o Organize, index, file, and store all quality systems documentation and quality records
o Receive, review, control, and track documents per established processes and procedures
o Create and control QA forms, issuing them as needed
o Order supplies and maintenance items as needed
o Maintain site training and equipment records
o Support client and company initiatives by providing basic QA support activities
o Support client, safety, and regulatory body audits as assigned
o Follow Bureau Veritas policies and procedures
o Identify gaps in the document control process and provide process improvements
o Ensure the document control system remains compliant with current regulations
o Maintain quality systems in company operations
- Review & Approval Authority
o Conduct quality review and approval of method validations
o Assist in review and approve OOS and deviation investigations, ensuring proper change control/CAPA implementation.
o Review approved Certificates of Analysis and calibration records
o Review and approve instrument qualification and method validation documents
o Manage the inspection and approval of laboratory data prior to release
- System Development & Management
o Develop, maintain, and enhance quality systems in company operations
o Develop and implement quality and document control system procedures
o Lead quality event tracking and trending activities
o Manage internal audit scheduling and task assignments for trained QA personnel
- Vendor & Equipment Management
o Evaluate and approve supplier surveys for laboratory vendor qualification
o Manage site laboratory equipment vendors providing repair, calibration, or preventive maintenance services
o Maintain site Training and Equipment Tracking Matrices
o Ensure site training and equipment systems are in an audit-ready state
- Cross-Functional Leadership
o Facilitate review and revision of procedures, specifications, and forms with functional departments
o Participate in formal audit activities
o Substitute for Quality I-III functions as necessary