Johnson & Johnson

Product Manager

• Delivery of tools and technology that automate repetitive tasks, leverage data, augment decision making and reimagine processes.
• Ensure deep integration, alignment & synchronization across the sector functions. Line up connections and collaboration of similar processes & capabilities (use cases).
• Execute rapid hands-on engineering (citizen development) to support delivery of benefits for sectors.
• Lead digital workshops, support Q&C proof of concepts & deliver on sector transfer products.
• Scout new opportunities for digital capabilities in partnership with JJT and sector digital functions.
• Establish and maintain digital product operational framework and digital lifecycle management.
• Distill business process needs, assisting with articulating the needs with technical partners​.
• Partner with and coordinate with SMEs to identify execution roadblocks – escalate to EQ LT for solutions where needed​.
• Act as a change agent for digital adoption, ensuring a digital perspective is considered in solution design on product teams​.
• Assist with cross-segment visibility to digital, AI, and IA-enabled solutions.
• Establish key metrics to track progress towards long-term digital product maturity.
• Help support and lead initiatives to drive execution of the Q&C digital strategy overall.
• Enables enterprise-wide innovation sharing while supporting segment needs.
• Feed in & out demand & supply of solutions across the Q&C workstreams.
• Accountable for timely and on-budget execution of products, where EQ has ownership.
• Stimulate "digital first" attitude in product teams and partner functions.
• Support communications & capability building for Enterprise Q&C population.
• Hands-on execution activities related to the digital deliverables.
• Act as a change agent for digital adoption, ensuring a digital perspective is considered in solution design on product teams.
• Distill business process needs, assisting with articulating the needs with technical partners​.
• Manage vendor resources where applicable.
• Promote and grow the EQ product portfolio.
• Coach, mentor and educate colleagues across the organization on EQ digital products and services.
• Identify opportunities for improvement to internal ways of working to support IA and collaborate with key stakeholders to implement aligned improvements.
• Collaborate with a broad team of segment & functional representatives and EQ to assist in connecting cross-workstream efforts.
• Understand the business problems/needs and help the business derive additional benefits through the identification of new and emerging services and capabilities.
• Provide input with the intent to influence product roadmaps.
• Consistently scan the internal and external environment to identify new capabilities to be delivered in support of the Q&C digital transformation and to enable value for the segments.

Business Product Owner, Digital Quality

Sales

• Lead therapy development to make Impella and Heart Recovery the ANZ standard of care by training clinicians, deploying toolkits, and building regional peer networks.
• Design and enforce clinical training and sign‑off pathways for physicians and support staff, tracking competency milestones and compliant documentation.
• Drive account adoption by prioritizing target hospitals, coordinating with commercial teams, and enabling clinical readiness and case reporting at key centres.
• Provide hands‑on clinical support in cath lab/OR/ICU, perform after‑action reviews, collect outcome data, and implement improvements to optimize patient outcomes.
• Forge strong partnerships with commercial and clinical stakeholders through weekly alignment, quarterly strategy meetings, and shared quality‑improvement initiatives.
• Travel across ANZ/APAC to monitor programs, lead trainings, support emergency cases, and scale therapy adoption regionally.

Senior Sales Manager

Customer Support

• Handle customer & stakeholder inquiries and complaints effectively taking ownership and escalating where required.
• Managing customer and commercial team interactions through telephony services.
• Contribute to achieving the team’s set KPIs by ensuring all customer orders, bookings & invoices are processed accurately in compliance with J&J Quality Systems & relevant SOP’s.
• Contribute to the National Customer Service Network providing support when needed.
• Collaborate with multiple departments including but not limited to Finance, Warehouse, Supply Chain, Commercial Team, Loan Kits etc.
• Effectively manage orders, consignment inventory, liaising with product specialists, hospital staff and warehouse to maintain stock availability at hospital locations.

Customer Service Representative

Communications

• Lead development and ongoing evolution of the integrated communications strategy for Accelerating Gamechangers.
• Serve as a strategic communications advisor to program and change leaders.
• Develop audience-centered communication frameworks, engagement strategies, and communication roadmaps.
• Apply insights, employee feedback, and communications metrics to refine strategies and improve program effectiveness over time.
• Counsel senior leaders on communication approaches that strengthen visibility, credibility, and engagement during organizational change.
• Develop and coordinate executive communications strategies and content for key leadership and governance forums.
• Ensure leaders are equipped with consistent, high-quality messaging and engagement resources.
• Establish and coordinate the transformation program's communications governance model.
• Provide subject matter expertise and consultation to project teams.

Senior Manager, Transformation Communications

Manager

• Lead regulatory affairs activities for the French market.
• Ensure compliance with local regulatory requirements.
• Enable timely, sustainable market access for DePuy Synthes products.
• Support product lifecycle activities.
• Manage regulatory risk.
• Partner with local, regional, and global stakeholders.
• Coordinate regulatory submissions, variations, renewals, and responses to health authority inquiries.
• Monitor regulatory changes and assess potential impacts to products, portfolios, and operations.
• Contribute to continuous improvement initiatives to enhance regulatory efficiency, consistency, and compliance.
• Ensure proactive engagement in shaping regional policy initiatives critical to business strategy, continuity, and growth.

