Jobs and Careers
ME

Principal Software Quality Engineer

Medtronic
United Statesfull_timeVerifiedPosted 14 May 2026
💰 $187,200/yr($124,800/yr$187,200/yr)

About the role


 

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

Principle Software Quality Engineer to support: AiBLE: Converged Planning

         

         

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 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

As a Principal Software Quality Engineer, you will play a critical role in ensuring the safety, reliability, and performance of software powering life-changing therapies. You will collaborate across R&D, systems, and cross-functional teams to drive quality excellence from concept through commercialization—directly impacting patient outcomes worldwide.

Key Responsibilities

  • Lead software quality engineering activities across the full product lifecycle, including requirements, design, development, integration, testing, and validation

  • Develop, implement, and maintain software quality standards, processes, and procedures to ensure compliance with internal and regulatory requirements

  • Drive software verification and validation (V&V) strategy, ensuring traceability, testability, and completeness of system requirements

  • Review software architecture, design specifications, and change requests to ensure alignment with quality, regulatory, and contractual requirements

  • Define and monitor key quality metrics to ensure product performance and continuous improvement

  • Ensure project and process documentation meets quality standards and supports audit readiness

  • Serve as a technical quality expert, influencing cross-functional decision-making and driving resolution of complex quality issues

  • Lead or contribute to large-scale, cross-functional programs with significant organizational impact

  • Mentor and provide guidance to engineers and team members within software quality and broader development teams

Basic Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Software Engineering, or related technical field

  • Minimum of 7+ years of software quality engineering experience, OR
    Master’s degree with 5+ years of experience, OR
    PhD with 3+ years of experience

Preferred Qualifications

  • Experience in medical device, regulated industry, or safety-critical systems (FDA, IEC 62304, ISO 13485)

  • Strong expertise in software verification & validation (V&V), validation strategy, and traceability

  • Deep understanding of software development lifecycle (SDLC), Agile methodologies, and DevOps environments

  • Experience with embedded systems, SaMD (Software as a Medical Device), or digital health platforms

  • Proficiency with test automation frameworks, scripting (Python, C++, MATLAB, or similar)

  • Experience working with risk management (ISO 14971), design controls, and regulatory submissions

  • Demonstrated ability to lead complex initiatives and influence cross-functional stakeholders

  • Prior experience in neuromodulation, neurotechnology, signal processing, or implantable systems strongly preferred

  • Strong analytical, problem-solving, and communication skills

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 Res

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Medtronic

View company profile →