Johnson & Johnson

Financial Planning and Analysis

• Support regional Regulatory Affairs compliance activities
• Coordinate and maintain regulatory documentation, trackers, and records for audits, inspections, and lifecycle management
• Monitor, analyze, and report on regional RA budgets, including forecasting, accruals, and variance analysis
• Support regional RA operational plans
• Track regulatory submissions, renewals, and commitments across countries in scope
• Prepare compliance and budget reports, dashboards, and presentations
• Partner with Quality, Finance, Supply Chain, and Commercial teams
• Contribute to continuous improvement of regulatory processes, controls, and budget transparency

Regional RA Compliance and Budget Analyst

• Serve as a finance partner to Indirect Procurement and Supply Chain leaders
• Provide financial planning, forecasting, and performance analysis across indirect spend categories
• Analyze procurement savings, productivity initiatives, and contract value realization
• Support annual budget, quarterly forecast, and long-range planning processes
• Develop and maintain financial models, dashboards, and KPIs for spend, savings, and cost drivers
• Provide financial governance and variance analysis
• Identify risks and opportunities and recommend corrective actions
• Collaborate with Procurement, Operations, and Finance teams on sourcing decisions and supplier negotiations
• Ensure compliance with internal financial policies, controls, and reporting standards
• Drive standardization, automation, continuous improvement, and enhanced financial transparency

Senior Financial Analyst, Indirect Procurement

Security Engineer

• Own the end-to-end penetration testing services program for products and connected platforms
• Develop the annual testing roadmap, prioritization model, and capacity plan
• Define and maintain penetration testing methodology, scoping standards, rules of engagement, and reporting templates
• Embed security testing gates into the product development lifecycle
• Execute and oversee assessments across medical devices, embedded firmware, wireless protocols, mobile and web applications, APIs, and cloud infrastructure
• Manage third-party penetration testing vendors, including scopes, statements of work, deliverable quality, and SLA performance
• Triage and validate findings, assess exploitability, and evaluate patient safety and clinical impact
• Drive remediation with R&D and engineering teams through retest and verified closure
• Conduct threat modeling and attack surface analysis
• Produce testing evidence for FDA premarket submissions, EU MDR technical files, and hospital security assessments
• Contribute testing results and residual risk analysis to product security risk files
• Build and report program metrics to leadership and product stakeholders
• Research emerging attack techniques, medical device vulnerabilities, and tooling; develop custom tooling and exploits as needed
• Assess testing implications of platform migrations, supplier changes, and separation/carve-out activity
• Deliver technical enablement and secure development training to engineering teams

Professional, Program Lead, PenTesting Services

• Integrate security requirements and controls into the design and development of digital and connected products
• Perform product security risk assessments, threat modeling, and vulnerability analysis across the product lifecycle
• Partner with product development, quality, and regulatory teams on secure design reviews and remediation activities
• Support security testing, including static and dynamic analysis, penetration testing coordination, and vulnerability validation
• Track, document, and manage product security findings to closure under internal governance processes
• Contribute to product security standards, procedures, and best practices
• Monitor emerging cybersecurity threats, vulnerabilities, and regulatory guidance relevant to medical devices and digital health
• Support audits, assessments, and regulatory inquiries related to product cybersecurity
• Partner with engineering, quality, regulatory, and IT teams to protect DePuy Synthes digital products and connected medical technologies

Experienced Security Engineer, Product Analyst

• Support regional Regulatory Affairs compliance activities to ensure adherence to applicable international and local regulatory requirements and internal procedures
• Coordinate and maintain regulatory documentation, trackers, and records for audits, inspections, and lifecycle management
• Monitor, analyze, and report on regional RA budgets, including forecasting, accruals, and variance analysis with QARA leadership and Finance
• Support development and execution of regional RA operational plans aligned with compliance priorities and budget constraints
• Track regulatory submissions, renewals, and commitments across countries in scope
• Prepare compliance and budget reports, dashboards, and presentations for regional and global stakeholders
• Partner with Quality, Finance, Supply Chain, and Commercial teams on regulatory initiatives and cost-effective execution
• Identify opportunities to improve regulatory processes, controls, and budget transparency

Manager

• Own, evolve, and realize value from sector and enterprise digital platforms and capabilities enabling MedTech R&D
• Manage the full lifecycle of digital platforms, including Product Lifecycle Management, Risk & Requirements, and adjacent R&D capabilities
• Own defined platforms, products, or capability areas
• Lead product deployments, operations, adoption, and value realization of sector R&D digital platforms
• Develop strategic plans, roadmaps, governance models, and stakeholder alignment
• Enable innovation through automation and adaptive, data-driven digital capabilities
• Evaluate and sponsor emerging technologies
• Own capability-level roadmaps and onboarding success
• Adapt platforms to changes in business scale, operating models, and technology
• Lead people or operate as a senior individual contributor with product accountability

