As part of the E&I Suite Team, the C&Q specialist is specifically
responsible for C&Q of E&I activities and assisting the Lead in the
Construction / FAT quality aspects of the Suite scope.
Responsibilities:
* Report to E&K Suite Team Lead and to the Project C&Q Lead on
technical matters
* Support suite team during C&Q program, incorporating E&I scope into
the overall project scope
* Develop, document, agree and implement an execution strategy to
deliver the C&Q scope in a controlled and well communicated manner
* Compile and execute SCDs and other test documentation
* Confirm SATs are suitably completed and category 1/2/3 items are
capable of being closed by the design team
* Review VTOPs form completeness
* Walk and confirm the installation/equipment is as per the supplied
design drawings and documents
* Confirm that all electrical / I&C connections drawings are
highlighted and walked down without issues
* Confirm the equipment has been built correctly, fully tested,
components installed as per design.
* Confirm the System construction has been documented and As
built/Redlined docs have been or are in the process of being updated
in CAD.
* Sign off documents at W2 & W3
* Input and confirm that all punch list category items are closed
* Provide coordination expertise during C&Q activities
* Facilitate mechanical completion in conjunction with the
construction team
* Coordinate 3rd party vendors during SAT execution. Review and
contribute to SAT protocols
Qualifications, Experience & Skills required:
* Bachelor**Apply on the website**;s degree in an Engineering,
Science or Technical field
* 5 years**Apply on the website**; experience in a similar role in
Pharmaceutical Facility / Building / Utilities systems
* Working knowledge of standards as they apply in biotechnology
processes industries
* Experience of design and construction/handover of pharmaceutical
process and building facilities
* Ability to work in design and construction of large project
environments within Ireland
* Working knowledge of control systems and automation
* Working knowledge of C&Q documentation required for cGMP project
delivery Pharmaceutical
As part of the E&I Suite Team, the C&Q specialist is specifically
responsible for C&Q of E&I activities and assisting the Lead in the
Construction / FAT quality aspects of the Suite scope.
Responsibilities:
* Report to E&K Suite Team Lead and to the Project C&Q Lead on
technical matters
* Support suite team during C&Q program, incorporating E&I scope into
the overall project scope
* Develop, document, agree and implement an execution strategy to
deliver the C&Q scope in a controlled and well communicated manner
* Compile and execute SCDs and other test documentation
* Confirm SATs are suitably completed and category 1/2/3 items are
capable of being closed by the design team
* Review VTOPs form completeness
* Walk and confirm the installation/equipment is as per the supplied
design drawings and documents
* Confirm that all electrical / I&C connections drawings are
highlighted and walked down without issues
* Confirm the equipment has been built correctly, fully tested,
components installed as per design.
* Confirm the System construction has been documented and As
built/Redlined docs have been or are in the process of being updated
in CAD.
* Sign off documents at W2 & W3
* Input and confirm that all punch list category items are closed
* Provide coordination expertise during C&Q activities
* Facilitate mechanical completion in conjunction with the
construction team
* Coordinate 3rd party vendors during SAT execution. Review and
contribute to SAT protocols
Qualifications, Experience & Skills required:
* Bachelor**Apply on the website**;s degree in an Engineering,
Science or Technical field
* 5 years**Apply on the website**; experience in a similar role in
Pharmaceutical Facility / Building / Utilities systems
* Working knowledge of standards as they apply in biotechnology
processes industries
* Experience of design and construction/handover of pharmaceutical
process and building facilities
* Ability to work in design and construction of large project
environments within Ireland
* Working knowledge of control systems and automation
* Working knowledge of C&Q documentation required for cGMP project
delivery
We need : English (Good)
Type: Permanent
Payment:
Category: Others