Director

• Support value evidence outcomes research plans and real-world evidence activities for in-line and pipeline products in prostate and kidney cancers
• Conduct prospective and retrospective observational studies on disease burden, epidemiology, treatment patterns, healthcare resource utilization and costs, satisfaction, clinical and patient-reported outcomes, systematic reviews, meta-analyses, and economic modelling
• Develop American Managed Care Pharmacy (AMCP) dossiers for U.S. payers and Global Value Dossiers
• Contribute to product development and marketing strategies across the product lifecycle to support market access and reimbursement
• Work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial, and country affiliates
• Develop and execute Value and Implementation plans and support reimbursement and market access
• Assess reimbursement and market access drivers and barriers and provide input into clinical, regulatory, payer/access, marketing, and evidence-generation strategies
• Design studies, author protocols, develop questionnaires, case report forms, data analysis plans, study reports, presentations, and publications
• Manage study-related contracting, budgets, vendors, and partners in accordance with company policies, SOPs, regulations, and Good Pharmacoepidemiology Practice
• Develop supplementary clinical data packages for HTA agency submissions
• Support country affiliates with local evidence-generation needs and adapt health economic evaluations and reimbursement dossiers
• Communicate outcomes research and health economic modelling data to internal and external stakeholders
• Maintain awareness of scientific and methodological developments
• Build relationships with scientific experts worldwide
• Present outcomes research data at national and international congresses and publish scientific articles

Director, Outcomes Research – Prostate and Kidney Cancers

Product Manager

• Set, own, and communicate product vision, strategy, and outcome-based roadmaps for Disease Biology and PharmTox digital capabilities
• Define and prioritize roadmaps for multimodal profiling across disease biology and preclinical research
• Manage product investments and contribute to business cases, including value, resources, risks, dependencies, and total cost of ownership
• Develop a cohesive strategy for a suite of scientific products and applications
• Align priorities across scientists, data scientists, lab operations, technology teams, and business leaders
• Collaborate across Lab Operations and Data & Analytics product lines on end-to-end multi-omics, preclinical, and imaging workflows
• Understand user needs through interviews, shadowing, and usage analytics
• Map processes and information architecture to identify pain points and automation opportunities
• Translate scientific and business needs into problem statements, requirements, user stories, acceptance criteria, success measures, and product requirements documents
• Drive solution discovery and rapid prototyping
• Prioritize features and trade-offs; manage backlogs and release planning
• Manage a portfolio of scientific applications and lead squads
• Evaluate tools, manage vendors, influence roadmaps, and integrate solutions with internal systems and the data lake
• Partner with product technology and engineering leads on ecosystem integration
• Apply industry standards and ontologies to develop FAIR applications and advance AI/ML approaches for drug discovery
• Create and maintain SDLC documentation, guidelines, SOPs, training materials, and user communications
• Support regulatory audits and inspections
• Drive adoption through metrics, user feedback, reports, visualizations, and user groups
• Promote capabilities and collaboration across teams
• Monitor competitive landscapes, standards, and emerging technologies
• Coach teams in customer-centered product practices and remove roadblocks

Product Manager/Associate Director – Disease Biology and PharmTox Product Line, Multimodal Integration and Biomarker Discovery

Product Designer

• Lead enterprise UX, research, web experience, and digital communications strategy across external digital properties
• Use audience research, journey mapping, usability testing, analytics, and stakeholder insights to improve digital experiences
• Set standards for site architecture, navigation, accessibility, inclusive design, content structure, and user journeys
• Guide web content strategy and governance with digital, editorial, analytics, platform, and regional teams
• Improve findability and reuse through taxonomy, metadata, tagging, and content classification standards
• Translate audience needs, pain points, performance data, and research findings into experience improvements
• Provide strategic oversight for major web initiatives and align scope, priorities, experience standards, and outcomes
• Build governance frameworks, workflows, compliance expectations, and operating practices
• Partner with IT and development teams on platform strategy, technology direction, and performance standards
• Define success measures and use analytics and performance data for decisions and continuous improvement
• Align Communications, IT, Legal, Privacy, analytics, regional teams, and external partners
• Advance GEO and AI-era discoverability for search, citation, and answer-engine visibility
• Build, coach, and lead a strong team and partner model
• Monitor UX, digital experience, AI search, and content innovation trends and translate them into opportunities
• Report to the Executive Director, Enterprise Brand Social Media and Digital Communications

