Technical support and reports writing of the QC routine laboratory for trouble shooting (e.g. HPLC)
Will be responsible for writing transfer and validation plans for Small and Large Molecules analytical methods
Support of the Track and Trend project in the release and stability analysis
Management of Standard Deviations
Processing inquiries about products
Profound experience in Quality Control
Experience in HPLC and chemo-physical analysis techniques
Extensive experience of analytical validation and protocols writing
Working knowledge of TrackWise system
Knowledge of the ICH or FDA guidelines for Small Molecules Drug Products and analytical validations, as well as knowledge of the compendial pharmacopoeia methods for Small Molecules Drug Products
Very good German and English (German = office language ; English = documentation to be written in English)
We will create a candidate profile containing your strengths and potential and thus increase your chance of being placed in a position
A very renowned 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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