Description
We are looking for a
CSV consultant for a medical device company (m/f)
Reference: -en
Start: asap
Duration: 6 MM++
Place: in West Switzerland
Branch: Herstellung von pharmazeutischen Grundstoffen
Your tasks:
- Verification of a MES (Manufacturing Execution System) for a medical device company
- Validation of a MES (Manufacturing Execution System) according to FDA regulations
- Consult the company from a compliance and quality point of view in the development of a MES
Your qualifications
- University Degree within engineering
- Deep understanding of CSV validation according to the FDA regulations
- Fluent in English
Skills:
- Software developer
- Qualification/validation specialist
Keywords: Spezialist Validierung und Qualifizierung