Eli Lilly and Company

Director

• Lead and manage large-scale programs from design, execution and delivery in a green field site
• Oversee the release train process, coordinating with various teams to ensure timely and efficient delivery of products and services
• Ensure all projects adhere to GxP standards, maintaining the highest levels of quality and regulatory compliance
• Engage with stakeholders at all levels, providing clear communication and regular updates on program status
• Identify potential risks and develop mitigation strategies to ensure program success
• Effectively allocate resources across projects to optimize productivity and performance
• Generate and present comprehensive reports on program progress, performance metrics, and outcomes

Associate Director – IT Systems Delivery Lead

Clinical Research

• Drive the execution of Lilly clinical trials through exceptional investigator engagement and site performance management
• Ensure Lilly’s portfolio is prioritized at high-performing sites and that trials are delivered with quality, speed, and insight
• Combine deep therapeutic and scientific knowledge with strategic agility to influence investigators, elevate protocol understanding, and co-develop tailored enrollment strategies
• Serve as trusted partners to investigators, building strong relationships that improve return on enrollment
• Partner closely with internal Lilly teams to ensure that insights from the field shape development strategies
• Lead site-level strategy and risk planning to ensure predictable enrollment and data delivery

Associate Director, Clinical Research Lead – East Coast/Midwest

Machine Learning Engineer

• Operationalize Data Foundry’s scientific tools and analytical methods into actionable prototypes
• Build the ML deployment pipelines, model serving infrastructure, API layers, and observability guardrails
• Ensure every scientific tool Data Foundry produces are analytics-ready, well-monitored, and exposed through APIs
• Maintain end-to-end ML deployment pipelines: experiment tracking, model versioning, containerized model serving
• Develop model registry infrastructure and feature engineering pipelines
• Implement monitoring and alerting for data pipelines, APIs, ML models, and agentic systems to ensure system reliability and performance at scale
• Productionize predictive and analytical methods from Methods4Insight with versioning and structured error handling
• Build serving infrastructure supporting both synchronous and asynchronous workloads
• Define and implement API contracts, documentation standards, and testing frameworks
• Build and operate cloud-native model serving infrastructure using containers, Kubernetes, and infrastructure-as-code
• Develop CI/CD pipelines for ML models and integrate model serving with Data Foundry’s data pipelines
• Collaborate with the Frontier AI team and Tech@Lilly to ensure Data Foundry’s scientific tools are exposed via well-defined interfaces

Engineer – MLOps, Scientific Platforms

Account Manager

• Acts as a role model for sales effectiveness, call quality, and customer‑centric engagement.
• Own territory: Based on data and insights develop and execute account planning.
• Achieve or exceed sales targets
• Actively supports team capability development on Lilly selling model through peer coaching, training and role plays.
• Lead through best practices.
• Demonstrates strong disease‑area knowledge and a deep understanding of treatment options, including Lilly and competitor products
• Engage customers with scientific credibility and fair balance through effective face‑to‑face, p2p and other digital channels.
• Operate as one team by building strong partnerships with peers and cross functional team
• Demonstrates high integrity and full compliance at all times

Metabolic Account Manager

QA Engineer

• Define and deliver the global CPQA reporting and analytics strategy, enabling scalable, compliant, and insight-driven decision making aligned to enterprise quality objectives.
• Partner with Tech@Lilly and the Global Quality Transformation Office to align reporting, data, and analytics solutions to enterprise strategy, architecture, and validation standards.
• Provide technical leadership to define the “art of the possible”, shaping innovative, scalable reporting and analytics solutions in partnership with Tech@Lilly and domain SMEs.
• Enable the analysis and interpretation of product complaint and quality data to deliver validated insights, signal detection, and decision support for quality, compliance, and business leadership.
• Design and deliver business intelligence and advanced analytics solutions, leveraging automation and AI to drive insight generation and continuous improvement.
• Conduct external benchmarking within and beyond pharma to identify leading practices and inform the CPQA analytics transformation roadmap.
• Establish and operate standardized reporting and analytics services, including routine performance reporting, standardized metrics, and regulatory / audit support requests.
• Ensure reporting and analytics solutions meet GxP, validation, and data integrity requirements, supporting reliable and compliant quality system outputs.
• Drive simplification, standardization, and automation of reporting activities to improve efficiency and reduce fragmented, manual processes across the organization.
• Act as system owner and build global reporting and analytics capabilities, including talent development, performance, issue resolution, and continuous improvement.

