Beschreibung
TRD QA Quality Specialist vacancy for a globally operating Basel based company in the pharmaceutical sector.Your tasks:
- Performing review of GMP relevant documents e.g. manufacturing master documents, executed batch records for material manufactured internally or at contractors, raw data
- Clarifying simple deficiencies in GMP documents with the line unit experts in own responsibility
- Uploading GMP documents into relevant quality electronic systems like DocStore Condor and iRelease
- Creating and completing GMP relevant documents in own area of responsibility while also filing and archiving documents owned by QA Operations
- Cooperating with other associates to support the function of QA Ops as well as contributing to knowledge exchange in TRD
Your experience/knowledge:
- Work experience with GMP in a pharmaceutical environment, ideally in the field of quality
- Bachelor degree or apprenticeship in chemistry or any other equivalent scientific education
- English and German, fluent in written and spoken
Your soft skills:
- Team-oriented and reliable personality
- Attention to detail and a motivated way of working
Location: Basel, Switzerland
Sector: Pharmaceuticals
Start:
Duration: 10MM+
Ref.Nr.: BH17983
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Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland.
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