Description
I'm currently recruiting on behalf of a leading Pharmaceutical company for a Validation Engineer based Scotland.This is an excellent opportunity to work with one of the countries leading Pharmaceutical providers in a strong Technical role.
Our client requires a contract Validation Engineer that can demonstrate experience of the following:
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
* 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. Multimillion 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.
This is a really pivotal role in a company that are looking to continue there impressive methods and processes that's allowed them to begin a leader in the Pharmaceutical industry.
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.