Consumer Product Quality Assurance – Reporting & Insights Lead

AI Engineer

• Develop and deploy agentic AI applications for clinical data interaction
• Build systems to extract patient phenotypes from clinical trial databases
• Construct AI and ML systems for data management and analysis
• Evaluate and monitor model performance in production
• Build pipelines for clinical trial databases

Applied AI Engineer, Clinical Informatics

Manager

• Work with Northern European (NE) HUB Consumer Engagement Team and local brand teams to lead the development, localization, and evolution of patient disease state education (DSE) campaigns across a variety of channels
• Own the planning, execution, and optimization of consumer campaigns & experiences across chosen & most relevant channels
• Work with internal cross-functional teams to drive capability, clarity, communication and own the execution of the consumer campaigns

Consumer Engagement Manager

Brand Manager

• Diseñar y ejecutar la estrategia de la marca en farmacias.
• Crear tácticas específicas para concienciación, derivación y mantenimiento del paciente.
• Gestionar campañas educativas y promocionales mediante medios digitales y físicos.
• Alinear acciones con equipos corporativos, médicos y de ventas.
• Planificar campañas orientadas a movilizar pacientes.
• Crear programas de Concienciación y soporte en farmacias.
• Establecer relaciones con farmacias, grupos farmacéuticos, mayoristas y Key Opinion Leaders.
• Impulsar acuerdos y colaboraciones para ampliar el alcance de las campañas.
• Realizar análisis de mercado, competencia y tendencias.
• Administrar el presupuesto y medir ROI de iniciativas.

QA Automation Engineer

• technical leader
• mentor process control team, including design, controls philosophy, implementation and commissioning
• process control work implementation and coordination
• develop and implement the Automation Engineering Project Plan
• technically lead and oversee the work of Site Area leads and System Integrator including Functional Requirements, Design Specifications, DCS Application Software, Test Specifications.
• lead/ participate in design reviews and DeltaV application software reviews, attend equipment and software FATs
• lead a team of automation engineers supporting commissioning
• provide periodic status updates to Project Management
• devising functional requirements and process control strategies for control systems in collaboration with Process Engineering
• DCS and SCADA software design, coding/ configuration and testing (sequence logic, graphics, batch software etc.)
• perform automation engineering activities including design, tuning and troubleshooting of control loops
• implement and support electronic systems (such as plant historians, applications and software integration) used to capture process automation related production data
• maintain the validated state of the site control systems in line with Lilly quality standards including the development and execution of validation strategies and associated documentation
• automation support for capital projects including new product introductions
• promoting the use of automation to improve productivity, operational efficiency and compliance
• developing a ‘network’ of corporate contacts and leveraging corporate expertise when needed

Senior Engineer – Automation Engineering

Compliance

• Define and own the global cyber compliance program, establishing a clear approach that transitions the function from reactionary audits and inspections toward continuous, risk-responsive, program-aligned assurance.
• Set the vision and drive execution for AI, automation and GRC platform capabilities to accelerate compliance delivery, reduce manual overhead, and improve compliance outcomes.
• Own and evolve Lilly's multi-framework compliance program spanning FDA 21 CFR Part 11, GxP, ISO 27001, SOC 2, NIS2, HIPAA, CCPA, PIPL/CSL/DSL, and emerging AI/ML governance requirements across global manufacturing, research, and commercial technology environments.
• Develop scope definitions for security controls and regulatory requirements that reduce task-driven overhead through technical innovation including AI and automation.
• Maintain a current-state, executive-ready view of how Lilly's cyber control environment satisfies each applicable regulatory framework, clearly mapping satisfied obligations and characterizing gaps with meaningful regulatory risk analysis.
• Drive effort to build and sustain inspection-ready documentation, evidence packages, and response protocols enabling confident engagement with authorities, ISO auditors, and other regulators globally with minimal lead time.

Senior Director – Global Cyber Compliance

Full-stack Engineer

• Design, build, and maintain data processing pipelines for complex scientific datasets, ensuring FAIR compliance and machine-actionability.
• Develop RESTful APIs and microservices providing unified programmatic access to LIMS, ELNs, instruments, data warehouses and analytical databases.
• Support continuous improvement of LIMS and adjacent systems to meet evolving scientific workflows, security, and scalability standards.
• Work directly with bench scientists to understand pain points and rapidly prototype custom applications, dashboards, and workflow tools.
• Validate prototypes through iterative scientist feedback, ensuring solutions are fit-for-purpose before transition.
• Partner with Tech@Lilly Product Engineering to hand off mature prototypes for enterprise scaling, defining transition criteria, documentation standards, and SLAs.
• Build integrations connecting lab automation equipment, scheduling systems, and instrument data streams to Data Foundry’s infrastructure.
• Develop software for robotic workflow control, instrument driver interfaces, and real-time data capture from automated platforms.
• Create modular, reusable automation workflow components scientists can configure without writing code.
• Build and operate cloud-native components supporting containerized workflows, infrastructure-as-code, CI/CD, and workflow orchestration.
• Apply DevSecOps standards including security scanning, code review, and automated testing.
• Participate in agile development with iterative improvement and cross-functional collaboration.

