Description
A global Biopharmaceutical leader is currently looking for an experienced commissioning qualification and validation (CQV) engineer to join their team on a new build project based in Ireland.The responsibilities of the commissioning, qualification and validation (CQV) engineer will include:
Commissioning Bio-process systems inclusive of reviewing and approving relevant automation systems.
Carry out and review test documentation
Ensure scheduling, tracking and reporting of activities are performed appropriately to achieve deadlines.
Understanding and leading compliance documentation such as risk assessment, root cause analysis and investigation
The successful commissioning, qualification and validation (CQV) engineer will possess the below experience
Experience in commissioning, qualification and validation in drug substance manufacturing facilities.
Experience with Delta V Automation platforms
Degree in Engineering/life sciences or equivalent (HND/HNC)
Proven track record in validation/verification documentation
Able to prioritise and manage tasks
The successful commissioning, qualification and validation (CQV) engineer will have the opportunity to join a global Biopharmaceutical organisation receive a competitive rate of pay.