Associate QA Auditor: GMP Compliance & Data Integrity

Charles River Laboratories; Charleston (SC); On-site; USD 30,000 - 32,000; Full time

Benefits offered by this job

Performance bonus

401K plan

Paid time off

Stock purchase

Health coverage

Wellbeing support

Work-life balance

Job summary

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,

Qualifications

• Associate’s degree (A.S./A.A.) or equivalent in life science or related discipline.
• 1–2 years of experience in a Quality Assurance role.

Responsibilities

• Participate in review of SOPs and controlled documents for GMP compliance.
• Perform raw data audits of documentation for temperature, humidity, and gauges in controlled areas; review autoclave/oven charts.
• Review incoming raw material receipt packages for compliance with specifications and testing procedures.
• Review accessory product records for compliance with product specifications and testing procedures.
• Review instrument release packages for compliance with product specifications and testing procedures.
• Review equipment and process logbooks and perform other related duties as assigned.

Skills

Quality Assurance

Education

Associate degree (A.S./A.A.) or equivalent

Bachelor’s degree preferred

Job description

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,