Scientific Software Developer

• The Engineer - Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry.
• The engineer will provide automation support for one or more operating areas across site and/or for capital projects.
• Process Automation is core to delivering a right first-time facility start up and continued support of ongoing manufacturing operations into the future.
• The Automation engineer will collaborate and partner with cross-functional peers to support successful delivery of robust control systems and instrumentation, business plan priorities, and compliance objectives.
• In the project delivery phase and startup phase of the project (startup expected 2025 to 2028), automation engineering roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture.

Engineer – Automation Engineering, Biologics

• Design and develop clinical trial protocols, statistical analysis plans, and other essential study documents for infectious disease programs
• Serve as a medical expert for assigned clinical trials, providing medical input and oversight throughout the study lifecycle, including site selection, investigator meetings, and data review
• Monitor and interpret clinical trial data, identifying safety signals, efficacy trends, and potential issues, and proposing appropriate actions
• Lead and participate in interactions with regulatory authorities (e.g., FDA, EMA) regarding clinical trial design, data submission, and labeling
• Collaborate effectively with cross-functional teams, including preclinical research, biostatistics, regulatory affairs, clinical operations, and commercial teams, supervising teams as assigned
• Contribute to the preparation of clinical study reports, publications, and presentations at scientific conferences
• Provide medical expertise and guidance to internal project teams and external investigators
• Stay abreast of scientific and clinical developments in infectious diseases and clinical research methodology
• Ensure compliance with all applicable regulations, Good Clinical Practice (GCP), and company standard operating procedures (SOPs)

Infectious Disease Clinical Research Physician

Engineer

• Partner with the Process Translation and Analytical Laboratories functional areas and site, group, and global IT teams to implement and support digital laboratory solutions that enable the Foundry’s operational objectives.
• Drive and support system design, configuration, validation, and release - serving as an IT domain expert (SME) for analytical laboratory IT systems at the Foundry.
• Lead system design and configuration sessions with analytical lab SMEs for LIMS, LES, ELN, and CDS platforms, translating business and scientific processes into validated technical solutions.
• Develop and implement Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols in compliance with 21 CFR Part 11 and EU Annex 11.
• Lead data integrity requirements across lab systems and ensure audit readiness for regulatory inspections.
• Coordinate instrument integration and data flows between lab equipment and LIMS/LES platforms.
• Support site deployment and upgrade of analytical laboratory IT systems throughout the facility’s startup and operational phases.
• Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks.
• Ensure systems remain in a validated state and lead their lifecycle through releases, recapitalization, and retirement.
• Collaborate with site and global IT system teams to ensure operational readiness of laboratory systems supporting the Foundry’s release objectives.
• Act as a key IT SME for analytical laboratory IT systems, organizing and educating peers on system use and best practices.
• Support audits and provide oversight for management reviews, laboratory metrics, equipment records, and laboratory documentation.

Principal Informatics Engineer

• Establish relationships within compound and cross-functional teams, across regions and geographies, development phases, and with alliance partners and vendors to resolve medical information strategy for launching molecules
• Understand the voice of the customer based on deep expertise and network within Medical Affairs, then applying that understanding to create a Global Medical Information launch strategy
• Use customer insights to develop Global Medical Information content that improve customer understanding across channels (Digital; Contact Centers)
• Ensure unsolicited verbal and written Medical Information inquiries from HCPs and consumers are answered in a timely, accurate, and compliant manner
• Lead the development of comprehensive medical information portfolio training for affiliate, regional, and call center partners that will improve the first customer touchpoint at product launch
• Provide functional coaching and lead ground-breaking initiatives that impact Global Medical Information processes, procedures, and systems
• Develop and maintain expertise in drug information practices across the industry, apply expertise and benchmarking to internal Medical Information discipline
• Provide staffing support and expertise at the Medical Information booth at scientific congresses