Biogen

Medical Director

• Define and govern GCM enterprise architecture standards across Commercial & Medical IT, ensuring alignment with enterprise architecture principles, security, compliance, and business strategy.
• Serve as the primary architecture leader for strategic GCM initiatives, shaping early solution designs and guiding key architectural decisions to ensure alignment with the target-state architecture.
• Lead GCM integration and data architecture strategy, defining how systems connect through scalable, secure patterns such as APIs, event-driven architecture, data-sharing models, and enterprise data flows.
• Develop multi-year enterprise architecture and business capability roadmaps that guide the evolution of Commercial & Medical platforms in line with business priorities, value streams, and capability needs.
• Identify opportunities to simplify and rationalize the application portfolio, including reducing overlapping systems, improving integration quality, lowering total cost of ownership, and avoiding unnecessary technology fragmentation.
• Provide thought leadership on emerging technologies, including cloud services, automation, data products, AI/ML, and generative AI, evaluating their fit for GCM business needs and integrating high-value capabilities with the appropriate security and compliance controls.
• Partner with cross-functional IT teams, including enterprise integration, data and analytics, security, infrastructure, delivery, and platform teams, to ensure architecture decisions are practical, scalable, and executable.
• Mentor and guide solution architects, platform architects, technical leads, and delivery teams to drive consistency in solution design and adoption of architecture best practices.
• Represent GCM in enterprise architecture forums, ensuring Commercial & Medical priorities are considered in cross-functional technology decisions.

Associate Director, Enterprise Architecture, Global Commercial & Medical IT

Business Operations

• Support site-level strategy development, planning, and prioritization in partnership with leadership
• Translate strategic priorities into operating plans, timelines, and materials
• Coordinate planning and delivery of key WCH Development forums and site forums beyond Development (e.g., all-hands, on-sites, R&D learning sessions)
• Track progress across priorities, highlighting risks, dependencies, and decisions for leadership visibility
• Support change management efforts, including communications and adoption activities
• Support execution of business operations initiatives aligned with Development priorities and site-wide priorities
• Contribute to process improvement and simplification to enhance team effectiveness
• Help maintain operating rhythms, planning cadences, and coordination across teams
• Assist in developing scalable approaches that enable efficient and compliant execution
• Support site leadership initiatives that strengthen culture and ways of working
• Partner with HR and site leadership to implement engagement activities and programs
• Coordinate logistics and execution of site events and leadership engagements
• Support external-facing site engagements in alignment with enterprise guidance
• Develop clear and concise materials to support leadership communications
• Support the preparation of updates, presentations, and storytelling on key initiatives
• Ensure alignment with enterprise communication standards and messaging

Senior Manager, Business Strategy & Operations – WCH Development

General

• Provides end-to-end leadership and oversight for commercial manufacturing and supply execution through external manufacturing partners, ensuring reliable supply, compliant operations, and sustained process performance across product lifecycle stages.
• Accountable for production strategy, production supply planning, manufacturing readiness, startup of external manufacturing operations in China, technology transfer, process validation support.
• Conducts on-site monitoring at CMO/CDMO partners, oversight of in-process testing and release testing in partnership with Quality Operations, deviation and change management, and continuous improvement across drug substance, drug product, and finished goods operations.
• Acts as the senior production representative for external manufacturing operations, leading cross-functional decision-making, risk management, escalation management, and cross-functional PO&T projects with internal and external stakeholders.

Production Lead

• Oversee strategy and execution of Quality operations for Biogen commercial products in China
• Act as Authorized Qualified Person for finished goods release and importation
• Ensure compliance with laws and regulations
• Manage China Site Quality team and RP release delegates
• Communicate quality issues to senior management and influence resolution
• Interact with cross-functional teams such as Planning, Logistics, Sourcing, etc.
• Manage Health Authority inspections and quality management activities
• Identify compliance gaps and collaborate to resolve issues
• Approve specifications, testing methods, and quality management procedures
• Ensure timely training of personnel in Quality Control and Quality Assurance

External Quality Lead – Authorized Qualified Person

Technician

• Perform preventive and corrective maintenance on manufacturing and laboratory equipment.
• Troubleshoot mechanical, electrical, instrumentation, and controls issues using established procedures and technical guidance.
• Support reliable equipment operation through root cause analysis and corrective action implementation.
• Partner with Engineering, Validation, Quality, Manufacturing, and Facilities teams to resolve equipment issues and improve system performance.
• Assist with validation activities and continuous improvement initiatives.
• Learn to navigate and utilize Computerized Maintenance Management Systems (CMMS).
• Read and interpret engineering drawings and technical documentation.
• Maintain training compliance and adhere to GMP, safety, and site procedures.
• Develop proficiency with industrial tools, maintenance practices, and manufacturing systems.