Director, UX – Digital Communications

Technician

• Execute production tasks for the appropriate area in a GMP manner under direction from Senior/Lead Technicians or Supervisors
• Identify appropriate tasks and perform basic functions independently
• Learn and perform more complex tasks related to the function of the area
• Maintain cGMP and safety training to site requirements
• Report potential quality events and GMP/SOP non-conformance
• Execute paperwork using Good Documentation Practices
• Perform incoming material receipt, clinical site drug returns, and sample management
• Receive, inspect, and store warehouse inventory
• Execute sample collection activities
• Perform weekly replenishment, excess and obsolete inventory posting, and min/max changes
• Coordinate and execute discard processes for expired and unavailable inventory
• Process orders and stage materials supporting packaging/labeling work centers
• Provide emergency cold vault coverage when needed
• Perform regular cycle counts and ensure system inventory accuracy
• Manage shipping, freight, and logistics functions, including pick, pack, label, schedule, and ship
• Coordinate and/or prioritize warehouse activities as assigned
• Create packaging documents according to SOPs
• Ensure correct documentation of transactions within SAP
• Check written GMP documents for correct content
• Interact with employees within the department and across other groups/departments

Warehouse and Distribution Technician – On-site

Software Engineer

• Initially support business needs at the Durham, North Carolina site for approximately 12–18 months, then relocate to Rahway, New Jersey based on business needs
• Provide on-site support for commercial drug product manufacturing operations, including formulation, filling, lyophilization, and visual inspection
• Troubleshoot shop-floor equipment and automation
• Support deviation investigations, change controls, equipment validation, technical protocol authoring and execution, and equipment maintenance
• Serve as technical SME for formulation, process development, scale-up, equipment troubleshooting, and maintenance
• Author quality investigations, change controls, SOPs, technical protocols, and validation documents
• Contribute to commissioning, qualification, and regulatory certification of the FLEx Sterile GMP clinical manufacturing facility
• Collaborate with formulation scientists, engineers, quality representatives, manufacturing, facilities, IT, and external vendors
• Support aseptic drug product formulation, filling, and lyophilization operations
• Manage project assignments and support facility and process equipment innovation
• Perform manual and/or automated operations, general maintenance, troubleshooting, and support functions
• Lead sterilization and cleaning validation programs, technical assessments, and regulatory inspection support
• Own change management, periodic reviews, deviation investigations, root cause analyses, and CAPA implementation
• Maintain GMP-compliant facilities, utilities, manufacturing equipment, automation systems, documentation, and configurations
• Support capital projects and new product introductions, including automation design, integration, FAT/SAT, commissioning, qualification, and acceptance testing
• Develop data, reporting, and visualization solutions to drive operational excellence and continuous improvement
• Manage work orders, contractors, purchase orders, budgets, asset tracking, and project closeout activities

Engineering Specialist

Representative

• Support customers by providing clinical information on company vaccines, education, and resources
• Help providers and systems address reimbursement, contract adherence, and immunization rates
• Serve as primary point of contact for healthcare providers, quality directors, immunization managers, and office managers within the assigned geography
• Execute customer visits across clinics, health departments, integrated delivery systems, and hospitals
• Deliver balanced product sales presentations aligned with product labeling, CDC recommendations, and professional society recommendations
• Provide Vaccine Management with updates on customer needs, feedback, marketplace dynamics, and quality-goal progress
• Maintain professional, healthcare-environment, product, and marketplace knowledge through self-study, workshops, conferences, and promotional-material review
• Use analytical tools to conduct quarterly business reviews regarding vaccine contracts
• Educate customers on maximizing contract performance across the company portfolio
• Assist customers with education and tools such as Vaccine IQ to improve immunization rates
• Monitor business performance against objectives using company-provided tools
• Develop territory-level business plans to improve immunization rates in accordance with company policies, standards, and ethics
• Maintain product knowledge and certification across the company vaccine portfolio and CDC pediatric and adult immunization schedules
• Manage selected customer accounts as primary point of contact and identify business opportunities
• Coordinate customer strategies with Account Executives, Integrated Delivery System teams, and Solutions support teams
• Collaborate with the local Customer Team and field-based employees
• Travel approximately 25%, varying by candidate location within the geography
• Report to Stacey Horne

Vaccines Customer Representative

Security Engineer

• Engineer, implement, and maintain security controls across strategic platforms including SAP, Salesforce, Databricks, Microsoft 365, ServiceNow, Veeva, AI platforms, and enterprise SaaS/PaaS services
• Support platform assurance through security assessments, control validation, risk reduction, and compliance readiness activities
• Integrate security capabilities into platform delivery, CI/CD workflows, and operational processes
• Develop automation, controls-as-code, and reusable security patterns
• Monitor platform security posture, investigate gaps, and drive remediation of findings
• Partner with platform teams to improve resilience, onboarding experience, and secure adoption
• Contribute to security standards, operational procedures, and engineering best practices

