Product Manager

• Lead the Value Team responsible for the Development Data Platform & Services
• Own three integrated product lines: Core Data Platform, Data Processing Services, and Platform Services
• Deliver trusted, governed, and AI-ready data products across the Research and Development (R&D) Division
• Governed access via the Data Integration & Access Layer (DIAL)
• Managed services for core clinical data operations
• Shared foundational capabilities enabling consistency and governance across the platform

Executive Director, Technical Product Management

Product Analyst

• Serve as the primary user-facing partner for advanced process analytics use cases, supporting investigations, monitoring, and continuous improvement through various applications (e.g. Seeq)
• Discover, document, and manage business processes, opportunity statements, use cases, and user requirements related to advanced process analytics
• Translate manufacturing and MS&T user needs into clear problem statements, requirements, and user stories that are traceable through delivery and testing
• Facilitate structured user feedback and synthesize insights into prioritized backlog items in partnership with Technical Product Managers
• Represent user needs in product planning and prioritization discussions, balancing business value, compliance expectations, and platform strategy
• Collaborate closely with manufacturing, engineering, digital, analytics, and platform teams to ensure solutions align with MPI standards and governance
• Participate across the product SDLC by supporting requirements refinement, backlog readiness, user acceptance testing, release planning inputs, and post-release feedback
• Develop and deliver training materials, documentation, and user enablement activities to drive adoption and effective use of analytics capabilities
• Build and maintain a strong domain understanding of manufacturing process data, analytics use cases, and workflows supported by the MPI ecosystem

Senior Product Analyst, Process Optimization

Project Manager

• Managing the end-to-end drug development process, including projects of significant complexity; driving cross-functional teams and leading by influence to develop comprehensive strategies and ensure successful execution.
• Act as enterprise leaders by guiding teams through the creation, approval, and execution of integrated project plans appropriate to the project's phase of development and complexity.
• Building and maintaining project schedules and critical project information in enterprise project management systems and databases.
• Using these tools to integrate activities across key team members, proactively identify risks, address uncertainty, escalate appropriately, assess program status, and ensure clear and effective communication with key team, management, and cross-departmental stakeholders.
• Leveraging relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results.
• Leading key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable.

Associate Director, Development Project Management

• Managing the end-to-end drug development process including routine projects that are of moderate complexity and/or partnering with a more seasoned lead project manager on higher complexity projects.
• Driving cross functional teams to develop comprehensive strategies and drive execution of aligned plans to achieve on-time delivery of critical milestones.
• Building and maintaining project schedules and critical project information in enterprise project management systems and databases.
• Preparing for, facilitating, and documenting outcomes of team meetings, ensuring meetings have clear purpose and objectives.

Senior Specialist, Development Project Management

Operations

• Responsible for the operational planning, feasibility, and execution of a clinical trial
• May serve as the clinical trial team lead
• May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities)
• Leads team for timeline management, risk identification and mitigation, issue resolution
• May facilitate and collaborate with key internal/external stakeholders (e.g., study team, country teams, vendors, committees) in support of clinical study objectives
• Accountable for managing any study specific partners and/or vendors

Senior Scientist, Clinical Operations

Research Scientist

• Lead downstream and/or integrated drug substance teams supporting late-stage clinical and commercial programs, with clear line of sight to licensure and commercialization.
• Provide technical leadership for laboratory scale and manufacturing scale studies supporting process characterization, validation, investigations, and continued process verification.
• Serve as a downstream subject matter expert across core unit operations, with a strong understanding of upstream, analytical, and GMP manufacturing interdependencies.
• Ensure process and product knowledge are developed, documented, and transferred in alignment with company standards and regulatory expectations.
• Support technology transfer activities to internal and external manufacturing sites, including scale-up, process validation, and manufacturing readiness.
• Contribute to manufacturing investigations and lifecycle management activities for commercial processes.
• Author and review technical and regulatory documentation, including sections supporting regulatory submissions.
• Drive division-wide initiatives aligned with biologics manufacturing and commercialization strategy.
• Influence multi-year planning: capability needs, digital systems, platform evolution.
• Represent BDSC on cross-functional and cross-divisional teams.
• Actively collaborate with internal stakeholders and external partners, including contract development and manufacturing organizations.
• Lead, coach, and mentor a team of downstream scientists, fostering scientific rigor, accountability, and professional growth.
• Promote a culture of innovation, continuous improvement, and operational excellence within the laboratory environment.
• Support the leadership team with resource planning, staffing strategies, and hiring decisions.
• Support talent development strategy, including developing future technical leaders and building a talent pipeline.

