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Verily

Senior Quality Engineer, Cybersecurity

Verily

Senior Quality Engineer in Cybersecurity at Verily Health focusing on integrating quality engineering practices with cybersecurity across medical devices. Leading initiatives in quality management systems and regulatory compliance.

Posted 7/21/2026full-timeDallas • California, Massachusetts, Texas • 🇺🇸 United StatesSenior💰 $113,000 - $170,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Software Quality Management Systems (QMS) and medical device cybersecurity, with a strong focus on ISO 14971, IEC 62366, and FDA guidance integration into the software development lifecycle. Proven ability to lead cross-functional teams and support compliance in the medical device industry.

Highest-signal resume keywords
Software Quality Management System (QMS)Medical Device CybersecurityISO 14971 Risk ManagementIEC 62304 ComplianceFDA Cybersecurity Guidance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Software Quality EngineeringDesign and Development Files (DDFs)Risk ManagementUsability EngineeringCAPA Management
Soft Skills
Cross-Functional CommunicationOrganizational SkillsLeadership Skills
Tools & Technologies
Google WorkspaceJiraGitHubDocument Control Systems
Industry Keywords
FDA QMSRISO 13485AAMI TIR57Post-Market Cybersecurity SurveillanceSoftware Development Lifecycle (SDLC)

Tech Stack

Tools & technologies
Cyber SecuritySDLC

About the role

Key responsibilities & impact
  • Lead ongoing implementation and continuous improvement of the Software Quality Management System (QMS)
  • Serve as the Quality Lead for the cybersecurity process
  • Guide software development teams in creation and maintenance of Design and Development Files (DDFs)
  • Support ISO 14971 risk management, IEC 62366 usability engineering, and FDA cybersecurity guidance integration into SDLC
  • Support post-market cybersecurity surveillance activities
  • Provide CAPA, complaints, audit, and QMS support related to software and cybersecurity incidents

Requirements

What you’ll need
  • Bachelor's degree in Computer Science, Software Engineering, Informatics, Biomedical Engineering, or a related technical field; or equivalent practical experience
  • 5+ years in software quality engineering within the FDA QMSR / ISO 13485 medical device industry
  • Proven expertise in medical device cybersecurity
  • Work experience with FDA premarket and postmarket cybersecurity guidance and applicable standards (e.g., AAMI TIR57)
  • Demonstrated experience applying IEC 62304, ISO 14971, IEC 62366, and AAMI TIR57
  • Experience collaborating with software development and security teams
  • Proficiency in Google Workspace, Jira, GitHub, and document control systems
  • Excellent cross-functional communication, organizational, and leadership skills

Benefits

Comp & perks
  • Flexible working hours
  • Professional development opportunities
  • Competitive salary
  • Health insurance
  • 401(k) matching