Johnson & Johnson

Robotics

• Instills and drives a vibrant regulatory culture, working among cross functional groups as a teammate and collaborator.
• Applies strategic regulatory thinking along with technical expertise to develop and implement regulatory strategies for new product clearances and approvals.
• Prepares and submits regulatory information required to obtain global market access, including preparation, writing and filing of FDA submissions (e.g., Q-submissions, IDEs, De Novo, 510(k)s) and global health authorities’ submissions technical documents.
• Serves as a Regulatory Affairs subject matter expert on new product development and engineering design control teams.
• This includes conducting reviews and providing expert regulatory feedback for specifications, device testing, risk management, and other relevant documentation in accordance with regulatory requirements and with positioning for regulatory submission.
• Proactively identify issues, effectively communicate timelines for project completion, and address complex issues that may impact registration status.
• Conduct regulatory evaluation of changes to devices in accordance with requirements of commercial/operating geography and generate the required regulatory submission (including Letters To File).
• Guides conformance with applicable regulations and guidance documents in product development, support of claims, content labeling, and promotional materials.
• Assists in the development of Regulatory Affairs processes.

Senior Regulatory Affairs Program Lead – Robotics & Digital Solutions, MedTech Surgery

Director

• Accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s).
• Oversee resource allocation, adherence to timelines and budget, compliance with relevant SOPs, policies, HCC and local regulatory requirements.
• Support the Site Enablement Leader in shaping and managing local organizational structure.
• Responsible for line management of Functional Managers (FM), and/or other Site Enablement staff.
• Oversee staff performance, development, training, project assignments, workload distribution, and supports issue resolution with direct reports.
• Ensure alignment of local goals with organizational objectives.
• Drive innovative solutions and process improvements for the Oncology therapeutic area, Site Enablement, and GD overall.

Director, Site Enablement – U.S. Oncology

Sales Operations Manager

• Lead the evolution of Johnson & Johnson's US Surgery sales enablement ecosystem.
• Drive the transition from legacy platforms to the next-generation Sales Enablement ecosystem.
• Own product strategy, roadmap execution, business alignment, and cross-functional delivery.
• Deliver a unified commercial experience that combines sales planning, opportunity intelligence, performance analytics, pricing optimization, and AI-powered recommendations.
• Ensure seamless integration with Microsoft's Dynamics-based Butterfly ecosystem and enterprise data platforms.
• Champion AI-enabled reporting and sales intelligence capabilities.

Manager – Sales Enablement, Product Management

Brand Manager

• Support day-to-day Brand Review operations and governance processes: Monitor the Brand Review inbox and queue
• Triage submissions, help organize review priorities
• Provide timely, practical guidance on campaign assets, program names and wordmarks, event collateral, and more.
• Manage routine requests and escalate complex issues to appropriate team members.
• Partner with Brand leads across business units to help implement the MedTech brand across assets and support consistent brand execution.
• Maintain Brand Review standard operating procedures (SOPs), helping keep them practical, clear, and reflective of current business needs.
• Support social media brand governance by reviewing social content, providing brand guidance, and partnering with social leads to help ensure platform-appropriate brand consistency.
• Help maintain and expand a reusable social media template library and component toolkit to support on-brand content production across teams.
• Identify and integrate appropriate AI capabilities into brand workflows, templates, and governance processes to improve efficiency, consistency, and scalable content development while maintaining brand and compliance standards.
• Coordinate production of the MedTech Brand quarterly newsletter: gather content, support layout development, and help coordinate distribution to keep partners informed of brand updates, wins, and guidance.
• Support creative explorations with agency partners by helping prepare briefs, coordinate timelines, and review concepts that broaden MedTech’s visual language and asset diversity.
• Assist with the development of new visual assets, including medical illustrations, hero product illustrations, photography, and iconography, and help ensure high-quality, metadata-tagged additions to the Brand Center.
• Coordinate with the Enterprise Brand team to help implement enterprise visual identity updates and support consistent, compliant MedTech applications.
• Track and report on brand consistency and the effectiveness of brand tools and processes, sharing observations and recommended improvements based on metrics and customer feedback.
• Build collaborative partnerships with business units by serving as a helpful brand resource, supporting teams with practical guidance while preserving brand integrity.
• Help educate stakeholders on brand standards to encourage consistent execution, stronger creative outcomes, and greater confidence using brand tools and guidance.
• Apply Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day work, decision-making, and partner interactions to support alignment with enterprise values.

