Who we are looking forPurposeTo verify and ensure the compliance and the correct application of Good Clinical Practices (GCP) being primarily responsible for the management of all the GCP CAPAs, preparation of the quality metrics, KPIs supporting the compliance inside Global R&D Departments, management of Quality Documents and by execution of first and second party audits.
Main ResponsibilitiesManagement of CAPA Plans from GCP auditsManagement of the requests for the collection of quality metrics, KPIs supporting Global R&D DepartmentsManagement of Trackwise, Suppliers and Audit workflowsSupport...