Johnson & Johnson

Research Scientist

• Provide CMC regulatory support for submissions in China
• Focus on antibody products and BLA preparation
• Ensure registration testing support at NIFDC or PFDA Laboratories
• Participate in task forces and comment on regulations
• Guide local, regional, and global associates

Senior Principal Scientist, CMC Regulatory Affairs - Biological

Compliance

• Ensure the timely registration and market access of medical devices across the MSM region in compliance with applicable European, FDA, national, and regional regulatory requirements.
• Provide strategic regulatory leadership and partner closely with business stakeholders.
• Lead regulatory affairs activities across the MSM region to support business growth and market access objectives.
• Drive regulatory shaping and outreach initiatives through engagement with Health Authorities, regulatory agencies, and industry trade associations.
• Assess and communicate the impact of changing regulatory requirements on products, registrations, licenses, and business operations.
• Act as Regulatory Affairs Lead on cross-functional projects and regulatory initiatives.
• Ensure compliance of the medical device portfolio with applicable regulatory requirements and company policies.
• Lead continuous improvement initiatives to strengthen regulatory processes and operational excellence.
• Ensure audit and inspection readiness and represent Regulatory Affairs during internal audits and Health Authority inspections.
• Communicate regulatory compliance updates, risks, and recommendations to leadership and key stakeholders.
• Oversee the Copy Review process and support compliant promotional and non-promotional communications.
• Lead, coach, and develop direct reports while fostering a high-performing and collaborative team environment.
• Identify opportunities for process optimization and cost efficiencies.
• Ensure compliance with all applicable quality, legal, ethical, and Healthcare Compliance (HCC) requirements.

Associate Director, Regulatory Affairs, Electrophysiology

Product Manager

• Manage products for AI-driven tools supporting regulatory and other R&D workflows, including regulatory strategy and innovation, productivity, document workflows, decision support, and automation.
• Develop and maintain product roadmaps aligned with business objectives and evolving AI capabilities.
• Collaborate with business and technology teams to define product strategy, vision, and execution with a cross-functional product team, translating human-centered workflows into clear requirements, wireframes, and user stories.
• Support prioritization across competing initiatives, balancing impact and feasibility.
• Identify opportunities where generative AI can streamline document creation, review, and knowledge access.
• Partner closely with regulatory teams to develop solutions fit-for-purpose and integrated into key workflows.
• Engage partners across R&D to understand and incorporate opportunities for synergy.
• Collaborate with data scientists, ML engineers, platform teams, UX, and business partners in a matrixed environment.
• Support alignment among technical and business teams.
• Provide product updates and insights to leadership across Data Science and Digital Health.
• Support end-to-end product lifecycle from concept to launch and iteration.
• Define user stories, acceptance criteria, and success metrics.
• Manage backlogs and coordinate sprints with technical and design teams.
• Ensure products meet quality, usability, security, and compliance expectations.
• Partner with engineering teams on model integration, data prep, and evaluation cycles.
• Apply knowledge of generative AI, RAG, agentic systems, and prompt engineering to shape product capabilities.
• Collaborate with data and platform teams to leverage AI-ready datasets and vector retrieval pipelines.
• Support change management and adoption of AI-enabled tools through onboarding and feedback loops.

Associate Director, Product Management

Insurance

• Supporting end‑to‑end Microbiological Quality & Sterility Assurance (MQ&SA) activities related to suppliers and external manufacturing processes
• Contributing to change requests and projects impacting controlled environments, cleaning, and sterilization processes
• Supporting contamination control strategies, including environmental monitoring and investigation activities
• Providing technical guidance and training on microbiological quality and sterility assurance
• Acting as subject matter expert for investigations, CAPA, non‑conformances, audit observations, and risk assessments
• Supporting due diligence activities (e.g., acquisitions, partnerships) by providing MQ&SA expertise and risk input
• Supporting development and updates of supplier quality agreements
• Coordinating and participating in supplier audits, including preparation, on‑site support, response review, and follow‑up activities
• Partnering with cross‑functional teams to support supplier qualification and lifecycle management
• Contributing to remediation activities following audits or regulatory findings
• Building strong relationships with external partners, including manufacturers, suppliers, sterilization providers, and testing laboratories
• Coaching and supporting colleagues and partners in MQ&SA practices

