Jobs at Johnson & Johnson

The Sales Consultant develops relationships with surgeons to drive sales of medical products, manages accounts, and provides case support to enhance patient care.

As a Clinical Representative, you will support surgeons by providing technical expertise, training, and procedural support within Orange County. Responsibilities include maintaining customer relationships, providing education, and assisting in account development for robotic-assisted urology solutions.

Lead and optimize escalation and field action processes and systems to ensure compliance with global regulations and J&J policies. Manage QRB/RMB activities, support field corrective actions, prepare regulatory reporting and recall documentation, monitor QMS performance, drive process improvements, and provide SME leadership and training across cross-functional teams.

Manage pricing and commercial contracts for MedTech customers including drafting, negotiation, execution, rebate-driven strategies, CPC governance, data analysis, compliance support, and cross-functional stakeholder coordination to enable sales and pricing decisions.

Lead labeling process improvements and projects for MedTech products: manage artwork design/approval/release, ensure regulatory compliance, drive system/process enhancements, mentor team members, coordinate global stakeholders, and partner with external vendors to optimize labeling operations.

Field-based sales consultant responsible for developing surgeon and account relationships, driving orthopaedic product sales, providing case coverage and OR support, implementing territory sales plans, managing inventory and promotional materials, and educating surgical teams to meet sales targets.

Lead cross-functional lifecycle management projects for medical devices, applying engineering and supply-chain expertise to improve processes, ensure continuity of supply, drive validations (IQ/OQ/PQ), implement corrective actions, mentor engineers, manage supplier relationships, and use Six Sigma/Lean methods to improve quality, productivity, and cost.

The Sr Engineer Quality Engineering ensures medical devices meet quality standards through leadership in design controls, risk management, and collaboration with product teams. Responsibilities include managing quality attributes, addressing quality issues in development, and supporting compliance with quality management systems.

Lead global communications and public affairs for J&J MedTech Electrophysiology. Set strategy across stakeholders, advise business leadership, manage a communications team, protect reputation, enable growth, drive employee engagement, and measure impact.

Lead and manage company‑sponsored neurovascular clinical trials end‑to‑end: feasibility, site selection, setup, conduct, monitoring, data review and closure. Develop trial documents, manage investigational devices and vendors, ensure regulatory and safety reporting compliance, support evidence generation and cross‑functional alignment, mentor study staff, and deliver projects on time and within budget.

Lead creation and delivery of scientific publications and congress materials for electrophysiology devices. Write manuscripts, abstracts, posters, and presentations; collaborate with cross-functional teams and external authors; interpret clinical data and develop figures/tables; ensure compliance with publication and regulatory guidelines; manage review/approval workflows; support congress planning and evidence dissemination.

Lead a Business Intelligence team supporting Electrophysiology and Cardiac Imaging & Structural Heart. Develop BI roadmap, build executive dashboards and self-serve analytics, translate data into executive recommendations, drive cross-functional commercial initiatives, ensure data quality and scalable solutions, and mentor analysts to deliver measurable commercial impact.

The Clinical Science & External Research Manager drives evidence generation strategies, manages external research programs, oversees study execution, and supports publication development while collaborating with cross-functional teams.

The Manager of R&D PMO leads global new product development programs, guiding cross-functional teams to ensure timely delivery aligned with regulatory standards and quality requirements, while managing risks and stakeholder communication.

Lead and scale knowledge management capabilities for R&D, focusing on GenAI retrieval strategies, data architecture, and collaboration with cross-functional teams.

Lead UX and product design for a next-generation surgical data and AI platform. Drive user research, define multimodal UX paradigms, build design systems, lead a team of designers, and partner with product, engineering, data science, and clinical stakeholders to deliver compliant, secure, enterprise-scale AI-enabled solutions.

The Senior Manager, External Manufacturing will manage global External Manufacturers to deliver quality, service, and financial performance for Electrophysiology products. Responsibilities include supplier performance management, strategy development, business engagement, and operational planning.

Provide clinical and technical support, training, and consultancy to physicians and EP lab staff on CARTO systems, catheters, and related equipment. Drive consultative sales, develop customer relationships, plan case support, mentor new team members, ensure compliance, document account activity, and collaborate with internal teams to grow account value. Requires frequent problem-solving in high-stress procedural environments.

Lead US Surgical Vision pricing strategy, deal desk, pricing committee, and contract compliance. Build tools and processes, drive adoption, manage rebate calculations and audit readiness, run commercial improvement projects, and coach a team of five while partnering with sales, marketing, finance, legal, and compliance to drive profitable growth.

Design and deliver robust electrical systems for ophthalmic medical devices across the product lifecycle. Develop mixed-signal, power, motor-control, and digital circuit designs and PCBs; create system algorithms and communication protocols; perform circuit simulation, prototype development, and IEC/EMC hardware testing. Lead subsystem projects, write requirements and test protocols, collaborate with cross-functional teams, and document hardware for regulatory-compliant formal release and post-launch support.