CQV Engineer

IE  ‐ Onsite
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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 following:
  • 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 and receive a competitive rate of pay.
Start date
ASAP
From
Quanta Consultancy Services
Published at
14.01.2017
Project ID:
1268983
Contract type
Freelance
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