Description
A QAV Specialist is required to join a Pharmaceutical organisation based in Ireland. The project is a new refurbishment assignment, which involves removing the current utilities and manufacturing lines and installing new utilities on site. This is a role that will require the successful QAV Specialist to review and approve the commissioning and qualification documents.The Role:
* To review and approve all commissioning and qualification documents.
* To review the documentation from a quality assurance perspective.
* To demonstrate project knowledge of equipment and utilities, along with some CSV knowledge.
Skills / Experience:
* Previous experience of working in a Pharmaceutical environment.
* Previous QA experience in a manufacturing environment.
* Previous experience of working with equipment and utilities validation.
* Knowledge of CSV would be an advantage.
To learn more about this excellent and rare opportunity to join a prestigious Global Pharmaceutical organisation and fulfil a unique and rewarding role, please send in your current CV.