Description
A C&Q Engineer is required to join a Global Biotech Manufacturing Organisation based in Ireland. The role will require the successful C&Q Engineer to work on Calibration 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:
* Reports to Calibration Lead
* Assist with Delivery of Calibration Program
* Tracking calibration activities against schedule
* Reviewing completed calibration packages
* Entering calibration execution/approval dates and creating calibration reports
* Managing approval of calibration packages
Skills / Experience:
* Previous C&Q experience with a GMP environment
* Experience within Calibration
* Experience of tracking Calibration activities
* Previous experience of using controls systems would be an advantage.
Please apply today to find out more about this fantastic opportunity.