Regulatory Affairs Manager

QA Engineer

• Support the design, development and testing of Medical Device Software, including Software as a Medical Device (SaMD) products.
• Provide leadership, guidance and expertise on the software development process, procedures and practices.
• Communicate business related issues or opportunities to next management level.
• Follow all Company guidelines related to Health, Safety and Environmental practices as applicable.
• Ensure that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
• Ensure personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.

Staff Quality Engineer – Product Quality

Director

• Actively contributes to Compound Strategy decision-making by ensuring relevant research, analysis, and expertise is available.
• Leads CDT in partnership with line functions to successfully develop the compound such that its value is maximized over its lifecycle while costs and time are minimized without sacrificing quality.
• Builds team effectiveness, and leads the Compound Development Team (CDT) to achieve its goals through the networks of people/functions represented on the team. When necessary, negotiates with function heads on functional deliverables.
• Challenges all functions on CDT to ensure that all issues and questions are being addressed, and that line function input into strategy and plans is adequate to meet the needs of the compound.
• Leads the development and maintenance of the compound development strategy in collaboration with the Project Manager (PM).
• Identifies potential issues and leads contingency planning; leads CDT problem solving and applies decision-making tools and techniques. Drives CDT to make effective and efficient decisions.
• Leads resolution of conflict at the CDT, Oncology Senior Leadership Team (Oncology SLT), Development Committee (DC), Investment Committee (IC), Group Operating Committee (GOC) and joint steering committees for partnered compounds and senior management levels.
• Ensures successful implementation of clinical supplies strategy.
• Accountable for overall budget and project plan deliverables.
• Acts as co-chair of global project teams with Alliance partners and aligns global strategy within a partnership, as applicable.
• Major collaborator for the internal Alliance Managers for partnered compounds.
• Ensures lessons learned at critical nodes in the development path.
• Leads the communication of strategy, issues, and plans to the PMC, Oncology SLT, DC, IC, GOC, alliance partners, JPKK, regional management boards, and other key stakeholders.
• Represents the interests of the compound/brand along with the global commercial lead at the Oncology SLT.
• Builds and maintains team effectiveness and satisfaction.
• Drives innovation by benchmarking.
• Secures the required resources for project success.
• Influences optimal team composition.
• Aligns goals and objectives with CDT members.
• Coaches and guides CDT members.
• Provides input for performance evaluation of CDT members.
• Align and implement on the Oncology SLT strategy.

Senior Director, Compound Development Team Leader – Oncology

• Assist DePuy Synthes sales organization in retaining and supporting further penetration with existing customers, while supporting product conversions with new customers.
• Assist in the attainment of established sales goals including market share objectives in prescribed territory.
• Apply knowledge of sales process, product portfolio and customer knowledge to improve sales outcomes.
• Guide and assist surgeons in the operating room through their clinical and product knowledge.
• Use product knowledge to present, demonstrate, and ensure proper utilization of DePuy Synthes products.
• Support customers by attending surgeries, assuring that the proper equipment is available and performing, including ways to optimize trays.
• Provide Operating Room and Sterile Processing Department consultation.
• Troubleshoot and provide other technical assistance; handle customer requests, effectively manage hospital billing, create/close purchase orders.
• Share key customer, procedural and marketplace insights with other sales, clinical, marketing and strategic account teams to improve on solutions/service levels.
• Prepare sales reports and documents as required.
• Maintenance, tracking and effective deployment of equipment, and assets throughout assigned area ensuring product availability.
• Ensure all promotional materials are maintained in a presentable manner.
• Ensure DePuy Synthes Services and offering meet highest quality standards.
• Focus on customer satisfaction and retention; and improving the customers’ insights into DePuy Synthes tangible and non-tangible value proposition and solutions.
• Differentiate DPS’s products versus competition by providing the customer unique insights.

Sales Associate, Trauma – Orthopaedics

• Provide strategic leadership for quality assurance and regulatory affairs across Latin America
• Ensure ongoing compliance with country‑specific regulatory requirements, applicable regional standards, internal policies, and DePuy Synthes quality management system expectations
• Provide strategic quality and regulatory guidance to support product registrations, renewals, variations, and full lifecycle management across LATAM markets
• Serve as the senior QARA escalation point for LATAM Local Market Support addressing regulatory, quality, and compliance risks
• Partner with cross‑functional stakeholders including Commercial, Operations, Supply Chain, Legal, and Global QARA to support product launches, supply continuity, and portfolio optimization
• Monitor, interpret, and communicate regulatory, quality, and enforcement trends across LATAM, proactively assessing business and patient safety impact
• Oversee and support regulatory inspections, quality audits, and health authority interactions, ensuring timely , consistent, and effective responses
• Drive continuous improvement, harmonization, and simplification of QARA processes across LATAM markets
• Lead, coach, and develop regional QARA leaders and teams, building strong capability, succession, and a culture of quality, compliance, and accountability
• Define distributor markets and design processes and systems that enable an efficient Distribution Management structure

