Jobs at Johnson & Johnson

Designs, implements, validates, and supports OT control systems (PLCs/SCADA/HMI) for regulated medical manufacturing. Leads OT lifecycle projects, integrates OT with MES/ERP, ensures OT security and regulatory validation (IQ/OQ/PQ, 21 CFR Part 11 awareness), troubleshoots production issues, manages vendors, performs risk assessments, and mentors teams to improve automation reliability and process stability.

Provide hands-on field service for robotic medical systems: install, commission, maintain, troubleshoot mechanical/electrical/software/firmware issues, perform preventive maintenance, upgrades, calibrations, maintain records, coordinate with hospital stakeholders, manage parts/tools, and support continuous improvement and customer satisfaction.

Lead electrical safety and basic safety verification for surgical robotic systems per IEC 60601-series and ISO 14971. Develop and maintain risk management, execute safety tests (hi-pot, leakage, structural), coordinate cross-functional safety reviews, support regulatory filings, supplier assessments, and external audits, and produce test plans, protocols, and compliance documentation.

Lead design, development, and delivery of surgical robotic capital hardware. Manage and mentor mechanical/electrical engineers, contribute hands-on to actuators, structures, and sensors, drive prototyping to commercial designs, and collaborate cross-functionally to ensure feasibility, testing, and regulatory compliance.

Lead upstream product marketing for core cardiovascular device technology: guide new product development, engage KOLs, run market research and advisory boards, assess competitive/clinical landscapes, inform R&D and commercial strategy, collaborate cross-functionally, and perform financial modeling. Support rollout of strategic programs and portfolio planning.

Design and develop robotic capital hardware for surgical environments, iterate prototypes to commercial products, collaborate with controls, software, and clinical teams, participate in design reviews and clinical labs, engage vendors, and mentor junior mechanical engineers.

Technical lead for sustaining and systems integration of deployed surgical robotics platforms. Triage field/manufacturing failures, perform root cause analysis, develop and deploy mitigations, manage component EOL activities, and drive cross-functional design changes to ensure safety, reliability, performance, and regulatory compliance.

Support and improve CI/CD, build systems, and cloud infrastructure for Ottava surgical robotics software. Maintain Jenkins pipelines, Terraform-managed AWS environments, Dockerized build/test environments, and Artifactory. Lead QNX OS image and software upgrade/migration efforts and automate build, release, and merge processes using Python and Bash.

The Senior Manager, OTTAVA Communications will lead strategic communications for surgical robotics, collaborating with cross-functional teams and driving business outcomes through diverse communication programs.

The Principal Electrical Engineer will lead the development of complex electronic systems for regulated medical devices, ensuring compliance with safety standards, and providing technical leadership within the team.

Lead business development for Robotics & Digital Surgery: define strategy, scout and evaluate opportunities, build and validate business cases, lead due diligence and complex deal negotiations, align internal stakeholders, and oversee integration and governance to advance MedTech robotic and digital healthcare initiatives.

Sell and expand Johnson & Johnson MedTech Neurovascular products within the Sacramento territory. Build and maintain surgeon and hospital relationships, demonstrate product use in OR/Radiology, meet sales quotas, convert competitors, execute ethical sales cycles, and support customers with product knowledge. Travel up to 40% and complete company training.

Design, architect, integrate, and test high-speed embedded audio/video and digital systems and PCBAs. Lead full lifecycle PCB design, perform EMI/ESD/thermal testing, develop test fixturing, create technical documentation, participate in design reviews and xFMEA, and collaborate with cross-functional teams to ensure reliability and compliance.

Lead data science efforts to build optimization and simulation models for supply chain network and planning improvements. Perform statistical analysis, machine learning, and scenario analysis on large healthcare datasets. Develop LP/MILP models, simulations, and production-ready solutions using Python/Julia and optimization solvers to drive data-driven decisions across supply chain.

Lead and grow the MONARCH software organization to deliver high-quality, regulatory-compliant medical device software. Drive technical strategy, manage budgets and resources, ensure software reliability across GUI, robotics, firmware, and cybersecurity, and align R&D with Quality, Regulatory, Commercial, and external stakeholders to support pre- and post-market product needs.

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.

Serve as strategic HR leader for Robotics & Polyphonic, partnering with business leaders on org design, talent strategy, workforce planning, culture and engagement, leadership coaching, change management, and succession planning. Drive data-informed talent decisions, support integrations and communications, and partner across OneHR to build capabilities and optimize organizational performance. Located in Santa Clara; 10% travel.

Lead scouting, evaluation, and onboarding of external biologics modality partnerships for DPDS in West North America. Provide scientific leadership in deal teams, assess early-stage innovation, drive due diligence, liaise with internal TA and business development stakeholders, and represent J&J externally. Support portfolio strategy, mentor cross-functional teams, and enable transactions from scientific and IP perspectives.

Manage supplier quality by investigating, resolving, and preventing supplier issues; run audits; drive SCARs, NCRs, and CAPAs; support component qualification, process validation, and supplier transfers; analyze supplier performance and train/monitor contract manufacturers to ensure compliance with medical device quality systems.

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.