Jobs at Medtronic

Lead UX/UI design for a cardiac mapping and ablation product, creating product design vision, user-centered experiences, prototypes, and collaborating with product, engineering, clinical, and hardware teams to deliver medically compliant software/hardware solutions.

Lead risk management and quality activities for new surgical medical devices: develop and maintain risk management files, conduct DFMEAs/PFMEAs, evaluate field issues and complaints, ensure design verification/validation and regulatory compliance (FDA, ISO), integrate product security, and mentor teams to embed patient safety across the product lifecycle.

Lead systems-level software architecture and MBSE work for the Affera Mapping and Ablation System. Develop and maintain SysML models, define interfaces and allocations, ensure V-model traceability from requirements through verification, perform FMEA and risk analysis, author/review software system requirements, and improve MBSE tooling and processes across engineering teams.

Lead design, development, testing, and deployment of software systems supporting manufacturing operations. Define system and database architecture, capture user requirements, implement automated/standardized processes, mentor engineers, conduct code reviews, collaborate cross-functionally, and drive continuous improvement to ensure product quality, reliability, and manufacturability.

Design and govern enterprise SAP architecture for S/4HANA and BTP, lead end-to-end ABAP development lifecycle, translate business requirements into technical designs, optimize custom code during ECC-to-S/4HANA transformation, support integrations, mentor architects, ensure coding standards and compliance, and collaborate with stakeholders to deliver high-quality SAP solutions.

Lead end-to-end strategic planning for the Surgical Operating Unit, delivering analyses, financial models, and executive presentations to influence portfolio prioritization, ROI/NPV, and long-term P&L alignment. Support governance, M&A, product strategy, and cross-functional decision-making with up to 30% global travel.

Lead global regulatory strategy and submissions for complex medical device programs, emphasizing AI-enabled and software-driven solutions. Prepare and coordinate regulatory filings, manage cross-functional workstreams, identify and mitigate regulatory risks, and interact with agencies to support timely approvals and market access. Mentor teams and build regulatory capability.

Senior Clinical Research Specialist designs, executes, and oversees global clinical studies for surgical products. Responsibilities include protocol and CRF authorship, site/vendor selection, trial operations per SOP/GCP and country regulations, data interpretation for regulatory/commercial submissions, project management, and stakeholder engagement and evidence dissemination.

Act as product owner for surgical robotics software, coordinating stakeholders, prioritizing and maintaining backlog, defining requirements, and planning releases. Work with hybrid HW/SW products, embedded systems, RTOS, firmware integration, and SDLC tools (JIRA, Git, Bitbucket, CMake, Simulink). Ensure regulatory compliance (ISO, ASPICE, FDA) through documentation, risk analysis (FMEA), test reporting, and audit readiness. Requires SAFe POPM certification and onsite presence in Boston four days per week.

Support regulatory strategy and documentation for medical devices across the product lifecycle. Assess regulatory impact of design and process changes, prepare submissions and renewals, support audits and inspections, maintain tracking systems, participate in risk management, stay current on regulations, and collaborate cross-functionally to keep regulatory activities on track and drive process improvements.

Lead research and development of signal and image processing algorithms for ultrasound-enabled medical devices. Design, implement, and evaluate real-time algorithms, analyze bench/preclinical/clinical data, and collaborate cross-functionally to translate concepts into validated clinical solutions while providing technical leadership and mentorship.

Lead DevOps efforts to accelerate software lifecycle: maintain build systems (CMake/ROS/Bazel), build and operate CI/CD pipelines, manage AWS cloud infrastructure, containerize with Docker/Kubernetes, implement artifact management (JFrog), monitoring (Grafana), ensure security and regulatory compliance, troubleshoot environments, document processes, and mentor team members.

Lead architectural design for real-time 3D visualization on the Prism Mapping platform, mentor engineers, and define the long-term visualization roadmap.

Lead the technical direction for integrating algorithms on the Prism Mapping platform, focusing on real-time signal pipelines and optimization strategies. Collaborate with teams to ensure robust clinical performance and timely delivery of new capabilities.

Lead the UI architecture for the Prism Mapping application, drive design and delivery of major subsystems, mentor engineers, and shape technical direction in a clinical environment.

As a Sr. Software Engineer - UI/UX, you will lead UI features in Qt/QML, collaborate with UX designers, mentor engineers, and contribute to architecture decisions.

Lead the technical direction and architecture for the core infrastructure of the Prism Mapping platform, ensuring reliability and performance in a medical device environment. Mentor engineers and drive technical improvements while communicating complex decisions to stakeholders.

As a Senior Software Engineer, you'll develop signals and algorithm interfaces, collaborate with developers, optimize algorithms, and mentor engineers in a regulated environment.

Support global import compliance by determining country of origin, assigning HTS classifications, applying rules of origin, and maintaining trade data in ERP. Analyze manufacturing/supplier information, prepare origin certifications, research customs regulations, support audits, and partner with engineering, sourcing, manufacturing, and suppliers to ensure compliant importation of medical devices worldwide.

Lead regulatory strategy and compliance for wound management devices across the product lifecycle. Prepare and support US and international submissions (Pre-Sub, 510(k), CE), review labeling and promotional materials, support registrations, collaborate cross-functionally, maintain regulatory documentation, and participate in audits to ensure regulatory compliance.