Spécialiste Qualité F/H
Core
Ensuring quality compliance and managing product safety issues for commercial entities in France, Belgium, and Luxembourg.
Role type
Quality Assurance Specialist
Builds
Quality management systems and regulatory compliance for medical devices
Domain
Medical devices / Healthcare
Required skills
ISO 13485, product complaint management, product recall management, internal audit management, CAPA management, scientific background (pharmacist, biomedical engineer, or Master's in Quality)
Preferred skills
English (oral and written)
Responsibilities
Implementing the Quality Management System (SMQ) in compliance with regulatory and internal requirements; Serving as the quality reference for France, Belgium, and Luxembourg; Managing product complaints and recalls; Managing non-conformities and CAPAs; Preparing and presenting quarterly quality reviews to the Executive Committee; Managing internal quality audits; Managing supplier quality; Writing and updating local operating procedures and processes; Leading and participating in continuous improvement projects.