Administer and maintain controlled documents including SOPs, work instructions, policies, forms, and quality records. * Coordinate document lifecycle activities including creation, review, approval, training, revision, archival, and retirement. * Support quality systems such as Document Management, Change Control, CAPA, Deviations, Training Management, Audit Management, and Supplier Quality. * Review document change requests and assess impact on existing quality processes. * Collaborate with Quality Assurance, Regulatory Affairs, Manufacturing, and business stakeholders to ensure timely document updates and approvals. * Maintain compliance with GMP, GxP, FDA, EU, and internal quality standards. * Support internal audits, external audits, and regulatory inspections by providing required documentation and evidence. * Monitor quality metrics, generate reports, and identify opportunities for continuous improvement. * ...