The responsability goes from Quality Assurance (i.e, create SOP, training plan, polivalent matrix, measurement and calibration, non conformance management, internal and external audits...) Quality control (incoming inspection, verification of documents...) and regulatory affairs of products (resgistration of product on health authority, health & Safety...) . Document Control: Create and update SOPs for the entirely Business Unit of Dornier MedTech Spain following standards coming from headquarters and aligned with ISO 13485. Manage the complains of Non-conformance Management: Control and manage...