Principal Scientist, Biologics Drug Substance Commercialization – Director

• Lead and/or execute analytical method development, improvement, validation and/or transfer activities
• Author analytical procedures and/or methods development and validation protocols, technical reports, experimental designs, regulatory submission documents, etc.
• Lead and/or perform investigations with strong technical troubleshooting skills and assist in developing/implementing CAPAs
• Provide documentation/technical input during inspections and audits (Regulatory and Internal)

Associate Principal Scientist, Supply Analytical Sciences

• Assessing, leading and managing the successful "end to end"(E2E) project management of major and complex supply chain changes
• Driving cross-divisional and cross-functional teams to ensure delivery of the targeted goals and timelines
• Developing detailed project plans for given changes using standard tools
• Managing multiple projects at any one time that have high complexity (global supply chain impact with many interdependencies)
• Proactively identifying and mitigating risks and participating in Integrated Risk Management (IRM)
• Ensuring inter-project communication and integrated execution

Associate Director – Project Manager, Manufacturing Network Strategy

Director

• supports the end-to-end pharmaceutical product strategy in our manufacturing and testing network
• ensures development and execution of a robust quality strategy for products supporting launch of the pipeline and/or uninterrupted supply of commercial products
• leads development and oversight of the Product Quality Strategic elements for the pharmaceutical franchises that includes short and long-term goals for the product franchise in alignment with the DCT/VCMT/Platform Councils/Product Councils
• acts as a quality designee for global product quality as needed
• ensures prioritization, progress, and escalation, as appropriate, of quality related strategic goals through periodic reviews and dashboards across products and manufacturing/testing sites across the network
• leads and/or participates in executing the VCMT/DCT aligned strategic goals with stakeholders and partners across our Research & Development Division and our Manufacturing Division
• reviews and approves franchise level documentation including Comparability Plans, CPV plans, Sister Site Evaluations, Post Marketing Product Reviews, Annual Management Review, Control Strategies, franchise level protocols/reports, filing/license submissions, franchise level regulatory observation responses, RTQs, franchise level change control, site and multi-site investigations, where appropriate

Director, Quality Product Strategy – Devices

Financial Planning and Analysis

• Provide financial guidance, planning, reporting and analysis in support of Global Quality
• Lead the forecast development process, including quarterly forecasts
• Evaluate and recommend resource allocation alternatives
• Present consolidated forecast submissions to Global Quality and Finance leadership
• Complete the monthly actuals reporting process, analyze variances and provide insightful commentary
• Identify opportunities to leverage digital tools for reporting forecasts and results
• Identify and deploy mitigation plans for significant business risks & opportunities
• Sponsor process improvements across Manufacturing Division's Finance
• Manage one direct report and collaborate with Global Quality Finance team

Finance Director – Global Quality

• supports the end-to-end pharmaceutical product strategy in our manufacturing and testing network
• ensures development and execution of a robust quality strategy for products supporting launch of the pipeline and/or uninterrupted supply of commercial products
• leads development and oversight of the Product Quality Strategic elements for the pharmaceutical franchises

Director, Quality Product Strategy – Small Molecule

• Define standard collection and mapping data definitions, ensuring alignment with industry (CDISC) standards and Health Authority regulations
• Ensure the definitions are maintained and aligned across the clinical lifecycle (e.g., data collection, analysis & report, and submission) deliverables
• Lead standards data governance reviews
• Contribute to the definition and maintenance of business processes related to the definition, use, maintenance, and sharing of clinical data standards
• Lead or participate in department initiatives, cross-functional working groups, and process improvement activities
• Participate in cross-functional project teams; establish collaborations/interactions with colleagues outside the department and make frequent contacts external to the area and/or company
• Maintain knowledge of new technologies, industry standards, regulatory requirements, and our company's guidelines and SOPs
• Work independently or as a team member with equal effectiveness
• Interact with staff across multiple company sites

