Johnson & Johnson

Brand Manager

• Brand activation & integration lead across all experience touchpoints - digital, social, content, and experiential
• Brand strategy & positioning - OTTAVA in category, brand platform, value prop, visual expression (collaborate with GSM on product positioning)
• Build & manage brand expression and guidelines (architecture, naming, etc)
• OTTAVA social strategy
• Balance high‑impact hero storytelling with efficient, scalable content production.
• Content operations and enablement (formats, production needs, scalable design solutions)
• Build high performing agency roster in collaboration with digital and creative lead
• Execute and deliver on marketing and communication asset needs and manage brand library
• Manage & lead brand campaigns, media, and collaboration with commercial on activation – partner on performance optimization with digital and creative lead
• High collaboration, coordination and leadership across internal and external teams required
• Lead day-to-day activities and management of external agency partners ensuring strong partnership and delivery on brand and experience mandatories
• Support Global Strategic Marketing and Regional Marketing teams in creation and execution of market enablement initiatives.
• Responsible to stay abreast of the latest market trends and research results and incorporation of key takeaways into messaging and communication initiatives
• Lead connection to Surgery, MedTech, Enterprise

Brand Director

Clinical Research

• Represent Clinical Science as core team member on critical projects, liaising between project and functional teams, and coordinating with Clinical Operations and Project Management partners to deliver on time, within budget, and in compliance with regulations and SOPs
• Activate and build collaborative relationships with across business platforms as well as key cross-functional partners (e.g., Global Strategic Marketing, Medical Affairs, Regulatory Affairs, R&D, etc.) to ensure consistent alignment in new product development and through product life cycle
• Lead initiatives for appropriate interpretation and dissemination of all evidence generated, including Clinical Study Reports, abstracts, manuscripts, and MDR-related documents (CER, PMCF, Clinical Plans, etc.)
• Contribute to clinical scientific discussions with regulatory agencies that support the clinical and regulatory strategy, including proposed investigations, review process of evidence to support marketing authorization, and support of regulatory inspections
• Engage and collaborate with industry's key opinion leaders, including KOLs and regulatory agencies, and build on relationships established through professional/technical societies

Principal Clinical Research Scientist – Surgical Implants

Account Manager

• Represent the organization by interacting with established customers and developing new prospects
• Apply a broad knowledge of the organization's products, services and marketing campaigns to close sales
• Understand customer’s strategic priorities, buying motives, end user needs,
• Participate in sales training activities and study marketing techniques
• Effectively communicate and utilize multiple resources and tools to deliver a clear and concise sales message

Territory Account Manager – MedTech

Manager

• Provide strategic, operational, and decision support to the Innovative Medicine Quality Leadership Team (IMQLT).
• Lead and/or support assigned projects, complex, cross-functional programs and key initiatives, across the Innovative Medicine Quality (IMQ) organization.
• Coordinate IMQ communication plans, leader meetings and forums.
• Champion change management, drive stakeholder and employee engagement and provide support to key leadership and executive meetings, presentations and engagements.
• Partner closely with the Global Communications team to develop and execute communications for the Innovative Medicine Quality organization.
• Manage the IMQ HOME page & Viva Engage community.
• Monitor the competitive landscape, provide insights and inform the IMQLT about company and industry developments, news, product launches, competitive moves, etc.
• Develop executive level, strategic messaging, and provide support for speaking engagements, key leadership meetings and executive presentations in partnership with Global Corporate Affairs.
• Create and maintain a high performing team culture within IMQ, champion change management and drive employee and stakeholder engagement.

