Jobs at Johnson & Johnson

Field-based medical affairs role executing KOL engagement and peer-to-peer education across the Northwest. Build relationships with academic and community KOLs, run compliant speaker programs, advisory boards, and congress activities, capture field insights, align with cross-functional partners, and drive brand priorities through disciplined execution and market understanding. Significant travel required.

Develops, validates, and scales supplier manufacturing processes for plastics components and subassemblies used in medical robotics and digital solutions. Leads supplier process development, tooling, inspections, qualification, corrective actions, and continuous improvement. Collaborates with R&D, Manufacturing Engineering, Quality, Purchasing, Supply Chain, and other teams to optimize manufacturing for performance, cost, and regulatory compliance. Applies engineering, statistical, risk-management, Six Sigma, Lean, and project-management methods while mentoring junior engineers and traveling up to 25%.

Supports administration, maintenance, monitoring, and continuous improvement of the Quality Management System. Responsibilities include document and records control, CAPA, nonconformance, change control, training management, audits, quality metrics, QMS reviews, inspection readiness, compliance monitoring, and remediation. Collaborates with Quality, Regulatory Affairs, Manufacturing, Engineering, Operations, Supply Chain, R&D, Service, and IT to ensure compliance with FDA QMSR, ISO 13485, company procedures, and related regulations.

Lead the Monarch Bronchoscopy medical device development program by managing cross-functional teams, timelines, budgets, milestones, risks, vendors, and stakeholder communications. The role coordinates project execution, drives quarterly goals, resolves issues, prepares management updates, and supports regulated product development. It requires substantial experience in regulated environments and program or project management, with medical device design control and regulatory knowledge preferred. The position is based in Santa Clara, California, with up to 10% domestic and international travel.

Sells and supports DePuy Synthes foot and ankle orthopaedic products across an assigned territory. Responsibilities include developing customer accounts, educating surgeons and hospital staff, providing operating-room case coverage, managing inventory and product delivery, building clinical relationships, collaborating on territory strategy, and achieving sales goals while maintaining compliance with applicable policies and regulations.

Leads tax planning strategy for intellectual property, product sourcing, business models, acquisitions, divestitures, and international expansion. Evaluates tax-efficient structures, advises business initiatives, supports transfer pricing and controversy matters, manages tax reporting and FIN 48 reserves, assesses effective tax rate impacts, oversees intercompany agreements, and advises on global mobility issues. Partners with Finance, Supply Chain, Tax Counsel, and regional business leaders.

Develop and maintain an AWS-based cloud data platform supporting medical robotics and software applications. Responsibilities include AWS infrastructure deployment and automation, data pipeline optimization, containerization, serverless solutions, infrastructure-as-code, incident resolution, root-cause analysis, troubleshooting, and architecture improvements. The role also supports feature planning and requires familiarity with cloud services, scripting, relational databases, Docker, Kubernetes, DevOps, and CI/CD practices.

MBA interns will complete 10–12-week MedTech marketing assignments in global strategic or U.S. marketing. Responsibilities include product launches, brand strategy, pricing, promotional and training plans, forecasting, customer insight development, product positioning, market research, and cross-functional collaboration with R&D, sales, customers, and vendors. Interns will address healthcare challenges, manage complex projects, influence stakeholders, and gain exposure to senior leaders. Successful interns may be considered for the full-time Marketing Leadership Development Program.

Lead manufacturing engineering for precision mechanical and electromechanical systems in surgical robotics. Responsibilities include developing and validating assembly processes, tooling, fixtures, metrology, fastening, bonding, and inspection systems; managing NPI and industrialization; troubleshooting robotic mechanisms; authoring regulated process documentation; and collaborating with R&D, Quality, Operations, and Production. The role also mentors junior personnel and ensures scalable, precise, and compliant manufacturing for robotic arm and instrument-drive assemblies.

