GLP QA Auditor – Nonclinical Studies
Listed on 2026-10-13
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Actalent seeks a Quality Assurance Auditor to support GLP compliance across nonclinical laboratory studies in a contract research environment. You will audit regulated studies, inspect facilities, and assist regulatory readiness for FDA and EPA inspections, contributing to cancer research and device-related testing.
The role requires 2+ years in GLP settings and 3+ years auditing GLP studies, with strong data integrity and documentation skills.
The GLP QA Auditor – Nonclinical Studies position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
As a GLP QA Auditor – Nonclinical Studies, you will play an important part at Actalent in South Brunswick, NJ, United States.
We invite applications for the GLP QA Auditor – Nonclinical Studies position located in South Brunswick, NJ, United States.
The following position is for a GLP QA Auditor – Nonclinical Studies with Actalent.
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