MedTech Brand Manager

Business Analyst

• Partner with Account Management and Offer Development team members to proactively support and influence contracting needs for our top customer segment.
• At the direction of management, direct and manage commercial contract terms and conditions negotiation.
• Support and help prioritize and manage workload queue.
• Draft, review, and negotiate terms and conditions in commercial contract documents, and participate in customer calls as necessary.
• Work with the Manager and Senior Manager, Contact Management to facilitate internal contract approval and stakeholder negotiation to resolve complex issues and assist in disputes (e.g., escalating complex legal and factual issues to the appropriate internal parties, e.g., Supply Chain, Human Resources, Corporate Risk Management, Health Care Compliance, Privacy, Commercial Programs Legal Group (CPLG)).
• Develop and maintain positive business partnering relationships with Legal, Offer Development, Health Care Compliance and Field Sales Organization.
• Proactively support the design and implementation of systems, processes, and controls to track and manage the contracting process to enhance efficiency and compliance.
• When assigned, facilitate effective communication and collaboration with internal partners, consistent with company mission and values, to ensure that actions taken reflect terms of contracts and agreements.
• Provide regular mentorship and training to Contract Management team members and to business partners to ensure they understand contractual requirements as well as the general legal and compliance environment.
• Ensuring conformity to business needs, accurate risk allocation, and compliance with DePuy Synthes Orthopedics’ policies and procedures.
• Partner with Offer Development and Field to resolve any discrepancy or gaps in pricing approvals.
• Implementation of price changes resulting from contract maintenance activity to include scheduled price increases stipulated in the contract and compliance price adjustments for noncompliant accounts.
• Generate contract price files, integrated delivery network (IDN) roster maintenance on contracts, creation of member-add letters, and draft amendments.
• Write and/or maintain assigned standard operating procedures and work instructions and help monitor adherence for related processes.
• Provide timely response to internal and external audit requests.

Lead Analyst, Contract Management

Data Scientist

• Be a hands-on scientific and technical leader, leading a portfolio of RWE projects, developing best practices, and mentoring team members.
• Identify common technical requirements for RWE projects, develop and maintain a common suite of tools that enable RWE data scientists to accelerate project delivery.
• End-to-end expertise in RWE studies including conceptualizing research questions, data feasibility, study design, analysis, programming, and interpretation.
• Provide thought leadership and hands-on programming expertise for developing and applying Real-World Data (“RWD”) methodologies to mitigate observed and unobserved biases in the execution of external control arm studies, hybrid control studies, comparative effectiveness analyses, etc.
• Provide thought leadership and hands-on programming expertise to generate actionable insights from post-hoc RCT analyses, observational databases, and literature reviews to support regulatory agency interactions.
• Independently create study protocols, statistical analysis plans, and statistical programming deliverables including analysis-ready data, tables and figures.
• Partner with the Data Science Therapeutic Area scientists to conceptualize, lead, shape and deliver Real World Evidence.

