Amgen

Strategy

• Lead venue strategy, hotel sourcing, contracting, and supplier relationship management for Amgen's U.S. Commercial internal meetings portfolio.
• Partner with internal stakeholders on venue strategy recommendation and execution for U.S. Commercial internal meetings.
• Serve as a trusted advisor to meeting sponsors and senior business leaders.
• Provide governance and oversight of hotel contracting activities.
• Develop strategic hotel partnerships that enhance value and service quality.
• Utilize meetings and spend data to identify venue strategy opportunities and continuous improvement.

Venue Strategy Manager, Global Meetings Management

Financial Planning and Analysis

• Lead the Finance technology, AI, data, and innovation roadmap aligned with CFO organization priorities
• Partner with Finance and cross-functional leaders to identify and deliver technology-enabled business improvements
• Translate Finance business needs into scalable technology, AI, automation, and analytics solutions
• Manage the Finance technology and innovation portfolio, including prioritization, governance, risk management, and value realization
• Lead the intake, prioritization, and execution of Finance AI, data, and automation initiatives
• Advance Finance data and analytics capabilities through improved reporting, dashboards, self-service analytics, and data governance
• Drive process simplification, reporting optimization, automation, and data-driven decision making across Finance
• Partner with Digital/IT and enterprise teams to develop, scale, and operationalize technology solutions and prototypes
• Ensure Finance technology initiatives comply with enterprise architecture, cybersecurity, privacy, compliance, and internal control standards
• Establish governance frameworks for Finance technology, AI, and data initiatives, including approvals, controls, adoption, and performance tracking
• Promote responsible AI adoption and strengthen technology, data literacy, and analytical capabilities across the CFO organization
• Lead change management, stakeholder engagement, communications, and training to accelerate adoption of new technologies
• Serve as the primary liaison between Finance, Digital/Technology, Data, Cybersecurity, and other enterprise functions
• Provide executive portfolio reporting, strategic recommendations, and oversight to support prioritization, execution, and delivery across initiatives

Associate Director, Finance Technology, AI Data & Innovation

Director

• Lead medical and clinical development activities for assets within the General Medicine therapeutic area
• Accountable for clinical strategy, study-level medical leadership, cross-functional decision-making, and support of program execution from early clinical development through late-stage studies
• Partner closely with Clinical Operations, Regulatory, Safety, Biostatistics, Medical Affairs, Data Management, and other functional teams
• Provide clinical and medical leadership for one or more General Medicine programs or studies
• Support the development, execution, and communication of global clinical development strategies for cardiovascular assets across all stages of development
• Collaborate with global teams to integrate medical, scientific, regulatory, commercial, and market access perspectives into development programs
• Build and maintain strategic scientific relationships with key opinion leaders and external experts
• Provide clinical and scientific leadership in the design, conduct, analysis, and interpretation of clinical trials
• Contribute to the authoring and review of clinical documents, safety evaluations, and risk-benefit assessments
• Participate in regulatory interactions and support submissions to global health authorities
• Interpret clinical trial results and contribute to data-driven development decisions
• Present scientific and clinical data at various forums as delegated by the Global Development Leader
• Identify emerging scientific opportunities and unmet medical needs in cardiovascular medicine to inform future development strategies
• Contribute to lifecycle management strategies and provide clinical content for regulatory submissions.

Clinical Development Director – Cardiovascular

Sales

• Have primary responsibility for regional sales activities and results
• Lead a sales force through District Sales Managers (DMs) and be responsible for achieving/exceeding sales goals
• Set the strategic vision for the region and effectively coach, motivate, hire and retain the right people
• Serve as key interface with senior sales management and marketing
• Maximize performance and conduct business in line with Amgen’s compliance and Business Conduct Standards
• Develop and maintain strong relationships with key customers in person and virtually
• Travel to locations such as doctor’s offices, clinics and hospitals as required

Regional Sales Director – Oncology

Manager

• Implementing HEOR strategy, aligned with the Access Strategy Lead (ASL), for one or several assets across the life cycle management
• Execution of deliverables whilst engaging with internal and external collaborators
• Generating global-impact payer-relevant evidence, patient reported outcomes (PRO), clinical outcomes assessment strategy (COA) and evidence synthesis
• Ensuring delivery of global materials to support Health Technology Assessment (HTA) submissions including the Global Value Dossier (GVD) and economic models
• Translating strategic objectives into concrete delivery via HEOR project plan
• Maintaining strong working relationships with top-10 countries, including the United States
• Ensuring compliance with HTA dossier governance
• Engaging with vendors and external experts to validate HEOR strategy and technical approach.

