CQV Engineer - Cpl Resources
  • Dublin, Leinster, Ireland
  • via BeBee.com
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Job Description

Job Description:

We are seeking a C&Q Engineer to join the team for an 11 month fixed term contract at Pfizer's state-of-the-art facility in Dublin, Grange Castle.



The DS2 Project involves the design, construction, and fit-out of a large-scale Cell Culture facility, including 6x bioreactors, associated scale-up trains, support equipment, and a single purification suite.



Key Responsibilities:

* Develop the C&Q package of documentation and install, commission, and qualify process equipment and utilities.

* Participate in design document reviews and ensure quality aspects are included in design.

* Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.

* Generate CQV documents and track and confirm closure of action items identified through reviews.

* Maintain a strong interface with the Automation and Engineering teams to ensure information flow meets their needs.

* Perform shakedown and commissioning and qualification of systems.



Requirements:

* B.Sc/B.Eng. degree in engineering discipline, with particular emphasis on mechanical or process engineering.

* Minimum of 4 years experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.

* Excellent interpersonal and communication skills.

* Familiarity with Delta-V & Navis Works is an advantage.



Skills:

* FAT

* HAZOP

* Delta V

* Mechanical Engineering

* Bioprocess Engineering

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