Senior Principal Scientist, Data Science RWE

Data Analyst

• Lead the design, implementation, and evolution of scientific data products and integration strategies supporting AI-enabled drug discovery and development
• Create scalable, interoperable, and AI-ready data products connecting discovery, preclinical, clinical, safety, and real-world evidence domains
• Establish data architecture, integration strategy, metadata framework, and productization approach for semantic reasoning, knowledge graphs, GraphRAG, advanced analytics, and agentic AI applications
• Define the future-state scientific data ecosystem
• Build AI reasoning models to support data-driven translational safety decision making
• Partner with Amazon engineering and deployed platform resources to deliver scalable data pipelines and data products
• Define implementation strategy for scientific data products deployed on AWS, ensuring alignment with enterprise architecture, security, governance, and AI-readiness requirements

Principal Scientist, Data Science – Data Products, Integration & Analysis

• Lead operational planning and execution of the enterprise AI Literacy strategy across multiple geographies and business functions.
• Develop and maintain scalable operating models, governance structures, processes, and delivery frameworks supporting AI Literacy initiatives.
• Manage the end-to-end delivery of virtual and in-person AI Literacy learning programs for approximately 15000 employees globally.
• Coordinate schedules, timelines, resources, dependencies, and implementation activities across multiple workstreams.
• Manage external vendors, agencies, and contractors responsible for training delivery and operational support.
• Monitor vendor performance, contractual obligations, service levels, and delivery outcomes.
• Manage program budgets, forecasts, resource plans, and operational expenditures.
• Drive continuous improvement initiatives focused on operational efficiency, scalability, and cost effectiveness.
• Implement processes and controls that support sustainable growth of the AI Literacy program.
• Lead continuous improvement efforts through data-driven decision making and performance analysis.

Director, R&D Data Science – Operations & Community Lead

Manager

• Execute real estate transactions including leases, renewals, expansions, and dispositions
• Manage transactions through full lifecycle
• Ensure all deals are executed on time, within financial targets, and aligned to business and portfolio strategy
• Lead negotiations with landlords, developers, and third-party providers
• Structure agreements balancing cost, flexibility, risk, and business requirements
• Ensure adherence to company policies, regulatory requirements, and country-specific considerations
• Partner with Governance & Strategy on business cases, approvals, and prioritization
• Support portfolio initiatives including site consolidations, expansions, relocations, and exits
• Maintain accurate, audit-ready lease and transaction documentation
• Provide clear decision support and trade-off recommendations to stakeholders
• Act as a trusted advisor to business and country leadership on transaction decisions
• Manage external brokers and transaction service providers
• Support execution of end-to-end site delivery lifecycle

Manager, Transaction Management – APAC

• Partner with cross-functional teams to define a neuropsychiatric digital health roadmap that integrates AI/ML (e.g., foundation models), data science, and company priorities across the patient journey, ensuring clinical relevance and patient-centered outcomes.
• Monitor emerging technologies in neuropsychiatry, digital phenotyping, remote assessment, passive sensing, and speech and language analytics to bring forward next-generation solutions for neuropsychiatry R&D.
• Execute the neuropsychiatry-focused digital health strategy by applying AI/ML, modeling, and longitudinal analytics to support patient stratification, endpoint development, and clinical trial optimization, in partnership with disease experts, statisticians, and platforms and clinical teams on study design and validation of digital measures, balancing their informativeness with low clinical burden for patients and study teams.
• Develop and apply sophisticated statistical/ML/AI models using digital health data to generate insights into disease and treatment outcomes.
• Develop multimodal approaches combining digital health data with imaging, blood-based biomarkers, omics, and real-world data to provide a more holistic picture of patients suffering from neuropsychiatric disease.
• Contribute to evidence packages to support regulatory qualification of digital endpoints and tools.
• Ensure validation and compliance with evolving global regulatory and data privacy standards.
• Collaborate with clinical operations to integrate digital health technologies into trial design, working cross-functionally to optimize data capture, integration, and interoperability of digital solutions.
• Partner with regulatory and medical affairs to build external collaborations with academic groups, technology partners, regulators, health authorities, and payers to advance digital health standards and novel endpoints.