Staff Scientist – Microbiology, Sterility Assurance

Manager

• leads the health economics activities for our Electrophysiology portfolio at Johnson & Johnson MedTech through the development and execution of robust health economic arguments and tools to support funding and procedural adoption.
• This regional role is responsible for Emerging Markets and works closely with local market-access and government-affairs teams.
• It ensures we have the necessary health-economics and market-access capabilities and that we convey a clear, value-based message to customers.
• Partner with key local and regional functional and external collaborators to contribute to the overall strategy, developing evidence and value communication tools and messaging aligned to the EP portfolio.
• Support the development of health economics tools, translating complex messages into simple statements that can easily be articulated by the sales force.
• Accountable for health economic input into novel local commercial initiatives requiring substantiation of value, including but not restricted to value-based procurement and value-based agreements.
• Work closely with the marketing, clinical, and sales teams to ensure the alignment of market access activities with overall business objectives.
• Provide input into the evidence generation strategy for new product development and identify local opportunities for health economic evidence generation.
• Support the adaptation and local approval of regionally developed HEMA tools, translating complex messages into simple statements that can easily be articulated by the sales force.

Health Economics & Market Access Manager, Electrophysiology, Emerging Markets

General

• Collaborate with J&J Oncology field teams peers to build relationships with key stakeholders in community accounts
• Educate and train staff on appropriate efficiency practices to support delivery of our products
• Act as Responsible subject matter expert (SME) on the economic value story and key private and public payer changes that impact delivery process for our products for both inpatient and outpatient settings
• Advise on patient affordability programs that are available to assist patients financially.
• Partner with J&J local teams to ensure staff in accounts have been trained using company approved materials to deliver pharmaceutical products in a safe and efficient manner
• Partner with J&J local teams to train appropriate clinical staff re: technical aspects of product delivery, administration, monitoring, and adverse event management and reporting.
• Assist members of sales force (e.g., Oncology Specialists, District Managers) in all aspects of product promotion, including but not limited to product access, pull-through and reimbursement.
• Support patient care and transition between sites of care to optimize patient adherence and ensure a mix of viable sites of care are available in the local marketplace.
• Mentor doctors and staff on practice management including but not limited to, how to develop and implement an end-to-end delivery of J&J products including overall operations management, scheduling, staffing, pre-authorization, reimbursement, capacity management, inventory management, and management/efficiencies.
• Help Community sites remove operational barriers with hematology products (EHR/Order Sets updated, transitions of care, partnerships).
• Drive the pull through of brand resources like professional education
• Implement EHR patient identification pull through and embed patient access & affordability resources into Community EHR systems in partnership with other Field teams
• Approach each customer from a total account management perspective, by leveraging resources appropriately, collaborating with business partners and accurately articulating the value proposition for the customer.

Oncology Area Business Specialist – Hematology

Systems Engineer

• Lead and execute multiple waves of integration between Transcend S/4 OTC and Planning Systems (APS), including design, build, testing, training, cutover, and go‑live activities.
• Collaborate with key workstreams—including Business SMEs, Product Owners, JJT, OMP, S/4, PLAN BPO, and business stakeholders—to drive day‑to‑day operations and maintain effective cadences.
• Ensure strong alignment with Business Units and central functions.
• Manage relationships with external vendors and integrators, including planning, and resource management.
• Provide effective stakeholder management through frequent updates on decisions, progress, risks, and key issues.
• Lead the operational delivery of the program, including managing team performance, schedules, and cross‑functional execution.
• Ensure all User Stories and KDDs in JIRA for Global Template processes are fully solutioned, tested, and successfully deployed.
• Own the creation and maintenance of training materials, and deliver training across the planning community as part of business adoption.
• Lead and coordinate project managers and indirect/external resources to deploy the program.
• Build strong alignment and collaboration with partner functions, including J&J Technology, MT SC Digital, Commercial, Business Unit Supply Chain, and Integrated Business Management.