Senior Manager, Global Health Economics & Outcomes Research

• Ensure incoming datasets are delivered according to defined data formats, metadata standards, and project requirements.
• Translate scientific and model development requirements into structured dataset preparation tasks with pathology scientists and pathologists.
• Ensure imaging data, annotations, and metadata are suitable for downstream AI/ML model development, validation, and scientific analysis.
• Execute computational pathology workflows across AI model development and discovery projects for image analysis workflows to generate quantitative readouts supporting discovery and program decision-making within cloud-based data platforms (e.g., Deciphex Patholytics, Procia-Concentriq).
• Identify opportunities to improve data workflows, tooling, and operational processes within computational pathology.
• Stay informed about emerging data management practices, digital pathology technologies, and AI data standards.
• Provide pathology expertise to the design and conduct of GLP and non-GLP nonclinical safety studies to enable progression of discovery and development programs to decision points inclusive of pathology peer reviews and report review of integrated toxicology reports for finalization.
• Serve as a contributing author to pathology sections of regulatory documents such as INDs, NDA/BLAs, IBs, and respond to Health Authority questions.

Senior Director – Pathology

Accounting Manager

• Perform the inventory accounting for certain Amgen manufacturing sites
• Will be accountable to manage and review the work of an outsourced provider that supports this team.
• Analyze complex inventory movements in SAP and verify that financials are accurate.
• Perform and analyze standard costing in SAP / S4 HANA
• Perform and review sophisticated journal entries, general ledger account analysis, and reconciliation for both SAP and consolidation tools.
• Prepare and review audit schedules and answer questions from internal and external auditors.
• Preparation and review of highly developed financial schedules such as footnote, month-end flash reports, accounting memos, and other ad hoc schedules, as required by the supervisor.
• May lead and review accounting control functions and reporting requirements such as: inventory reserves, pre-approval manufacturing, standard costing including absorption tests, and excess capacity analysis among others.
• Special projects to improve accounting processes including digital projects and integration support.
• Consolidate, analyze, and report global inventory balances by product/site and perform detailed monthly variance analysis.
• Leverage various AI tools to increase efficiency and compliance.

Cost Accounting Manager

Communications

• Lead global and U.S. communications for Amgen’s cardiovascular portfolio, ensuring strategies are integrated, business-relevant, and aligned across key internal partners.
• Serve as a senior communications advisor and point of accountability to global and U.S. cardiovascular leadership teams.
• Develop and execute integrated communications strategies that support business objectives, strengthen Amgen’s cardiovascular story, and engage priority audiences across global and U.S. channels.
• Lead communications for marketed products, future launch readiness activities, and stakeholder-facing campaigns.
• Partner across Corporate Affairs, including Advocacy, Enterprise Media, Internal Communications, Digital and Social, Policy Communications, and other key functions, as well as Investor Relations, Medical Affairs, Legal, Regulatory, Commercial, Government Affairs, and Value & Access, to deliver integrated strategies.
• Translate scientific, clinical, and business information into clear, credible, audience-relevant communications for patients, healthcare professionals, media, advocacy partners, internal audiences, and other stakeholders.
• Successfully use data, analytics, social listening, audience insights, and measurement to inform strategy, optimize execution, and demonstrate impact.
• Identify opportunities to responsibly use AI, digital tools, and emerging technology to improve planning, content development, stakeholder engagement, workflow efficiency, and measurement.
• Inspire and manage a high-performing team by setting clear priorities, supporting development, strengthening ways of working, and maintaining high standards.
• Anticipate and navigate emerging issues, new information, stakeholder dynamics, and rapid changes in the external environment.
• Oversee PR agencies, providing clear direction, ensuring high-quality execution, and measuring results and impact.

Senior Director, Corporate Affairs, CV Communications

• As a member of the Global Quality Strategy organization team, this individual will manage projects and initiatives in Global Quality portfolio in support of the end-to-end GxP operating model.
• Partner with cross functional senior management to ensure successful execution, tracking and value realization of critical initiatives and projects aligned with Global Quality GxP operating model.
• Stand up, own and facilitate governance and processes intended to advance Global Quality strategy and objectives.
• Perform analysis to identify improvement opportunities and make recommendations to management.
• Apply emerging technologies, such as AI, to the lifecycle management of global Quality projects and strategic initiatives.
• Analyze critical path items and constraints to schedules, recommending solutions to remove any roadblocks using a proactive approach.
• Identify core KPIs aligned with pivotal initiatives and projects.
• Provide leadership to key initiatives and strategic projects, including driving program management, content creation, and presentation.
• Continuously track and communicate progress and adherence to strategic initiatives and projects.

