Description
A Commissioning, Qualification and Verification Engineer is required to join a global Pharmaceutical organisation based in Ireland. This is a role that will require the successful CQV Engineer to work on a new build syringe line. They will require the support of all CQV efforts in multiple disciplines.The Role:
* To monitor and co-ordinate all quality risk assessments ready for final report issued.
* To liaise with documentation team and lead to ensure that all documentation is delivered, approved and signed off.
* To liaise with vendors and suppliers to support GDP requirements and to review all vendor site change controls for final testing phase.
* To assist with quality audits for all vendors and suppliers.
Skills / Experience:
* Previous CQV experience in a Pharmaceutical / Biopharmaceutical environment.
* Previous experience of executing protocols such as FAT/IV/SAT/FV
* Experience of commissioning summary reports for executed documentation
* Strong communication skills to be able to liaise with vendors and suppliers
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.