<ul><li>Ensure all laboratory documentation is accurate, complete, and up-to-date.</li><li>Manage document control processes, including document creation, approval, revision, and archiving.</li><li>Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.</li><li>Prepare and maintain documentation required for regulatory inspections and audits.</li><li>Implement and monitor corrective and preventive actions (CAPA) related to documentation issues.</li><li>Verify the accuracy and completeness of laboratory records, including test results, observations, and calibration records.</li><li>Ensure data integrity and compliance with data management policies.</li></ul>

QA Lab Documentation