist HR functions, knowledge of Austrian labor law, and proficiency in HR systems.

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 is for a Pharmaceutical Sales Representative specializing in Gastroenterology in Germany. The responsibilities include identifying and building relationships with key customers, conducting sales discussions, performing strategic account analysis, developing multi-channel access plans, and implementing sales and marketing strategies. The role requires a certified pharmaceutical representative or a natural science degree, several years of experience as a pharmaceutical representative, strong sales and interpersonal skills, and experience with account-based selling and multi-channel approaches.

This role is for an Operations Associate in pharmaceutical manufacturing. The responsibilities include implementing continuous improvement projects, monitoring operational performance, investigating operational problems, conducting root cause analysis, managing deviation investigations and CAPA, leading process improvement projects, and collecting production data. The role also involves collaborating with supervisors on production plans and ensuring their execution, as well as providing education on MSOE concepts and assigning tasks to team members. It requires a Bachelor's degree or equivalent experience and 2-5 years of experience in pharmaceutical manufacturing or support.

Senior Application Support Engineer for a healthcare company, focusing on advanced technical support, troubleshooting, and incident resolution for a suite of products. The role involves collaboration with development teams, monitoring application health, and ensuring compliance with regulations like HIPAA.

Automation Technician role focused on maintaining and supporting automated equipment in a pharmaceutical manufacturing environment. Responsibilities include ensuring equipment performance, supporting engineering initiatives, and adhering to cGMPs. Requires experience in automation, PLC/HMI programming, and GMP manufacturing.

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 Vice President, Head of Transactions and M&A for a specific therapeutic area within Eli Lilly, responsible for identifying, evaluating, and executing business development transactions including M&A, in-licensing, and out-licensing to drive external innovation and company growth. This role requires close collaboration with internal business and research leaders and managing deal teams.

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.

This role supports the management, implementation, and maintenance of a cross-functional learning strategy to enhance organizational capabilities within GBS, aligning with emerging business needs. It involves the full HRD cycle (design, development, implementation, evaluation) and focuses on leadership and people development, including adapting to AI-enabled environments.

This role is for a Sr Manager/Manager of MRP Planning in Eli Lilly's manufacturing facility in Suzhou, China. Responsibilities include coordinating regulatory changes, managing material procurement for filling lines and projects, and supporting the affiliate bidding process. The role involves SAP system usage for PO release and payment tracking, and ensuring material availability for projects.

This role is for a Director of ExploR&D Translational Medicine at Eli Lilly, focusing on the medical strategy and oversight for drug development programs. The incumbent will lead early-phase clinical development, work with external biotech companies and internal experts, and be responsible for medical and safety leadership from candidate selection to proof-of-concept. Key tasks include constructing and executing clinical development plans, integrating scientific concepts, evaluating literature, providing medical leadership for clinical plans, and ensuring compliance with regulations and GCP.

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.

Sales Representative role focused on promoting pharmaceutical products, managing multichannel resources, analyzing business performance, and visiting healthcare professionals. Requires a degree, intermediate-high English, a driver's license, and experience with technology platforms for information analysis and virtual communication.

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.

Scientist/Senior Principal Scientist role in Bioanalytical Research at Eli Lilly, focusing on quantitative bioanalysis, metabolite identification, and biotransformation characterization for small molecule therapeutics. Requires method development, structural elucidation using mass spectrometry, and cross-functional collaboration.

This is an internship role in Corporate Health Management at Eli Lilly, focusing on developing and implementing health and safety programs. The role involves supporting projects, maintaining intranet pages, planning internal events, and assisting with health offerings. A key responsibility is creating training materials, preferably using AI. The ideal candidate is a student in a health-related field with Microsoft Office proficiency and some experience with AI tools.

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 is for a Pharmaceutical Sales Representative specializing in obesity treatments. The responsibilities include consulting and selling to general and specialist physicians, implementing sales and marketing strategies, building networks, and organizing educational events. The ideal candidate has a background in life sciences or business, is a certified pharmaceutical representative, has at least 2 years of experience in pharmaceutical sales, and possesses strong sales and networking skills.

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.

This role is for a pharmaceutical sales representative responsible for promoting and selling company products within a specific territory, managing customer relationships, and achieving sales targets. It involves understanding drug features, market conditions, and maintaining a professional image.

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.