Senior Quality Engineer - Minneapolis

About this role

We anticipate the application window for this opening will close on - 15 Aug 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 ENT operating unit provides innovative technologies for sinus, otology, neurotology, head & neck, skull base, and airway care. With advanced instruments, image-guided systems, and implants, we enhance precision, safety, and efficiency, supporting clinicians with education and clinical guidance to improve patient outcomes.  Check us out on LinkedIn: Medtronic ENT

This is a seasoned individual contributor role responsible for developing, implementing, and maintaining rigorous quality standards and protocols during the sustaining and post-market phases of the product lifecycle. The Specialist serves as a key technical expert, working with limited supervision, who must demonstrate substantial expertise in risk management (e.g., assessing product risk and supporting field actions). This role involves providing design-quality oversight for product changes (including design change analysis and DHF maintenance), and using advanced inspection, testing, and statistical analysis methods to ensure product precision, accuracy, and compliance with all required standards and documentation.

A successful candidate will drive process improvements within the Quality function, manage projects, use specialized knowledge to influence internal stakeholders and external vendors, often requiring travel to design sites within the US, and provide guidance and mentorship. The core mission is to proactively assess, mitigate, and resolve complex technical issues to guarantee product reliability and regulatory adherence.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

Responsibilities may include the following, and other duties may be assigned. • Develops, modifies, applies, and maintains rigorous quality standards and protocols for processing materials into finished products, with a specific focus on the sustaining and post-market phases of the product lifecycle.

• Collaborates with engineering, design, and manufacturing functions to ensure quality standards are established and maintained, including providing Design Quality oversight for product changes, design change analysis, and Design History File (DHF) maintenance.

• Demonstrates strong expertise in risk management by devising and implementing methods and procedures for inspecting, testing, and evaluating product precision and accuracy, and supporting complex risk assessments (e.g., product risk and field action support).

• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.

• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with all regulatory requirements.

• Required to travel to design and manufacturing sites within the USA to support technical projects, audits, and design quality reviews.

• May specialize in design quality, product evaluation, reliability engineering, and process quality as they apply to the management of released product portfolios.

Required Knowledge and Experience: • Requires a Baccalaureate degree 

• Minimum of 4 years of relevant experience OR an advanced degree with a minimum of 2 years of relevant experience

Nice to have: • Site transfer experience

• Pharma or combination product 

• Risk Management.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work a

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