Senior Specialist, Cybersecurity Engineering

• Report to the Chief Privacy and Digital Trust Officer
• Partner with the Chief Information Security Officer and advise the enterprise on AI and cybersecurity matters
• Provide legal counsel on AI/ML development, deployment, governance, cybersecurity risk management, incident response, and regulatory compliance
• Advise on AI design, development, procurement, deployment, governance frameworks, transparency, bias mitigation, and human oversight
• Develop and implement AI governance policies, risk assessment frameworks, third-party AI due diligence, and AI incident reporting processes
• Monitor and interpret global AI regulations, including the EU AI Act and FDA guidance
• Serve on divisional AI committees
• Lead AI contract negotiations and advise on technology transactions, data rights, and generative AI platforms
• Represent the company with regulators, trade associations, and industry organizations
• Serve as primary legal advisor to the CISO and Information Technology Risk Management organization
• Support cybersecurity incident response and assess breach notification obligations
• Advise on SEC cybersecurity disclosure rules, NIST frameworks, and industry standards
• Provide guidance on vulnerability disclosure, threat intelligence sharing, and engagement with law enforcement and regulators
• Support cybersecurity policies, vendor security assessments, and security provisions in commercial agreements
• Partner with privacy, compliance, and legal colleagues on AI, cybersecurity, regulatory, commercial, and data protection matters
• Advise on data governance and data-sharing arrangements
• Support M&A, licensing, and collaboration transactions through cybersecurity and AI due diligence and integration guidance
• Train business stakeholders on AI legal risks and cybersecurity legal obligations

Director, AI – Cybersecurity Legal

Sales

• Support and service the Animal Health product portfolio
• Support and promote Animal Health products and services, including Bio-Pharma products, Allflex ID products, and livestock monitoring services
• Support veterinarians, dealers, resellers, and livestock producers in using products
• Provide logistical support for market field trials with Sales and Tech Services
• Develop and execute plans to engage customers and meet customer needs
• Participate in field-based events, including trade show support and customer education
• Communicate clearly, concisely, and promptly
• Identify and communicate problems to Sales and Tech Services
• Actively support sales strategy across the region and territories through sales support activities

Animal Health Sales Intern

• Serve as a key analytics partner to US vaccines marketing, aligning analyses and insights to brand and portfolio priorities
• Work with business stakeholders to understand key questions, clarify objectives, and translate them into analytical use cases
• Enable prioritization and scoping conversations by assessing business demand, requests, and potential use cases
• Analyze claims, EMR/EHR, CDC, IQVIA, digital, and CRM data to generate actionable commercial insights
• Propose analytical approaches and AI/ML/NLP/modeling techniques, including methods and trade-offs
• Collaborate with data scientists, engineers, and onshore and offshore DHH teams
• Support the design, development, and refinement of AI/ML and NLP solutions, including Agentic AI
• Ensure analyses are delivered with high quality, timeliness, compliance, and an excellent user experience
• Keep clients updated on progress
• Synthesize findings into concise stories and visualizations
• Present insights to support data-driven decisions
• Stay current on vaccine market dynamics and advances in analytics, AI, and machine learning
• Lead a team of data scientists and analytics professionals

Director – US Market Engagement, Vaccines & ID

Medical writer

• Develop, author, edit, and lead the review of accurate, clear, and compliant clinical, regulatory, and/or public-facing documents
• Partner with project leads to support multiple programs and therapeutic areas across the company portfolio
• Apply medical writing best practices, including lean writing and health literacy principles
• Contribute scientific expertise and collaborate on cross-functional teams
• Apply critical thinking, problem-solving, and negotiation skills to complex medical writing challenges
• Provide program oversight and keep project leads and/or management informed of issues affecting timelines, quality, or compliance
• Use medical writing-specific tools and technology platforms
• Lead initiatives to improve medical writing processes and standards
• Apply knowledge of clinical development, relevant regulations, disease areas, and company products
• Provide scientific and operational mentorship, coaching, and/or project oversight to other medical writers
• May manage direct reports, including workload, professional development, and performance management