Plan Systems Integration, Senior Analyst

• Execute regulatory submissions (registrations, variations, renewals) and support product lifecycle management
• Ensure compliance with local regulations, GxP standards, and company SOPs; maintain inspection-ready documentation
• Support audit and inspection readiness, including responses to Health Authority queries and CAPA tracking
• Maintain regulatory documentation and manage data in regulatory and quality systems
• Monitor regulatory changes and support implementation across the portfolio
• Collaborate cross-functionally (Medical, Safety, Quality, Supply Chain) to ensure compliance and supply continuity

Regulatory Affairs & Compliance Specialist

• Supporting chamber monitoring readiness
• Yokogawa panel replacement activities
• Change control execution
• Financial planning within Biologics AD
• Ensuring operational continuity and compliance
• Maintaining and verifying chamber monitoring tracking information
• Supporting change controls related to chamber updates
• Partnering with chamber owners and service providers
• Serving as a business lead and subject matter resource for COMET change control processes
• Maintaining reports, dashboards, and periodic updates
• Supporting monthly financial close and reporting activities
• Developing and managing capital and expense budgets
• Monitoring project performance against forecasts and updating budgets

Scientist, Biologics Analytical Development, Proteins

• Technology Ownership - Own the technology and its future! Develop and routinely update the global strategy and roadmap for the designated manufacturing process, considering external market, competitor, and technology trends.
• Process Standardization & Optimization - Drive global process excellence by ensuring that process changes and improvements are effectively communicated and adopted across all manufacturing sites. Establish and maintain global validation strategies and support relevant audits specific to the process, fostering continuous improvement and compliance.
• Subject Matter Expertise - Act as the go-to expert for all technical aspects of Machining processes across all sites, with an unparalleled understanding of the existing process and the opportunities that can be harnessed to drive step-change improvements. Approve and endorse process changes, including new equipment, upgrades and modifications, ensuring compliance with internal standards and regulatory requirements.
• Support, Collaboration & Governance - Provide technical support and governance on existing initiatives within the business, working collaboratively with cross-functional teams to resolve challenges and streamline operations.
• Capability Building - Work collaboratively with the business to ensure that it has the investments, infrastructure, capital and talent required to implement the technology strategy and roadmap.
• New Initiatives - Support the development of new programme charters and initiatives by providing expert guidance on timelines, costs, risks, and benefits during development and implementation of new innovations.
• Data & Metrics Reporting - Collect, analyze, and report metrics related to the process, such as performance trends, aligning these insights with overall business metrics.

Global Process Owner – Machining & Finishing

Financial Planning and Analysis

• Own budget management and forecasting for multiple groups simultaneously, each with distinct goals, stakeholders, and reporting needs.
• Partner cross-functionally with department leaders to build, track, and adjust budgets in accordance with planning cycles.
• Provide financial leadership – translating data into clear recommendations that shape strategic and operational decisions.
• Influence stakeholders at varying levels of seniority, even without direct authority, to drive sound financial decision-making.
• Identify risks, variances, and opportunities across budgets, and proactively flag them to leadership.
• Build financial models and reporting tools that scale across multiple business groups.
• Drive month-end/quarter-end close activities including variance analysis and forecasting updates.
• Manage, coach, and develop team members, fostering a culture of accountability, collaboration, and continuous improvement.
• Lead a team of 1-2 Analysts.

Finance Manager – Commercial Excellence

• Represents Deliver through balanced role with other E2E pillars (Plan-Source-Make).
• Connects BU strategies and requirements into Deliver Center Operations and Capabilities teams, as well as the other way around.
• Partners with regions for critical processes and accountabilities, including Performance Mgmt., BP/LRFP, Flow Optimization, NPI execution, Margin Expansion.
• Partners with GSCS teams (GTTO, Trade Compliance) focusing on transportation / lane optimization, tariffs management and budget control.
• Infuse business specific priorities into the overall MedTech SC Deliver strategy and capability roadmap to accelerate BU growth.
• Incorporate and collaborate with E2E SC team to drive MedTech SC Deliver strategic plans associated with the respective BU ( i.e. product flow optimization, efficiency and productivity initiatives for hubs and transportation, capacity and capabilities improvement, etc.).
• Ensure visibility into global Hubs priorities and performance, and drive global aggregation through partnership with Regional SC Leads.
• Shared accountability for performance metrics, including OTIF-SC and OTIF-D as part of E2E SC; drives continuous improvement against failure modes linked to Deliver including partnering to address E2E issues.
• Ensure on time delivery of NPI and new capabilities through Deliver Playbook adherence and maturity.
• Shared accountability with E2E SC for optimizing inventory levels through improvement on unproductive inventory reductions at Hubs, international lanes reliability and leadtime compression and E2E product flows design.
• Shared accountability with Global E2E SC for driving COGS reduction in freight and warehousing and margin expansion across; ensures a process is in place to provide visibility to Deliver cost performance and improvement, jointly sets and works to achieve cost optimization targets.
• Shared accountability with Global E2E SC to ensure a robust foundation in compliance including trade compliance, Quality, EH&S, financial compliance.
• Develops talent and maintains leadership pipeline; actively sponsors and mentors key talent across E2E supply chain, builds leadership competencies in team.
• Responsible for Deliver integration into core global processes (e.g., STEM, issue management / escalations, strategic capacity planning, S&OP, IBP and E2E flow optimization).

