Jobs at Johnson & Johnson

Provides strategic legal counsel to MedTech teams across medical device regulatory strategy, clinical research, approvals, market access, commercialization, promotion, post-market surveillance, quality compliance, inspections, field actions, healthcare interactions, privacy, cybersecurity, and fraud and abuse laws. Collaborates with global legal, regulatory, compliance, and business teams and supervises promotional-material review. Travel within the United States is required up to 10% of the time.

Leads manufacturing engineering for precision electromechanical assemblies used in surgical robotics. Designs, validates, and documents assembly processes, tooling, fixtures, inspection methods, and manufacturing readiness activities. Owns DFM, NPI, troubleshooting, root-cause analysis, process optimization, quality documentation, and cross-functional transitions with R&D, Quality, and Production. Requires deep expertise in robotic mechanisms, harmonic drives, motors, encoders, CAD, GD&T, statistical methods, regulated medical-device environments, and mentoring junior personnel.

Manages the global Supply Chain Collaboration template and leads supplier onboarding, enablement, and deployment activities. Oversees requirements, fit-gap assessments, solution design, testing, training, cutover, hypercare, and ongoing optimization using SAP collaboration platforms. Partners with supply chain, procurement, technology, suppliers, and deployment teams to expand capabilities, integrate with S/4HANA, adopt AI, and improve inventory visibility and collaboration. The role also supports governance, compliance, change management, and global business transformation programs.

Lead the mechanical and electromechanical design of robotic medical device hardware from concept through verification, validation, and production release. Responsibilities include designing precision assemblies, actuator and sensor-integrated mechanisms, tolerance analysis, DFM/DFA, prototype testing, failure analysis, quality documentation, risk assessments, manufacturing transfer, supplier collaboration, and production issue resolution. Provide technical leadership, collaborate cross-functionally, and mentor junior engineers.

Manages OTTAVA contract intake, drafting, revisions, negotiation support, execution, redlining, legal reviews, compliance, pricing alignment, and audit-ready documentation. Partners with Finance, Legal, Pricing Operations, and CPC governance teams to resolve escalations, standardize templates, reduce cycle times, and maintain the contract database. Requires extensive contract management experience, strong commercial and compliance knowledge, and familiarity with security amendments, BAAs, PHI, and data security.

Manufacturing Engineer leading new product introduction for robotic medical device systems. Responsibilities include designing and validating assembly processes, tooling, gauges, and fixtures; maintaining manufacturing and quality documentation; troubleshooting electromechanical systems; conducting root cause analysis; supporting process characterization and validation; and driving continuous improvement with cross-functional R&D, Quality, and Production teams.

Leads U.S. commercial finance for the OTTAVA platform, including forecasting, budgeting, long-range planning, reporting, variance analysis, governance, compliance, and business-case development. Partners with commercial leaders to identify risks and opportunities, support strategic decisions, improve financial processes, and ensure SOX and accounting compliance. The role also provides team leadership, coaching, executive insights, and support for launch readiness and growth initiatives.

Leads and develops a sustaining engineering team while providing hands-on technical guidance for electronics, PCBA, test equipment, and electromechanical fixtures. Oversees manufacturing engineering deliverables across new product introduction, sustaining, validation, reliability, repair, rework, and production support. Drives documentation, quality compliance, process improvements, equipment and fixture design, troubleshooting, and cross-functional execution in a regulated medical device environment.

Provides hands-on mechanical engineering support for medical-device robotic capital equipment, including sustaining design, global BOM management, engineering changes, manufacturing transfers, quality investigations, CAPA, obsolescence management, CAD, drawings, tolerance analysis, DFM/DFA, validation, and continuous improvement. Partners cross-functionally with R&D, Manufacturing, Quality, Service, suppliers, and external manufacturing partners. The role is fully onsite in San Jose and requires up to 10% travel.

Provides remote and occasional onsite technical support for J&J MedTech robotic capital equipment. Troubleshoots and triages product issues, supports customers and field engineers through multiple communication channels, performs remote diagnostics, escalates unfamiliar problems, and participates in 24/7 on-call coverage. The role also serves as a product specialist, supports training, manages product-specific processes, coordinates technical information, and contributes to continuous improvement while ensuring compliance with medical device regulations.

Leads a team of robotic technical support engineers providing remote support for medical capital equipment and digital technologies. Oversees support operations, escalations, performance metrics, workforce planning, process improvements, customer experience, and cross-functional issue resolution. Develops team capability, supports product launches, and presents operational updates to leadership. The role requires experience with complex medical devices or healthcare technology, people leadership, customer escalations, and data-driven operational improvement.

Provides advanced technical support for robotic surgical capital equipment through phone, email, and call center channels. Troubleshoots complex product issues, coordinates resolutions with field and cross-functional teams, supports customers during emergency on-call coverage, manages product processes and projects, mentors technical support staff, reports performance metrics, and maintains quality procedures. The role also serves as a product specialist and supports customer training, with approximately 20% domestic travel.

Leads the end-to-end design, integration, verification, validation, deployment, and lifecycle support of complex mechatronic equipment in a regulated MedTech environment. Integrates mechanical, electrical, controls, software, sensing, robotics, machine vision, and automation systems. Owns requirements, architecture, risk management, troubleshooting, supplier technical direction, equipment qualification, manufacturing readiness, and change control while mentoring engineers and technicians.

Leads electrical and electronics engineering for complex robotic medical equipment. Owns root-cause investigations, PCB/PCBA failure analysis, sustaining design changes, obsolescence management, manufacturing test support, risk documentation, CAPA, validation, and regulatory compliance. Partners with R&D, Manufacturing, Quality, suppliers, and contract manufacturers to resolve production, service, and field issues, improve reliability, and maintain production continuity.

Develops and executes ANSYS and Abaqus simulations for robotic medical device assemblies and electromechanical systems. Performs structural, vibration, thermal, dynamic, and stress analyses; optimizes precision motion components; correlates models with physical test data; and supports design validation, troubleshooting, root-cause analysis, and risk reduction. Collaborates with multidisciplinary engineering, manufacturing, quality, and vendor teams while preparing technical reports and engineering change documentation in an ISO and FDA-regulated environment.

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%.

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.

Own supply chain, manufacturing, and lifecycle strategies for OTTAVA robotic surgical platform subsystems. Develop roadmaps for sourcing, cost, capacity, quality, manufacturing, and lifecycle management. Lead obsolescence planning, product changes, supply continuity, technology transitions, and issue resolution. Coordinate cross-functional task forces and align Procurement, Engineering, Manufacturing, Quality, Planning, Service, and Program Management teams to ensure subsystem readiness and long-term performance.

Supports manufacturing execution for the OTTAVA surgical robotic platform. Provides hands-on shop-floor support for system integration, manufacturing tests, troubleshooting, root cause analysis, production continuity, and quality-system activities. Partners with Manufacturing, Test, Quality, NPI Engineering, and R&D teams to resolve hardware, software, and system-level failures, implement corrective actions, and maintain compliant production documentation.

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.