Amgen

Full-stack Engineer

• Lead the Global Reliability Network
• Lead a network of site reliability engineers, maintenance leaders, system owners, and technical SMEs.
• Develop and execute the Reliability Network strategy, goals, milestones, and maturity plans.
• Share reliability KPIs, bad actor trends, equipment improvements, lessons learned, and reusable solutions.
• Represent reliability priorities and recommendations in senior engineering governance forums.
• Turn data insights into equipment improvements
• Use CMMS data, Asset Performance Monitoring, Plant Pulse, PdM findings, and site input to identify recurring failures, high-risk assets, downtime drivers, and bad actors.
• Convert reliability insights into corrective actions, equipment improvements, PM/PdM optimization, spare parts strategies, and capital recommendations.
• Track improvement actions, verify benefits, and scale successful practices across sites.
• Advance asset criticality and maintenance strategy
• Define and maintain a standard risk-based asset criticality approach across sites.
• Use criticality to prioritize maintenance strategies, work execution, spare parts, lifecycle planning, and performance monitoring.
• Standardize maintenance strategies based on criticality, failure modes, operating context, and performance history.
• Support RCM, FMEA/FMECA, PM optimization, predictive maintenance, and condition-based maintenance approaches.
• Lead Asset Performance Monitoring and PlantPulse adoption
• Define business requirements for asset health, criticality, failure modes, risk ranking, performance monitoring, and continuous improvement.
• Partner with SAP EAM, Technology/IS, site engineering teams, the Reliability Network, and SMEs to support deployment, training, adoption, and data quality.
• Serve as PlantPulse business owner to ensure tools address reliability pain points, support troubleshooting, and generate actionable equipment insights.
• Connect reliability to business value
• Partner with OPEX teams to identify reliability improvements that unlock capacity and reduce downtime.
• Translate recurring failures and reliability constraints into business impact.
• Support lifecycle risk visibility for critical assets, including deterioration, obsolescence, maintenance cost, reliability concerns, and end-of-life planning.
• Integrate reliability principles into capital projects from conceptual design through turnover.

Principal Engineer – Global Reliability Network Lead

Clinical Research

• Support late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring, and analysis activities
• Working collaboratively with the study team and clinical leadership to ensure high-quality, decision-ready clinical data
• Assist in authoring clinical protocols, Investigators Brochures, and other regulatory documents ensuring consistency and clarity
• Provide input into & implementation of data management plan, CRF design, and data review oversight
• Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
• Assist Development Lead and Clinical Scientist Director in medical monitoring and management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
• Anticipate and actively manage problems across a broad spectrum of cross-functional teams
• Work cross-functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
• Support appropriate training, recruitment, and development requirements for matrix team resources

Clinical Scientist Associate Director, Late Development, Obesity

Director

• Responsible for the development, characterization, scale‑up, and support of drug substance cell culture and purification processes
• Lead and develop a multi‑site organization of 30+ scientists and engineers
• Drive program success, safety culture, technical excellence, innovation, automation, and digital strategies
• Support a diverse portfolio of biologics, including monoclonal antibodies (mAbs), BiTEs, bispecifics, biosimilars, and other novel protein‑based modalities
• Play a key role in advancing late‑stage and commercial drug substance strategies across Amgen’s manufacturing network
• Lead a high‑impact, multi‑functional drug substance organization integrating cell culture and purification disciplines across multiple sites
• Recruit, develop, and retain a strong and diverse team; manage portfolio prioritization and organizational resourcing
• Advance integrated drug substance processes through commercial process development, process characterization, lifecycle management, and control strategy development
• Partner with engineering, manufacturing, and external network collaborators to enable successful process transfer and commercialization
• Author and review global regulatory filings (IND/INDa/MA) and respond to regulatory agency questions
• Drive ideation, development, and deployment of innovative and differentiating bioprocess technologies
• Contribute to Amgen’s scientific and regulatory eminence through publications, patents, and participation in external conferences and forums.

Senior Director, Bioprocess – Process Development

• Lead Amgen’s business development efforts in identifying and evaluating innovative therapeutics being developed outside of Amgen
• Develop and nurture a network of key industry and academic contacts
• Ensure robust communication of ideas, interests and information between the external community and internal groups
• Manage the search and identification of opportunities through networking and reviews of the external landscape
• Assess and prioritize based on Amgen’s therapeutic area strategy
• Lead the technical evaluations of opportunities by creating and managing cross-functional review teams
• Provide recommendations based on robust scientific and drug industry knowledge
• Ensure appropriate and efficient decision-making processes
• Engage in business negotiations and work with legal to execute contractual agreements for certain projects
• Responsible for leading strategic discussions and presentations with senior management, R&D, and Commercial.

