Johnson & Johnson

QA Engineer

• Drive and deliver audit strategies and capabilities for applicable therapeutic program level(s), Clinical System, Clinical Supplier, or Local Operating Company audits.
• Foster 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.
• Monitor 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.
• Maintain and share expert-level GCP knowledge with the ability to provide critical information, advice and guidance on complex quality and compliance issues.
• Conduct GCP audits & support GxP Audits as applicable (expected up to 50% time) with a focus on audits relevant to the responsible therapeutic areas.

Manager, Clinical QA Program Lead

• Drive and deliver audit strategies and capabilities for applicable therapeutic program level(s)
• Conduct GCP audits & support GxP Audits
• Develop tactical and operational audit plans to implement and deliver domain-specific audit strategies
• Independently lead and manage the domain-specific compliance audit programs
• Serve as the primary contact for applicable Clinical QA domain specific activities

Manager

• Serve as the primary Healthcare Compliance Officer for assigned APAC markets, including South Korea, Hong Kong, and Taiwan
• 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

Director

• Own and continuously evolve the global commercialization readiness framework.
• Define launch criteria, risk identification standards, and execution governance models.
• Lead pre-launch workshops focused on positioning, workflow integration, and technical differentiation.
• Translate product roadmap features into field-relevant technical-commercial execution models.
• Align deployment strategies with regional commercial leadership.
• Lead coordinated early-launch commercial readiness and execution in partnership with regional and global core teams (i.e. Education and Service).
• Provide in-field presence during priority launch waves to ensure execution consistency across countries / regions.
• Identify execution risks and drive corrective actions during early commercialization phases.
• Define early adoption performance indicators aligned to utilization trajectory, workflow reliability, and competitive differentiation.
• Standardize post-launch escalation pathways and mitigation strategies across markets.
• Partner with regional leadership to ensure launch execution supports sustained commercial performance.
• Establish post-launch evaluation cadence to ensure accountability and continuous improvement.
• Provide structured leadership updates on launch readiness, execution quality, and commercialization performance.
• Build model, capabilities, and team to support global strategic expansion initiatives, early launch experiences and on-going success.
• Institutionalize repeatable launch templates applicable across Bronchoscopy, Urology, and Digital Solution initiatives.
• Capture field insights and integrate learnings into global playbooks and training standards.

Director – Global Commercialization, Launch Excellence

Operations

• Support the Latin America S&OE operating model, ensuring consistent execution routines, escalation paths, and decision cadence.
• Provide visibility of risks (service, inventory, capacity, backorders) and ensure alignment across sites and stakeholders.
• Support trade-off discussions and ensure clear communication, tracking, and follow-through of decisions and actions.
• Partner with Customer Service and site operations to support prioritization and maintain transparency of customer-impacting decisions.
• Ensure alignment between site-level execution and regional governance, reinforcing consistency, accountability, and readiness.
• Track adherence to processes, identify recurring gaps, and support continuous improvement initiatives.

Service Ops Lead – Market Execution

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
• Own and support Intercompany financial processes and system integrations
• Lead solution architecture and design for SAP S/4HANA Supply Chain Finance capabilities
• Partner with Finance, Manufacturing, Planning, and Supply Chain leaders to translate business requirements
• Provide technical leadership to project teams, system integrators, and offshore delivery partners
• Ensure systems meet SOX, audit, and data governance requirements
• Lead and develop a team of IT professionals and managed service partners
• Collaborate with enterprise architecture and cybersecurity teams

Senior Technology Manager, SC Finance

Accounts Receivable

• Serve as the primary field-based lead for education, assistance, and issue resolution with healthcare providers
• Invest time (up to 50%) on-site with HCPs
• Educate HCPs on product coverage, prior authorizations, and reimbursement processes
• Collaborate with field support team members
• Address critical access and affordability issues for patients
• Build strong, trust-based relationships with customers
• Manage territory logistics, routing, and account business planning
• Maintain and grow knowledge of national, regional, local, and account market dynamics
• Collaborate with internal J&J departments

Field Reimbursement Manager – Immunology, Dermatology

Solutions Engineer

• Lead the International digital customer experience strategy across EDI, DSOS, customer insights, and supporting satellite systems
• Oversee and optimise the satellite systems supporting Customer Services and external customers
• Own the International customer experience narrative by translating business requirements into customer expectations
• Lead the development, prioritisation, and delivery of the digital customer experience capability and technology roadmap
• Partner end to end with Commercial, Customer Service, Supply Chain, Finance, Technology, and external customers
• Provide people, virtual team, and cross‑functional leadership
• Drive governance, adoption, enhancements, and user experience improvements

Senior Manager, Customer Service Digital Solutions

• Accountable for the successful development of EP Clinical Account Specialists (CAS)
• Directly supervises new CAS hires throughout their early development
• Partners closely with the Regional Business Director to enable all aspects of developing CAS talent
• Oversees the region’s training effectiveness and optimizing clinical coverage
• Implements strategic hiring and development plans aimed at improving regional CAS performance
• Works in close alignment with the Regional Technology Specialist (RTS) and Territory Managers (TM)
• Provides strategic oversight and continuity in CAS development

Clinical Manager – Electrophysiology

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

• 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.

Manager, Clinical QA Program Lead

Manager, Clinical QA Program Lead

Manager, HCC Other APAC

Director – Global Commercialization, Launch Excellence

Service Ops Lead – Market Execution

Senior Principal Engineer – Packaging

Senior Technology Manager, SC Finance

Field Reimbursement Manager – Immunology, Dermatology

Senior Manager, Customer Service Digital Solutions

Clinical Manager – Electrophysiology

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

Director, Site Enablement – U.S. Oncology

Manager – Sales Enablement, Product Management

MedTech Brand Manager

Lead Analyst, Contract Management