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Job description
As a Quality Engineer II at Medtronic, you will lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. You will develop, modify, apply, and maintain quality standards and protocols for processing materials into partially finished or finished materials product.
Responsibilities may include developing quality standards and protocols, collaborating with engineering and manufacturing functions, devising and implementing methods and procedures for inspecting, testing, and evaluating products and production equipment, and ensuring corrective measures meet acceptable reliability standards.
This role is ideal for an individual contributor with responsibility in technical functions to advance existing technology or introduce new technology and therapies. You will work independently with general supervision on larger, moderately complex projects and contribute to the completion of project milestones.
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Healthcare • Manufacturing
Covidien, now part of Medtronic’s Minimally Invasive Therapies Group, is a global leader in medical devices and surgical solutions. The business delivers a comprehensive portfolio that includes advanced surgical tools, medical supplies, respiratory monitoring systems, and vascular therapy devices, all designed to enable clinicians to perform less‑invasive procedures with greater precision and safety. The organization’s commitment to innovation, evidence‑based outcomes, and worldwide reach creates a dynamic environment for professionals seeking to advance their careers in minimally invasive medicine. Employees benefit from access to cutting‑edge technologies, collaborative research initiatives, and the opportunity to impact patient care on a global scale.