Johnson & Johnson

Operations

• Responsible for the timely, efficient and accurate coordination, creation and maintenance of various master data elements (e.g. Material Master, BOM/Recipes, Production Versions, etc.) in SAP/ECC directly and/or through automated workflow system(s).
• Execute the data operations and data quality process.
• May include coordination of testing, error handling, data conversion and/or validation, and audit/compliance actions (Non-Conformance (NC) and/or Corrective Action Preventive Action (CAPA)).
• Engage with partners on tactical matters.
• Provide tactical guidance and knowledge transfer to third-party team(s) and serve as point of escalation.
• Participate in the completion of projects and departmental goals by tactically focusing on business outcomes.
• Execute tools and processes that improve master data management operations execution.
• Collaborate on the preparation of metrics, dashboards, and tracking to facilitate the efficient operations of the department.
• Participate in, and sometimes lead, operational and governance meetings including end-to-end, value capture, and third-party reviews.
• Deliver training to educate partners on detailed procedures, data flows, etc.

Data Operations Analyst

Compliance

• 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.
• Write and file FDA submissions (e.g., Q-submissions, IDEs, 510(k)s).
• Serves as a Regulatory Affairs subject matter expert on new product development and engineering design control teams.
• Proactively identify issues, effectively communicate timelines for project completion, and address complex issues that may impact registration status.
• Guide conformance with applicable regulations and guidance documents in product development, support of claims, content labeling, and promotional materials.
• Assists in the development and enhancement of Regulatory Affairs processes.

Senior Regulatory Affairs Program Lead – MedTech Surgery

Procurement

• Develop and drive the Procurement vision for, with and through the stakeholder community
• Developing the vision, strategy and implementation plan for specific categories of spend that will effectively meet the long range requirements of the business partners and deliver the maximum value for Johnson & Johnson.
• Lead Supplier Relationship Management of strategic supplier to assure alignment of Johnson & Johnson's objectives are met, including quality, reliability, innovation and cost
• Understand long range requirements of the business partners and engage in strategic planning and partnering to ensure alignment
• Deliver on financial, service, reliability, quality, innovation, and growth commitments
• Build and manage relationships throughout Johnson & Johnson that results in dynamic interactive dialogue on a broad range of perspectives and information critical to the development of optimal approaches and solutions
• Develop deep supplier relationships with strategic suppliers to include data review and analysis, performance management and development and improvement of end to end value, and bring innovation to the business
• Identify, develop and direct the implementation of Procurement goals and category strategies, based on deep subject matter expertise and an informal understanding of industry/market dynamics
• Leverage data analytics and technology to develop and drive Procurement strategies that are aligned with the business/sector needs
• Handle supplier relationships, communicate changes to category strategy, execute joint collaborative initiatives, and monitor supplier negotiations
• Lead team meetings and provide updates to Procurement Leadership
• Lead & prioritize portfolio of Procurement segment-specific initiatives (Innovative Medicine, MedTech)