Leads a manufacturing engineering team and provides hands-on technical direction for electronics, PCB/PCBA, electromechanical fixtures, test equipment, validation, production support, and documentation. Oversees manufacturing deliverables across new product introduction and sustaining programs, ensures quality and regulatory compliance, drives continuous improvement, and partners cross-functionally on equipment, process, and manufacturing readiness. The role is fully onsite in San Jose and includes up to 10% travel.

Leads end-to-end software program execution for the Ottava surgical system, including schedules, quarterly objectives, risk mitigation, contingency planning, conflict resolution, and stakeholder alignment. Drives Agile teams toward development milestones, communicates strategic tradeoffs, promotes team effectiveness, and manages and develops personnel. The role requires technical and program management experience in regulated environments, with medical device experience preferred.

Leads Pacific Northwest key opinion leader engagement and medical education strategy for lung and head and neck oncology. Builds relationships with healthcare leaders, shapes brand strategy and local market insights, coordinates cross-functional initiatives, manages budgets and agencies, supports educational programs and congresses, and ensures compliance with ACCME, HCC, and PhRMA guidelines. The role requires extensive field travel, oncology expertise, strategic thinking, and collaboration with medical, commercial, brand, and analytics teams.

Design and develop electrical systems for medical robotic platforms, including PCAs, power electronics, motor control, sensing, communications, and fault-tolerant systems. Own hardware development from architecture and schematic design through PCB layout, prototyping, verification, documentation, and release. Conduct testing, EMI/ESD evaluations, thermal analysis, troubleshooting, and design validation while collaborating with multidisciplinary engineering teams.

Systems and Simulation Engineering Interns will support the development and testing of robotic surgical systems through systems engineering, modeling, simulation, requirements development, verification, and performance analysis. Responsibilities include collaborating with multidisciplinary engineering teams, analyzing simulation and test data, supporting architecture and tradeoff studies, documenting results, correlating simulations with laboratory tests, and creating automation tools for robotics R&D.

Design and implement real-time control software and algorithms for next-generation medical robotic systems. Collaborate with cross-functional teams to prototype, test, and evaluate human-robot interaction, control algorithms, and hardware. Participate in design reviews, code reviews, procedure development, and clinical procedure support while ensuring safety-critical system performance.

Develop, implement, and test control algorithms for robotic surgical systems. Build C++ software for real-time, safety-critical applications, participate in code reviews and debugging, collaborate on software architecture and system requirements, and document algorithms and designs. Work with robotics hardware, kinematics, dynamics, control theory, estimation, perception, AI/ML, and embedded systems in support of the OTTAVA surgical robotic platform.

Supports clinical engineering and human factors activities for robotic surgical systems and medical devices. Responsibilities include researching clinical workflows, defining user needs, conducting usability and product evaluations, analyzing qualitative and quantitative data, preparing risk and traceability documentation, developing task analyses and test methods, and communicating findings through reports and presentations. Collaborates with physicians, healthcare professionals, engineers, and end users to improve product safety, usability, and performance.

Software Engineering Interns will design, develop, test, document, and maintain software for real-time, safety-critical robotic surgical applications. Responsibilities include software architecture, embedded and firmware development, application and UI components, robotics algorithms, debugging, code reviews, performance optimization, and collaboration with systems, electrical, mechanical, quality, and clinical engineering teams. Interns will apply software quality, cybersecurity, reliability, and maintainability practices throughout the development lifecycle.

Supports surgical robotics R&D through system and subsystem integration, testing, troubleshooting, design characterization, and development of test methods and fixtures. Collaborates across mechanical, electrical, software, controls, and clinical engineering domains to develop and improve robotic surgical platforms.

Electrical Engineering Interns will design, prototype, test, debug, and integrate PCBAs for surgical robotic platforms and medical device systems. Responsibilities include creating technical documentation, conducting root-cause analysis, presenting design concepts, collaborating across electrical, mechanical, software, controls, and clinical engineering teams, and participating in robotic device assessments. Projects may involve electrical design, assembly, manufacturing, firmware, and testing.