QA Specialist (2-Year Fixed-Term Contract)

Work Flexibility: Hybrid Supports the effectiveness and compliance of the local Quality Management System by maintaining QMS processes, managing quality records, CAPAs, supplier quality activities, and driving continuous improvement in accordance with ISO 13485 and medical device regulatory requirements. What you will do Maintain and continuously improve the local Quality Management System (QMS) in accordance with ISO 13485:2016, company objectives, and applicable regulatory requirements. Develop, revise, and maintain local QMS procedures, work instructions, and related documentation. Ensure EEMEA quality procedures and document updates are reviewed and appropriately implemented locally. Execute quality assurance activities in compliance with established procedures and processes.…