Description
Our global pharmaceutical client require an experienced Validation Engineer to provide documentation writing support.Project Overview
Global Integration Programme where new sites are being integrated into the client's network. As the role is primarily one of documentation, some home office work is a possibility.
Duties/Deliverables/for the role:
- Write SOPs for equipment facility standards
- Develop overall validation standards
- Prepare other necessary Validation documentation
- Liaise with team on other tasks
- Having worked extensively within Validation in a GMP environment
- Biotechnology Process Equipment Validation documentation
- Some CSV documentation exposure
- Native/fluent English speaker
- French language skills a bonus
- All-inclusive hourly rate in €s.