Beschreibung
GMP Auditor Plasmalieferanten (m/f/d)
Reference: -en
Start: 01/08
Duration: 6 MM
Main tasks:
- Conducting GMP-compliant audits and inspections of plasma suppliers in Europe and America
- Creation of audit reports and monitoring of the supplier database used for regulatory submissions
- Project-related communication with external suppliers, internal (international) departments
Main qualifications
- Sound knowledge of the regulations of plasma production and the associated supply chain
- Fluent spoken and written English
- You have experience in dealing with the current EMA guidelines/requirements
Main advantages:
- Interesting assignments at renowned national and international companies
About us:
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
My contact at Hays:
My contact person:
Sarah Zwisler
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