We anticipate the application window for this opening will close on - 30 May 2026

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

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, corrective and preventive actions) 

• Partner with global functions and contract manufacturers to ensure designated suppliers are monitored on a regular basis (via audits, onsite reviews, continuous improvement initiatives etc.) for ensuring continued adherence to good manufacturing pract