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.