Johnson & Johnson

Program Manager

• Responsible for the strategic leadership, governance, long-term evolution, and overall performance of the GOLD Program.
• Serve as the primary global leader for GOLD and is accountable for program strategy, governance, stakeholder engagement, workforce planning, development architecture, program outcomes, and continuous improvement.
• Lead the GOLD Program Office team, providing direction, prioritization, oversight, and escalation support.
• Ensure operational excellence, participant experience, and program outcomes are delivered at a best-in-class level.
• Build and maintain strong partnerships with Executive Sponsors, Program Champions, senior leaders, HR partners, Talent Acquisition, and key business stakeholders.

Senior Manager, Supply Chain Leadership Development – GOLD Program

Manager

• Educate HCPs on reimbursement processes, claims submissions, procedures, and coding requirements of payer organizations (local payers, government payers, etc.) for core and launch products.
• Collaborate with field support team members such as sales representatives and key account managers and serve as reimbursement expert for the local team.
• Act with a sense of urgency to address critical access and affordability issues for patients.
• Partner with managed care colleagues to understand current policies and potential future changes.
• Conduct field-based reimbursement and access support, education and creative problem-solving aligned to FRM Rules of Engagement.
• Build strong, trust-based relationships with customers in all assigned Oncology accounts.
• Manage territory logistics, routing, and account business planning.
• Maintain and grow knowledge of national, regional, local, and account market dynamics including coverage and coding requirements.
• Grow the knowledge of hub and specialty distribution channels to improve practice and patient support needs.
• Collaborate with internal J&J departments such as marketing, sales, medical science, SCG, IBG, HCC, and PECS.
• Serve as subject matter expert regarding education and insights on access and affordability solutions across multiple payer types and plans (i.e., Medicare, Medicaid Managed Care, Commercial).
• Execute business in accordance with the highest ethical, legal, and compliance standards, including timely and successful completion of all required training.

Field Reimbursement Manager – Oncology

General

• Evidence-based decision making for the severity of harms as a result of device-associated hazardous situations and associated probabilities of harm.
• Documenting, explaining, and defending device risk assessment decisions made, and updating Product Risk Management (PRM) deliverables based on new evidence and inputs from cross-functional peers and stakeholders.
• Representing Global Medical Safety at RMTs and quality event meetings convened for device assets.
• Review and sign off on device Product Risk Assessments (PRA) and other PRM deliverables requiring medical input.
• Leading standardization initiatives, including the development and maintenance of a global harms list.
• Ensuring a complete and comprehensive knowledge base of in-scope device assets and programs across the portfolio and product lifecycle, including but not limited to integral and non-integral medical devices, in vitro diagnostics, and software-as-a-medical device.
• Ensuring successful and compliant resolution of competing priorities and objectives across multiple stakeholders and programs.
• Meeting performance and risk metrics for device workflows that support strategic decision-making.
• Supporting special projects and initiatives as needed.

Device Safety Officer

• Lead Product Strategy Roadmap development and alignment, partnering with Value Stream leadership to prioritize initiatives that support VS objectives and E2E supply chain goals.
• Drive execution of strategic programs and LCM project plans, to deliver defined business outcomes.
• Define, manage, and communicate performance metrics, diagnostics, and control tower insights to track progress, identify risks, and surface improvement opportunities.
• Partner with VS teams and functional leaders to deliver Continuous Improvement, cost improvement, JJOS deployment, and Value Capture Planning initiatives tied to operational and financial targets.
• Collaborate with supply chain functions, commercial teams, R&D, Finance, Product Management, and NPI launch leads to enable strategic decision-making and seamless integration of new products through Stage Gates 3–6.
• With VS teams, advance key LCM processes, including Product Risk Assessment, Issue Management, and Value Stream Optimization, to improve execution discipline and value stream performance.
• Facilitate Lean Six Sigma and operational excellence events for the Value streams, including Lean-driven workshops and problem-solving sessions, to deliver breakthrough process improvements, strengthen standard work, and drive measurable business results.

