Sterile Drug Product Facility Project CQV Engineer

2 weeks ago


Dublin, Dublin City, Ireland beBeeCqv Full time €55,000 - €75,000
Job Summary

We are seeking a highly skilled CQV Engineer to join our Sterile Drug Product Facility project team in Dublin, Ireland.

This is an exciting opportunity for a professional to develop current skills and learn new technology within a fast-paced project environment.

To succeed in this role, the ideal candidate will have:

  • A minimum of a BS qualification in a scientific, technical, or engineering discipline
  • Previous CQV experience is an advantage; previous GMP experience is essential
  • Biopharmaceutical Process/Validation knowledge
  • Exposure to cGMP in a fast-paced environment

In this role, you will play a vital part in supporting the commissioning and qualification of equipment and systems. You will be responsible for developing and executing protocols, maintaining validation documentation, and ensuring it is up-to-date and audit-ready.

The successful candidate will be able to demonstrate their expertise in equipment and system start-up activities, including functional testing and troubleshooting. They will also be able to develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.

This role offers an excellent opportunity to grow professionally and contribute to the success of our project team.


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