Beschreibung
Quality Assurance Specialist GCP / GLP (m/f/d)
Reference: -en
Start: asap
Duration: 6 MM
Main tasks:
- Manage the external audit contractors (e.g. contract writing, contract amendment writing, WO preparation, price proposal requests)
- Accurately file GxP documents in GxP computer system
- Support Quality Managers and Quality Specialists in Quality Unit with tracking of GxP relevant documents/tasks
- Act as contact person for vendors and internally in respect to administrative QA issues
- Deputize for QA Specialist
- Write and review clinical QA related documents
- Manage sub-contracting of external audits at vendor/investigator sites
- Organize and prepare internal GCP/PV/GLP audits according to approved schedule
- Divers administrative help for QA team
Main qualifications
- Strong IT skills especially in Word, Excel and document management systems
- GCP/GLP/PV basic knowledge
- Experience with review of GxP-documents
- Service-oriented
Main advantages:
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, 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 professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Tina Maric
Referencenumber:
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