Beschreibung
QC Manager in Analytics (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Writing of SOP’s and analysis instructions
- 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
Main qualifications
- 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)
Main advantages:
- 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
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:
Mihai-Lucian Burcea
Referencenumber:
Make contact:
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