Principal Medical Writer

Medical Director

• Lead a team and provide portfolio-level oversight of study-integration delivery across programs and regions
• Serve as senior technical authority by approving high-impact designs, governing standards at scale, balancing demand and capacity, and driving automation and operational excellence
• Own integrated plans from design through closeout across in-scope studies; synchronize releases and dependencies
• Ensure technical components are production-ready before first-patient-first-visit and monitor status and quality before and after release
• Oversee decommissioning and archival with complete, audit-ready documentation
• Lead critical or high-risk studies and cross-program integrations to unblock delivery and model best practices
• Set program and therapeutic-area technical strategy aligned to GDMS/DI&A goals
• Participate in governance, present recommendations and trade-offs, and communicate status, risks, and decisions to sponsors and governance forums
• Define and manage SOWs, SLAs, and SLOs; track service-provider delivery health and hold partners accountable
• Champion risk-based computer system validation and inspection readiness
• Coordinate internal audits, including evidence, responses, and action plans
• Build business cases, prioritize initiatives, define OKRs/KPIs and dashboards, and track realized value
• Act as design authority for data collection, flows, integrations, and validation patterns
• Provide technical consultancy on data architecture, metadata, and cross-system interoperability
• Mentor and coach team members; review plans and specifications and improve agile, testing, and automation practices
• Sponsor communities of practice and reusable assets/templates
• Lead strategic improvement initiatives involving automation, CI/CD in validated contexts, test efficiency, and metadata enablement
• Set objectives, assign work, conduct check-ins and reviews, coach performance, and provide recognition
• Develop career plans, create growth opportunities, and ensure training and mentoring
• Lead recruiting and hiring and oversee performance management and sensitive employee-relations matters with HR
• Coordinate onshore, offshore, and contingent resources and ensure effective handoffs
• Manage operating budget and optimize spending against priorities
• Support and empower team leaders

Director, Clinical Data Management

General

• Perform direct and indirect activities supporting the manufacture of media, antigen and final vaccine material in line with the production schedule and local regulatory and GMP requirements
• Perform manufacturing activities for intermediates and final vaccine material
• Prepare, stage, use and maintain mechanical and laboratory equipment
• Ensure materials and equipment are available and within date prior to manufacture
• Support production planning, batch documentation and schedule adherence
• Assist with maintenance and validation activities to minimise downtime
• Conduct batch record review and verification, including timely BPR corrections
• Support cycle counts, inventory accuracy and SAP master data review
• Follow SOPs and maintain Good Documentation Practices
• Contribute to hazard and near miss identification, incident investigations and CAPA
• Participate in Safe by Choice discussions and model inclusive behaviours
• Support compliance audits, event investigations, change management and environmental monitoring
• Maintain good housekeeping and ensure equipment is fit for purpose and safe to use
• Support adherence to relevant quality standards and manufacturing requirements
• Apply MPS tools and methodologies to support investigations and CAPA implementation
• Contribute to technical process advancement and growth strategies in Production
• Participate in Site Tier communication processes and cross-functional tier meetings
• Support cost mitigation and innovation initiatives that improve manufacturing performance
• Participate in competency-based training, priority setting and development planning
• Escalate issues that may impact the production schedule
• Coordinate activities during periods of leave or offsite work where required
• Raise purchase requisitions and manage limit orders as needed
• Perform SAP transactions within required timeframes
• Report to the Line Lead

Production Technologist

Accounting Manager

• Execute and review month-end, quarter-end and year-end close activities in accordance with corporate accounting policies and local statutory requirements
• Ensure accuracy and integrity of general ledger balances and financial reporting
• Prepare and review complex journal entries, accruals, provisions and balance sheet reconciliations
• Support the preparation of statutory financial statements and other local reporting obligations
• Coordinate audit requests and provide support during external and internal audits
• Partner with Tax teams in the preparation and review of corporate income tax calculations and tax provisions
• Monitor changes in accounting and tax regulations and assess potential impacts on financial reporting
• Identify and implement opportunities for process simplification, standardization and automation
• Lead and participate in cross-functional and global projects impacting finance processes and reporting
• Serve as a key liaison between Finance, Tax, Business Services and external stakeholders
• Leverage data, automation and digital solutions to improve financial processes, strengthen controls and generate actionable insights

Accounting Specialist

Research Scientist

• Support the strategic design, development, and delivery of efficient, flexible, and modular analysis, reporting, and submission standards and tools for drug and vaccine projects across therapeutic areas
• Drive data structures encompassing analysis and reporting data standards and submission standards
• Lead and contribute to departmental strategic initiatives
• Collaborate with Biostatistics, Statistical Programming, Data Management, Clinical Research, Regulatory, Observational Research, Clinical Safety, and PK/PD Modeling and Simulation organizations
• Develop and drive adoption of a scalable, reusable multilingual standards library based on R, Python, and SAS
• Emphasize open-source adoption, automation, and appropriate use of AI
• Address operational challenges through strategic, standards-based solutions
• Facilitate global adoption of standards and programming best practices
• Provide technical consultation and analytical support to statistical programmers and statisticians
• Represent the company in relevant industry initiatives, including CDISC and PHUSE

MSD