Description
I'm looking for a Validation Engineer to work on a 6 month contract based in the Midlands for the following role:Key Responsibilities:
* Responsible for Validation (Equipment and Facility) activities within the projects group. Ensure projects relating to facilities and equipment Validation are validated in line with regulatory and company requirements.
* To produce the necessary Validation documents (IQ, OQ, RTM, etc.) in conjunction with the equipment suppliers and CSV
You must have experience with the following:
* Writing and execution of Validation documents IQ, OQ, RTM, etc.
The right person will:
* Be a graduate (or equivalent) qualification in a scientific discipline.
* Possess good knowledge of Pharmaceutical Validation working to GAMP/GMP guidelines.
* Have a proven track record in planning and executing validation activities for complex engineering. projects (i.e. Multi-million pound capital projects.)
* Have excellent facility and equipment validation knowledge.
* Expert knowledge in Pharmaceutical Validation, from Laboratory & plant equipment through to Networked IT enterprise software and PCS and PLC systems.
* Have a proven ability to communicate at most levels of management.
* Have a proven track record of problem solving.
* Possess knowledge and application of the principle of the QMS.
Moreover, I have a couple of Computer System Validation positions that are on the horizon; if you would like to discuss these or the above in more detail, please send me through your updated CV and I will give you a call.