Johnson & Johnson

QA Engineer

• Design and implement automated and manual QA strategies for GenAI systems
• Build regression tests, generate synthetic test data, build test harnesses and evaluation pipelines for accuracy
• Validate prompt logic, model behavior and evaluation metrics
• Execute tests and debug pipelines
• Support deployment of GenAI products
• Lead system design reviews
• Collaborate closely with data scientists and developers
• Establish testing standards and workflows for continuous integration and deployment
• Conduct code reviews and document system design decisions

Senior Engineer – GenAI Quality Assurance

Supply Chain

• Defining and executing the digital strategy and multi-year roadmap for Clinical Supply Chain.
• Leading major transformation initiatives that modernize systems, processes, data, and ways of working across Clinical Supply Chain and R&D.
• Driving simplification, standardization, and end-to-end process integration across planning, manufacturing, packaging, labeling, logistics, and clinical supply operations.
• Ensuring transformation efforts deliver measurable improvements in reliability, agility, productivity, compliance, and patient experience.
• Leading and developing a global organization of approximately 70+ employees and contractors across digital solutions, systems, and business transformation.
• Building a high-performing, inclusive culture focused on innovation, collaboration, accountability, and continuous development.
• Developing the talent, leadership capabilities, and succession pipeline needed for the future of digital clinical supply.
• Serving as a trusted partner to senior leaders across Clinical Supply Chain, Global Development, Innovative Medicines Supply Chain, Advanced Therapies Supply Chain, Quality, Manufacturing, Johnson & Johnson Technology, and the Transcend organization.
• Representing Clinical Supply Chain and R&D in enterprise governance, transformation, and industry forums.
• Building strategic partnerships with technology providers, service partners, and industry consortiums to accelerate innovation and adoption of industry standards.
• Overseeing the portfolio of digital products, platforms, and technology solutions supporting Clinical Supply Chain and R&D transformation.

Senior Director, Digital – Clinical Supply Chain

Supervisor

• Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
• Responsible for scheduling all activities of the Field Specialists to ensure customers technical needs are met.
• Responsible for the scheduling of all reactive calls, committing arrival time to customers to ensure J&J meets our Service Level Agreements.
• Responsible for scheduling all proactive calls to ensure all preventative maintenance, required updates, and appropriate retrofits are completed within specified time frames.
• Responsible for initiating technical escalations as necessary to ensure timely repair of equipment.
• Responsible for level loading work across the Field Specialists, managing overtime, approving time off, and scheduling training for all assigned Field Specialists.
• Responsible for approving expenses, monitoring individual team member performance and area metrics.
• Responsible for driving regulatory compliance and auditing of Field Specialist's tools, parts and administration.
• Other duties as assigned.

Territory Supervisor, Northeast

Analyst

• Conduct literature searches, systematic reviews, evidence synthesis, and landscape assessments for trauma, foot and ankle, and CMF products, including fracture fixation, plating systems, and craniomaxillofacial reconstruction technologies
• Perform targeted evidence searches to support competitive intelligence, product positioning, and stakeholder engagement across the trauma portfolio
• Maintain and update evidence libraries, reference databases, and bibliographic files for the trauma portfolio
• Summarize and critically appraise published clinical and economic evidence, identifying key findings and implications for HEMA strategy
• Support the development and updating of health economic models and cost calculators for trauma-related procedures and technologies
• Gather and validate model inputs from published literature, clinical data, claims analyses, and internal data sources
• Analyze clinical, claims, and real-world data to generate evidence supporting the value of trauma products
• Assist in the preparation of value briefs, evidence summaries, and case stories
• Prepare presentations, data summaries, infographics, and reports for internal teams, advisory boards, and external audiences
• Develop and maintain standardized templates for HEMA deliverables to ensure consistency across the trauma portfolio
• Monitor the competitive landscape, clinical guidelines, reimbursement trends, and emerging evidence in the trauma market
• Track and summarize key congress presentations, competitor publications, and clinical practice updates relevant to the trauma segment
• Coordinate with cross-functional teams including Marketing, Medical Affairs, R&D, and Regulatory on evidence needs and project timelines
• Maintain organized project trackers, timelines, and documentation to ensure on-time delivery of HEMA projects
• Participate in team meetings and professional development activities to build expertise in health economics and the trauma market