Senior Manager, R&D Data, Data Science, AI – Digital Health for Neuropsychiatry

Supervisor

• Oversee daily warehouse operations and domestic transportation managed by 3PL
• Coordinate cold chain operations in collaboration with internal teams and external partners
• Monitor shipment execution and ensure proper documentation and filing
• Manage inventory accuracy through reconciliation and cycle counts
• Resolve operational issues in day-to-day activities
• Monitor and manage KPIs through regular review meetings with 3PL partners
• Drive continuous performance improvement at DCs
• Control logistics costs within budget
• Manage warehouse capacity planning and optimize transportation flows
• Ensure compliance with GDP, Trade & Customs, and EHS&S requirements
• Maintain adherence to Korean regulations for pharmaceutical storage and distribution
• Coordinate internal and external audits at 3PL facilities
• Lead warehouse and distribution-related projects
• Drive Cost Improvement Projects (CIP) to achieve productivity and efficiency gains
• Partner with regional/global teams to implement new initiatives
• Improve end-to-end supply chain performance
• Collaborate with internal stakeholders including EM Planner and Cold Chain teams
• Build strong partnerships with 3PL and external stakeholders to support business growth

Warehouse & Distribution Supervisor

• Provide strategic and technical leadership to ensure the scientific rigor of data generation initiatives across the Johnson and Johnson portfolio of innovative medicines.
• Maintain deep expertise in evolving methodologies, including proactive awareness of regulatory, Payer/HTA, and guideline/formulary evidentiary requirements.
• Review, synthesize, and disseminate external case studies and precedents to shape internal strategy and analyses.
• Act as key reviewer for the Global RWE Methods Review Board, ensuring robust governance and methodological consistency across programs.
• Lead the design of advanced study designs and statistical analyses aligned with Payer/HTA expectations (e.g., indirect treatment comparisons, causal inference methods, surrogate endpoint validations, etc.) to support market access and launch strategies for key assets.
• Provide key contributions to capability building, including training for team on Payer/HTA requirements and new methodologies and also in the development of coding libraries and AI/ML advanced analytics scaling and platforms, etc.

Director, HTA Statistics – RWE Methods

Consultant

• Responsible for the success of the sales territory
• Lead, motivate and inspire the team
• Responsible for the personal and professional development of the team
• Implement commercial and clinical strategies
• Build and maintain long-term customer relationships
• Collaborate with other departments and the Regional Business Manager

Regional Consultant Manager – Electrophysiology

• Maintain deep expertise in evolving methodologies, including proactive awareness of regulatory, Payer/HTA, and guideline/formulary evidentiary requirements.
• Review, synthesize, and disseminate external case studies and precedents to shape internal strategy and analyses.
• Act as key reviewer for the Global RWE Methods Review Board, ensuring robust governance and methodological consistency across programs.
• Lead the design of advanced study designs and statistical analyses aligned with Payer/HTA expectations (e.g., indirect treatment comparisons, causal inference methods, surrogate endpoint validations, etc.) to support market access and launch strategies for key assets.
• Provide key contributions to capability building, including training for team on Payer/HTA requirements and new methodologies and also in the development of coding libraries and AI/ML advanced analytics scaling and platforms, etc.

Director HTA Statistics – RWE Methods

Financial Planning and Analysis

• Supporting and optimizing global intercompany pricing processes across complex supply chain structures while ensuring compliance with Tax and SOX requirements.
• Combining finance, data analytics, and project support, including ICP calculations, standard cost and data loads, subsidy reporting, year-end close activities, and ERP system coordination.
• Working closely with cross-functional teams and strategic initiatives.
• Developing data workflows, dashboards, and reporting solutions to provide business insights and support decision-making.
• Partnering with Tax, Planning, Supply Chain, and IT teams to document processes, maintain master data integrity, support audits, and ensure accurate implementation of pricing models across multiple systems.
• Mapping out and documenting impacted supply chain flows to ensure adherence to the tax model in close collaboration with the tax planning group.
• Coordinating the timely loading of the calculated data including ICP and Std Cost in the various ERP systems (i.e., JDE 8.12, S/4Hana) and building necessary checks to ensure flawless data set-up and go-live without delays in servicing customer orders.