Description
The Compliance Associate will provide guidance, leadership, and training to business-unit personnel to maintain GMP and quality compliance in a biomanufacturing CDMO facility. The role covers GMP documentation, procedures, KPI reporting, vendor management, investigations, deviation and change-control reporting, risk assessments, CAPA plans, SOP reviews, training, audits, regulatory frameworks, and compliance issue resolution. It requires a technical education or equivalent experience, at least six years of practical and related experience, and at least five years in a GMP environment at a biopharmaceutical CDMO or in a compliance, documentation, or technical role.