Business Excellence Program Manager

Analytics Engineer

• Design and maintain production-grade data pipelines and curated datasets that directly support pharmacovigilance activities, including safety monitoring, analytics, and regulatory reporting.
• Ensure data engineering solutions produce reproducible, explainable, and trusted analytics outputs suitable for safety decision support and inspection readiness.
• Enable AI/ML and GenAI workflows for safety analytics, including: Feature engineering and feature store enablement, Embeddings, vectorized representations, and semantic retrieval, Retrieval-Augmented Generation (RAG) patterns for safety analytics tools.
• Own the end-to-end data lifecycle for safety analytics, from source system intake through transformation, serving, and downstream analytical consumption, ensuring data continuity, traceability, and integrity.
• Lead architectural decisions across ingestion, transformation, storage, and serving layers on GCP (e.g., BigQuery, Dataform, object storage).
• Design, implement, and automate scalable, reusable data pipelines and architectures to support evolving safety analytics needs.
• Establish and enforce data quality, validation, lineage, and observability standards for safety analytics datasets.
• Define and implement data governance practices, including data contracts, schema versioning, access control, stewardship, and lifecycle management.
• Ensure safety analytics data and systems meet Global Medical Safety requirements for reliability, auditability, and regulatory use.
• Apply GxP validation expertise to data pipelines, analytics services, and supporting infrastructure.
• Partner with quality and compliance teams to implement CSV/CSA-aligned controls, audit trails, documentation, and organizational change.
• Design and build APIs and microservices-based architectures to operationalize safety analytics and ML capabilities (e.g., feature serving, retrieval services, analytics backends).
• Deploy and operate services on GCP (e.g., Cloud Run, GKE) with a strong focus on security, scalability, and observability.
• Serve as a technical authority and data engineering leader for Safety Analytics within Global Medical Safety.
• Review and influence designs across pipelines, services, feature stores, and AI/ML integrations to maintain a high technical bar.
• Collaborate closely with safety scientists, epidemiologists, biostatisticians, analytics teams, IT, and platform partners to translate safety needs into scalable technical solutions.
• Communicate complex technical concepts and tradeoffs clearly to both technical and non-technical stakeholders.

Principal Data Engineer – Safety Analytics

Operations

• Manage the day-to-day execution of GD communications activities, including planning, drafting, formatting/editing, coordinating inputs and approvals, preparing content for distribution, sending emails, managing calendar invitations, and tracking what needs to go out and when
• Maintain the GD communications calendar, global distribution lists, communications trackers, and follow-up processes to ensure timely execution and clear accountability
• Manage GD communications channels and platforms in partnership with enterprise teams, including serving as liaison to the Home team, coordinating Home postings, maintaining GD SharePoint sites, supporting channel governance, and ensuring content is current, accessible, organized, and aligned to enterprise and GD standards
• Support communications operations, reporting, and continuous improvement by developing, tracking, and reporting key performance indicators and metrics, including quarterly communications KPIs
• Pull external engagement updates from the GD tracker for monthly updates to the Head of GD, maintain deliverables trackers, monitor progress against timelines, and identify opportunities to improve communications processes, templates, and standards
• Support GD communications forums, meetings, and employee engagement channels, including coordinating monthly GD Communications Council meetings, managing monthly newsletter article submissions, supporting Senior Manager town halls and GD town halls, coordinating logistics for leadership forums and other meetings, and supporting people leader communications, toolkits, and related resources

Manager, Global Development Communications Operations

• Draft and produce high-quality, engaging GD-specific content across multiple channels and modern approaches to enable employee engagement and comprehension — inclusive of articles, newsletters, town halls, leadership memos, executive and leader communications (Head-of-GD, SBP cascades, 100-day plans), Viva Engage, and other internal channels as needed.
• Help coordinate the delivery and tracking of GD business communications across all functions in partnership with the Director, Global Development Strategy and Operations; align with Enterprise GCA on macro-level communications when appropriate; manage newsletter development and to facilitate effective delivery of communications.
• Ensure communications plans align to active change initiatives and support consistent messaging across GD without owning change methodology, frameworks, or governance.
• Support development and execution of select external initiatives including annual Clinical Trials Awareness Week and GD leader LinkedIn posts.