Manager, Digital Transformation

• Own, evolve, and realize value from sector and enterprise digital platforms and capabilities enabling MedTech R&D
• Manage the full lifecycle of digital platforms, including Product Lifecycle Management, Risk & Requirements, and adjacent R&D capabilities
• Own defined platforms, products, or capability areas
• Lead people or operate as a senior individual contributor with product accountability
• Own capability-level roadmaps and onboarding success
• Manage product ownership and lifecycle of sector R&D digital platforms, including deployments, operations, adoption, and value realization
• Conduct strategic planning, roadmap development, governance, and stakeholder alignment
• Enable innovation through automation and adaptive, data-driven digital capabilities
• Evaluate and sponsor emerging technologies
• Adapt platforms to changes in business scale, operating models, and technology

Project Manager

• Lead and manage MDRIM and document management projects from initiation through completion
• Coordinate cross-functional stakeholders across Regulatory Affairs, Quality, R&D, Manufacturing, and external partners
• Oversee planning, tracking, and reporting of project milestones, risks, issues, and dependencies
• Ensure document management processes comply with global regulations, internal quality standards, and inspection-readiness expectations
• Identify process gaps and implement standardized, efficient MDRIM and documentation workflows
• Maintain project documentation, dashboards, and metrics for transparency and leadership decision-making
• Facilitate governance meetings, project reviews, and stakeholder communications across QARA International
• Apply Johnson & Johnson Credo values and quality principles in project activities

Project Manager, MDRIM – Document Management

• Lead and manage MDRIM and document management projects from initiation through completion
• Coordinate cross-functional stakeholders across Regulatory Affairs, Quality, R&D, Manufacturing, and external partners
• Plan, track, and report project milestones, risks, issues, and dependencies
• Ensure document management processes comply with global regulations, internal quality standards, and inspection-readiness expectations
• Identify process gaps and implement standardized MDRIM and documentation workflows
• Maintain project documentation, dashboards, and metrics for transparency and leadership decision-making
• Facilitate governance meetings, project reviews, and stakeholder communications across QARA International
• Apply Johnson & Johnson Credo values and quality principles in project activities

Project Manager, MDRIM, Document Management

• Translate enterprise and regional direction into district strategy with clear priorities, measurable outcomes, and disciplined execution
• Drive district performance across the Neuroscience portfolio through customer-focused execution aligned with patient and business needs
• Lead and develop a high-performing team through hiring, performance management, and development planning
• Coach and mentor the team to strengthen selling effectiveness, clinical execution using approved resources, and business acumen
• Drive demand generation and care transitions across outpatient and inpatient settings
• Build relationships with key customers and stakeholders and strengthen cross-functional partnerships
• Anticipate market dynamics using internal and external data to adjust strategy and remove barriers
• Influence Sales leadership, Medical Affairs, and Marketing using field insights
• Reinforce accountability, inclusion, team health, and clear expectations through change
• Adhere to Healthcare Compliance policies and guidelines
• Use approved AI-enabled tools to scale best practices, strengthen strategic planning, and elevate team execution while maintaining privacy and data integrity

Senior District Manager, Neuroscience

• Lead the UDI Program Management Office, establishing governance, roadmaps, milestones, and performance metrics aligned with global regulatory requirements
• Provide strategic oversight for UDI-related technology initiatives across ERP, labeling, master data, and regulatory submission systems
• Partner with Quality, Regulatory Affairs, Supply Chain, IT, and Commercial teams to drive end-to-end UDI compliance and execution
• Maintain documentation, risk management, change control, and audit support processes to ensure inspection readiness
• Lead and develop PMO and UDI professionals, fostering accountability, continuous improvement, and quality culture
• Monitor global UDI regulatory changes, assess business impact, and drive timely implementation of updates
• Manage program risks, dependencies, and resource planning for on-time, compliant delivery
• Drive process optimization and standardization using PMO best practices and quality system principles

Senior Manager, UDI PMO

• Lead the UDI Program Management Office, establishing governance, roadmaps, milestones, and performance metrics aligned to global regulatory requirements
• Provide strategic oversight for UDI-related technology initiatives across ERP, labeling, master data, and regulatory submission systems
• Partner with Quality, Regulatory Affairs, Supply Chain, IT, and Commercial teams to drive end-to-end UDI compliance and execution
• Ensure inspection readiness through documentation, risk management, change control, and audit support processes
• Lead and develop a team of PMO and UDI professionals
• Monitor global regulatory changes related to UDI and assess business impact
• Manage program risks, dependencies, and resource planning for compliant delivery of UDI initiatives
• Drive process optimization and standardization using PMO best practices and quality system principles

