Description
Quality Project Specialist wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Several years of working experience in a relevant area
- Compliance with GMP, ethical, health safety and environment (HSE) and information security (ISEC) standards
- Awareness of TRD as well as GMP relevant IT tools and processes
- Languages: fluent English both written and spoken
Your tasks:
- Recognizing and clarifying simple and complex deficiencies in GMP documents
- Providing support for quality relevant electronic systems (e.g. GLIMS, TQW, TEDI, ESOP)
- Writing and completing GMP documents (e.g. CoAs, CoCs , BRR sheets, test scripts, SOPs)
- Filing and archiving documents owned by QA (e.g. audit reports, CoAs, CoCs, BRR sheets)
- Coping with CoA needs from different customers, such as CMC, Qualified Persons and distribution of TEDI documents to external customers
Start: ASAP
Duration: 12MM+
Location: Basel, Switzerland
Ref.Nr.: BH11673
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.
Going the extra mile…
New to Switzerland? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more