Top Tech Jobs & Startup Jobs

Supports Medtronic’s global property and casualty insurance programs by preparing and validating insurance data, reviewing policies and contracts, administering certificates, supporting workers’ compensation reporting, maintaining records and SharePoint content, responding to insurance inquiries, and assisting with merger and acquisition due diligence and integration.

Leads the design, integration, optimization, troubleshooting, and support of automation and control systems for advanced medical-device manufacturing. Provides technical leadership across PLCs, HMIs, robotics, machine vision, motion control, and industrial networks. Partners with R&D, Manufacturing, Quality, and Operations on equipment development, qualification, new product introduction, scale-up, validation, reliability, and regulatory compliance. Also leads suppliers and system integrators and implements solutions improving uptime, efficiency, quality, and safety.

Provides technical leadership for automation and controls in advanced medical-device manufacturing. Designs, integrates, optimizes, and supports PLC, HMI, robotics, motion control, machine vision, and industrial network systems. Leads equipment development, qualification, NPI, manufacturing scale-up, troubleshooting, root-cause analysis, reliability improvements, and regulatory compliance while partnering with R&D, Manufacturing, Quality, and Operations.

Defines and governs information architecture for Medtronic’s digital health platform. Leads data strategy, modeling, integration, stewardship, metadata, data quality, access governance, and enterprise data standards. Partners with engineering, product, quality, regulatory, cybersecurity, legal, and business teams to document data flows, ensure secure and compliant data practices, and enable reporting, analytics, and future AI/ML initiatives.

Leads Privacy by Design across connected medical devices and supporting systems. Responsibilities include privacy risk assessments, DPIAs, compliance documentation, regulatory evidence, incident investigations, corrective actions, privacy incident response, stakeholder consultation, and alignment with product security engineering. The role mentors professionals and advances privacy governance, training, metrics, and continuous improvement while ensuring compliance with global privacy laws and medical device standards.

Principal Reliability Engineer responsible for improving product and manufacturing-process reliability across machining, finishing, and assembly. Conducts reliability studies, design of experiments, risk analyses, PFMEA, statistical process control, drawing and inspection reviews, gauge design, supplier quality reviews, and corrective action assessments. Develops inspection procedures, analyzes process data, supports environmental testing, resolves production issues, and mentors engineers and suppliers. Requires an engineering degree, substantial reliability experience, advanced English, and travel availability.

Leads phased integration of Medtronic’s Interventional Cardiology Therapies portfolio while protecting therapy-area execution. Develops integration strategy, future-state operating models, governance, decision rights, and cross-functional alignment across R&D, clinical, regulatory, marketing, quality, finance, and HR. Establishes and leads the integration PMO, manages milestones, dependencies, risks, leadership communications, and operating reviews, and advances targeted opportunities supporting long-term portfolio integration.

Leads and scales a multidisciplinary systems engineering organization for complex ENT medical devices. Owns systems architecture, requirements, integration, lifecycle management, risk oversight, and platform strategy across hardware, software, and firmware. Develops engineering talent, drives compliant product launches, standardizes processes, and aligns technical direction with clinical, regulatory, commercial, and executive stakeholders.

Leads cross-functional data enablement programs for connected surgical products, managing scope, schedules, dependencies, risks, vendors, roadmaps, and executive reporting. Partners with hardware, software, product, quality, regulatory, IT, and commercial teams to define telemetry, connectivity, data requirements, and cloud architectures. Guides analytics and machine learning applications for device and clinical data while ensuring compliance with medical device quality, privacy, regulatory, and cybersecurity requirements.

Lead and develop mechanical engineers supporting released neuromodulation and pelvic health products. Oversee sustaining engineering, technical investigations, root cause analysis, CAPA, design changes, risk mitigation, supplier issues, manufacturing support, and cross-functional resolution. Manage priorities, resources, workload, and execution while ensuring product quality, reliability, regulatory compliance, and patient safety.