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.