Senior Software Quality Engineer

Restorative Neurotechnologies

Sr. Software Quality Engineer at Echo Neurotechnologies ensuring quality compliance and support in medical device development.

Posted 7/17/2026full-timeSan Francisco • California • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Quality Management Systems (QMS) in compliance with FDA and ISO standards, with a strong focus on risk management, software validation, and collaboration across multi-disciplinary teams in the medical device industry.

Highest-signal resume keywords

Quality Management System ImplementationRisk Management ActivitiesSoftware Validation and VerificationMedical Device Regulations ComplianceDesign History File Creation

ATS Keywords

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Hard Skills

Quality EngineeringRisk Management ToolsDesign ControlsFailure Modes and Effects AnalysisCybersecurity DocumentationTraceability MatricesDesign Verification and ValidationRoot Cause AnalysisContinuous Improvement InitiativesAI/ML Technology

Soft Skills

CollaborationCritical ThinkingBuilding TrustNavigating AmbiguityPromoting Quality Culture

Industry Keywords

FDA QMSRISO 13485IEC 62304ISO 14971IEC 62366-1Medical Device DevelopmentRegulated EnvironmentDesign Transfer ActivitiesInternal and External AuditsManagement Review

Tech Stack

Tools & technologies

Cyber Security

About the role

Key responsibilities & impact

Participate in ongoing implementation of the Quality Management System (QMS) in conformance with US FDA QMSR, ISO 13485, IEC 62304, and IEC 62366-1 and other relevant standards.
Support the product development team in creation of design history files (DHFs) including product requirements, software architecture and design specifications, design verification and validation test protocols and reports, risk management file, cybersecurity documentation, traceability matrices, etc.
Guide and lead risk management activities, including failure modes and effects analysis (FMEA) and hazards analysis, in alignment with ISO 14971.
Guide and lead computerized system assurance and validation activities for SW tools and systems.
Engage and collaborate with suppliers and support design, development and design transfer activities.
Support and participate in internal and external audits, coordinating and providing documentation and evidence of compliance.
Support root cause analysis for nonconformances, defects and CAPAs, issue management, management review and quality data analysis.
Foster a collaborative environment, champion continuous improvement initiatives and promote a quality culture across the organization.

Requirements

What you’ll need

Bachelor’s or Master’s degree in Engineering (e.g., Biomedical, Computer Science, Electrical, or related field).
8+ years of quality engineering or in medical device development from concept development to production release.
Strong understanding of medical device regulations and standards (FDA, ISO 13485, IEC 62304, ISO 14971, IEC 62366-1) and experience working in a regulated environment.
Experience with software V&V activities, experience with AI/ML technology is a plus.
Hands-on experience with risk management tools (e.g. FMEA, risk analysis) and design controls.
Experience in establishing work relationships across multi-disciplinary teams and with partners in different time zones, building trust and demonstrating critical thinking.
Experience in navigating ambiguity, bringing clarity to complex situations and thriving in a fast-paced environment.

Benefits

Comp & perks

Competitive compensation, including stock options.
Comprehensive benefits package.
401(k) program with matching contributions.