Description
Two C&Q Engineers are required to join a Global Pharmaceutical organisation based in Ireland. The roles will require the successful C&Q Engineers to work on vial syringe filling line in a sterile manufacturing environment. This project is part of a new build site and they are currently in the process of transferring a number of new products in preparation for production.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:
* A Degree in Chemical /Mechanical or related industry would be desirable.
* Previous C&Q experience in a GMP environment
* Experience in utilities in either black or clean utilities is desirable but not essential
* Background in Thermal mapping would be desirable but not essential
* Previous experience of using MCS, SCADA systems or Delta V would be an advantage.
To learn more about this excellent and rare opportunity to join a prestigious Pharmaceutical organisation and fulfil a unique and rewarding role, please send in your current CV.