Jobs at Medtronic

Architect, design, implement, test, document, and maintain embedded firmware for patient monitoring platforms using mixed-signal MCUs. Collaborate with system engineering, clinicians, and stakeholders to capture requirements, apply regulatory/quality processes, and prioritize design tradeoffs informed by physiological signal measurement and human physiology.

Lead systems engineering for a robotic-assisted surgery platform: translate user needs into requirements, perform functional analysis and allocation, document system/subsystem architecture, manage risk and regulatory design controls, use MBSE, oversee integration and verification, and support lifecycle activities including field issue investigation and design-change impact analysis.

Lead and grow a software engineering team for regulated medical device products: recruit and mentor staff, drive engineering execution and quality, enable AI-assisted development and local LLMs, coordinate cross-functional product efforts, improve processes and reliability, and resolve customer/field issues in partnership with quality, systems, and product teams.

Lead system-level verification, integration, and test development for electromechanical medical devices. Develop test strategies, design and validate fixtures using CAD, implement automated or semi-automated tests (LabVIEW/Python/MATLAB), execute and document test plans, troubleshoot hardware and test equipment, support manufacturing transfer, mentor junior engineers, and ensure quality-system compliance.

Lead enterprise automation and continuous-improvement initiatives for Global Supply Chain Finance. Identify and prioritize process improvements, design and deploy automated reporting and dashboards, partner with cross-functional teams, build business cases, measure business impact, standardize global processes, and lead change management from concept through implementation.

Lead hardware system design for Digital Health R&D: define electrical requirements, design and verify PCBs and schematics, drive hardware debugging and integration, ensure regulatory and standards compliance (medical device), mentor engineers, and collaborate cross-functionally to deliver scalable, manufacturable patient-contacting products.

Lead a global team to design and deliver supply chain data solutions and digital transformation programs. Own data architecture, analytics, process improvement, and program execution to improve planning, manufacturing, inventory, logistics, and order fulfillment. Mentor teams, communicate KPIs to executives, manage risks, and ensure data accuracy and predictive analytics drive operational decisions.

Lead downstream marketing for cerebrospinal fluid management products, owning strategic planning, product lifecycle, launches, pricing, demand generation, and event marketing. Collaborate cross-functionally with sales, clinical, regulatory, quality, operations, and supply chain. Use market and clinical insights to develop value propositions, drive commercial effectiveness, and present data-driven updates to leadership. Manage annual marketing plans, budgets, and forecasting. Travel up to 30% and work onsite a minimum four days per week.

Lead a global Product Release team within Regulatory Affairs to drive product release strategy, ensure compliance with global regulatory requirements, improve processes through standardization and automation, manage data quality and distribution controls, establish KPIs and reporting, and build organizational capability in regulatory systems and operations.

Lead end-to-end Procure-to-Pay transformation: optimize and standardize P2P processes, drive automation and digital initiatives, strengthen governance and controls, partner cross-functionally, set KPIs, and lead a team of managers to deliver operational excellence, compliance, and measurable cost/value improvements.

Design, develop, test, and document system solutions for computer- and robotic-assisted surgery. Define user needs, use cases, requirements, and system architecture. Lead engineering analysis, risk mitigation, integration troubleshooting, and formative user evaluations in lab surgical environments. Provide SME input across cross-functional teams to support clinical workflow integration and surgical procedure introduction.

Lead a clinical quality team to ensure compliance with clinical research regulations and internal QMS. Drive audit and inspection readiness, investigations, CAPA management, risk identification, and cross-functional alignment to improve clinical quality processes and data integrity.

Lead mechanical design and development of custom machines, automation, tooling, and fixtures for medical device manufacturing. Create detailed 3D CAD models, drawings, and BOMs in SolidWorks; support equipment qualification/validation (IQ/OQ/PQ); perform tolerance and failure analyses; lead cross-functional design reviews, FAT/SAT commissioning, troubleshooting, and project management; mentor engineers and ensure design controls and documentation discipline in a regulated environment.

Lead systems engineering for computer-assisted ENT surgical systems: define user and business needs, architect solutions, direct design/trade studies, run lab user evaluations, mitigate risks and hazards, support integration and surgical introduction, and provide cross-team technical leadership.

Lead regulatory operations, compliance, and technical communications for the Acute Care & Monitoring portfolio. Build roadmaps, automate processes, manage IFUs/UDI/EUDAMED, ensure audit/inspection readiness, oversee labeling/translation, and develop a high-performing RA and technical communications team.

Lead a team to develop and execute operations sourcing strategies ensuring raw material supply continuity, supplier risk mitigation, capacity planning, and cost reduction. Drive supplier negotiations, performance management, inventory optimization (VMI/SMI), cross-functional collaboration, escalation resolution, and continuous improvement to support Colorado Campus manufacturing operations.

Deliver Robotic Assisted Surgery (RAS) training to surgeons, first assistants, and OR staff; manage training center logistics, equipment maintenance, and troubleshooting; build relationships with training partners; support continuous improvement of curricula and training research initiatives.

Plan, coordinate, and execute medical education and consultative meetings for CST. Manage budgets, vendor sourcing/negotiation, logistics (travel, visas, AV/production), registration and attendee experience, event reporting, and ensure regulatory/compliance alignment. Role requires up to 30% travel and occasional weekend/night work.

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 product programs for clinical cloud software and AI solutions for spine and cranial treatments. Define product vision, roadmaps, and business cases; translate surgeon and market insights into requirements; align technical capabilities with clinical workflows; drive go-to-market and cross-functional commercialization; and influence stakeholders while managing matrixed teams and vendors to deliver AI-enabled surgical solutions.