Senior Software Quality Engineer

Primary Responsibilities

• Support software quality activities across the full lifecycle, from requirements and design through verification, validation, release, and post-market support.
• Collaborate with project and development teams to ensure compliance with company procedures, applicable standards, and regulatory requirements.
• Provide early quality input on software requirements, architecture, algorithms, code, and technical design reviews.
• Review requirements, design outputs, test cases/results, and traceability documentation for completeness, clarity, and compliance.
• Support software risk management activities, including SFMEA, hazard analysis, risk mitigation, and verification.
• Support verification and validation planning, execution, documentation, defect investigations, root cause analysis, and CAPA activities.
• Contribute to software configuration management, change control, release readiness, and documentation consistency.
• Support internal/external audits and regulatory readiness while monitoring software quality metrics and driving process improvements.
• Provide quality input on reliability, cybersecurity, usability, and other software quality considerations throughout development.

Required Qualifications

• Bachelor’s degree in Engineering, Computer Science, Software Engineering, Science, or a related technical field.
• Experience in software quality, software development, verification and validation, or a related engineering/quality role.
• Working knowledge of software development lifecycle activities.
• Understanding of design controls, requirements traceability, verification and validation, and risk management.
• Strong analytical, documentation, and problem-solving skills.
• Effective communication skills and ability to work across multiple functions and organizational levels.
• Ability to manage multiple priorities and deliver work on time.

Preferred Qualifications

• Experience in medical device or other regulated product development environments.
• Familiarity with standards and regulations such as ISO 13485, ISO 14971, IEC 62304, 21 CFR 820, and IEC 60601-1.
• Knowledge of Agile development methodology.
• Experience with embedded software, mobile applications, or medical device software.
• Familiarity with cybersecurity evaluations and how threats can translate to patient safety risks.
• Experience supporting audits, inspections, or regulatory submissions.

In-person exchanges are invaluable to our work. We’re working a minimum of 3-4 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.

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.

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Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.

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Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package

A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: United Kingdom: 76,800.00 GBP - 115,200.00 GBP |

The final salary within this range will be determined based on objective, job-related criteria, including relevant experience, skills and qualifications, in accordance with our compensation framework.

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This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).