Manager, Procurement

• Provide strategic healthcare compliance guidance and support for assigned Global Functions, partnering with business leaders early in strategy development, business planning, and pre-commercial initiatives to identify compliant pathways that support innovation, growth, evidence generation, launch readiness, and long-term business objectives through proactive, risk-informed guidance.
• Assess emerging risks associated with strategic growth initiatives, evolving healthcare environments, external stakeholder engagement strategies, and novel business models, helping leaders navigate ambiguity and make informed decisions.
• Provide guidance regarding healthcare compliance laws, regulations, industry codes, company policies, and evolving enforcement expectations, translating complex requirements into practical business solutions.
• Advise stakeholders on interactions and engagements involving healthcare professionals (HCPs), healthcare organizations (HCOs), government officials (GOs), patient organizations, advocacy groups, advisory boards, consulting arrangements, grants, sponsorships, and other external stakeholders.
• Lead and support strategic risk management activities, including risk assessments, root cause analysis, mitigation planning, and ongoing risk reviews, while advising business partners on risk considerations associated with evidence generation activities, disease-state initiatives, stakeholder engagement strategies, launch readiness efforts, strategic planning activities, and future-state business opportunities.
• Support healthcare compliance program effectiveness through governance, monitoring, investigations, issue management, corrective actions, internal controls, and continuous improvement activities.
• Provide healthcare compliance guidance and risk assessment support for Global Business Development activities, including strategic partnerships, licensing opportunities, acquisitions, collaborations, due diligence activities, and integration initiatives.
• Support the development and implementation of compliance controls, governance structures, and risk mitigation strategies related to Global Business Development activities and integration efforts.
• Promote compliance-by-design principles by embedding compliance considerations into strategic planning, governance frameworks, operating models, decision-making processes, and evolving ways of working.
• Partner effectively across Global Functions, Legal, Finance, Business Development and cross-functional stakeholders to support strategic priorities, mitigate risk, and enable compliant business outcomes.
• Drive awareness of healthcare compliance expectations while supporting organizational initiatives, change management efforts, and stakeholder engagement activities that strengthen a culture of integrity and responsible decision-making.
• Work with industry associations and other external organizations, as applicable, to influence/develop industry policies and standards in close partnership with HCC Sector Leads, to help shape the external environment.
• Sponsor, lead and engage in a variety of tasks and project initiatives to advance Health Care Compliance and/or business-related goals.
• Drive alignment across diverse stakeholders operating within a matrixed global environment.

Director, Health Care Compliance Officer – Global Functions

• Serve as the designated Patient Service Center (PSC) Operations point of contact for assigned Field Reimbursement team members
• Participate in regular business reviews, pipeline calls, and regional FRM/FRAD meetings to discuss access trends, payer changes, and field-identified barriers
• Clearly communicate PSC services, workflows, SLAs, escalation paths, and documentation expectations with HCP offices and patients
• Compile and share PSC performance data to support field strategies and account planning
• Triage & coordinate resolution of complex access and reimbursement issues raised by the Field Reimbursement partners
• Support implementation of new patient access programs, payer policy updates, and field reimbursement playbooks by ensuring team readiness
• Ensure all communications and materials align with non-promotional requirements and compliance standards.

Field Liaison, PSC Operations

Analyst

• Analyze order management scenarios and interdependencies across Commercial, Logistics, Quality, and Finance.
• Identify interfaces, data flows, and exception handling scenarios.
• Support local fit-gap validation against the global template and draft business user requirements.
• Identify functional risks, gaps, and improvement opportunities, and escalate as needed.
• Support deployment readiness, including SME onboarding, review of training materials, SOP updates, and data validation.
• Coordinate business simulation and user acceptance testing activities with business SMEs across the Order to Cash domain.
• Support defect triage, root cause analysis, and issue resolution.
• Provide functional support during deployment and hypercare.

Order to Cash Deployment Analyst

Marketing

• Manage key projects including but not limited to quarterly ”Plan of Action Live” meetings, All Field Calls and major conference and events and general marketing team coordination
• Work in a highly collaborative manner with marketing managers and marketing communication team members in campaign strategy development and execution
• Help drive and execute the creation, review and approval and dissemination of marketing assets
• Manage key communication channels with the sales organization including “Weekly Rounds”, managing materials placed on Showpad and general Showpad curation, and general email correspondence
• PO & Invoice Management for outside vendors (Fenway / Dorothy Monares / etc.)
• Install and maintain systematic and scalable approach to conference engagement from a messaging and branding perspective
• VAC Submission Process management

Senior Commercial Marketing Specialist

Manager

• Managing a team of field based Oncology Sales Specialists who will plan and execute territory business plans for breakthrough products in Oncology.
• Demonstrating business and clinical expertise while building a strategic plan and guiding the team to deliver sales results within an assigned budget.
• Possessing strong leadership skills and building a high-performing, motivated and engaged team while developing individual talent and managing performance.
• Connecting with internal and external customers and shaping our business to help the appropriate patients.
• Working in the field with minimal supervision, adapting quickly to change and demonstrating an understanding of pharmaceutical/biotech regulatory and promotional guidelines.

