Jobs at Medtronic

Lead global supply chain IT strategy and execution across planning, logistics, warehousing, transportation, and fulfillment. Drive digital transformation using cloud, data, AI/ML, analytics, automation, and modern platforms while ensuring secure, scalable delivery, governance, vendor and financial accountability, and developing a high-performing global team to achieve measurable supply chain outcomes.

Leads cross-functional value stream and sustainment initiatives supporting product availability, supply continuity, and operational performance. Develops project plans, schedules, action trackers, and stakeholder communications; coordinates operations, supply chain, quality, engineering, planning, and R&D teams. Identifies and mitigates risks, manages dependencies, monitors KPIs, supports regulatory compliance, and drives process improvements across the product lifecycle.

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.

Designs and develops custom machines, automation systems, tooling, fixtures, and manufacturing equipment for regulated medical device environments. Creates controlled SolidWorks models, assemblies, drawings, and bills of materials; supports qualification, validation, commissioning, FAT, SAT, and troubleshooting. Performs tolerance analysis, failure investigations, root-cause analysis, and design-for-manufacturability assessments. Leads design reviews and collaborates with electrical, software, controls, manufacturing, quality, and operations teams to deliver safe, reliable, compliant equipment.

Lead design and implementation of embedded OS layer software and platform infrastructure. Develop Yocto-based embedded Linux distributions, BSPs, hypervisors, device drivers, CI/CD pipelines, and security features (secure boot, OTA). Act as platform point of contact, collaborate with product teams, and produce engineering policies and documentation.

Designs, develops, validates, and supports digital manufacturing architectures connecting plant-floor equipment, PLCs, databases, MES, ERP, and enterprise systems. Builds Ignition applications, HMIs, dashboards, SQL databases, reports, alarms, historian systems, and KPI monitoring tools. Troubleshoots connectivity issues, supports equipment launches, integrates OPC-UA communications, collaborates on secure OT/IT architectures, and documents system changes.

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.

Leads global sourcing strategy for MRO, capital equipment, and manufacturing services across approximately 60 sites and $700 million in annual spend. Directs supplier negotiations, contracts, performance programs, category strategies, cost optimization, working capital initiatives, and enterprise transformation. Partners with manufacturing, engineering, quality, finance, and supply chain leaders while managing and developing a geographically distributed team of 20 sourcing professionals.

Leads clinical development support for neurovascular medical devices by authoring clinical, scientific, and regulatory documents; developing evidence strategies; analyzing and communicating clinical data; conducting literature reviews; supporting regulatory submissions; managing publication planning; and coordinating cross-functional projects with clinical, regulatory, quality, medical, and commercial stakeholders.

Provide strategic IP counsel for M&A, divestitures and investments: lead IP due diligence, assess IP portfolios and risks, draft and negotiate IP provisions, advise senior leaders and deal teams, and manage cross‑functional transaction workstreams to meet objectives within budget and timeline.

Leads regulatory affairs for Wound Management medical devices across the full product lifecycle. Responsibilities include developing Pre-Sub, 510(k), CE Mark, and international submissions; advising on US and global regulatory requirements; interacting with regulatory authorities; reviewing labeling, promotional materials, and technical documentation; supporting audits and product registrations; and collaborating with engineering, quality, clinical, marketing, and international regulatory teams.

Provides strategic leadership for clinical quality systems, compliance, governance, inspection readiness, audits, investigations, remediation, and quality data reporting across Medtronic’s Surgical CMAH organization. Leads and develops a quality team, drives standardized business processes, manages risks, supports regulatory submissions, and advances operational excellence and continuous improvement across Clinical, Medical Affairs, and HEPR functions.

Leads mechanical design and development of manufacturing equipment, automation systems, tooling, and fixtures for regulated medical device production. Creates SolidWorks models and engineering documentation, supports qualification and validation, performs tolerance and failure analyses, and leads design reviews, commissioning, troubleshooting, and technical project execution. Collaborates with multidisciplinary teams, manages project risks and deliverables, and mentors engineers while ensuring manufacturability, compliance, and design-control discipline.

Lead software quality engineering across the full development lifecycle for Medtronic’s AiBLE medical technology portfolio. Responsibilities include software verification and validation, requirements traceability, test coverage, design control compliance, risk documentation review, quality process development, metrics analysis, audit documentation, and cross-functional issue resolution. The role supports regulated product development and commercialization, including AI-enabled software and medical device quality requirements.

Manages post-sale customer relationships for Medtronic’s HealthCast intelligent patient manager portfolio. Leads clinical workflow discussions, implementation, training, adoption, retention, executive business reviews, KPI reporting, issue resolution, and expansion opportunities. Serves as a strategic advisor and customer advocate while coordinating with Sales, Product Management, Engineering, Technical Support, Marketing, and other internal teams. Requires clinical credentials, strong presentation skills, enterprise software experience, and extensive travel.

Coordinates enterprise account meetings, executive engagements, business reviews, customer visits, events, and special projects. Supports account managers with scheduling, agendas, presentations, reports, communications, documentation, timelines, budgets, contracts, and status tracking. The role facilitates collaboration across Sales, Marketing, Finance, and operating teams while managing multiple priorities and maintaining project information and deliverables.

Lead global supplier integration initiatives to improve supply continuity, inventory performance, lead times, safety stock, and operational efficiency. Responsibilities include scaling supplier-managed inventory, consignment, and supplier portal capabilities; conducting supplier assessments and value-stream mapping; building business cases and implementation roadmaps; presenting recommendations and value realization to executives; monitoring KPIs; and managing cross-functional change across suppliers, sites, and internal teams. The role requires up to 75% travel.

Leads complex neurovascular clinical studies and development programs, overseeing strategy, execution, timelines, quality, risks, and outcomes. Partners with Clinical, R&D, Regulatory, Quality, Medical Affairs, Marketing, and external investigators. Develops clinical evidence strategies, authors regulatory and scientific documents, interprets clinical data, presents findings to executive leadership, and leads publications and dissemination activities.

Leads Supplier Quality Engineering teams across Medtronic’s Colorado sites. Oversees supplier quality, purchased-product conformity, nonconforming materials, supplier changes, CAPA, audits, inspections, corrective actions, and risk-reduction initiatives. Develops performance monitoring systems, leads cross-functional investigations, ensures compliance with purchasing controls and FDA requirements, and manages employee development, coaching, performance goals, and departmental priorities.

Develop and advise on regulatory strategies for complex medical devices, novel technologies, software, and AI-enabled products. Partner with regulatory and operating-unit teams on submissions, health-authority interactions, evidence expectations, risk management, market expansion, and post-market commitments. Support mergers, acquisitions, licensing, and remediation activities by identifying regulatory risks and opportunities. Translate evolving global regulations and deficiency trends into practical guidance, training, and recommendations for senior leaders and cross-functional teams.