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Senior Quality Engineer – CST – Lafayette, CO (Onsite)

Medtronic
USA-CO, United States, United Statesfull_timeVerifiedPosted 30 Jun 2026
💰 $147,600/yr($98,400/yr$147,600/yr)

About the role

We anticipate the application window for this opening will close on - 11 Jul 2026


 

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

As one of three comprehensive portfolios at Medtronic, Neuroscience is dedicated to improving the lives of people living with neurological disorders, spine conditions, and chronic pain. Guided by our Mission—to alleviate pain, restore health, and extend life—we develop technologies and therapies that help people regain function, reduce pain, and return to the activities that matter most.

         

         

Our Cranial & Spinal Technologies (CST) Operating Unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging, and data-driven planning tools for complex spine and cranial procedures. Platforms such as AiBLE™ connect these technologies to enhance surgical precision, streamline workflows, and support improved patient outcomes across the globe.

Check us out on LinkedIn: Medtronic CST

A Day in the Life

The Senior Design Quality Engineer plays a critical role in ensuring product quality, safety, and regulatory compliance throughout the medical device product lifecycle, with a primary focus on product design, development, and sustaining engineering. As the quality representative on cross-functional project teams, you will provide technical leadership in design controls, risk management, verification and validation, and quality system compliance, partnering closely with Research & Development, Manufacturing, Regulatory Affairs, and Supply Chain to deliver safe, effective, and compliant medical technologies.

Responsibilities include, but are not limited to:

  • Serve as the Design Quality representative on new product development and sustaining engineering projects, ensuring compliance with design control and quality system requirements.

  • Lead design quality activities, including design controls, risk management (DFMEA, hazard analysis, risk controls), verification and validation strategies, and design traceability.

  • Review and approve design documentation, engineering changes, protocols, reports, and technical documentation to ensure product quality and regulatory compliance.

  • Partner with R&D and cross-functional teams to develop risk-based verification and validation strategies and assess the quality impact of design changes, nonconformances, and CAPA activities.

  • Support design transfer, supplier integration, manufacturing readiness, and product transfers to ensure successful commercialization and sustaining operations.

  • Collaborate with Engineering, Manufacturing, and Supplier Quality teams to establish inspection methods, testing strategies, and quality standards that ensure product reliability and performance.

  • Support internal and external regulatory inspections and audits, including FDA, ISO 13485, EU MDR, and other applicable regulatory requirements.

  • Provide technical quality leadership, influence cross-functional decision-making, and drive continuous improvement initiatives that enhance product quality, compliance, and operational excellence.

Location: Lafayette, CO (Onsite)

Onsite: At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. We’re working onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. This role will require <10% of travel to enhance collaboration and ensure successful completion of projects.

Minimum Requirement (Basic Qualifications):

To be considered for this position, the following Basic Qualifications must be evident on your resume

  • Bachelor’s degree in Engineering or Technical discipline with minimum of 4 years of relevant experience, OR

  • Master’s degree in Engineering or Technical discipline with minimum of 2 years of relevant experience, OR

  • PhD in Engineering or Technical discipline with minimum of 0 years of relevant experience.

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Company

Medtronic

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