Senior District Manager, Genitourinary (GU) – Southern California

• Lead, mentor, and motivate team members to achieve performance goals and high customer satisfaction.
• Oversee day-to-day operations, ensuring adherence to policies, procedures, and service level agreements (SLAs).
• Monitor key performance indicators (KPIs) and identify areas for operational improvement.
• Ensure all operations follow industry regulations and company standards.
• Analyze customer feedback to drive service enhancements and resolve issues.
• Collaborate with cross-functional teams and external partners to streamline processes and improve workflow in a respectful and positive manner.
• Supervise, coach, and mentor a team of 50+ direct and indirect reports, ensuring excellent patient service.
• Foster a positive, inclusive, and high-performance work culture.
• Responsible for the creation and delivery of presentations to internal stakeholders related to compliance, status of patient care, successes in operations, opportunities for improvement, and quarterly business reviews.
• Strong compliance approach, ensuring teams have a clear understanding of patient privacy laws.
• Stay abreast of industry trends and regulatory updates that may impact program delivery.
• Up to 25% travel required, primarily to Pittsburgh, PA.

Associate Director, PSC Operations

• Implement the pre-defined global Functional process template across regions and business units, ensuring compliance with industry regulations and SAP standard processes.
• Lead the deployment of a functional template within S/4HANA, avoiding customizations unless strictly required by legal or regulatory requirements.
• Ensure that all design decisions conform to SAP Clean Core principles—favoring configuration over custom development and using standard extensibility frameworks where needed.
• Lead cross-functional teams including business SMEs, IT, SAP consultants, validation experts, and system integrators in the execution of Value Stream-related project deliverables.
• Collaborate with other value stream leads (e.g., Order To Cash, Finance, Master Data) to ensure fully integrated end-to-end process design.
• Act as a key liaison between business units, program leadership, and technical teams, ensuring alignment on scope, timeline, and business readiness.
• Oversee detailed solution design, configuration reviews, data migration validation, testing strategy (including GxP and CSV compliance), and business process walkthroughs.
• Manage Value Stream-related testing activities including Functional Testing, User Acceptance Testing (UAT), and validation activities in alignment with SDLC.
• Support the creation and approval of Value Stream-related validation deliverables in accordance with QA and regulatory requirements.
• Collaborate with the Change Management team to drive user readiness and adopt the global Value Stream template.
• Support creation and delivery of training materials and process documentation tailored to the needs of regulated users and business partners.

Deploy Process Manager – Plan & Source

Medical Director

• Leads the project scientists, ensuring appropriate training, mentoring, and supervision across the assigned study/studies within the clinical development program
• Works closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders
• Provides support for clinical study/studies within a development program including: Working closely with clinical project scientists in collaboration with GCO and GMS to ensure comprehensive medical monitoring, thorough and timely responses to address site issues and eligibility questions, and detailed, real time review of serious adverse events and deaths
• Working in partnership with clinical project scientists to ensure development of high quality study protocols including use of consistent processes/standards across studies
• Collaborating with the Clinical Leader, Clinical Project Scientists and Procurement on key study design elements including assessment of complexity and cost of protocol-required evaluations
• Participating in strategic study start-up planning in collaboration with GCO and C&G including early site assessment, feasibility, and use of simplified contract and budget templates to accelerate rate of site activations
• Co-leading and overseeing clinical development/authorship of informed consent forms, eCRFs, study manuals, clinical study reports, and regulatory submission documents
• Working closely with Medical Writing to support protocol or protocol amendment completion
• Working closely with Clinical Leader, Regulatory and GCO to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion
• Working closely with GCO to track study recruitment and implement action plans to address early impediments to study enrollment
• Working closely with Quality Management & Quality Assurance to review audit findings and implement effective corrective action plans
• Working closely with clinical scientists and data management to support medical review and data query resolution
• Interacting with clinical investigators and Key Opinion Leaders as appropriate
• Working with GCO to provide oversight of CRO/study vendors’ performance as it relates to study start-up and conduct
• Working with the Clinical Leader, with Data Management and with Statistics on analysis of study results and completion of study reports
• Works with the Clinical Leader to support the development and compilation of NDA/MAAs and to support responses to Health Agency questions and HA presentations post-filing
• May review/co-author medical publications emerging from clinical trial results
• May interact with medical consultants in concert with senior clinical staff, in conducting IDMC and Investigator meetings as well as Advisory Boards

