Description
A biotech manufacturing facility in the South East of England requires a Validation Engineer to focus on Cleaning Validation activities. 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 the 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
* Cleaning Validation Experience
* 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 today with an covering letter highlighting your key skills and relevant experience aligned to this opportunity.