Description
A biotech manufacturing facility in the South East of England requires a Validation Engineer to focus on cleaning validation. The work will be to review, write and execute documentation.Key Responsibilities:
* Protocol writing (including IQ, OQ, PQ and also have hands on experience of executing cleaning validation), documentation reviews
* Good planning, organisational and time management skills along with an ability to make decisions, solve problems, negotiate, influence and communicate with others is required.
You must have the following:
* Knowledge and experience working in a GMP environment
* Biotech manufacturing experience
* Knowledge and experience within cleaning validation
* Be able to demonstrated excellent oral and written communication skills, and must be able to work in both a team environment as well as independently.
This is an exciting position for an individual who is ready to step up and deliver exciting projects on time and on schedule within a highly regulated industry. Please apply now for more information.
To apply please contact Andreea Chitiu on or