Description
We are looking for a
Quality Assurance Manager (m/f)
Reference: -en
Start: asap
Duration: 5 MM
Place: in Central Switzerland
Branch: Pharmazeutische Industrie
Your tasks:
- Support Operations to achieve sustainable compliance with medical device regulations in the production of market products
- Conduct Quality Reviews for change management, deviation management and CAPAs
- Review and release specifications and verification documents
- Review Device History Records and release products
- Quality representative for PFMEA
- Actively participate in knowledge management and contribute to continuous process improvement initiatives
Your qualifications
- Professional experience in a regulated environment (ISO 13485 and regulatory requirements of United States Food and Drug Administration)
- Bachelor in a technical field (science, engineering, etc.), advanced degree preferred but not required
- Very good German and good English skills
Skills:
- Quality manager