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Senior Quality Engineer - CST - Memphis, TN (Onsite)

Medtronic
USA-TN, United States, United Statesfull_timeVerifiedPosted 7 Jul 2026
💰 $147,600/yr($98,400/yr$147,600/yr)

About the role

We anticipate the application window for this opening will close on - 9 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

Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey. 

         

         

Our Cranial & Spinal Technologies (CST) operating unit advances surgical care for spine and cranial conditions through an integrated ecosystem of implants, navigation, robotics, imaging, and planning tools. Platforms like AiBLE enhance precision, efficiency, and outcomes for complex procedures worldwide.  

 

Check us out on LinkedIn: Medtronic CST 

 

#Neuroscience 

 

Careers That Change Lives  

We are seeking an experienced and driven Senior Quality Engineer to join our dynamic cross-functional team within the Spine and Biologics Portfolio, Cranial and Spinal Technologies (CST) operating unit. CST is at the forefront of developing innovative spinal medical technologies that address evolving clinical needs and enhance patient care, supported by a strong portfolio of trusted solutions known for quality, integrity, and reliability in cranial and spinal procedures.  

In this high-impact role, you will lead and coordinate quality assurance activities across multidisciplinary teams, ensuring compliance, continuous improvement, and excellence throughout the product lifecycle. You will also be instrumental in driving production and supplier quality strategies, partnering closely with internal and external stakeholders to optimize processes, strengthen product performance, and support operational excellence in a fast-paced, collaborative environment. 

Responsibilities may include the following and other duties may be assigned. 

  • Collaborate with internal and contract manufacturing engineering teams to ensure purchased products and/ or components are manufactured and qualified in accordance with applicable industry standards and regulatory requirements. 

  • Develop and maintain quality records per established processes - design history files, risk management, change requests across the product lifecycle. 

  • Collaborate with engineering and extended teams to lead Product Acceptance, Approved Supplier List coordination, Supplier Owned Quality deployment, Production Parts Approval Process, as applicable. 

  • Perform duties as the technical liaison between contract manufacturers and Medtronic site(s) - devise and implement methods/ procedures for inspecting, testing and evaluating the precision, accuracy, stability and control of products and/ or production equipment. 

  • Monitor parts through the development and production value stream, communicate and resolve issues in a timely manner (including leading nonconformance assessments, investigations, corr

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Company

Medtronic

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