Director of External Research – Development

Administrative Assistant

• Support Executive Directors within the Global Marketing organizations for General Medicine and Inflammation.
• Manage complex and frequently changing calendars for Executive Directors across multiple time zones.
• Coordinate domestic and international travel arrangements, including itineraries, visas, meeting logistics, and expense reporting.
• Support document management, including compliance-related administrative activities, presentations, and briefing materials.
• Screen and prioritize communications, ensuring timely responses, follow-up, and escalation when needed.
• Process purchase orders, invoices, and contracts in accordance with Amgen policies.
• Support onboarding activities for new team members and contractors.
• Maintain organizational charts, distribution lists, team calendars, and shared resources.
• Support leadership meetings, global team meetings, offsites, workshops, and virtual events.
• Coordinate logistics for cross-functional and international meetings, including scheduling, catering, technology support, attendee management, and congress support.
• Prepare meeting minutes, track action items, and ensure follow-through across stakeholders.
• Identify opportunities to streamline processes, improve team operations, and bring forward practical ideas that enhance coordination, engagement, and ways of working.
• Support team culture, engagement activities, and recognition efforts with positive energy, sound judgment, and a collaborative spirit.
• Partner effectively with Commercial, Medical, Value & Access, Corporate Affairs, Finance, HR, Legal, and other functions.

Administrative Coordinator – Global Marketing, General Medicine, Inflammation

• Supports the design, execution, and oversight of cardiovascular trials and other late-phase global clinical studies.
• Contributes to protocol development, study execution, medical monitoring support, and clinical data review, ensuring delivery of high-quality, decision-ready clinical data for regulatory submissions and scientific dissemination.
• Support the design, start-up, and execution of global cardiovascular trials, ensuring adherence to protocol, regulatory requirements, and data integrity standards.
• Contribute to development of clinical protocols, statistical analysis plans, investigator brochures, and regulatory documents, with particular focus on cardiovascular endpoints and safety outcomes.
• Collaborates with cross-functional teams to support endpoint strategy, event adjudication processes, and cardiovascular safety monitoring.
• Participates in development and oversight of endpoint adjudication charters, safety monitoring plans, and Data Monitoring Committee (DMC) interactions.
• Provides clinical input into data management plans, CRF design, and clinical data review, with focus on cardiovascular outcomes endpoints (e.g. MACE, hospitalization events, mortality) and/or cardiac imaging endpoints.
• Conducts ongoing clinical data review and signal detection, supporting identification and resolution of safety and data quality issues across global trial sites.
• Supports preparation and interpretation of interim analyses, database lock activities, and top-line data readouts.
• Assists Development Lead and Clinical Scientist Director with medical monitoring activities and oversight of CROs, vendors, and adjudication committees.
• Collaborates with clinical operations, biostatistics, safety, regulatory, and medical affairs teams to ensure successful delivery of cardiovascular outcomes and/or cardiac imaging studies.
• Contributes to clinical study reports, regulatory submissions, scientific publications, and presentations for internal and external stakeholders.
• Identifies operational or scientific risks and proactively implement mitigation strategies across cross-functional teams.

Clinical Scientist Associate Director, Cardiovascular

• You’ll help shape how marketing tactics are planned, produced, and deployed across channels, working in close partnership with U.S. Brand teams and cross-functional partners.
• As a key connector between brand strategy and execution, you’ll drive more consistent, efficient, and impactful commercial delivery — while contributing to implementation of new processes, tools, and ways of working.
• You’ll work cross-functionally with Brand Marketers, Content Production teams, Media and Channel Operations teams, and Data & Analytics partners to deliver coordinated, effective and efficient commercial activation.
• Work closely with the Obesity brand marketing team to drive coordinated execution of customer capabilities in collaboration with GCCI Transformation teams, Media, Production, and Channel Operations teams, and Business Analytics & Insights partners.
• Lead weekly pod interactions across GCCI channel operations teams to uncover insights for optimization and expand capability utilization for brand benefit.
• Educate and drive usage of new self-service tools and centralized capabilities to enable the brand team to efficiently find, re-use, create, and deploy content as technology evolves.
• Share channel-specific best practices and toolkits to enable Brand team execution at scale.
• Support development and implementation of cross-channel pilots or test-and-learns related to new formats, journeys, and automation.
• Document results, learnings, and best practices to uplift content capabilities, including contributing to global standards and Amgen Brand Management training curriculum.
• Monitor and keep pace with the latest industry content innovations and recommended practices.
• Partner with GCCI BAI and decision science teams to deliver performance tracking and operational dashboards to assess execution quality, content utilization, and deployment efficiency.
• Act as a key liaison to enterprise platform owners (e.g., DAM, Veeva, MLR systems) to ensure system alignment and content flow.

