Qualitätsmanager (m/w/d) X
Core
Managing the quality management system, including document control, audit preparation, CAPA handling, and customer complaint analysis.
Role type
Quality Management Specialist
Builds
Quality management system processes and compliance documentation
Domain
Manufacturing / Medical Devices (ISO 13485, ISO 9001, FDA 21 CFR 820)
Required skills
Quality management system administration, internal and external audit coordination, CAPA management, customer complaint analysis, process optimization, validation planning and documentation, error analysis
Preferred skills
Knowledge of DIN EN ISO 13485, DIN EN ISO 9001, FDA 21 CFR 820, technical degree or technician training, English proficiency