Assist in reviewing and updating Standard Operating Procedures (SOPs) under the guidance of the Quality Manager., Support the preparation of materials for management reviews., Help monitor QMS process documentation for completeness and compliance with ISO 13485., Learn and apply structured quality thinking (risk-based approach, CAPA, process awareness) in day-to-day tasks., Shadow and assist during internal audit preparation activities., Help compile evidence packages and document findings for audit readiness., Research regulatory updates (MDR, EU AI Act, ISO standards) and summarise implications for the team., Support IT security awareness activities tied to the QMS (e.g., documentation, training materials)., Assist in maintaining records relevant to data privacy compliance (GDPR)., Collaborate with engineering, clinical, and operations teams to understand how quality requirements apply across the product lifecycle., Prepare summaries, reports, and presentations on quality and regulatory topics for internal stakeholders.