Beschreibung
Documentation Specialist (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM+
Main tasks:
- Provide compliant, accurate and timely documentation support (GMP pharmaceutical environment (Quality Systems))
- Timely generation and approval of all key documents supporting the program schedule
- Coordinating and managing approval of SOPs documents and acting as SOP Steward
- Maintaining a site system for the tracking of documentation progress (including archiving of paper records)
- Generation of metric reports
- Provide support and collaborate with Source Areas and local/global Counterparts
Main qualifications
- High level technical writing skills
- Advanced PC skills such as Excel, MS Access, Word, PowerPoint, Office 365
- Familiarity with automated approval systems such as Trackwise, Documentum (MIDAS, Veeva Vault) etc.
- English speaking required; German speaking (nice to have)
- Ability to work with minimal work direction
Main advantages:
- Reputable international 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:
Yves Fabien Deschamps
Referencenumber:
Make contact:
Email: