The Associate Quality Assurance Auditor is responsible for supporting regulated GCP & GLP activities, including developing and implementing the site's Audit Program.
Requirements
- Bachelor’s Degree OR 3+ Years’ experience in a laboratory, pharmaceutical, medical device or clinical research organization
- Independently performs document audits
- Manages the receipt and review of necessary documentation
- Develops Quality metrics
- Serve as a resource for the promotion and compliance with regulations, guidelines, Quality Management System and Standard Operating Procedures
- Monitors and assesses all required standards, laws and guidelines
- Support client, regulatory and sub-contractor audits
- Collaborate with QA Auditors, Sr. QA Auditors, QA Supervisor and QA Manager as needed
- Participate in monthly laboratory Quality Assurance meetings
- Perform other duties as assigned