Medical Director/Senior Medical Director, Oncology Late Development

Financial Planning and Analysis

• Own the end-to-end product strategy and roadmap for FP&A and Reporting technology solutions
• Partner with Finance, Supply Chain, and Commercial stakeholders
• Lead the delivery and continuous improvement of FP&A applications
• Ensure solutions support accurate forecasting, budgeting, cost management
• Drive vendor and system integrator relationships

Technology Senior Manager, Finance (FP&A)

• Lead the end‑to‑end management of strategic IT vendors, including onboarding, performance management, renewals, and exits, to ensure reliable and cost‑effective technology services.
• Establish and govern vendor performance through SLAs, KPIs, scorecards, and regular business reviews, driving accountability and continuous improvement.
• Partner with IT service owners, sourcing, procurement, finance, and legal teams to align vendor strategies with business and technology roadmaps.
• Identify, assess, and mitigate vendor‑related risks, including operational, financial, cybersecurity, and compliance risks, in alignment with enterprise policies.
• Support contract negotiations and commercial discussions to optimize cost, value, and service outcomes across the vendor portfolio.
• Drive standardization of vendor management processes, tools, and reporting across Technology Services.
• Lead and develop vendor management team members, fostering a culture of accountability, collaboration, and continuous learning.
• Provide executive‑level insights and reporting on vendor performance, risks, and financials to IT and business leadership.

Technology Manager – IT Vendor Management

Director

• Lead and oversee IT Quality strategy for North America, including quality governance, testing, validation, and continuous improvement across enterprise and commercial systems.
• Direct managers and senior individual contributors in a matrix environment, providing coaching, performance management, and talent development.
• Establish and maintain quality standards, processes, and metrics for software development, system validation, and release management.
• Partner with IT, Digital, and business stakeholders to ensure quality is embedded throughout system design, development, testing, deployment, and support.
• Oversee risk identification, mitigation planning, and issue escalation related to system quality, compliance, and reliability.
• Ensure compliance with applicable regulatory, corporate, and internal quality requirements impacting IT systems and data integrity.
• Use data, dashboards, and KPIs to monitor quality performance and drive improvements across IT platforms and services.
• Collaborate with external vendors and internal partners to align on quality expectations, testing approaches, and delivery standards.

Technology Director, Quality

• Define and own the global WMS strategy and roadmap, ensuring alignment with enterprise IT and Supply Chain priorities.
• Lead global WMS operations, including system stability, performance, upgrades, and continuous improvement across distribution centers and regions.
• Partner with Supply Chain, Manufacturing, Quality, and Commercial teams to deliver technology solutions that improve warehouse efficiency, accuracy, and service levels.
• Oversee global WMS implementations, enhancements, and integrations, including vendor coordination and delivery governance.
• Lead the application of AI, advanced analytics, and automation to modernize supply chain platforms, improving demand forecasting, planning accuracy, and end-to-end decision-making while driving efficient and resilient supply chain operations at scale.
• Ensure WMS solutions meet regulatory, quality, and compliance requirements applicable to medical device supply chains.
• Manage external technology partners and service providers to deliver cost-effective, high-quality outcomes.
• Lead, coach, and develop a high-performing global team of supply chain technology professionals.
• Drive data-driven decision-making and standardization to improve global warehouse visibility and performance.