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Verily

Quality Systems and Compliance Lead

Verily

Quality Systems and Compliance Lead driving quality excellence and managing QA domains at Verily Health, a data platform focused on AI-enabled precision health solutions.

Posted 7/21/2026full-timeDallas • California, Massachusetts, North Carolina, Texas • 🇺🇸 United StatesSenior💰 $142,000 - $213,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Quality Assurance and Quality Management Systems (QMS) within the medical device and life sciences sectors, with a strong focus on ISO 13485:2016 compliance and FDA regulations. Proven ability to lead cross-functional teams and implement quality initiatives that enhance product development and commercialization.

Highest-signal resume keywords
Quality Management System (QMS) LeadershipISO 13485:2016 ComplianceFDA QMSR KnowledgeCross-Functional Team LeadershipSaMD and AI/ML Product Quality Assurance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Quality AssuranceQuality Metrics AnalysisCorrective Action ImplementationQuality System DesignRegulatory Affairs
Soft Skills
Strategic LeadershipCollaborationAnalytical Thinking
Industry Keywords
Medical DeviceDigital HealthLife SciencesQuality ExcellenceProduct Development

About the role

Key responsibilities & impact
  • Drives quality excellence at Verily by owning one or more Quality Assurance domains and leading strategic QA initiatives
  • Responsible for designing and advancing robust quality systems
  • Ensures that products are developed, commercialized, and sustained to the highest standards of quality
  • Analyzes quality metrics and performance data to identify trends and implement effective corrective actions
  • Partners with engineering and product teams to embed quality practices into development workflows

Requirements

What you’ll need
  • Bachelor's degree in a scientific, engineering, or related field
  • 8+ years of experience in quality assurance or regulatory affairs within the medical device, digital health, or life sciences industry
  • Demonstrated experience leading or managing a QMS in conformance with ISO 13485:2016 and FDA QMSR
  • Experience supporting or managing quality across SaMD and/or AI/ML-enabled products
  • Proven ability to lead cross-functional quality initiatives

Benefits

Comp & perks
  • health insurance
  • retirement plans
  • paid time off
  • flexible work arrangements
  • professional development
  • bonuses
  • stock options
  • wellness programs