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QPS

Auditor I – Laboratory

QPS

. Audit scientific data for clinical and nonclinical study records and reports .

Posted 9/24/2026full-timeNewark • United StatesMid-LevelSenior💰 $45,000 - $50,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in auditing scientific data and ensuring compliance with protocols, SOPs, and quality management systems. Proficient in identifying noncompliance and formulating corrective actions within laboratory settings.

Highest-signal resume keywords
Audit Scientific DataQuality Management System InspectionGLP ComplianceGCP ComplianceGMP Quality Assurance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Data AuditingCorrective Action FormulationLaboratory Procedures InspectionAnalytical ProceduresRaw Data Documentation
Soft Skills
CommunicationAttention to DetailProblem-Solving
Industry Keywords
BiologyBiochemistryImmunologyAnalytical ChemistrySOPs

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Audit scientific data for clinical and nonclinical study records and reports
  • Ensure study conduct and raw data comply with protocols, SOPs, validated methods, study plans, lab manuals, and analytical procedures
  • Inspect laboratory work in situ, including procedures, facilities, equipment, personnel training, computer systems, and raw-data documentation
  • Audit and inspect the Quality Management System
  • Identify noncompliance and formulate corrective and preventive action recommendations
  • Issue audit reports to scientists, personnel, and management
  • Verify audit follow-up responses and close audits
  • Assist with client and government audits and departmental goals as directed by line management

Requirements

What you’ll need
  • Bachelor’s degree in a related scientific discipline such as Biology, Biochemistry, Immunology, or Analytical Chemistry preferred
  • Lab experience and/or experience working within GLP, GCP, or GMP Quality Assurance preferred but not required
  • Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis
  • No visa sponsorship will be provided now or in the future

Benefits

Comp & perks
  • After hours incentive work potential
  • Great learning opportunities and support for career goals
  • Structured Career Ladders with growth opportunities
  • Bonuses and merit increases linked to individual, team and company performance
  • Company-matched 401(k)
  • Company-sponsored Group Life/AD&D insurance
  • Short- and Long-term Disability Insurance
  • Internal committees designed for QPS employees