Director, Cross Channel Engagement Lead

General Counsel

• Develop, implement, and execute global intellectual property strategies for Amgen’s therapeutic products and product candidates (e.g., small molecules and peptides), related to, for example, compositions, polymorphs, formulations, processes, and methods of manufacturing.
• Working with Amgen scientists to identify patentable subject matter
• Drafting, filing, and prosecuting patent applications worldwide
• Conducting prior art searches
• Analyzing patents and preparing freedom-to-operate opinions
• Conducting due diligence in support of licensing activities
• Negotiating and drafting research agreements
• Providing legal advice and counsel to R&D and business partners on a variety of IP related matters
• Assisting with litigation-related matters and challenging/defending patents in PTAB, opposition, and other forums.

Senior Counsel – Patent Medicinal/Pharmaceutical Chemistry

Architect

• Be accountable for helping drive the successful design, architecture, build, test and implementation SAP S/4 Transportation management solution across all the Amgen manufacturing and distribution sites
• Partner with business leads, business engagement teams to support the development of business cases for delivering the IT roadmap and Business strategy
• Collaborate with Business, Operations IS and ERP solution architects (Order-to-Cash, Record to Report, Source to Settle) for cross functional integrations and E2E solution design
• Serve as solution owner for the SAP transportation management solutions within the global ERP architecture team
• Lead continuous improvements to drive IT effectiveness with the business and IT
• Collaborate with business and operations IS teams to identify future business needs and prioritize resources/effort to support the delivery of business-critical projects, enhancements and process improvements
• Deliver on portfolio investments and ensure business value outcomes are realized based on prioritized business needs
• Drive implementation of cross functional initiatives required for regulatory compliance
• Uses deep business knowledge to drive engagement on major IT initiatives
• Influence architecture decisions and solution choices with business stakeholders and enterprise architects
• Manage Implementation vendor to ensure the effective execution of the projects and services, holding them accountable to project scope, SLAs and critical metrics
• Drive configuration and development activities to meet business requirements through a combination of internal and external teams
• Ensure all the required functional, configuration and technical design documents of SAP TM capabilities are created in compliance with GxP requirements and ERP architecture standards
• Support Validation/QA teams on ensuring GxP compliance of SAP TM capabilities with the corporate standard for IT change management and IT SOPs following 21 CFR Part 11 and Annex 11 requirements
• Promotes adoption of SAP industry best practices within in S/4 transportation management and logistics execution workstream.

SAP Principal Architect, Transportation Management

Manager

• Handling industry leading transformation of overall patient support offerings
• Engaging directly with health care professionals and matrix partners to establish options for financial assistance / reimbursement
• Making outbound calls to health care professionals (HCPs), when required
• Entering data into supporting systems to initiate enrollment of new and existing patients
• Reviewing Patient Enrollment Forms for completeness and accuracy, identifying any potential barriers and following all processes outlined in SOP
• Initiating patient’s benefits verification by reviewing patient data and insurance material
• Ensuring that data entry process into the supporting system is completed accurately and in a timely manner
• Monitoring potential delays or pending cases

Intake Case Manager – Rare Disease

• Lead a team of epidemiologists to conceptualize, design, conduct, analyze, interpret and publish observational research supporting drug development programs and regulatory submissions
• Identify evidence needs and develop the RWE plan to support product development and commercialization strategy
• Design and execute studies to support evidence generation such as identifying appropriate patient populations
• Find opportunities to substitute for and/or complement interventional studies to reduce time and cost of drug development
• Influence cross-functional team members regarding the appropriate use and timing of non-interventional research
• Leverage real-world data and CfOR analytic approaches to inform high-value business decisions
• Track business and functional priorities and align resources against those priorities
• Develop and maintain relationships with key leaders in observational research

