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Dayforce

Quality Audit Specialist

Dayforce

Quality Audit Specialist executing internal and external audits for compliance in clinical trials. Interacts with cross functional groups and external partners to ensure compliance initiatives are met.

Posted 7/29/2026full-timeRemote • Tennessee • 🇺🇸 United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in executing internal and external audits, ensuring regulatory compliance in clinical trials, and managing electronic Quality Management Systems. Proficient in driving post-audit actions and maintaining key performance indicators for quality assurance.

Highest-signal resume keywords
Regulatory ComplianceClinical Trials Audit ExperienceEQMS Software ExperienceQuality ManagementVendor Assessment

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Internal AuditsExternal AuditsPost-Audit ActionsQuality ManagementKey Performance Indicators
Tools & Technologies
EQMSVeeva Vault
Industry Keywords
GCP ComplianceClinical TrialsVendor AuditsQuality Assurance

Tech Stack

Tools & technologies
Google Cloud PlatformVault

About the role

Key responsibilities & impact
  • Execute internal and external audits
  • Support vendor and client audits
  • Drive post-audit actions to completion
  • Assist Quality Management in monitoring GCP regulatory compliance
  • Schedule and organize internal and external assessments of LabConnect
  • Perform internal and external assessments of LabConnect critical vendors
  • Update and maintain QRS Key Performance Indicators
  • Support the electronic Quality Management System (eQMS)

Requirements

What you’ll need
  • Bachelor’s degree with 4-6 years in quality-related roles, specializing in regulatory compliance required
  • Experience with clinical trials audit activities (hosting audits and conducting audits)
  • eQMS software experience preferred (Veeva Vault is ideal)

Benefits

Comp & perks
  • Fully remote role.