Description
QC Technical Writer (m/f/d)
Reference: -en
Start: asap
Duration: 3 MM++
Main tasks:
- Writing of specifications (raw materials, DS,DP) and SOP's
- Writing of Analytical methods, stability protocols and reports
- Creation and post-processing of production documents / quality-related technical documents
- Plan, support and track process and document changes / create a document overview
- Support the team with transfer- and technical issues
Main qualifications
- Good English knowledge written and oral
- GMP-knowledge
- Profoud experience in a pharmaceutical company and in physico- chemical analysis.
Main advantages:
- A highly motivated team and an open way of communication
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:
Marc Peter Linder
Referencenumber:
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