Entry-Level GLP QA Auditor

Charles River Laboratories, Inc.; Shrewsbury (MA); On-site; USD 60,000 - 64,000; Full time

Job summary

Charles River Laboratories is seeking a QA Auditor in the United States to perform audits of basic records and inspections to ensure GLP compliance. You will communicate risks to your supervisor and maintain audit records for traceability.

The role requires reviewing SOPs and reports for accuracy, identifying deviations, and supporting scheduling of QA audits. A strong eye for detail and solid written/verbal communication are essential.

Qualifications

• Bachelor’s degree in life science or related discipline.
• 1-2 years experience in QA role.
• Must comprehend regulations and guidance documents and apply critical thinking.
• Detail oriented with ability to communicate findings verbally and in writing.
• Experience with audits and inspections is preferred.

Responsibilities

• Assure Charles River’s compliance with GLP. Communicate all identified compliance and quality risks to supervisor.
• Perform data audits to ensure records are attributable, legible, contemporaneous, original, accurate, and in compliance with regulations, SOPs, and protocols.
• Review SOPs, protocols, reports, and other quality and regulated records for accuracy, completeness, and compliance with all applicable GLP regulations.
• Maintain written and signed records of all audits and inspections and sign records documenting the performance of audits and inspections and reporting to management.
• Identify deviations from GLP regulations, protocols and SOPs.
• Independently perform inspections to monitor processes, facilities, equipment, personnel, materials, methods, practices, records, and controls to assure compliance with GLP regulations.
• Assist in scheduling and tracking QA audits, inspections and procedures as requested.
• Perform all other related duties as assigned.

Skills

Data audits

GLP compliance

Quality assurance

Documentation

Education

Bachelor's degree in life science

Tools

Microsoft Office

Job description

Charles River Laboratories is seeking a QA Auditor in the United States to perform audits of basic records and inspections to ensure GLP compliance. You will communicate risks to your supervisor and maintain audit records for traceability.

The role requires reviewing SOPs and reports for accuracy, identifying deviations, and supporting scheduling of QA audits. A strong eye for detail and solid written/verbal communication are essential.