Trauma Analyst, F&A, CMF HEMA

Operations

• drive operational excellence across Global Market Access, with a primary focus on EU HTA Regulation readiness and execution.
• operationalize EU HTA across a global portfolio and support timely, high-quality execution of Joint Clinical Assessments and Joint Scientific Consultations.
• refine, adapt, and implement the internal end-to-end JCA process, including governance, submission readiness, and compliant document management.
• coordinate and align with Regulatory Affairs on EMA submission and post-submission process steps.
• lead operational execution and cross-functional coordination of JCA internal PICO scoping, dossier preparation, submission, and post-submission activities, including follow-up interactions with (co-) assessors for relevant assets across Therapy Areas.
• ensure linkage to related activities such as scientific advice, and partner closely with R&D.
• drive continuous improvement in the efficiency, quality, and consistency of dossier preparation, quality checks and workflow automation, including appropriate use of artificial intelligence and other digital solutions.
• support resource planning for JCA-related activities across assets and functions, including budget, FTE capacity, and vendor planning.
• ensure proactive planning for internal pipeline assets in scope for upcoming EU JCAs.
• review and synthesize JCA reports to distill key insights and learnings for future programs and understand potential implications for HTA markets globally.
• support external stakeholder engagement, including interactions with trade associations.
• deliver training for relevant global stakeholders to enhance understanding of EU JCA processes, roles, responsibilities, and operational requirements.
• manage submission and post-submission activities for JSCs, including cross-functional coordination and compliant document management.
• implement and maintain planning, milestone tracking, and knowledge management tools to support transparency, coordination, and compliant ways of working across the HTA & Decision Science team and broader Global Market Access organization.

Associate Director – Market Access Operations & Excellence

• Drives and delivers audit strategies and capabilities for applicable therapeutic program level(s), Clinical System, Clinical Supplier, or Local Operating Company audits, ensuring connectivity and holistic alignment of strategies.
• Fosters the partnership between audit strategy and execution teams and enhance the value of Clinical audit programs through enhancing the audit report peer review process and the analysis and communications of meaningful audit outcomes.
• Monitors audit outcome trends and identification of pro-active collaboration opportunities with stakeholders to resolve and address compliance related matters and identify opportunities to enhance audit strategy and overall quality and compliance of clinical programs across therapeutic areas.
• Maintains and shares expert-level GCP knowledge with the ability to provide critical information, advice and guidance on complex quality and compliance issues.
• Leverages data analytics tools to analyze relevant data sources.
• Evaluates and analyzes the data to identify any relevant trends and insights as an input for the development of the appropriate audit program.
• Conducts GCP audits & supports GxP Audits as applicable (expected up to 50% time) with a focus on audits relevant to the responsible therapeutic areas.
• Develops tactical and operational audit plans to implement and deliver domain-specific audit strategies.
• Ensures the relevant standard procedures, audit scopes and audit plans are fully understood and applied in audit activities.
• Independently leads and manages the domain-specific compliance audit programs as laid down in a comprehensive audit schedule, through planning, conducting and reporting of QA audits of activities, data, internal and external facilities and processes in GxP/non-regulated areas to assure adherence to company internal standards and policies/requirements, and compliance with applicable (Health Authority) regulatory requirements.
• Guides auditors in the scope definition, planning, conduct and reporting of audits, providing regulatory and process expertise within the applicable therapeutic area program(s).

Manager, Clinical QA Program Lead

• Audit strategy: Drives and delivers audit strategies and capabilities for applicable therapeutic program level(s), Clinical System, Clinical Supplier, or Local Operating Company audits.
• Fosters the partnership between audit strategy and execution teams and enhance the value of Clinical audit programs.
• Monitors audit outcome trends and identifies collaboration opportunities with stakeholders to resolve compliance related matters.
• Conducts GCP audits & supports GxP Audits as applicable (expected up to 50% time).
• Develops tactical and operational audit plans to implement and deliver domain-specific audit strategies.
• Independently leads and manages domain-specific compliance audit programs as laid down in a comprehensive audit schedule.
• Guides auditors in the scope definition, planning, conduct and reporting of audits.
• Prepares and reviews audit summary reports to share/escalate significant information with senior leaders.

