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
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
Reputable international company
Über Hays: 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.
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