Senior Manager, Strategy & Insights

Operations

• Lead the integration and management of healthcare compliance initiatives
• Oversee the compliance of HCC data management and operations
• Collaborate with global teams in the implementation of compliance strategies
• Develop and provide training related to compliance standards
• Analyze and mitigate compliance risks affecting the organization

Director, HCC Data Management – Tech Operations

Director

• Provide medical affairs support for Craniomaxillofacial platform
• Deliver medical and surgical input across product development and life-cycle management
• Collaborate cross-functionally to support evidence generation and market registration
• Provide clinical guidance and expertise as a medical expert
• Research and prepare responses to medical information requests

Senior Manager – Medical Affairs, LCM

Communications

• Leading global communications for neuroscience, cardiovascular, and established products
• Managing strategy, launch execution, growth brand messaging, and issues management
• Maximizing commercial opportunities through orchestrated communications and market shaping
• Influencing policy, stakeholder engagement, and brand visibility in high-revenue markets
• Overseeing a global team with 10 direct reports and 14 indirect reports
• Accountable for global messaging for therapeutic areas and products
• Ensuring impactful communications that drive revenue generation and brand growth

Vice President, Global Neuroscience & Cardiovascular – Established Products Communications & Public Affairs

• Represent Clinical Science as core team member on critical projects, liaising between project and functional teams, and coordinating with Clinical Operations and Project Management partners to deliver on time, within budget, and in compliance with regulations and SOPs
• Activate and build collaborative relationships with business platforms as well as key cross-functional partners (e.g., Global Strategic Marketing, Medical Affairs, Regulatory Affairs, R&D, etc.) to ensure consistent alignment in new product development and through product life cycle
• Lead initiatives for appropriate interpretation and dissemination of all evidence generated, including Clinical Study Reports, abstracts, manuscripts, and MDR-related documents (CER, PMCF, Clinical Plans, etc.)
• Contribute to clinical scientific discussions with regulatory agencies that support the clinical and regulatory strategy, including proposed investigations, review process of evidence to support marketing authorization, and support of regulatory inspections
• Engage and collaborate with industry's key opinion leaders, including KOLs and regulatory agencies, and build on relationships established through professional/technical societies

Principal Clinical Research Scientist – Equipment Platform Vision

• Represents Deliver through balanced role with other E2E pillars (Plan-Source-Make).
• Connects BU strategies and requirements into Deliver Center Operations and Capabilities teams, as well as the other way around.
• Partners with regions for critical processes and accountabilities, including Performance Mgmt., BP/LRFP, Flow Optimization, NPI execution, Margin Expansion.
• Partners with GSCS teams (GTTO, Trade Compliance) focusing on transportation/lane optimization, tariffs management and budget control.
• Infuses business specific priorities into the overall MedTech SC Deliver strategy and capability roadmap to accelerate BU growth.
• Collaborates with E2E SC team to drive MedTech SC Deliver strategic plans associated with the respective BU (i.e. product flow optimization, efficiency and productivity initiatives for hubs and transportation, capacity and capabilities improvement, etc.).
• Ensures visibility into global Hubs priorities and performance, and drives global aggregation through partnership with Regional SC Leads.
• Shared accountability for performance metrics, including OTIF-SC and OTIF-D as part of E2E SC; drives continuous improvement against failure modes linked to Deliver including partnering to address E2E issues.
• Ensures on time delivery of NPI and new capabilities through Deliver Playbook adherence and maturity.
• Shared accountability with E2E SC for optimizing inventory levels through improvement on unproductive inventory reductions at Hubs, international lanes reliability and leadtime compression and E2E product flows design.
• Shared accountability with Global E2E SC for driving COGS reduction in freight and warehousing and margin expansion across; ensures a process is in place to provide visibility to Deliver cost performance and improvement, jointly sets and works to achieve cost optimization targets.
• Shared accountability with Global E2E SC to ensure a robust foundation in compliance including trade compliance, Quality, EH&S, financial compliance.
• Develops talent and maintains leadership pipeline; actively sponsors and mentors key talent across E2E supply chain, builds leadership competencies in team.
• Responsible for Deliver integration into core global processes (e.g., STEM, issue management/escalations, strategic capacity planning, S&OP, IBP and E2E flow optimization).

