We are looking for a Quality & Regulatory Affairs Specialist to support the local operations of a global medical device organisation. This role sits at the intersection of Quality Assurance, Regulatory Affairs, and Post‑Market activities , ensuring compliance with national and European medical device requirements.

Key Responsibilities

• Manage product quality complaints , including assessment, documentation, coordination of returns, and follow‑up with internal teams.
• Support Field Safety Corrective Actions (FSCA) , including handling Field Safety Notices and reconciliation activities.
• Maintain and improve the local Quality Management System in alignment with ISO 13485 and internal procedures.
• Drive and support CAPA , deviations, issue evaluations, and continuous improvement initiatives.