Details
Category: Biotechnology- Location: French- speaking part of Switzerland
- Starting date: Feb 01, 2019
- Domain of experience: Biotechnology
- Level required:
- Years of experience: 1+
Your Role
As a Validation Specialist, you will be working on an independent position directly at our Client’s site. Our Client is an international biotechnology company based in the French- speaking part of Switzerland. You will be working on creating validation protocols for USP/DSP processes and cleaning.
Your Tasks
- Develop and implement GxP-compliant protocols for biotechnology process and cleaning validation
- Ensure compliance with international regulations
- Ensure timely processing of related deviations, investigations and changes
- Competent and timely creation of validation documents for USP/DSP in collaboration with the Quality teams
Your Profile
- Minimum 1 year of relevant experience in biotechnology industry
- Excellent command of French is mandatory
- Experience working in a GxP regulated environment
- Deep understanding of upstream and downstream processes
- Knowledge of cGMP requirements