Headcount Solutions is recruiting a C&Q Engineer for our clients
biotech facility in Leinster.
Reporting to the E&I Suite Team Lead, this person will be specifically
responsible for Commissioning & Qualification (C&Q) of E&I activities
and assisting the lead in the construction/FAT quality, aspects of the
Suite scope
He/she will be required to work closely with a cross-functional team
and coordinate activities between Design, Construction, Process,
Technical Operations, C&Q, IPT and Maintenance.
Main Responsibilities:
* Support a suite team during a commissioning and qualification
program, incorporating Electrical and Instrumentation 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 SCD&#**Apply on the website**;s and other test
documentation
* Confirm SAT&#**Apply on the website**;s are suitably completed and
category 1 /2/3 items are capable of being closed by the design team.
* Walk and confirm the Installation /Equipment is as per the supplied
design drawings and documents.
* Confirm that all electrical /I+C connection drawings are highlighted
and walked down without issues.
* Confirm the System construction has been documented and As
built/Redlined docs have been or are in the process of being updated
in CAD.
* Provide coordination expertise during C&Q activities as needed.
* Assist in the coordinating of C&Q start-up activities , punch list
follow-up.
* Facilitate/expedite Mechanical Completion in conjunction with the
Construction team. (Liaise with construction contractors towards
successful completion of Construction Turn Over Documentation).
* Coordinate third party vendors during SAT execution. Review and
contribute to SAT protocols.
* Support of the Suite Leads in clear, and documented, definition of
scope and scope boundaries
* Delivery of stakeholder agreed scope for Suite facilities to
Commissioning Qualification or as appropriate Process Qualifications.
Requirements:
* Minimum of **Apply on the website** years&#**Apply on the website**;
experience similar role in Pharmaceutical Facility/ Building/Utilities
systems within Pharmaceutical industry.
* Working knowledge of standards as they apply in biotechnology
processes industries and a working knowledge of FDA and EU regulations
is preferred.
* Experience of design and construction/handover of pharmaceutical
process and building facilities for pharmaceutical facilities.
* Working knowledge of C&Q documentation required for cGMP project
delivery.
* Ability to generate and communicate project plans and schedules.
For further information please contact Mick on (phone number removed)
or forward details in confidence to C&Q Engineer
Headcount Solutions is recruiting a C&Q Engineer for our clients
biotech facility in Leinster.
Reporting to the E&I Suite Team Lead, this person will be specifically
responsible for Commissioning & Qualification (C&Q) of E&I activities
and assisting the lead in the construction/FAT quality, aspects of the
Suite scope
He/she will be required to work closely with a cross-functional team
and coordinate activities between Design, Construction, Process,
Technical Operations, C&Q, IPT and Maintenance.
Main Responsibilities:
* Support a suite team during a commissioning and qualification
program, incorporating Electrical and Instrumentation 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 SCD&#**Apply on the website**;s and other test
documentation
* Confirm SAT&#**Apply on the website**;s are suitably completed and
category 1 /2/3 items are capable of being closed by the design team.
* Walk and confirm the Installation /Equipment is as per the supplied
design drawings and documents.
* Confirm that all electrical /I+C connection drawings are highlighted
and walked down without issues.
* Confirm the System construction has been documented and As
built/Redlined docs have been or are in the process of being updated
in CAD.
* Provide coordination expertise during C&Q activities as needed.
* Assist in the coordinating of C&Q start-up activities , punch list
follow-up.
* Facilitate/expedite Mechanical Completion in conjunction with the
Construction team. (Liaise with construction contractors towards
successful completion of Construction Turn Over Documentation).
* Coordinate third party vendors during SAT execution. Review and
contribute to SAT protocols.
* Support of the Suite Leads in clear, and documented, definition of
scope and scope boundaries
* Delivery of stakeholder agreed scope for Suite facilities to
Commissioning Qualification or as appropriate Process Qualifications.
Requirements:
* Minimum of **Apply on the website** years&#**Apply on the website**;
experience similar role in Pharmaceutical Facility/ Building/Utilities
systems within Pharmaceutical industry.
* Working knowledge of standards as they apply in biotechnology
processes industries and a working knowledge of FDA and EU regulations
is preferred.
* Experience of design and construction/handover of pharmaceutical
process and building facilities for pharmaceutical facilities.
* Working knowledge of C&Q documentation required for cGMP project
delivery.
* Ability to generate and communicate project plans and schedules.
For further information please contact Mick on (phone number removed)
or forward details in confidence to
We need : English (Good)
Type: Permanent
Payment:
Category: Others
