Ingénieur Sr Systèmes Logiciels

Ingénieur Sr Systèmes Logiciels Nous utilisons des cookies nécessaires et des cookies de mesure d’audience pour assurer le fonctionnement de ce site et produire des statistiques anonymes. Nous souhaitons également utiliser des cookies et des technologies similaires pour améliorer le fonctionnement du site, analyser de façon plus précise l’activité des visiteurs et afficher des publicités personnalisées. Nous définirons ces cookies et technologies uniquement si vous les acceptez.

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Sur site:
Fridley, Minnesota, United States of America:
Temps plein:
Offre publiée aujourd'hui:
Date de fin : 2 novembre 2026 (Il reste 6 jour(s) pour postuler):
R74046

We anticipate the application window for this opening will close on - 2 Nov 2026

Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.
** Journée type
** 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.
The Senior Software Systems Engineer on the Neuromodulation and Pelvic Health Premarket Design Quality team will partner with cross-functional development teams to ensure software and system-level design activities are planned, executed, and documented in compliance with applicable quality and regulatory requirements.  This role supports new product development by providing quality oversight and technical guidance throughout the design control lifecycle, with a focus on software-intensive medical device systems.

** Key Responsibilities
*** Provide design quality support for software and software-enabled medical device development programs from concept through transfer to manufacturing.
* Ensure compliance with applicable design control, software lifecycle, and risk management requirements.
* Review and contribute to system requirements, software requirements, architecture, and design documentation.
* Participate in the development of verification and validation strategies for software, system, and integration testing.
* Partner with engineering, product development, regulatory, clinical, manufacturing, and quality teams to resolve design quality issues.
* Evaluate software development deliverables for completeness, traceability, and regulatory readiness.
* Lead software-related risk evaluation and mitigation verification to support risk management activities, including hazard analysis
* Participate in design reviews and provide constructive feedback to improve product quality, safety, and compliance.
* Assist in root cause analysis and corrective action activities related to design or software quality issues.
* Mentor less experienced engineers on design quality practices, documentation expectations, and compliance requirements.
* Contribute to continuous improvement initiatives for design quality processes, tools, and templates.  
** Required Qualifications
*** Bachelor's degree in Software Engineering, Computer Engineering, Electrical Engineering, Systems Engineering, or a related technical field and minimum of 4 years…