Description
I'm looking for a Validation Engineer for a 6 month contract based in Scotland 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.
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.
If you are interested in this role then please do not hesitate to submit your CV and if your right for the role I will give you a call to discuss the role further.