Associate Director, Strategic Planning – Operations

Compliance

• Serve as a microbiology and contamination control subject matter expert for Quality Compliance, QC laboratories, manufacturing, and site teams.
• Support the contamination control program, including site engagement, network participation, metrics review, risk identification, and escalation of significant concerns.
• Contribute to the development, revision, and implementation of global microbiology and contamination control standards, procedures, technical guidance, and quality intelligence documents.
• Support periodic contamination control reviews, trend evaluations, and state-of-control assessments for in-scope sites, processes, and products.
• Provide technical input for environmental monitoring, bioburden control, endotoxin, microbial identification, disinfectant efficacy, cleaning and disinfection, gowning, aseptic practices, utilities, facilities, and laboratory controls.
• Partner with site Quality, Manufacturing, Engineering, and QC laboratories to promote consistent application of contamination control expectations.
• Provide technical review and recommendations for microbiology investigations, deviations, CAPAs, risk assessments, change controls, audit observations, and inspection commitments.
• Support evaluation and implementation of new or improved microbiology methods, technologies, laboratory practices, and contamination control tools.
• Contribute to Microbiology Center of Excellence activities, technical forums, communities of practice, and network alignment discussions.
• Support regulatory inspections, internal audits, health authority commitments, and inspection-readiness activities related to microbiology, contamination control, QC laboratories, and manufacturing controls.
• Provide technical input to audit responses, regulatory inspection responses, CAPA plans, and effectiveness checks.
• Review regulatory filings, responses, or technical documents for microbiology-related content, as assigned.
• Monitor relevant regulatory, compendial, and industry developments and help translate them into practical expectations for sites and functions.
• Lead or support cross-functional projects related to microbiology, contamination control, laboratory practices, inspection readiness, or quality improvement.

Associate Director, Quality Compliance – Microbiology

• Serve as a aseptic processing and contamination control subject matter expert for Quality Compliance, Manufacturing, and site teams.
• Support the contamination control program, including site engagement, network participation, metrics review, risk identification, and escalation of significant concerns.
• Contribute to the development, revision, and implementation of global aseptic processing and contamination control standards, procedures, technical guidance, and quality intelligence documents.
• Support periodic contamination control reviews, trend evaluations, and state-of-control assessments for in-scope sites, processes, and products.
• Provide technical input for environmental monitoring, bioburden control, endotoxin, microbial identification, disinfectant efficacy, cleaning and disinfection, gowning, aseptic practices, utilities, facilities, and laboratory controls.
• Partner with site Quality, Manufacturing, Engineering, and QC laboratories to promote consistent application of contamination control expectations.
• Provide technical review and recommendations for microbiology investigations, deviations, CAPAs, risk assessments, change controls, audit observations, and inspection commitments.
• Support evaluation and implementation of new or improved technologies, practices, and contamination control tools.
• Contribute to Global Aseptic Council activities, technical forums, communities of practice, and network alignment discussions.
• Support regulatory inspections, internal audits, health authority commitments, and inspection-readiness activities related to microbiology, contamination control, QC laboratories, and manufacturing controls.
• Provide technical input to audit responses, regulatory inspection responses, CAPA plans, and effectiveness checks.
• Review regulatory filings, responses, or technical documents for aseptic processing -related content, as assigned.
• Monitor relevant regulatory, compendial, and industry developments and help translate them into practical expectations for sites and functions.
• Lead or support cross-functional projects related to aseptic processes, contamination control, laboratory practices, inspection readiness, or quality improvement.

