Beschreibung
QA Quality Specialist (m/f/d)
Reference: -en
Start: asap
Duration: 4 MM+
Main tasks:
- Perform review of GMP relevant documents (e.g. manufacturing master documents, executed batch records for material manufactured internally or at contractors, raw data)
- Clarify simple deficiencies in GMP documents with the line unit experts in own responsibility
- Upload GMP documents into relevant quality electronic systems (e.g. DocStore Condor, iRelease)
- Write and complete GMP relevant documents in own area of responsibility (e.g CoAs, archiving checklists)
- File and archive documents owned by QA Operations
- Collaborate with other associates to support the function of QA Ops
- Participate in knowledge exchange in TRD
Main qualifications
- Bachelor degree or apprenticeship in chemistry (or any other equivalent scientific education)
- Relevant GMP experience in a pharmaceutical environment, ideally in the field of quality
- Languages: fluent in English and German
- Soft skills: team-oriented, reliable, motivated, attention to detail
Main advantages:
- Workload: 100%
- Onsite positon / No homeoffice
About us:
With over 15 years of experience in the pharmaceutical and chemical industry as well as in 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 experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
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