Description
Responsible tasks:- Manage supplier related documents (NC's, CAPA's, change requests)
- Manage supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)
- Perform product investigations
- Maintain validation plans from Process Validation at suppliers
- Supplier transfer projects
Supporting tasks:
- Supplier preparation for FDA inspections
- Supplier selection
- Quality Agreement
Requirements:
- Experienced in Supply Management in Medical Devices
- FDA 21CRF part 820 and ISO 13 485
- Excellent knowledge of German and English
For more information on this vacancy, and also Freelancer Quality Management roles in Switzerland in the medical devices field, please contact Burcu Parilti on , and email her your CV in WORD format, scanned copies of Certifications, and Zeugnisse to