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Quality Assurance Specialist

Your responsibilities :
Implementing, training, and monitoring QMS compliance
Applying a risk-based approach to QMS processes
Managing internal and external audits
Conducting regulatory intelligence
Supporting Management Review and quality objectives
Overseeing eQMS (Quality Computerized Systems)
Contributing to continuous improvement projects

Your profile:
An engineering degree or equivalent
8+ years of experience in Quality and Regulatory within the Medical Devices industry
ISO19011 internal auditor qualification
Deep knowledge of relevant regulations and standards
SAP experience (a plus)
Strong communication skills in French and English (German is a plus)

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