Jobs at Medtronic

Lead and coordinate end-to-end manufacturing value stream for cardiovascular and neuroscience products. Drive safety, quality, delivery, cost targets, workforce planning, budgets, continuous improvement (MPS/Lean), cross-functional alignment, and day-to-day operations in a regulated medical device environment.

Field-based Spine Sales Representative responsible for selling Medtronic spinal implants and biologics, providing case coverage, managing consignments and loaner inventory, maintaining customer records, meeting sales quotas, creating business plans, training and supporting accounts, and traveling frequently within the assigned territory (about 50%).

Lead pricing strategy and governance for Neuroscience, Pelvic Health, ENT and Neurovascular portfolios. Build pricing and revenue models, manage approvals, forecast ASPs, analyze market and competitive pricing, support product launches, train sales/contracting teams, and drive pricing programs to optimize margin and portfolio performance.

Provide technical, clinical, educational, and sales support for Cardiac Ablation Solutions; deliver and oversee projects, assist region sales and customer service, mentor junior staff, and liaise with internal and external stakeholders to meet objectives.

Seasoned individual contributor responsible for developing and maintaining quality standards and protocols for sustaining and post-market product lifecycles. Provide design-quality oversight (DHF maintenance), lead risk assessments and field actions, design inspection/test methods, perform statistical analysis, drive corrective actions and process improvements, mentor peers, and support technical projects across US design and manufacturing sites.

Support global interventional cardiology clinical trials by organizing study documentation, managing regulatory submissions, using clinical systems (EDC/CTMS/Veeva), assisting site compliance and training, coordinating stakeholders, and contributing to process improvements and inspection readiness.

Support and sustain manufacturing processes for Nitinol stent production: troubleshoot equipment, design operations, identify process improvements, ensure regulatory compliance, apply DOE/statistical and lean tools, guide operators, and participate in process validation and continuous improvement projects.

Design, develop, and test high-integrity cloud software for implantable cardiac device systems. Define technical requirements and architecture, build distributed cloud-based microservices, ensure regulatory-quality standards, support design reviews, and participate in Agile ceremonies. Collaborate with cross-functional teams to deliver scalable, secure CRM and patient-facing solutions.

Lead post-market reliability for cardiac pacing and defibrillator products. Design and run reliability studies and DOEs, analyze performance and process-control statistics, perform risk analyses for complaints and CAPA, produce quality/reliability reports, develop quality documentation for audits, support manufacturing sites globally, and build models to identify problematic units/batches. Collaborate cross-functionally to maintain product safety and performance.

Develop and execute sales enablement strategies and content to prepare sellers, optimize buyer interactions, build pipeline, and use sales metrics to improve selling effectiveness. Create training, tools, and coordinate with Sales, Marketing, and Communications to support sales goals.

Lead industrial engineering strategy for a high-volume medical device manufacturing site, driving Lean/Six Sigma continuous improvement, capacity planning, labor optimization, line design, and cross-functional change. Mentor engineers, facilitate improvement projects, support NPI and site expansions, and ensure measurable gains in safety, quality, delivery, and cost while communicating results to site leadership. Onsite role with strong operational and change-leadership responsibilities.

Design, build, test, and document web applications in a cloud IaaS environment. Work on agile, cross-site teams to develop high-reliability neuromodulation software, support test automation, meet project milestones, and participate in continuous improvement.

Sell Medtronic medical devices within an assigned territory, build and maintain customer and distributor relationships, pursue leads, provide product education, conduct market research, implement market development plans, and relay customer feedback to internal teams to meet sales targets.

Support a cardiovascular product production line by designing manufacturing processes and layouts, reducing scrap, investigating nonconforming product, maintaining SPC, verifying equipment performance, specifying operations, and ensuring regulatory compliance.

Lead and deliver technical and clinical training on Medtronic Robotic Assisted Surgery technologies and related therapies. Design, develop, and evaluate blended learning programs; perform competency assessments; support new-hire progression; collaborate with MedEd, Marketing, Sales, and cross-functional teams; monitor market and competitor activity. Travel up to 50% and work nontraditional regional hours in Asia.

The Senior Quality Engineer will develop quality standards, collaborate on manufacturing processes, and ensure compliance in medical device manufacturing.

Support clinical data collection and management for studies: design and implement protocols and CRFs, test and validate reports/dashboards (SQL, Spotfire, Power BI), develop data quality plans, review and resolve discrepancies, and prepare internal validation reports. Entry-level individual contributor role with mentorship and close supervision.

As a Spine Technical Consultant at Medtronic, you'll provide clinical and technical support to operating room teams, promoting spinal therapy devices and conducting training to ensure safe and effective usage.

Design, develop, and maintain Qt-based GUI and Windows desktop test applications; build automated validation and test frameworks; integrate DAQ, sensors, hardware controllers, and computer vision for manufacturing. Create verification/validation protocols and compliance documentation, support hardware-software integration, troubleshoot defects, collaborate cross-functionally, and drive continuous improvement in regulated medical device manufacturing environments.

Provide legal counsel to Medtronic EurAsia business units, draft and review commercial, real estate, employment, M&A and other contracts, monitor legislation, assess litigation risk, advise on antitrust and regulatory matters, support corporate governance, train stakeholders, and coordinate with outside counsel.