• Translate enterprise and regional direction into district strategy with clear priorities, measurable outcomes, and disciplined execution
• Drive district performance across the Neuroscience portfolio through customer-focused execution aligned with patient and business needs
• Lead and develop a high-performing team through hiring, performance management, and development planning
• Provide advanced coaching and mentoring to strengthen selling effectiveness, clinical execution, and business acumen
• Drive demand generation and care transitions execution across outpatient and inpatient settings
• Build relationships with key customers and stakeholders and strengthen cross-functional partnerships
• Anticipate market dynamics using internal and external data to adjust strategy and protect or grow performance
• Influence Sales leadership, Medical Affairs, and Marketing through field insights
• Reinforce accountability, inclusion, and team health while supporting the team through change
• Adhere to Healthcare Compliance policies and guidelines
• Use approved AI-enabled tools to scale best practices, strengthen strategic planning, and elevate team execution while maintaining privacy, data integrity, and policy alignment

• Lead, develop, and engage direct and matrixed teams; set priorities, assess performance, and build succession and capability plans
• Own end-to-end regional outbound transportation execution, service recovery, escalation management, crisis response, and business continuity
• Serve as the primary outbound transportation leader for MedTech businesses, establishing governance, service expectations, decision rights, and executive reporting
• Partner with Procurement on supplier RFPs and contracting, evaluate suppliers, identify required capabilities, monitor supplier performance, and execute remediation plans
• Lead carrier governance, including SLAs, KPIs, business reviews, corrective actions, capacity, contracts, and sourcing implementation
• Own service, customer, patient, quality, and cost performance, including OTIF-D, claims, premium freight, accessorials, and remediation plans
• Partner with Quality on claims, OS&D investigations, quality events, SOP compliance, audit readiness, root-cause analysis, and corrective actions
• Own budget planning, forecasting, accruals, variance and savings delivery, freight-payment controls, invoice exceptions, and billing disputes
• Partner with transportation technology, data quality, reporting and analytics, and IT teams to drive regional capabilities and support transformation initiatives
• Drive lane, mode, carrier, and network optimization; lead transportation workstreams for site transitions and strategic supply-chain programs
• Standardize regional processes, SOPs, escalation protocols, and controls using structured problem-solving and continuous improvement
• Monitor transportation regulations, trade requirements, market conditions, and carrier-network changes; implement required controls

LATAM Transportation Manager

Research Scientist

• Design, build, and scale simulation, optimization, digital twin, and decision-support capabilities across Therapeutics Development & Supply, including CMC and Clinical Supply Chain
• Translate development, manufacturing, portfolio, capacity, resource, and clinical supply processes into rigorous computational models
• Formulate and solve optimization problems involving portfolio prioritization, resource allocation, capacity planning, and resource scheduling
• Apply linear and mixed-integer programming, nonlinear optimization, stochastic programming, decomposition, heuristics, and multi-objective methods
• Develop models that make constraints, uncertainty, risk, and tradeoffs explicit and convert outputs into decision recommendations
• Design, build, validate, and maintain digital twins of TDS and CSC operations
• Develop discrete-event, Monte Carlo, agent-based, system dynamics, and hybrid simulations
• Establish practices for model verification, validation, calibration, sensitivity analysis, uncertainty quantification, and performance monitoring
• Create reusable modeling components and platforms across products, programs, sites, and business processes
• Develop robust, reusable modeling workflows and decision-support products using Python, scientific computing, optimization, simulation, and cloud-based tooling
• Apply software engineering best practices including modular design, version control, testing, documentation, reproducibility, code review, and maintainable interfaces
• Partner with data engineering, product, architecture, and platform teams to integrate models with enterprise data and workflows
• Partner with leaders and subject-matter experts across TDS, CSC, technical operations, portfolio management, finance, and digital organizations
• Lead technical work across multiple initiatives as a hands-on modeler and developer
• Communicate assumptions, limitations, results, and recommendations to technical and non-technical audiences
• Mentor colleagues and provide technical direction to internal teams, consultants, and external collaborators

Regional RA Compliance and Budget Analyst

Senior Financial Analyst, Indirect Procurement

Professional, Program Lead, PenTesting Services

Experienced Security Engineer, Product Analyst

Regional RA Compliance and Budget Analyst

Manager, Digital Transformation

Manager, Digital Transformation

Project Manager, MDRIM – Document Management

Project Manager, MDRIM, Document Management

Senior District Manager, Neuroscience

Senior Manager, UDI PMO

Senior Manager, UDI PMO

Senior District Manager, Neuroscience

LATAM Transportation Manager

Principal Scientist, Operations Research – Decision Science