Director, Observational Research – Obesity

Supply Chain

• Manage assigned end-to-end processes and ensure their readiness for execution of clinical supply chain processes.
• Partner with DTI to assist with the resolution of technical incidents utilizing the Integrated Service Management-ServiceNow (ISM-SN) application.
• Point of contact for application issues, incidents, and troubleshooting.
• Manage timely closure of incidents.
• Troubleshoot technical incidents with end users utilizing both internal resources and outside organizations such as External Trial Operations (ETO).
• Monitor iDoc failures and determine the root cause of issues.
• Work with the business and/or DTI team to implement corrective actions.
• Act as a change record owner to support continuous improvement initiatives.
• Manage documentation and maintenance of clinical customization requirements to support readiness for key projects, audits, and inspections.
• Manage audit readiness playbooks for assigned processes.
• Interpret customers’ needs to identify potential opportunities for improvements.
• Generate Business Requirements (BRD) documents to initiate enhancements per the intake process.
• Support development of business cases for proposed system enhancements.
• Support and/or lead enhancement implementation.
• Develop project milestones, adhere to timelines, utilize project management tools such as Smartsheet, communicate issues, ensure issue resolution, and ensure change management for business end users.
• Act as primary tester for system enhancements and upgrades, which includes script authoring/approval, data preparation, test execution, and defect resolution test approval.
• Support training in the clinical OTC and/or PTS process at Amgen to DSC and cross functional staff.

Supply Chain Manager – Development Supply Chain Technologies

• Achieve results through detailed goal setting, accountability measures, effective partnership, performance management, collaboration with other groups, and dedication to serving customers
• Independently lead sophisticated studies in the General Medicine therapeutic areas ensuring statistical aspects of clinical activities meet required standards and are robust and valid
• Influence and supply to strategy development
• Defend statistical approaches
• Represent GBS through participating in and collaborating with multidisciplinary study teams

Biostatistics Manager, General Medicine

Engineer

• Own and manage Citrix Virtual Apps and Desktops infrastructure, ensuring performance, availability, scalability, and compliance.
• Administer and maintain Citrix ADC (NetScaler) environments, including: Global Server Load Balancing (GSLB)
• Load Balancing services
• Content Switching policies
• SSL offloading and certificate management
• Web Application Firewall (WAF)
• Multi-factor authentication (MFA) using nFactor authentication policies
• Maintain the health and resiliency of Citrix environments, including Citrix Cloud and Citrix ADC platforms.
• Design and implement secure remote access solutions leveraging Citrix Gateway and advanced authentication integrations.
• Perform patching, firmware updates, and platform upgrades in line with enterprise change management policies.
• Troubleshoot and resolve complex technical issues involving Citrix infrastructure, user sessions, authentication flows, networking, and backend integrations.
• Serve as the technical escalation point for Citrix and NetScaler-related incidents within IT operations.
• Collaborate with network and security teams to implement enterprise traffic management and application delivery strategies.
• Document configurations, SOPs, architecture decisions, and operational runbooks to support audits and operational continuity.
• Monitor system alerts, identify systemic issues, and implement long-term corrective and preventive actions.
• Mentor support teams and transfer knowledge to ensure consistent operational support coverage.

IS Engineer – Citrix Specialist

Security Engineer

• own global QMS processes for Warehousing & Distribution (W&D) and Supply Chain Security (SCS), ensuring standardization and consistency across the network.
• Define, maintain, and continuously improve global QMS processes for W&D and SCS, including standards, process flows, and documentation.
• Assess and implement changes to processes to meet evolving regulatory, compliance, and business requirements.
• Establish and manage process governance, including metric frameworks, performance tracking, and reporting.
• Monitor process performance, analyze trends, and identify risks or gaps requiring corrective or preventive actions.
• Lead and execute CI and OE initiatives across the GSC network.
• Own and manage business systems supporting QMS processes (e.g., lane management, distribution complaints), including enhancements and lifecycle oversight.
• Manage supplier-related processes for distribution materials to ensure quality, compliance, and performance standards are met.
• Lead cross-functional collaboration to align processes and improve E2E performance.
• Plan and support audits and MRs, ensuring processes meet quality expectations.
• Drive change management activities related to process and system updates, ensuring adoption across regions and functions.