Description
Two C&Q Engineers are required to join a Global Biotech Manufacturing Organisation based in Ireland. The roles will require the successful C&Q Engineers to work on Utilities activities in a new sterile manufacturing environment. This project is part of a new build site and they are currently in the Commissioning and Qualification stage.The Role:
* To plan, organise and prioritise and review vendor documentation as well as create and execute the test documentation in line with GMP standards.
* To prepare and execute IC, OC, IQ and OQ documentation, including the dealing with the exception/ deviation handling and closeout.
* To work with construction contractors and vendors to be able to compile and review the construction turnover IQ support binders.
* To work on your own initiative to deal with construction turnover related issues and take closure for discreet projects.
Skills / Experience:
* Previous C&Q experience with a GMP environment
* Experience within upstream and/or downstream
* Experience in utilities in either grey or clean utilities is desirable
* Previous experience of using controls systems would be an advantage.
If you would like to hear more about these C&Q Engineer Utilities opportunities, please apply today.