General

• Optimize IT/OT infrastructure for plant automation, process control, industrial automation, and manufacturing automation
• Build, maintain, and support OT infrastructure for GMP manufacturing and pilot plant operations
• Lead or support project scoping, technical requirements, infrastructure deliverables, commissioning readiness, estimates, and automation infrastructure solutions
• Partner with scientists, automation engineers, process engineers, controls engineers, infrastructure teams, and vendors to translate needs into technical requirements
• Contribute to solution architecture for plant automation, OT infrastructure, industrial networks, SCADA, MES, PI Historian, virtualization, on-premises systems, and cloud-connected components
• Provide technical support, troubleshooting, incident resolution, root cause analysis, and continuous service improvement
• Map, design, and maintain IT/OT service architecture diagrams, control networks, servers, virtualization, backups, archival, data flows, interfaces, and integrations
• Collaborate with R&D scientists and engineers to identify automation, manufacturing, and data integration needs
• Work with instrument vendors, automation suppliers, system integrators, and equipment manufacturers to evaluate and implement technologies
• Provide timely IT support for investigations, diagnostics, troubleshooting, and resolution with infrastructure, engineering, security, risk, quality, and compliance teams
• Support other sites from the primary location

Senior Specialist, OT Research Infrastructure

Research Scientist

• Implement Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for antibody-drug conjugates and other biologics conjugate product franchises
• Serve as Regulatory CMC Lead for synthetic moieties, including drug-linkers, in assigned ADC and bioconjugate programs
• Provide regulatory leadership within Regulatory and cross-functional teams
• Deliver regulatory milestones through product development and post-approval lifecycle
• Develop and execute phase-appropriate global Regulatory CMC strategies for drug-linkers, payloads, linkers, peptides, and other chemically synthesized moieties
• Assess global regulatory CMC requirements and identify potential risks
• Integrate synthetic-moiety regulatory strategy with targeting components, conjugation processes, conjugated drug substance, and drug product
• Align dossier content, data requirements, and regulatory milestones
• Manage preparation and execution of CMC documentation for IND/IMPD, original BLA/MAA, post-approval variations, agency meeting packages, and health-authority responses
• Manage change controls and develop regulatory filing strategies
• Conduct activities with a focus on compliance
• Complete detailed global regulatory assessments according to guidelines, policies, and timelines
• Collaborate with partner groups on authoring and reviewing submissions
• Resolve project issues collaboratively and escalate to CMC leadership as appropriate
• Participate in early- and late-development programs and cross-functional efforts to improve CMC content and processes

Associate Principal Scientist, Regulatory CMC – Biologics, Synthetic Moieties, Drug-Linker, ADCs, Bioconjugates

Compliance

• Serve as Regulatory CMC Lead for the synthetic moiety (Drug-Linker) of assigned ADC and other bioconjugate programs
• Provide regulatory leadership within Regulatory and cross-functional teams
• Deliver all regulatory milestones through product development and post-approval lifecycle
• Develop and execute phase-appropriate global Regulatory CMC strategies for drug-linkers, payloads, linkers, peptides, and other chemically synthesized moieties
• Assess global regulatory CMC requirements and identify potential risks
• Integrate synthetic-moiety regulatory strategy with targeting component, conjugation process, conjugated drug substance, and drug product strategies
• Align dossier content, data requirements, and regulatory milestones
• Manage preparation and execution of CMC documentation, including INDs, IMPDs, BLAs, MAAs, post-approval submissions/variations, agency meeting packages, and responses to health authority questions
• Manage change controls and develop regulatory filing strategies
• Conduct activities with an unwavering focus on compliance

Senior Scientist, Regulatory Affairs – CMC, Synthetic Moieties, ADCs, Bioconjugates

Chief Marketing Officer

• Support the alliance business operations framework, including planning cycles, operating cadence, milestones, deliverables, execution tracking, and ongoing operational governance
• Lead preparation and execution support for governance committees and decision-making forums
• Develop agendas, assess decision readiness, manage issues, track escalations, and follow through on agreed actions
• Ensure alliance activities comply with contractual obligations, governance structures, decision rights, operating procedures, and compliance requirements
• Coordinate internal and external stakeholders to facilitate alignment, transparency, and informed decision-making
• Lead coordination of alliance-related portfolio lifecycle management activities
• Facilitate integration of portfolio processes into alliance ways of working
• Drive alignment of marketing operations approaches, processes, tools, and technologies across alliance environments
• Integrate partnered promotional assets and portfolio content into broader portfolio planning and execution processes
• Identify, surface, and help resolve cross-company alignment issues involving priorities, timelines, resources, assumptions, dependencies, and execution risks
• Build trusted relationships with senior leadership, cross-functional partners, regional and market stakeholders, external alliance partners, and governance committee representatives