Senior Manager, Global Development Communications Operations

Robotics

• Collaborate with systems engineering to ensure requirements clarity, testability, and traceability from user needs, system and sub-system requirements, through verification and validation.
• Define minimum testable requirements post-change (risk-based, essential performance, basic safety).
• Develop and execute comprehensive V&V strategies and master system test plans for complex medical devices, including system verification protocols and regression plans that ensure robust requirements coverage; this includes investigational, integration, reliability, and formal V&V testing.
• Prepare and deliver system-level V&V documentation, including summary reports and verification results.
• Reviewing and approving sub-system verification deliverables to ensure alignment with overall system requirements.
• Design, validate, and implement test methods, including manual and automated test setups, to ensure they are suitable for verifying product requirements, including repeatability, reproducibility.
• Oversee the maintenance of robotics test lab facilities, ensuring all equipment and infrastructure are properly calibrated, serviced, and compliant with company safety, quality, and procedural standards; proactively identify and resolve issues to support uninterrupted testing and development workflows.
• Ensure compliance with regulatory standards (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 60601, ISO 14971).
• Support design transfer and product launch activities including complaints investigations.
• Investigate and document non-conformances, deviations, and test failures, drive root cause analysis and corrective actions.
• Interface with regulatory, quality, and manufacturing teams to support audits and inspections.
• Responsible for communicating business-related issues or opportunities to next management level.
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams.
• Support project resource and schedule planning.

Senior Robotics Verification and Validation Engineer

Medical Director

• Assessing the medical safety of assigned Janssen products
• Work closely with an experienced Medical Safety Officer to strategically lead cross-functional matrix teams responsible for product safety and benefit risk oversight
• Ensure proactive and timely assessments of safety data to characterize the emerging and known safety profiles
• Communicate potential and known risks and changes to benefit/risk to relevant stakeholders
• Lead in the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen products

Associate Director – Medical Safety Officer, Oncology

Director

• The Field Director is responsible for leading the Caplyta US Northeast Medical Science Liaison (MSL) team in providing scientific, clinical, research, and educational support to health care professionals and internal partners related to Caplyta, while ensuring customer centric, insight driven, and compliant scientific engagement across the region.
• The Field Director will partner with the MSL Head to set and drive strategy for their region/organized providers, translating TA and Medical Affairs strategy into clear regional priorities, measurable objectives, and executional excellence.
• The Field Director is responsible for ensuring strong clinical engagement strategy for each territory within their region and will conduct routine strategy reviews with each MSL direct report, leveraging data, insights, AI tools, and performance trends to guide decision making.
• The primary role of the Field Director is to provide support, coaching, and development to each of their direct reports (MSLs), utilizing the skills framework, routine feedback, and periodic field observation, with a strong emphasis on strength-based coaching, continuous improvement, and career development planning.
• The Field Director will be responsible for the execution of field Medical Affairs programs, including product launches, proactive initiatives, and HCP engagement.
• The Field Director is responsible for ensuring that each direct report is functioning at the expected level of scientific acumen/expertise, presentation skills, and soft skill abilities, including professional credibility and command, stakeholder influence, adaptive communication, and effective scientific storytelling.
• In addition, the Field Director plays a critical role to remove barriers and aligning field activities to ensure impactful scientific engagement.
• The Field Director is responsible for staying abreast of scientific information and disease states to ensure proficient interaction model, and coach with their team.
• They will also ensure their direct reports execute collection and analysis of high quality, actionable Medical Insights and effectively communicate them to inform strategy, evidence generation, and lifecycle planning.
• The Field Director will demonstrate effective change leadership by upholding professionalism, performance, and integrity in challenging situations, and by guiding the team with resilience, accountability, and engagement through ambiguity and shifting priorities.
• The Field Director will coordinate closely with Medical Affairs, Scientific Affairs, and cross functional partners to align objectives and execution as appropriate.
• The Field Director is expected to identify possible solution(s) and make a recommendation to the MSL Head for action, demonstrating strong critical thinking, risk assessment, and sound judgment.
• The recommendations are expected to support the company’s scientific objectives.

