MedTech Quality & Regulatory Manager – Vigilance & QMS

KARL STORZ France is seeking a Quality & Regulatory Manager to implement regulatory strategies for medical devices and oversee post-market activities. The role requires a strong background in MDR/ISO 13485 and experience with QMS, audits, and continuous improvement.

Fluency in English and French is essential, along with excellent communication and training skills to guide cross-functional teams and ensure regulatory compliance across the organization.