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Vice President, Quality Assurance – Regulatory Affairs
DayforceVice President managing Quality Assurance and Regulatory Affairs for AirStrip's SaMD portfolio. Leading regulatory strategy and ensuring compliance and quality operations.
Posted 7/29/2026full-timeSan Antonio • Texas • 🇺🇸 United StatesLead💰 $160,000 - $205,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and executing global regulatory strategies, ensuring compliance with FDA and international standards while leading a high-performing Quality Assurance and Regulatory Affairs team. Proven ability to manage quality processes, regulatory submissions, and inspections effectively to support organizational growth.
Highest-signal resume keywords
Regulatory Strategy DevelopmentQuality Management System (QMS)Regulatory Compliance FrameworksFDA EngagementLeadership in Quality Assurance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Regulatory SubmissionsQuality AssuranceRisk ManagementRegulatory InspectionsAudit ManagementMarket Expansion StrategyContinuous ImprovementProactive PlanningCompliance ProgramsTeam Development
Soft Skills
Relationship BuildingCoachingAccountabilityStrategic DirectionCommunication
Industry Keywords
Medical DevicesSaMDISOMDSAPRegulatory AgenciesQuality ProcessesGlobal SubmissionsIndustry StakeholdersRegulatory TrendsExecutive Oversight
About the role
Key responsibilities & impact- Own and evolve AirStrip’s global regulatory strategy aligned to business goals and product roadmap
- Build and maintain strong relationships with regulatory agencies and industry stakeholders
- Represent AirStrip externally through regulatory engagement, industry participation, and strategic partnerships
- Monitor regulatory trends and translate them into proactive, actionable plans
- Provide strategic direction for global submissions, approvals, and market expansion
- Lead the continued development and continuous improvement of AirStrip’s Quality Management System (QMS)
- Ensure quality processes are scalable, efficient, and aligned with organizational growth
- Maintain consistent readiness for regulatory inspections and audits (e.g., FDA, ISO, MDSAP)
- Provide executive oversight of risk management, quality performance, and compliance programs
- Lead Management Review activities and ensure appropriate escalation and resolution of quality and compliance risks
- Lead, coach, and develop a high-performing QA/RA organization
- Set clear expectations, accountability, and development pathways for team members
Requirements
What you’ll need- Bachelor’s degree in a scientific, engineering, clinical, or related discipline (advanced degree preferred)
- 10+ years of progressive leadership experience in Quality Assurance and Regulatory Affairs within medical devices and/or SaMD
- Demonstrated experience working directly with FDA and global regulatory agencies
- Proven track record leading successful regulatory inspections and audits
- Deep working knowledge of quality management systems and regulatory compliance frameworks
- Experience developing regulatory strategy and guiding global submissions and approvals
Benefits
Comp & perks- Health insurance
- Bonuses