Chemiker (m/w/d)
Core
Develop and maintain the Quality Management System (QMS) and support international regulatory approval for In-vitro Diagnostic (IVD) products.
Role type
Quality Management Specialist (Regulatory Affairs)
Builds
IVD products for diagnostics and research
Domain
Medical Devices / In-vitro Diagnostics
Required skills
Quality Management Systems (ISO 13485), Regulatory Affairs (IVDR), Audit Management, Product Registration, Document Preparation, Research & Evaluation
Preferred skills
MDSAP experience, Natural Sciences Degree (Chemistry/Biochemistry/Biology/Biotechnology/Medical Engineering)
Technologies
Microsoft Office