Manufacturing Maintenance Technician Apprentice – 24-Month Program

Procurement

• The Purchasing Intern will be a member of the Purchasing team within the Procurement department, supporting the team in the completion of activities within the request to purchase order process.
• Responding to stakeholders in the ServiceNow ticket management tool.
• Performing changes on Purchase Orders in the Oracle system.
• Various ad hoc tasks provided by the Analysts.
• Exposure to compliance ensuring activities, such as checking potential purchases against vendor contracts.
• Provide answers and solutions to end users via the ServiceNow ticketing system, emails, Teams chat, and calls.
• Issue Purchase Orders in Oracle.
• Support ad hoc requests from Purchasing Analysts and Purchasing manager.
• Review the internal documentation while performing the tasks, ensuring the accuracy of the process description, and make corrections or suggestions as needed.
• Escalation of system technical issues and process issues.

Purchasing Intern, Procurement Operations – 12 Months

Data Scientist

• Define and lead analytics and AI strategy using modern methodologies, including LLMs, GenAI applications, agentic workflows, and RAG-based solutions.
• Research, test, and implement new technologies, data sources, and AI/ML approaches for pharmacovigilance, regulatory submissions, quality, and clinical data insights.
• Establish AI governance, validation protocols, and responsible AI practices aligned with GxP and regulatory requirements.
• Collaborate with cross-functional R&D analytics groups to advance standards, innovation, and analytics governance.
• Present findings, model evaluations, and business impact of AI-enabled solutions to technical and non-technical stakeholders.
• Mentor and upskill junior staff in data science, GenAI, LLMs, prompt engineering, RAG architectures, and responsible AI practices.

Associate Director, AI/Data Science

Clinical Operations

• Serve as the quality lead for assigned clinical studies and programs, providing guidance on GCP compliance and quality expectations.
• Lead and support the Study Risk Assessment (SRA) process and proactively engage in inspection readiness activities.
• Conduct and manage investigations, root cause analyses, and the development and oversight of CAPAs and Effectiveness Checks.
• Collaborate with stakeholders to evaluate and escalate quality risks, and contribute to the development of mitigation strategies.
• Partner with internal and external teams to ensure appropriate documentation, risk management, and audit/inspection response planning.
• Support audit planning and regulatory inspection preparation, contributing to inspection management strategies and coordination.
• Participate in cross-functional and process improvement initiatives to enhance quality system effectiveness across RD&M.
• Review and approve controlled documents, CAPAs, and SOPs in alignment with quality standards and regulatory requirements.

Senior Manager, Clinical Quality Compliance

Operations

• Lead and manage the relationship with Franchise Leadership Team
• Drive insights agenda: Scope, lead, and deliver cross-functional projects across core insights functions, including market research, forecasting support, competitive intelligence, brand analytics, and field analytics
• Deliver high quality ad hoc analyses to leadership that offer clear recommendations in support of brand strategy
• Proactively provide actionable insights to key stakeholders for both short term resource allocation decision and long-term strategy development
• Collaborate with Advanced Analytics and Orchestration team and other Business Intelligence and Operations (BIO) teams to support initiatives to guide brand strategy and execution
• Lead Integrated Customer Plan (ICP) and Annual Operating Plan (AOP) for CD&I, and provide commercial team with comprehensive performance, target audience, and market insights to support strategy & resource investment
• Cultivate strong relationships and effective ways of working within MS Marketing team and amongst cross-functional teams (Sales, Marketing, Market Access, Medical, etc.), building consensus/buy-in amongst teams
• Manage insights spend to allocated budget; pursue novel research methodologies that offer new capabilities and ways to optimize project efficiency
• Partner effectively with leadership to ensure that key business decisions are based on data/fact-based analysis
• Drive innovation in analytics and business execution to have impact on the business performance and investment strategy

Sr Director, Insights & Analytics, Neuropsychiatry/Women’s Health

• Building and maintaining strong relationships with medical business stakeholders to understand learning needs and implement effective solutions.
• Partnering with regional medical teams to assess field medical training needs and develop learning solutions.
• Ensuring content accuracy, alignment with strategic objectives, and compliance with Biogen policies.
• Leveraging Digital technologies including AI to create innovative and efficient learning solutions tailored to Field Medical capabilities.
• Managing content review processes to maintain quality and adherence to regulatory standards.
• Collaborating with Commercial and Global training counterparts to ensure cross-functional alignment and resource efficiency.
• Designing and implementing diverse training formats, including e-learning modules, virtual sessions, and in-person workshops.
• Identifying and coordinating internal and external speakers for training programs.
• Delivering or supporting foundational, continuing, and advanced training offerings as needed.
• Developing and tracking standardized training compliance metrics and generating reports to meet business demands.
• Overseeing project-specific budgets, managing vendors, and reporting on training activities and outcomes.

