Validation project engineer required to join a global pharmaceutical company located in the South West UK for an initial 6 month duration.
A fast paced and exciting environment which is seeing a lot of internal investment currently this is the chance to get involved with a global client who is going from strength to strength.
With a number of exciting refurbishment projects in the pipeline this is a great chance to be involved in the full project lifecycle with the opportunity to move into other projects and areas of the business.
Validation project lead required to focus on one particular client on site. The validation engineer will be responsible for running an expansion project on site from a validation perspective.
This senior validation engineer will responsible for writing the Validation master plans, impact assessments, reviewing and amending documentation, FATs.
They need someone who is a project leader and able to complete the validation hands on work themselves. They need to be able to write validation documentation and drive the validation to completion in this project.
- 5+ years experience within the life science industry
- Previous experience within fill finish / bulk drug substance environment would be usefu
- Hands on experience writing VMP (validation master plans), Impact assessments and reviews.
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