Jobs at Intuitive

Lead a team delivering safety-critical embedded and firmware software for advanced energy medical devices across product lifecycles. Own requirements, risk assessment, prototyping, development, testing, release, and process improvements (CI, code review, static analysis). Interface with cross-functional teams to coordinate hardware/software schedules and mentor engineers.

Lead strategy, delivery, and support of service-focused business systems for Global Services. Manage a global team of product owners and analysts, own CRM and integrated service technologies, drive process standardization, ensure regulatory compliance and system validation, and oversee program/portfolio delivery, governance, and stakeholder engagement to improve field and technical support operations.

Lead AI, automation, and digital transformation strategy for Global Services. Define roadmaps, identify automation opportunities, oversee design and delivery of AI-enabled and RPA solutions, ensure regulatory compliance and validation, drive analytics and ROI measurement, manage vendors, and build a high-performing team.

Lead post-marketing vigilance and complaint handling for medical devices in Japan. Prepare and implement GVP, manage filings and communications with regulatory agencies (MHLW/PMDA), oversee outsourced contractors, maintain SOPs and documentation, support QA and continuous improvement of safety/quality processes, and manage package insert documentation and PMDA web updates.

Design, implement, and operate a Bazel-based unified build system for large C/C++ embedded codebases. Implement and optimize remote caching/execution, write tooling in Rust/C++/Python, improve build performance and observability, debug distributed builds, integrate on-prem and cloud infrastructure, and mentor engineers on scalable build practices.

Lead planning and execution of pre‑market and post‑market clinical trials for medical devices. Develop protocols, manage site selection/start‑up/monitoring, oversee CROs and CRAs, ensure GCP/FDA compliance, liaise with KOLs and biostatisticians, drive study deliverables, prepare clinical study reports and regulatory submissions, mentor junior staff, and support publications and cross‑functional alignment.

Develops clinical and commercial skills by supporting sales reps with surgeon training, technical in-services, territory management, and selling technology benefits to existing robotic users. Handles administrative reporting, expense submission, and prepares for a future quota-bearing role while gaining clinical, technical, and sales experience.

Lead a team of supplier engineers to ensure supplier manufacturing processes are capable, compliant, and scalable. Oversee component/process qualification, supplier nonconformance and CAPA/SCAR, drive DFM and risk mitigation, govern supplier change requests, and partner cross-functionally to maintain validated medical device state and support launches and volume ramps.

Support EMEA regulatory operations for medical devices including registrations, EUDAMED/Swissdamed implementation, compliance (CAPA, audits, inspection readiness), labeling/eIFU, documentation, and cross-functional regulatory support on-site in Aubonne, Switzerland.

Lead the Multiport Business Unit regulatory affairs function across the product lifecycle. Develop and execute regulatory strategies for US/Canada and global markets, oversee premarket submissions (510(k), IDE, registrations), manage sustaining activities, build and develop regulatory teams, advise executive leadership, influence regulatory policy, support clinical data planning, manage budgets/resources, and ensure compliance with standards and guidance.

Manage logistics and operational projects for Commercial Enablement: coordinate training facility logistics, forecasting, scheduling, travel and visa planning, optimize costs and attendee processes, administer training technologies, maintain training records, run and analyze testing reports (e.g., Questionmark, Qstream).

Manage APAC trade compliance for medical device imports/exports: develop policies, oversee classification, customs clearance, broker/forwarder management, audits, risk assessments, SAP/data governance, and cross-functional training to ensure regulatory compliance and smooth international trade operations.

Lead and optimize regional customer training center operations for da Vinci robotic systems. Hire, develop, and mentor trainers; design and measure training programs; collaborate with sales, marketing, surgical societies, and global peers; manage schedules, resources, and training center strategy; support surgeon and OR staff education and occasional OR system support. Travel up to 30%.

Serve as technical liaison for endoluminal reprocessing solutions, drive regional research and program implementation, provide customer feedback into product design and launches, lead stakeholder engagement and training, and manage project execution to enable sustainable reprocessing programs across healthcare sites.

Lead global clinical evidence strategy for Endoluminal products, design and execute pre- and post-market clinical trials (including first-in-human/IDE), ensure regulatory and GCP compliance, manage budgets and KPIs, partner cross-functionally for reimbursement and regulatory interactions, and lead and coach Clinical Affairs team members.

Lead enterprise ServiceNow architecture and strategy across multiple modules. Design scalable integrations, CMDB and data models, enforce governance and best practices, mentor teams, run pilots, and drive platform innovation including AI/automation.

Lead human factors research, usability testing, and risk analysis for medical device product teams. Translate user needs into usability requirements, author regulatory usability documentation, conduct formative and summative evaluations, mentor junior HF staff, and collaborate with cross-functional teams to ensure safe, usable clinical products.

Lead supply chain readiness, launch, and scaling of high-value new robotic systems. Manage supplier selection, contracts, cost negotiations, capacity and risk mitigation, inventory strategies, and supplier performance. Drive cross-functional program roadmaps, executive reviews, and long-term supplier strategies to meet cost, capacity, and speed-to-market goals in a regulated manufacturing environment.

Develop and deploy ML algorithms on the da Vinci surgical robot by writing C++ applications, connecting models to robot data streams, integrating outputs with other teams, and using Linux command-line and build systems to run and maintain software.

Serve as a technical advisor to digital and capital sales, driving implementation of Intuitive's digital portfolio. Lead integration planning, stakeholder engagement, network and cloud architecture discussions, project scheduling, risk mitigation, and documentation in SFDC. Coordinate cross-functional teams, manage customer technical reviews, and ensure successful activation and sustainment of digital solutions across hospital environments.