Associate Director, Global Field Medical Training, Excellence

Compliance

• Develop and deliver impactful compliance education and awareness programs for US Commercial employees and managers.
• Communicate emerging trends, new policies, and expectations to the US Commercial organization consistently.
• Collaborate with business units to identify and prioritize compliance risks and craft solutions to mitigate them effectively.
• Develop and execute monitoring plans based on identified compliance risks and oversee any necessary remediation.
• Conduct live compliance monitoring and use findings to discern trends and address compliance risks.
• Facilitate the implementation of remediation related to compliance investigation findings.
• Provide support for US commercial brands and functions on compliance issues and initiatives.
• Assist with US Speakers Bureau compliance and promotional program compliance initiatives.
• Participate in Internal Audits and help in implementing corrective actions based on audit outcomes.
• Contribute to critical compliance initiatives and projects.
• Undertake additional projects or activities as the need arises within the business.

Compliance Officer

Medical Science Liaison

• Be a credible medical/ scientific expert who engages with KME and HCP to increase confidence in making the best clinical decisions pertaining to disease state and Biogen’s products in the near and long term for the benefit of patient care.
• Focus on building deep, strategic, long-term relationships with internal & external stakeholders to be viewed as a partner rather than transactional.
• Be a “partner in the trenches”—be responsive, engage often and be a solutions-driven conduit to leaders in the medical community.
• Engage in projects and/or initiatives aligned to US Medical strategy, objectives and tactics.
• Be highly accountable to qualitative and quantitative medical excellence performance goals, standards, and measurements.
• Deliver against KME engagement plans that add high value by navigating resources at the office in collaboration with field and non-field colleagues.
• Capture and report KME/HCP medical insights using Veeva with the highest level of consistency and accuracy to help inform the medical and clinical strategies.

Senior Medical Science Liaison, Multiple Sclerosis

• Lead development and continuous improvement of CSO business processes, governance, and operational infrastructure
• Translate priorities into execution plans and track outcomes, risks, and delivery
• Drive initiatives across country delivery, site engagement, monitoring oversight, and continuous improvement
• Synthesize insights and data into actionable recommendations to improve decision-making and performance
• Lead resource planning, forecasting, and tracking across CSO sub-functions
• Develop dashboards and executive-ready reports on performance, capacity, and priorities
• Serve as Sub-Process Owner for key CSO processes, ensuring governance and compliance
• Support process and system enhancements to improve execution and scalability
• Strengthen onboarding, knowledge sharing, and ways of working across CSO

Senior Manager, CSO Business and Process Lead

Full-stack Engineer

• Lead end-to-end manufacturing strategy, scale-up, and lifecycle management, ensuring alignment with program and organizational objectives.
• Define and implement manufacturing standards, control strategies, and best practices across IDU programs.
• Serve as the primary technical authority with contract manufacturers, driving performance and innovation.
• Influence cross-functional and organizational decisions, providing SME input to development, quality, regulatory, and supply chain strategies.
• Drive manufacturing technology roadmaps, process innovation, and continuous improvement initiatives.
• Represent the organization externally through industry engagement and collaboration to bring in leading practices.
• Transfer new product designs into scalable and robust manufacturing processes.
• Establish inspection strategies, validation plans, and compliance documentation.
• Evaluate suppliers, manage contract manufacturers, and optimize supply chain processes.
• Select and optimize manufacturing processes, tooling, and assembly approaches.
• Approve routine engineering documentation and resolve day-to-day manufacturing issues.

Principal Manufacturing Engineer – Implantable Device Unit

Marketing Operations

• Manage the day-to-day leadership of the TA-specific committee, ensuring high-quality and compliant materials reach the market efficiently.
• Collaborate effectively with business partners to ensure successful PRC execution and maintain beneficial relationships.
• Capture, report, and analyze business metrics and TA-specific performance, recommending improvements to enhance processes.
• Partner with stakeholders to manage the annual plan through quarterly forecasting, addressing potential volume surges proactively.
• Conduct ongoing collaboration with Marketing teams to plan and approve content timelines, tracking adherence for key events.
• Facilitate PRC and escalation meetings to ensure a collaborative approach to promotional review.
• Develop expertise on emerging content review concepts and promotional tactics, including system refresh and relaunch.
• Manage contracted PRC Coordinator to ensure efficient meeting facilitation and documentation.
• Develop and deliver training programs for TA stakeholders and review teams, including agency partners.