Quality Compliance Associate Director – Aseptic Processing

• Foster a culture of innovation, identify and implement data and analytics solutions that drive value to our stakeholders
• Co-ordinate end-to-end service delivery from the acquisition and cataloguing of data to the ingestion, quality control, and readiness of that data for consumption into analytics published by Global Commercial Capabilities & Innovation (GCCI)
• Create roadmaps with Technology, AI&D, and Commercial leaders to implement and maintain next generation of data and analytics platforms and technologies
• Plans closely with Technology and AI&D leadership across the Enterprise to drive development of new capabilities and/or continuous improvement anywhere commercial data is required (i.e. product launches, field execution, etc)
• Develops cross-functional governance plans to ensure executive alignment of technology prioritization for GCCI. This includes active relationship-building and engagement with leadership at VP and ED level and down.
• Conducts joint-planning with Technology and business owners to mature and evolve the operating model using the Scaled Agile Framework (SAFe)
• Manages execution of initiatives with CEO staff level visibility such as AI Data Scaffolding, Performance Analytics, and reporting platform buildout within the Neural Nexus initiative
• Conducts interdependency analysis across multiple product teams in the solution train to ensure coordinated value delivery
• Manages a team of Product Owners that drive prioritization and delivery execution across the portfolio
• Drive the design, development, deployment, and sustainment of scalable data and analytics platforms and reusable accelerators that enable and increase the value of application and product teams

Director, GCO Technology, Data & Analytics

DevOps Engineer

• Take ownership of complex software projects from conception to deployment.
• Manage software delivery scope, risk, and timeline.
• Possesses strong rapid prototyping skills and can quickly translate concepts into working code.
• Contribute to both front-end and back-end development using cloud technology.
• Develop innovative solutions using generative AI technologies.
• Conduct code reviews to ensure code quality and adherence to best practices.
• Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations.
• Identify and resolve technical challenges effectively.
• Stay updated with the latest trends and advancements.
• Work closely with product team, business team, and other stakeholders.
• Design, develop, and implement applications and modules, including custom reports, interfaces, and enhancements.
• Analyze and understand the functional and technical requirements of applications, solutions, and systems and translate them into software architecture and design specifications.
• Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software.
• Identify and resolve software bugs and performance issues.
• Work closely with cross-functional teams, including product management, design, and QA, to deliver high-quality software on time.
• Maintain detailed documentation of software designs, code, and development processes.
• Customize modules to meet specific business requirements.
• Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
• Provide ongoing support and maintenance for applications, ensuring that they operate smoothly and efficiently.

Senior DevOps Engineer – Senior Associate Software Engineer

Account Manager

• Representing Amgen products to physicians and healthcare professionals
• Establishing product sales and performing total territory account management
• Providing disease information and education to medical professionals and all external customers involved in the care of patients
• Consistently achieving assigned sales objectives through the promotion of patient-centered disease and product education to HCPs
• Implementing goals of the marketing plan through execution of strategic account business plan
• Demonstrated experience working in a matrix environment
• Effectively utilizing all available resources and programs
• Proven ability to navigate and identify opportunities through the healthcare landscape
• Establishing productive business relationships with key local, regional, and national KOLs
• Developing and maintaining a high-level, in-depth disease and therapeutic clinical and scientific knowledge
• Utilizing a consultative selling approach involving a highly technical, solution oriented selling technique
• Executing all responsibilities with a strong understanding and adherence to compliance and corporate policies

Account Manager, Specialty Account Manager – Rare Disease

Risk

• Support the development, execution, and continuous improvement of enterprise GxP Quality Risk Management programs and processes across multiple GxP domains (GMP, GCP, GLP, GVP, GDP, etc.).
• Support implementation and continuous improvement of enterprise Quality Risk Management (QRM) frameworks aligned with global regulatory expectations.
• Facilitate risk identification, assessment, mitigation, escalation, and monitoring activities across GxP functions and sites.
• Partner with cross-functional stakeholders to identify emerging compliance and operational risks across the product lifecycle.
• Support development and monitoring of Key Risk Indicators (KRIs), quality metrics, and risk dashboards to enable proactive decision-making.
• Conduct risk trending, signal analysis, and data evaluation to identify systemic issues and opportunities for mitigation.
• Assist with governance and oversight of enterprise risk registers, risk review forums, and escalation pathways.
• Collaborate with Digital and Quality Systems teams to support risk management process integration within Veeva or other quality technology platforms.
• Support inspection readiness activities and provide SME support during internal audits and regulatory inspections related to risk management processes.
• Contribute to development of training materials and risk management capability-building initiatives across the organization.
• Monitor industry trends, regulatory updates, and emerging technologies related to Quality Risk Management and digital quality transformation.
• Support execution and continuous improvement of enterprise GxP Governance and Management Review processes.
• Coordinate governance meetings, governance committee materials, metrics reporting, and follow-up actions.
• Assist in maintaining governance frameworks, charters, roles/responsibilities, and escalation models.
• Support preparation of executive-level governance reports and presentations summarizing quality risks, trends, compliance status, and key decisions.