Manager, Delivery Business Unit Integration, Med Tech

• Own the end-to-end customer success strategy for MedTech Supply Chain digital products, from onboarding through ongoing adoption and value optimization.
• Serve as the primary escalation point and trusted partner for internal customers, ensuring alignment between business needs and product capabilities.
• Proactively identify adoption risks and drive mitigation plans to ensure long-term product success.
• Establish and manage a product analytics framework to monitor usage, adoption, performance, and business impact of digital solutions.
• Translate data and insights into clear, actionable recommendations for product teams, leadership, and customers.
• Develop executive-ready dashboards and narratives that clearly articulate product health and value.
• Lead onboarding as a structured program, including scope, timelines, dependencies, risks, and organizational change.
• Coordinate cross-functional teams (IT, Product, Data, Operations, Training) to ensure seamless deployments.
• Standardize onboarding playbooks, templates, and protocols to enable scalable product launches.
• Act as a liaison Supply Chain Operations, Digital/Product teams, Data & Analytics, and IT.
• Influence without authority to align diverse collaborators around shared outcomes and priorities.
• Communicate clearly and credibly with senior leaders, translating technical concepts into business value.
• Coach and mentor customer success and project management resources, fostering a high-performance, customer-centric culture.
• Define and evolve the Customer Success operating model for Supply Chain Digital, including roles, processes, and governance.
• Drive continuous improvement through lessons learned, retrospectives, and feedback loops.
• Contribute to broader digital transformation efforts by shaping standards, metrics, and ways of working.

Senior Manager, Program Success

Executive Assistant

• Provide comprehensive, proactive administrative support to the Vice President, Results & Impact, including complex calendar management, meeting prioritization, and scheduling across global time zones.
• Serve as a strategic gatekeeper for the VP’s time, using judgment to appropriately sequence, prioritize, and resolve competing demands.
• Prepare the VP for internal and external engagements by coordinating pre-reads, briefing materials, agendas, and follow-ups.
• Anticipate needs and resolve issues independently to support effective executive decision-making.
• Coordinate leadership meetings, working sessions, and cross-functional forums, including agenda development, material consolidation, note-taking (as needed), and action-item tracking.
• Manage end-to-end logistics for high-stakes meetings (in person and virtual), including participant coordination, room reservations, technology support, and follow-ups.
• Ensure timely flow of information between the VP, direct reports, peers, and stakeholders.
• Act as a key liaison between the Global RE, FM & Corporate Operations team and broader Supply Chain & Operations leadership, Enterprise partners (e.g., Finance, HR, IT), and other business stakeholders.

Senior Principal Scientist, CMC Regulatory Affairs - Biological

Associate Director, Regulatory Affairs, Electrophysiology

Associate Director, Product Management

Staff Scientist – Microbiology, Sterility Assurance

Health Economics & Market Access Manager, Electrophysiology, Emerging Markets

Oncology Area Business Specialist – Hematology

Plan Systems Integration, Senior Analyst

Regulatory Affairs & Compliance Specialist

Scientist, Biologics Analytical Development, Proteins

Oncology Area Business Specialist – Hematology

Global Process Owner – Machining & Finishing

Finance Manager – Commercial Excellence

Manager, Delivery Business Unit Integration, Med Tech

Senior Manager, Program Success

Executive Admin