A global pharmaceutical company based in a french speaking region of Switzerland is currently searching for two CSV Consultants.
The contract duration will be 3 months with a high possibility of extension.
The company is experiencing high workload due to the success of their product, so they are needing additional support urgently. Please see the responsibilities and details below:
- Support project documents (URS, FS process, P&IDs, tracability Matrix)
- Evaluation of deviations, CAPA, Change control
- Support the validation strategy
- Take part in Validating IT and CQV activities
- Fluent in French and English
Please apply directly