Director, Global Marketing Alliance Portfolio Lead

Program Manager

• Develop a DS&I-specific strategy aligned with enterprise objectives
• Support informed portfolio decisions that enhance digital capabilities
• Create business cases for potential technologies across GSMG & GWES
• Capture scope and value drivers for project prioritization
• Align digital priorities with IT and GSMG & GWES stakeholders
• Build marketing and communication content for product releases
• Maintain communication plans based on the digital roadmap
• Maintain relationships with leadership and stakeholders
• Review and update project value drivers, milestones, dates, risks, actions, and related data
• Analyze the digital portfolio backlog and identify opportunities
• Define and monitor value realization measures
• Complete ad-hoc portfolio projects and identify process improvements
• Establish standardized tools across DS&I, GSMG, and GWES
• Support programs that raise digital acumen across GSMG & GWES

Senior Digital Portfolio Program Manager

Director

• Lead, manage, and develop a team of field-based health-systems Medical Affairs professionals
• Recruit, onboard, train, coach, and evaluate Payer & Health Systems Medical Affairs Directors
• Manage performance against objectives and competencies through field observation, coaching visits, discussions, feedback, and metric analysis
• Develop and monitor individual development plans
• Oversee portfolio product launches and in-line product medical affairs plans
• Execute medical affairs plans and prioritize payer and health-system accounts
• Provide insights to headquarters from internal and external health-system stakeholders
• Coordinate with Commercial, Country Medical Affairs, V&I Global Medical and Value Capabilities, and Outcomes Research leadership
• Oversee strategic account plans and medical account plans
• Collaborate on national and regional medical account coverage
• Monitor the healthcare landscape and allocate medical affairs resources
• Facilitate communication with senior headquarters leadership for key accounts
• Represent the Payer & Health Systems team on cross-functional workstreams
• Ensure compliance with regulations, company policies, ethical guidelines, and standard operating procedures
• Support development and execution of the Payer & Health Systems medical account plan across the portfolio and account segments
• Lead medical account planning and management for prioritized health-system regional accounts
• Contribute to annual resource development and medical meeting coverage plans
• Provide project support to the Country Medical Affairs organization
• Contribute to annual budget planning and support management of the team budget
• Review and approve routine expense reports

Senior Director, Team Lead – Medical Affairs, Payers & Health Systems

Clinical Research

• Plan and direct clinical research activities involving new or marketed medicines in Atherosclerosis
• Manage the full cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication
• Evaluate pre-clinical and translational work to generate early clinical development plans and Investigational New Drug applications
• Develop clinical development strategies for investigational or marketed Atherosclerosis drugs
• Plan clinical trials, including design, operational plans, and settings
• Monitor and manage ongoing or new clinical trials
• Analyze and summarize clinical findings to support safety and efficacy decisions, new drug applications, clinical study reports, and publications
• Participate in internal and joint internal/external research project teams
• Support business development assessments of external opportunities
• Supervise clinical study execution
• Collaborate with commercialization, regulatory affairs, statistics, and manufacturing experts
• Assist senior leadership in communicating study progress and relevant scientific information
• Maintain scientific knowledge and awareness of research methodologies
• Identify strong investigators and establish communications with prominent clinical investigators
• Attend scientific meetings
• Author development documents, presentations, budgets, and position papers
• Facilitate collaborations with external researchers around the world
• Travel on company business approximately 20% of the time