Director, QARA LATAM – Distribution & Ops

• Target Assessment and Antigen Strategy Lead evaluation of therapeutic targets, including: Structural, sequence, and domain architecture analysis Integration of internal and external data (literature, databases, structural repositories) Define antigen and engineered-cell design strategies to support antibody discovery: Construct design and domain selection Epitope exposure and conformational state optimization Strategies for difficult targets (e.g., multi-pass membrane proteins) including Nanodisc technology and nucleic acid immunogen design
• Protein Design & Engineering Apply computational and structural biology approaches to protein design: Homology modeling, structural analysis, and rational mutagenesis Integration of emerging AI/ML-based protein design tools Engineer proteins to improve: Stability and expression Functional relevance for discovery assays and immunization

Director, Protein Sciences

Medical Officer

• Assess the medical safety of Innovative Medicine products
• Strategically lead cross-functional matrix teams
• Communicate potential and known risks to relevant stakeholders
• Lead design and implementation of risk mitigation strategies
• Collaborate with relevant functions to ensure timely assessments of safety data
• Provide medical and scientific expertise on clinical teams
• Anticipate safety concerns and influence clinical protocols
• Review and approve medical assessment reports
• Participate in department-wide initiatives and lead work process improvement

Medical Safety Officer, Immunology

• Assess medical safety of Innovative Medicine products
• Lead cross-functional matrix teams for product safety and benefit risk oversight
• Proactively assess safety data to characterize safety profiles
• Communicate potential and known risks to relevant stakeholders
• Lead design and implementation of risk mitigation strategies
• Provide medical expertise on development teams
• Collaborate with Clinical teams to minimize patient impact
• Contribute to key regulatory and clinical documents
• Actively participate in meetings with Health Authorities and external leaders
• Provide medical oversight on due diligence teams for Licensing & Acquisition
• Align and improve common processes across teams
• Create, review and implement safety assessment SOPs and tools
• Lead or participate in department-wide initiatives

Medical Safety Officer – Immunology

Operations

• Lead the design, implementation, and continuous improvement of Talent Acquisition processes, systems, and tools to enhance efficiency and scalability.
• Manage day-to-day TA operations, ensuring consistent execution of recruiting workflows, policies, and compliance standards.
• Partner with TA leadership and HR stakeholders to analyze workforce needs and align operational strategies with business objectives.
• Develop and track key recruiting metrics and dashboards, providing insights that inform decision-making and improve performance.
• Oversee TA technologies (e.g., ATS/HRIS) to ensure optimal functionality, data integrity, and user adoption.
• Drive continuous improvement initiatives by evaluating current programs and identifying opportunities based on industry best practices.
• Lead and mentor a team of TA operations professionals, fostering a culture of accountability, collaboration, and development.
• Collaborate cross-functionally with HR, IT, and business leaders to implement strategic TA initiatives and process enhancements.
• Ensure compliance with local labor laws and company policies related to recruitment and hiring activities.
• Support change management initiatives, including the implementation of new tools, processes, or organizational structures.

Senior Manager, TA Operations

Medical Director

• Responsible for the development and execution of the clinical development plan and has ownership for the design of clinical trials and for the content of clinical study reports
• Leads Cross-functional Clinical Team; supervises, develops and recruits junior medical staff
• Molecule responsible physician; Responsible for the oversite of medical monitoring/reporting and safety activities; Evaluates adverse events (pre and post-marketing) for relationship to treatment.
• Responsible for overseeing content for the Independent Data Monitoring Committee (IDMC) and adjudication meetings as needed
• Interprets, reports and prepares results of product research in preparation for global health authority submissions and external communication
• Responsible for assessment of medical publications emerging from the Team and its affiliates
• Assists Regulatory Affairs in the development of drug/device regulatory strategies and determining requirements for any corrective actions or health authority reporting
• Acts as medical contact at company for global health authorities concerning clinical/medical issues
• May act as company spokesperson regarding publication of clinical research findings and presentations to relevant global health authorities and advisory committees
• Helps explore and evaluate new product ideas to assist in identifying new marketing opportunities
• Supports general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance
• Supports early clinical development involving product potential and development for registration
• Manages the budget for all project related clinical activities

Executive Director, Clinical Leader – Neuropsychiatry

Clinical Specialist

• Provide case support to physicians within certain territories.
• Cover procedural case coverage for peripheral and coronary interventional procedures in the pre-market and post-market phases.
• Play a critical role in clinical studies including device training, case support,
• Ensure timely data collection for clinical programs.
• Present clinical study training materials based on investigational plans to support the safe and effective use of medical devices.
• Manage key study investigators and foster relationships with medical advisors.
• Partner with clinical research colleagues to meet business needs including site re-training and data collection.
• Administrative activities including training to procedures, manage territory travel and budgets.