Manager, Deliver Business Unit Integration, Med Tech

Analyst

• Manage outbound transportation operations for customer shipments, including domestic and international distribution from J&J distribution centers
• Coordinate shipment planning and execution to ensure timely and accurate delivery to end customers, including hospitals, wholesalers, and specialty care providers
• Track and trace outbound shipments, providing proactive communication and resolving delivery exceptions to maintain service levels
• Support development, implementation, and analytics as well as provide analysis and recommendations to support strategic supply chain decisions
• Partner with distribution centers, customer service, and logistics teams to align shipping priorities with customer requirements and order fulfillment timelines
• Monitor carrier performance and compliance with service level agreements (SLAs), escalating issues and driving corrective actions as needed
• Lead cost improvement initiatives by identifying opportunities to optimize routing, mode selection, consolidation, and carrier utilization
• Drive service improvement initiatives to enhance delivery reliability, visibility, and customer satisfaction
• Analyze and report transportation metrics related to service, cost, and efficiency to support operational and strategic decision-making
• Ensure compliance with transportation regulations, company policies, and customer-specific requirements for outbound shipments

Transportation Analyst

• Driving continuous quality improvements
• Maintaining Service & Repair compliance
• Providing global multi-site support
• Presenting internal and external customer-facing needs to site leaders and business unit partners
• Coordinating regional efforts related to compliance, technology investments, regulations, and resource management/optimization

Director, Service & Repair Quality

• Lead a global team of PV Quality Management experts overseeing the end-to-end delivery of process, qualification, and training
• Enable Business Partners to conduct R&D/Medical Safety efficiently and compliantly
• Set the vision and strategy for process and personnel qualification management in collaboration with R&D senior leaders
• Act independently to drive results and organizational performance
• Represent IMQS-PDM as a champion to key business partners and stakeholders
• Manage staff for process/qualification/training design

Director – PV Quality Management

Compliance

• Responsible for supporting a robust regulatory compliance program for the worldwide headquarters, manufacturing sites, and R&D sites within the Surgery Segment of J&J MedTech
• Understands the factors contributing to compliance risk profiles, based on metrics and data analysis and other intelligence (e.g., escalations, regulatory inspection outcomes, etc.), to proactively identify, communicate, prioritize, address/prevent/reduce compliance risk
• Conducts Follow-up activities for the JJRC independent audit program, field action assessments, significant health authority inspections, post-acquisition assessments, and regulatory actions
• Provides leadership and expertise to interpret and evaluate audit observations and provides guidance and support to develop risk-based action plans
• Identifies opportunities for cross-regional/site remediation activities collaborate with Segment Quality and Compliance professionals to develop risk-minimizing strategies
• Support supplier/EM compliance activities through the review of supplier audit reports and follow-up reports
• Participates in early engagement activities with stakeholders
• Assists with escalation and alignment activities associated with supplier/EM outcomes as needed
• Provides oversight and compliance review of remediation programs (MCAP/SDCAP/QEP, PAM, etc.)
• Ensures partnership with JJRC and other Q&C groups to leverage work / resources to minimize duplication
• Interprets and communicates current and emerging regulatory and J&J requirements at a global level
• Partners with Q&C and Enterprise Regulatory Outreach teams to continuously monitor the changing regulatory climate to proactively assess and communicate industry trends and emerging areas with potential impact to compliance programs
• Serves as a key advisor and subject matter expert for critical compliance activities, including due diligence, mock inspections, regulatory agency interactions, decommissioning, divestiture, Compliance Data Reviews, special investigations, and business strategies, as needed
• Supports Health Authority inspection readiness activities at high-risk sites, ensures subject matter expert preparedness, and reviews significant communications with Health Authorities
• Engages with high risk sites, as needed, to oversee and, if necessary, verify remediation efforts.

Brand Director

Principal Clinical Research Scientist – Surgical Implants

Territory Account Manager – MedTech

Senior Manager, Strategy & Insights

Brand Director

Director, HCC Data Management – Tech Operations

Senior Manager – Medical Affairs, LCM

Vice President, Global Neuroscience & Cardiovascular – Established Products Communications & Public Affairs

Principal Clinical Research Scientist – Equipment Platform Vision

Manager, Deliver Business Unit Integration, Med Tech

Principal Clinical Research Scientist – Surgical Implants

Transportation Analyst

Director, Service & Repair Quality

Director – PV Quality Management

Director, Compliance