Senior Director, Clinical Research – Atherosclerosis

• Develop professional relationships and engage with national and regional Scientific Leaders
• Conduct peer-to-peer scientific discussions and provide approved medical and scientific information
• Address scientific questions and direct out-of-scope inquiries to appropriate company resources
• Maintain current knowledge of the scientific and clinical environment in COPD/Respiratory
• Initiate scientific and data exchanges with potential investigators and assess research alignment, study concepts, scientific merit, and qualifications
• Enhance understanding of investigator-sponsored research foundations and goals
• Identify barriers to patient enrollment and retention
• Recommend study sites and identify potential investigators for Phase II-IV clinical development programs
• Conduct Site Initiation Visits
• Serve as protocol lead in collaboration with Global Clinical Trial Operations
• Address investigator questions and provide information about Company-sponsored clinical studies
• Engage in scientific congresses and medical meetings and facilitate scientific/data exchange
• Gather scientific insights about medical or scientific needs, priorities, and concerns of Scientific Leaders and/or patients
• Liaise between the scientific community and the Company
• Support onboarding and share therapeutic expertise with other field medical team members
• Adhere to field and corporate policies, GMSA strategy, SOPs, GCP guidelines, and administrative/operational responsibilities
• Work independently and as a team member while modeling integrity, inclusion, and empowerment

Regional Medical Scientific Director, MSL, COPD/Respiratory

• Work closely with Publication Managers, agency partners, and internal and external publication stakeholders
• Support tracking, capturing project updates, reporting, budgets, and communications for SCIS publications and outputs
• Attend monthly publication team meetings and assist with note taking and meeting summaries
• Update meeting agendas and obtain updates from publication team members
• Assist in developing and maintaining publication planning slide decks
• Support congress planning, presentation trackers, document trafficking, archival, QR code processes, compendia, abstract planning decks, and study statement slides
• Provide onsite support at major conferences when requested, including poster hanging
• Complete ad hoc publication slide deck requests and update the slide repository
• Manage document flow with internal and external service providers and publication reviewers
• Track and report publication projects not led by SCIS
• Maintain journal and congress listings
• Create, maintain, and reconcile Datavision records through final publication
• Support agency contracting, budget tracking, reference requests, bibliography management, and study data package or protocol document delivery
• Develop and maintain publication MS Teams sites/channels and manage access requests
• Assist with publication compliance activities and maintain department documents, repositories, and archives
• Communicate proactively with Publication Managers, agency partners, and stakeholders to support timely completion of publication activities
• Assist with quarterly record maintenance and other requests as needed

Publication Management Specialist

• Set the strategic direction for the product source management and network execution portfolio within NS&E
• Lead execution of network rationalization strategies and global product source changes
• Translate business objectives into actionable portfolio plans, priorities, and performance expectations
• Oversee and develop a team of Directors and their respective teams
• Build the leadership pipeline through coaching, mentoring, stretch assignments, succession planning, and role development
• Oversee the integrated portfolio of network actions and global source change projects
• Manage project plans, risks, dependencies, governance, reporting, and escalations
• Serve as senior leader and primary escalation point for Operating Unit and site leaders
• Partner with Operations, Supply Chain, Quality, Regulatory, Technical, Finance, Global Engineering Services, and other functions
• Provide updates to executive sponsors, senior leadership, and governance forums
• Guide business case development and evaluate strategic network options
• Drive risk identification, issue resolution, mitigation planning, and performance management
• Serve as process owner for assigned NS&E systems and business processes
• Drive continuous improvement, standardization, efficiency, and best-practice sharing
• Ensure compliance with company policies, ethical business practices, and applicable laws and regulations

Executive Director, Network Strategy Execution, Product Source Management

AI Engineer

• Design, develop, test, and maintain software applications supporting scientific research and business operations
• Collaborate with software engineers, scientists, and product teams to deliver solutions addressing real-world challenges
• Learn and apply cloud platforms, AI-assisted development tools, web frameworks, and data platforms
• Contribute to applications using AWS, React, Python, Databricks, Power Platform, GitHub, and SharePoint
• Support adoption of AI-enabled solutions and explore emerging technologies that create business value
• Participate in code reviews, testing, troubleshooting, and continuous improvement
• Document solutions and share knowledge with team members
• Contribute to Agile product teams through planning, development, and delivery activities

