Quality ManagerMDR/ IVDRISO13485:2016Good Manufacturing Practice
Quality Manager
Development and integration of a quality management system in accordance with ISO13485:2016 and cGDP standards
Preparation and processing of technical documentation for the approval of in-vitro diagnostic tests (class D) in accordance with IVDD 98/79/EC and IVDR 2017/746
Supplier qualification in accordance with cGMP and cGDP specifications
Project management of the various suppliers and review of documentation, as well as initiation of required measures
Reporting and preparation of summary to the management
Quality ManagerMDR/ IVDRISO13485:2016Good Manufacturing Practice
Quality Manager
Development and integration of a quality management system in accordance with ISO13485:2016 and cGDP standards
Preparation and processing of technical documentation for the approval of in-vitro diagnostic tests (class D) in accordance with IVDD 98/79/EC and IVDR 2017/746
Supplier qualification in accordance with cGMP and cGDP specifications
Project management of the various suppliers and review of documentation, as well as initiation of required measures
Reporting and preparation of summary to the management
In-Vitro Diagnostics Class D
MDR/ IVDRISO13485:2016Good Manufacturing Practice
X1 Pharma GmbH + Pharmact AG
Remote / Mannheim
Kompetenzen
Kompetenzen
Qualitätssicherung
GMP
GDP
Medical Devices
Branchen
Branchen
Pharma, Biotech, Medtech
Vertrauen Sie auf Randstad
Im Bereich Freelancing
Im Bereich Arbeitnehmerüberlassung / Personalvermittlung