Jobs at Medtronic

The eManuals Release Administrator manages the release of electronic manuals, coordinates product launches, participates in testing, and monitors project progress while ensuring quality and meeting stakeholder requirements.

The Senior Global Product Manager will develop and execute global market strategies for pancreaticobiliary initiatives, ensure revenue targets, manage partnerships, and collaborate cross-functionally for product launches and growth.

Lead marketing program management for Core Spine & Biologics at Medtronic, overseeing product lifecycle, portfolio management, and cross-functional collaboration to enhance surgical care.

The Supplier Quality Engineer II ensures suppliers deliver quality materials, develops audit schedules, and collaborates with teams to enhance quality and compliance standards.

The Systems Engineer II collaborates on medical device development, assisting in requirements, architecture documentation, integration issues, and working with cross-functional teams throughout the product lifecycle.

Lead the downstream marketing of AiBLE, an AI ecosystem for spine surgery, translating complex procedures into value-driven solutions while enhancing customer experience and collaboration with diverse teams.

The Regulatory Affairs Program Manager leads regulatory strategies for OEM and ACM distributed products, coordinating regulatory activities and documentation while managing multiple programs effectively.

The Sr Financial Analyst will provide financial planning and analysis for the Acute Care & Monitoring FP&A organization, focusing on forecasting, budgeting, and reporting processes while partnering with business leaders.

The Principal Market Development Specialist will lead regional marketing efforts for renal denervation therapy, focusing on patient access, strategic planning, and collaboration with healthcare providers.

The Principal Regulatory Affairs Specialist leads regulatory strategies for the Core Respiratory portfolio, interacting with various departments to ensure compliance and support business objectives.

As a Senior Business Process Improvement Analyst, you'll use Lean Six Sigma to improve manufacturing processes, lead cross-functional teams, and drive operational excellence through structured methodologies and collaboration with various departments to meet business goals.

The Sr. Category Manager for Chemicals will lead global sourcing strategies, manage supplier relationships, negotiate contracts, and drive cost reductions while ensuring compliance and quality oversight.

The IT Manager for Threat Intelligence will develop strategies for threat intelligence, oversee cyber threat analysis, and collaborate with security teams to enhance organizational defenses against cyber threats. Responsibilities include guiding team members, managing threat intelligence programs, and ensuring compliance with regulatory standards.

The Senior Manufacturing Engineer will manage manufacturing optimization projects, focusing on process design, validation, and collaboration with cross-functional teams to ensure quality and efficiency.

As a Senior Software Engineer, you'll design, develop, and support software components for innovative surgical products, collaborating with cross-disciplinary teams.

Lead the development team for patient monitors, ensuring software quality and collaborating with various stakeholders to deliver product updates and enhancements.

The role focuses on enhancing product reliability for medical devices through design tests, risk analysis, and compliance with regulations.

The role involves designing and delivering sales training for medical technologies, enhancing commercial teams' ability to sell complex equipment through effective instructional methods.

The Strategic Accounts Director leads efforts to develop relationships with key accounts and drive Medtronic's revenue and solutions. Responsibilities include strategic planning, collaboration with regional leaders, achieving fiscal targets, and fostering partnerships to meet healthcare needs.

The Sr Regulatory Affairs Manager will lead global regulatory strategies, ensure compliance, and collaborate with teams for product approvals. Responsibilities include team management, regulatory agency interaction, and oversight of submissions for medical products.