One of our clients is looking for a Q&V Consultant for a 6-month project. The position is based in the German-speaking region of Switzerland.
Requirements:
- Independent creation and updating of qualification and validation documentation including statistical analysis and evaluation (risk analyses/FMEA, plans, reports)
- Support in risk analysis (P-FMEA) of manufacturing processes
- Experience in the pharmaceutical environment and in dealing with GMP requirements (EU-GMP Annex 11, data integrity, GAMP 5, etc.) and good documentation practices are a Plus
- Good command of English and German is required
For further information about this position please apply.
Please note, only those with the right to work in Switzerland can apply!