Research Analyst

• Acts as primary local company contact for assigned sites for specific trials
• Participates in site feasibility and/or Site Qualification Visit
• Responsible for executing activities within site initiation and start-up
• Ensures site staff are trained and the corresponding training records are complete and accurate
• Contributes to site level recruitment strategy and contingency planning
• Ensures that clinical drug supplies are appropriately used, handled, and stored
• Ensures compliance with all data collected
• Tracks costs at site level and ensure payments are made

Associate Clinical Research Associate – Site Manager

Manager

• Serve as the primary EMEA Operate State contact for the supported Distribution and Transportation business area, ensuring effective coordination between business stakeholders, Super Users, Global Product Owners, Technical Owners, and JJT
• Build strong, collaborative relationships with end users, Super Users, and global platform teams to foster alignment, adoption, and effective use of the SAP S/4HANA platform
• Coordinate and support standardized regression testing processes within the business function, ensuring consistency, quality, and alignment with release and deployment timelines
• Support persona-based security role design and maintenance in alignment with global standards, business requirements, and compliance expectations
• Identify, track, and analyze business errors, coordinate resolution efforts, support escalation management, and identify trends for continuous improvement
• Partner with the Super User community to manage platform enhancement requests, ensuring alignment with global design governance, business value, and functional priorities
• Support smooth transition of newly deployed users from hypercare to Operate State, ensuring readiness, adoption, and a positive onboarding experience
• Develop and implement an Operate State transition model as part of the continuous design, build, test, deploy, and support methodology framework
• Lead intake, assessment, and prioritization of platform demands from the supported area, managing funding alignment, governance interdependencies, and backlog prioritization
• Collaborate with JJT to deliver a unified business-technology support model covering enhancements, capability building, issue resolution, and escalation management
• Partner with the Master Data Governance team to implement a coordinated data support model that strengthens data quality, consistency, and operational reliability
• Manage KPIs and Control Tower metrics for the supported business function(s), partnering with stakeholders to ensure visibility, issue tracking, proactive risk mitigation, and continuous improvement
• Lead the design and delivery of the Super User Certification program, including curriculum development, training execution, engagement tracking, and competency validation
• Oversee Super User communities within the assigned area, ensuring ongoing training, onboarding, engagement, knowledge sharing, and proactive succession planning
• Maintain and continuously improve tools, processes, and governance routines within the Operate State support model to enhance efficiency and effectiveness
• Provide functional support for projects impacting SAP S/4HANA in the supported area, collaborating with cross-functional teams to ensure business requirements are reflected in system design, testing, deployment, and sustainment

MT SC ERP D&T Manager, EMEA

• Support the Latin America S&OE execution capability across the Distribution Center (DC) network
• Ensure consistent, timely, and exception-based execution across distribution operations
• Support the coordination of execution decisions by connecting site operations, Customer Service, Deliver Planning interfaces, and partner functions
• Contribute to aligning execution priorities and help ensure that DC operations operate in a coordinated and disciplined manner across Latin America
• Monitor Performance & Improvement: Track adherence to processes and support continuous improvement initiatives

Service Ops Lead – LATAM

Engineer

• Lead packaging initiatives and programs across secondary and tertiary packaging, ensuring clear scope, milestones, stakeholder alignment, risk management and execution discipline.
• Own and maintain packaging roadmaps aligned with product lifecycle needs, site priorities, capacity plans, sustainability objectives, and evolving regulatory expectations, including ownership of budget planning and preparation of CARs.
• Drive innovation and change by identifying, evaluating and implementing new packaging materials, technologies, processes and ways of working that improve robustness, efficiency, sustainability and business continuity.
• Act as the secondary and tertiary packaging engineering subject matter expert, providing technical guidance on materials, pack structures, protective strategies, equipment interfaces, manufacturability and distribution requirements.
• Provide technical oversight for packaging development, qualification, validation and lifecycle management activities to ensure packaging integrity, manufacturability and reliable performance across internal sites and external partners.
• Monitor current and emerging packaging regulations, standards and industry expectations; assess their impact on packaging operations, documentation, processes and site implementation plans.
• Partner with Quality, Regulatory, Manufacturing, Procurement, Planning, Logistics, Product and MSAT stakeholders to align packaging decisions, communicate risks and drive timely implementation of mitigations.
• Lead technical assessments, investigations and problem-solving activities related to packaging materials, processes, suppliers, distribution performance and operational issues.
• Coach and support packaging engineers and cross-functional partners by sharing expertise, strengthening technical capability and promoting consistent application of packaging standards and best practices.
• Represent MSAT Packaging in cross-functional forums and contribute to governance, prioritization and decision-making for packaging initiatives.

