The role involves maintaining and improving the Quality Management System to ensure compliance with GxP, GMP, and GDP regulatory standards. You will manage document control, handle deviations and CAPAs, support audits, and oversee product quality complaints.
The role involves supporting GMP compliance, supplier assurance, and Marketing Authorisation Holder oversight within the pharmaceutical quality system. You will coordinate audit activities, manage quality documentation, and track performance metrics to ensure regulatory compliance and continuous improvement.
