Beschreibung
We are searching for QA Consultant to support a project with our Pharmaceutical client in North Rhine-Westphalia. I have included details of the area for support below:Documentation Management (QA)
- Document review and management in preparation for GMP inspection.
- Experience working with both paper based and electronic systems
- Start: June - End 2020
- German speakers required
- ~40 hours per week, site-based
If you are Interested, Apply via the link below and don't hesitate to contact me on LinkedIn.