Description
We are looking for a
CSV Specialist (m/f)
Reference: -en
Start: 08/16
Duration: 5 MM+
Place: in Hesse
Branch: Wettbewerber
Your tasks:
- Support the RIMS Data Quality Framework initiative as well as the implementation of the next major RIMS version
- Project management support
- Update existing process documentation/training documentation
- User Acceptance Test organisation and execution for next major RIMS version and for new reports
- Update of existing validation documentation
- Data entry in different systems
Your qualifications
- Business fluency in English
- Good experience in business process analysis, computerized validation, regulatory procedures (worldwide & EU), Regulatory Affairs and Regulatory Information Management
- Experience within the pharmaceutical industry and Quality Assurance is beneficial
Skills:
- Qualification/validation specialist
Keywords: Spezialist Validierung und Qualifizierung