Posted Jan 11
Quanta Consultancy Services
Dublin, Dublin, Ireland
This employer requests that only candidates in
Ireland apply to this job.
You appear to be located in
United States, not Ireland, so you will not be able to apply for this job.
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 (CQV) Engineer will possess the following 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 candidate will have the opportunity to join a global Biopharmaceutical organisation receive a competitive rate of pay, please apply today!
Employment Type: Contract
Other Pay Info: Competitive