Associate QA Auditor: GMP Compliance & Data Integrity
Listed on 2026-10-06
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Charles River Laboratories in Charleston, SC is seeking an Associate Quality Assurance Auditor to join our Quality team. The shift is M-F from 11:30 AM to 8:00 PM, and the role involves auditing quality control data for routine assays, materials, and documentation to ensure GMP and SOP compliance.
Ideal candidates have an AS/AA or equivalent, with 1–2 years of QA experience. Responsibilities include SOP reviews, raw data audits for environmental controls, material receipts, product records,
As a Associate QA Auditor: GMP Compliance & Data Integrity, you will play an important part at Charles River Laboratories in Charleston, SC, United States.
This role, Associate QA Auditor: GMP Compliance & Data Integrity at Charles River Laboratories, could be your next opportunity.
Are you ready to take on the Associate QA Auditor: GMP Compliance & Data Integrity role at Charles River Laboratories?
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