Senior Principal Engineer, Packaging

Financial Planning and Analysis

• Lead strategy, delivery, and ongoing optimization of Supply Chain Finance, ensuring alignment with business objectives and IT standards.
• Own and support Intercompany financial processes and system integrations, including eliminations, transfer pricing support, and cross‑entity transactions.
• Lead solution architecture and design for SAP S/4HANA Supply Chain Finance capabilities, including Intercompany, Product Costing, Material Ledger, Inventory Valuation, Manufacturing Finance, Profitability Analysis, and Financial Planning processes.
• Partner with Finance, Manufacturing, Planning, and Supply Chain leaders to translate business requirements into scalable SAP S/4 solutions and integrated business processes.
• Provide technical leadership to project teams, system integrators, and offshore delivery partners, ensuring solution quality, design consistency, and successful delivery.
• Ensure systems meet SOX, audit, and data governance requirements, maintaining strong controls and documentation.
• Lead and develop a team of IT professionals and managed service partners, fostering high performance and accountability.
• Collaborate with enterprise architecture and cybersecurity teams to ensure solutions are secure, reliable, and future‑ready.

Senior Technology Manager, Supply Chain Finance

• Serve as the primary Healthcare Compliance Officer for assigned APAC markets
• Execute healthcare compliance strategies aligned with regional and global priorities
• Identify, assess, and manage compliance risks related to commercial, promotional, professional education, and other business and operational activities
• Provide practical, risk-based guidance to business leaders on healthcare compliance requirements and ethical decision-making
• Partner with cross-functional stakeholders to embed compliance controls into business processes and market activities
• Support core compliance program elements, including governance, risk assessments, monitoring, reporting, and training programs
• Collaborate with Legal and other functions to support investigations, audits, and regulatory or health authority interactions
• Monitor regulatory developments and industry trends across APAC and escalate emerging risks as appropriate
• Prepare compliance risk assessments, insights, and updates for regional leadership
• Promote a strong culture of integrity, accountability, and speak-up across supported markets

Manager, HCC Other APAC

Accounts Receivable

• Serve as the primary field-based lead for education, assistance, and issue resolution with healthcare providers
• Educate HCPs on product coverage, prior authorizations and appeals, reimbursement processes
• Act with urgency to address critical access and affordability issues for patients
• Collaborate with field support team members such as sales representatives
• Conduct field-based reimbursement and access support, education, and creative problem-solving

Field Reimbursement Manager – Immunology, Dermatology

Field Engineer

• Perform Technical Support to internal and external customers through the Customer Support Call Center
• Manage account schedule and perform the installation, operation, repair and upgrades of equipment within assigned territory.
• Devises and implements preventative maintenance programs and maintains performance and service records for equipment.
• Manage region and schedule to facilitate all aspects of technical / engineering work required to support all products supported and serviced by the technical department.
• Responds to customer requests for emergency service.
• Determines cause(s), troubleshoots and takes corrective action.
• Provides guidance to customers to include Doctors, Nurses and hospital Biomedical engineers along with Field Service Specialists and/or Representatives and assists when customer satisfaction issues arise.
• Manage customer expectations on a regular basis before and after various interactions to ensure customer satisfaction.
• Completes paperwork, documentation and administrative tasks per policy and procedures.
• Complete, clear and timely update in the Service Management System related to Workorder, Orders.
• Complete all processing of RMA returns to support individual usage of parts and equipment.
• Manage allocated inventory and complete required audits to support thereof.
• Completes required training for supported products and processes.
• Acts as customer advocate to represent customer needs internally
• Participate in incident investigation.
• Support installation and support of products in clinical trials, external evaluations, regulatory testing or similar.
• Responsible for communicating business-related issues or opportunities to next management level
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Be familiar with and adhere to J&J environmental and safety policies and guidelines.
• Immediately inform supervisors If there are any violations, deviations or hazards present
• Project Management, Presentation, Good communication Skills

Senior Engineer – GenAI Quality Assurance

Senior Director, Digital – Clinical Supply Chain

Territory Supervisor, Northeast

Trauma Analyst, F&A, CMF HEMA

Associate Director – Market Access Operations & Excellence

Manager, Clinical QA Program Lead

Manager, Clinical QA Program Lead

Associate Clinical Research Associate – Site Manager

MT SC ERP D&T Manager, EMEA

Service Ops Lead – LATAM

Senior Principal Engineer, Packaging

Senior Technology Manager, Supply Chain Finance

Manager, HCC Other APAC

Field Reimbursement Manager – Immunology, Dermatology

Field Service Engineer