Associate Director, Clinical Data Management

Marketing

• Lead consumer marketing for Sac‑TMT; build acquisition, activation, and retention strategy across the patient journey
• Set consumer priorities and roadmap aligned to brand goals and launch milestones
• Align consumer strategy, messaging, and omnichannel plans with the HCP team/CAT to ensure a cohesive, compliant go-to-market approach across audiences and touchpoints
• Lead consumer campaigns, with emphasis on digital, social, multicultural, CRM, and web
• Own DTC/acquisition strategy (segmentation, targeting, creative direction, channel plan) to drive awareness, enrollment, and adherence
• Ensure consumer touchpoint readiness (web, CRM, call center, patient support assets)
• Own KPIs/ROI; partner with Data & Analytics to build dashboards and the measurement framework
• Use research and performance insights to test/learn and optimize creative, channel mix, and audiences
• Represent the voice of the consumer to inform priorities and investment decisions
• Build and lead the Consumer CAT; coach and develop direct reports
• Drive adoption of agile ways of working across Consumer and HCP CATs; Partner with Sales, Medical Affairs, Market Access, Organized Customer, Analytics, Global Marketing, and Regulatory/Legal to deliver compliant, on‑time launch execution
• Lead agencies/vendors to deliver quality, on‑time work aligned to strategy
• Maintain strong Legal/Compliance partnership; ensure consumer materials meet promotional/non‑promotional and regulatory requirements
• Drive consumer launch readiness and lifecycle planning to support uptake and adherence
• Identify risks/dependencies and adjust priorities to achieve launch and lifecycle goals
• Embed health equity and Social Determinants of Health (SDoH) in consumer strategy
• Ensure outreach is culturally competent and accessible for diverse patient populations

Director, US Oncology Consumer Marketing

• Define and shape PSP strategies tailored to the unique needs for individualized therapies, translating insights into actionable solutions for the patient journey.
• Partner across our company Access Program, Data Strategy, Customer Experience & Innovation teams to ensure PSP design optimizes integration opportunities across teams, and maps data accessibility across platform so that patient and operational barriers are mitigated.
• Establish and oversee PSP measurement frameworks and dashboards that enable data driven decision making and continuous patient journey optimization.
• Lead PSP launch planning, process mapping, and cross-functional coordination to ensure seamless go-to-market implementations and continuous improvement post-launch
• Develop a comprehensive overview of the end-to-end intismeran treatment experience, and use patient, operational, and market insights to identify barriers and drive continuous improvement to the journey.
• Identify emerging analytical capabilities to enhance PSP and future-state design for intismeran Treatment Completion Strategy.
• Define support strategies that help patients successfully progress through key milestones in the intismeran treatment journey, including coordination at critical handoffs, mitigation of logistical barriers, and support for timely treatment initiation and completion.
• Manage budget and spend across agencies, and campaign development and execution while managing key AOR and vendor relationships.
• Synthesize and translate complex data sets to identify drivers and opportunities to optimize the patient journey by uncovering patient barriers and generating actionable recommendations for improvement.

Associate Director, Oncology Marketing – Patient Experience Strategy Lead, Intismeran Autogene

Data Scientist

• Lead end‑to‑end data science and statistical projects to address manufacturing challenges, applying advanced methods (DOE, SPC, regression, GLMs, multivariate analysis, optimization, simulation, predictive modeling, machine learning, etc.)
• Perform data quality assessments, maintain metadata awareness, and prepare reports for stakeholders and regulatory submissions
• Develop reproducible, well‑documented code and data science pipelines
• Automate repeatable tasks and integrate data science into operational workflows
• Mentor colleagues and upskill stakeholders in statistical and data-driven thinking
• Communicate complex statistical and modeling results clearly, to both technical and non-technical audiences, and provide actionable recommendations
• Stay current with modern predictive modeling, statistical methods, machine learning and AI methodologies
• Collaborate closely with Operations, Quality, Engineering, and Regulatory teams across regions

MSD