Description
Our client, the world's oldest independent biotechnology company, which researches, develops and manufactures biological products for the treatment of serious diseases with a focus on neurological disorders, currently requires a C&Q Engineer to work on their new build project in Denmark.The Role:
* To plan, organise, 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 downstream processes and Equipment. Filtration (Skids) and Harvest Trains.
* Previous experience of using controls systems would be an advantage. (Delta-V)
Please apply now for more information!