MSL Field Director

• The Product Safety Head is responsible for safety oversight and strategic direction for multiple products within the Oncology solid tumors therapeutic area.
• Oversee a team of Medical Safety Officers (MSOs) leading product safety strategy and risk management activities in Global Safety Strategy & Risk Management (GSSRM).
• Help ensure consistency of safety strategy execution and communications across multiple products within the assigned product.
• Maintain compliance with legal and regulatory requirements.

Product Safety Head – Solid Tumors

Data Analyst

• Act as a main point of contact for business users seeking data for analytics, reporting, or operational decisions
• Guide customers on what data exists, where it resides, and how to access it across enterprise platforms
• Translate business questions into data solutions and recommend appropriate datasets or data products
• Educate users on data definitions, appropriate usage, and limitations
• Support users in navigating data catalogs and semantic layers
• Promote adoption of the Digital Brain and associated data standards
• Guide users toward certified, governed data sources vs. shadow or siloed data
• Work closely with data engineering, data quality, and platform teams to stay aligned on available data assets
• Feed recurring business needs into data product development and prioritization
• Support intake processes by helping shape business requests into structured data requirements

Lead Analyst, Data Advisor

• Own and lead real estate delivery across the Americas, ensuring transactions and projects are executed on time, on budget, and to standard
• Serve as the single point of accountability for regional execution performance
• Lead and develop regional RE delivery teams and matrixed partners
• Drive standardization, governance, and best-practice sharing across RE delivery teams to improve speed, quality, and controls
• Execute real estate transactions including leases, renewals, expansions, exits, dispositions, and residential housing arrangements
• Oversee project execution across the region, ensuring adherence to scope, cost, schedule, and quality expectations
• Deliver strategic space planning and site initiatives aligned to workplace standards and portfolio strategy
• Ensure all regional activities comply with global RE governance, approval thresholds, and controls
• Act as the regional escalation point for compliance, execution risk, and delivery challenges

Director, RE Delivery – Americas

Full-stack Engineer

• Lead technical solutioning for Therapeutic Area products
• Define end-to-end technical architectures across scientific workflows, data platforms, AI solutions, and knowledge management ecosystems.
• Ensure alignment to enterprise architecture, data, and security standards
• Promote reuse of existing platforms and shared capabilities
• Partner with Product Managers
• Shape product designs to ensure feasibility, scalability, and maintainability
• Quickly validate technical assumptions before investment decisions
• Provide technical input into backlog prioritization, sequencing, and roadmap planning
• Build lightweight proof-of-concepts and technical spikes to assess new technologies and integration approaches
• Enable delivery across teams
• Work closely with engineering teams to ensure designs are clearly understood and implemented effectively
• Align with enterprise architects, platform teams, and vendors on solution direction
• Identify and manage technical dependencies across products
• Drive continuous improvement
• Identify opportunities to simplify, standardize, and scale solutions across TA products
• Bring forward and evaluate relevant emerging technologies (e.g., data platforms, AI/GenAI, workflow orchestration) and recommend build, buy or partner approaches.
• Contribute to evolving architecture frameworks and best practices

Technical Lead, Therapeutic Area Enabling Innovation

Account Executive

• Attend all portions of the ACAS fellowship training program without exception.
• Engage in dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during training.
• Understand the dynamics of an EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
• Prioritize and appropriately respond to requests in a high-stress environment.
• Maintain composure and problem-solving focus during stressful interactions.
• Respond daily to requests by email and voicemail.
• Drive collaboration and maintain consistent, open lines of communication across the assigned responsibilities with the local team/Pod (i.e. TM and other CAS), as well as the support team (i.e. field trainers, site trainers, RBD) and other internal and external partners
• Responsible for following all company guidelines related to health, safety and environmental practices and that all resources needed to do so are available and in good condition.
• Responsible for adhering to company compliance with all federal, state, local and company regulations, policies, and procedures.