Software Engineer – AI Development

Sales

• Engage customers to address identified needs and educate key stakeholders about oncology products
• Communicate with the broader oncology community and achieve or exceed assigned sales goals
• Manage the Omaha, Nebraska territory, including Des Moines, Iowa
• Travel to visit customers in person and attend national sales meetings and industry conferences
• Work with territory team members to attain or exceed assigned sales goals
• Meet key stakeholders to understand practice structure, business models, influencers, priorities, and needs
• Build business relationships and trust to uncover customer needs
• Use approved resources and messaging to communicate patient-centered product value for indicated uses
• Apply knowledge of multidisciplinary care teams, cancer staging, treatment options, pathways, and disease guidelines
• Analyze trends in complex buying environments and drug distribution channels
• Review patterns for products purchased and prescribed across outpatient and inpatient infusion settings, hospitals, and GPO contracts
• Develop and execute short- and long-term plans with the local team and district manager
• Ensure a consistent customer experience across divisions and functional areas
• Share key learnings and collaborate with the customer team, including Customer Team Leader, Key Account Manager, Nurse Educator, Field Reimbursement Associate, and Medicare Account Executive

Oncology Sales Representative

Account Executive

• Liderar la ejecución del plan de Monitoreo Ganadero en el país, adaptando las prioridades globales y regionales a iniciativas locales.
• Impulsar el crecimiento del negocio identificando clientes, oportunidades y acciones para fortalecer resultados.
• Trabajar con los equipos comerciales para apoyar la planificación, demos, propuestas y cierre de oportunidades.
• Aportar conocimiento del portafolio y del mercado, incluyendo procesos de producción lechera, salud animal, nutrición y tecnologías conectadas.
• Ser responsable del portafolio de Monitoreo en el país, incluyendo tecnologías de ordeño, identificación animal, software, dispositivos conectados y nuevos desarrollos.
• Colaborar con Customer Success y Soporte Técnico para mejorar la adopción, el uso y la experiencia del cliente.
• Compartir y adaptar materiales de capacitación, técnicos y de marketing para apoyar los lanzamientos y necesidades locales.
• Fortalecer el conocimiento del equipo con capacitaciones, recursos técnicos y acompañamiento en campo.
• Actuar como punto de contacto con equipos regionales y globales para proyectos, lanzamientos, feedback y prioridades del negocio.
• Reunir y comunicar información clave sobre clientes, mercado, competencia y tendencias para apoyar la toma de decisiones.
• Asegurar el uso correcto y eficiente de los recursos, siguiendo políticas, estándares y procesos de la compañía.

Representante de Ventas, Soluciones Tecnológicas – Corral de Engorda

Customer Success Manager

• Liderar la estrategia de Customer Success en el país, alineada con las prioridades del negocio.
• Asegurar una buena experiencia del cliente desde la entrega comercial hasta la adopción, uso y expansión.
• Dar seguimiento al valor entregado, la satisfacción del cliente y los riesgos de abandono.
• Liderar, desarrollar y acompañar al equipo local de Customer Success.
• Coordinar con equipos regionales y globales para aplicar procesos, herramientas y mejores prácticas.
• Trabajar de forma transversal con Ventas, Marketing, Soporte y otras áreas para asegurar una experiencia fluida.
• Detectar oportunidades de crecimiento comercial y derivarlas al equipo correspondiente.
• Apoyar lanzamientos de nuevos productos y cambios en el mercado, asegurando adopción y capacitación.
• Impulsar la mejora continua del área con datos, reportes y seguimiento de indicadores.
• Gestionar indicadores de onboarding, adopción, salud de cartera, satisfacción, valor entregado, retención, expansión, operación y desarrollo del equipo.

Líder Posventa y Satisfacción del Cliente – Soluciones Tecnológicas para Ganado Lechero

Data Engineer

• Design, build, and maintain the data foundation powering data-driven modeling of sterile drug product development
• Capture, curate, and deliver experimental and process data from Sterile Product Development teams into machine learning, statistical, and hybrid modeling workflows
• Partner with SPD experimentalists, process engineers, and analytical scientists to gather requirements for data solutions
• Design and implement scalable data pipelines ingesting experimental and process data from SPD teams
• Translate data-driven model requirements into analysis-ready, feature-rich datasets
• Define and enforce data standards, metadata schemas, and ontologies
• Automate data ingestion from laboratory instruments, electronic lab notebooks, PAT systems, and manufacturing systems
• Integrate data with cloud-based storage and compute environments
• Develop data analysis and visualization workflows
• Design and build dashboards, reports, and data exports
• Curate data and define requirements for automating data ingestion at scale
• Influence the digital data strategy for sterile product development
• Collaborate across scientific, engineering, and digital disciplines and multidisciplinary teams
• Deliver scientific innovation and build trusted partnerships across stakeholder networks

MSD