About the RoleWe are looking for a motivated and detail-oriented Quality Engineer to join our team. This is an exciting opportunity for an experienced quality professional to play a key role in maintaining and improving our Quality Management System (QMS) while ensuring compliance with applicable Medical Device Regulations, International Standards, and customer requirements.The successful candidate will work closely with internal teams, suppliers, and external stakeholders to support quality assurance activities, drive continuous improvement initiatives, and help ensure the highest standards of product quality and regulatory compliance.Key ResponsibilitiesMaintain and support the effectiveness of the Quality Management System (QMS), including:Document ControlCAPA (Corrective and Preventive Actions)Change ControlRisk ManagementInternal AuditsVigilancePost-Market Surveillance (PMS)Supplier ManagementSupport product monitoring, assessment, and release activities.Review and maintain quality records and documentation to ensure compliance with applicable regulations and standards.Prepare, analyse, and present quality data to identify trends, support investigations, and drive continuous improvement initiatives.Participate in root cause investigations, non-conformance management, CAPA activities, and implementation of corrective actions.Collaborate with suppliers and subcontractors to ensure product and process quality requirements are met.Review supplier quality documentation, ..... full job details .....