Job Details: Commissioning & Qualification Engineer/C&Q


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
Commissioning & Qualification Engineer/C&Q
Position: Commissioning & Qualification Engineer (C&Q / E&I)

We are one of the largest, best known Pharmaceutical companies in the
industry and our products are known globally.

We are looking to recruit a Project Engineer with prior experience of
Commissioning & Qualifying electrical and instrumentation equipment to
join us on an initial **Apply on the website** month contract.

You will be responsible for the Commissioning & Qualification
(C&Q) of E&I activities and assisting the lead in the
construction/FAT quality, aspects of the Suite scope and will
coordinate activities between Design, Construction, Process, Technical
Operations, C&Q, IPT and Maintenance.

You will hold responsibility for coordinating the preparation of the
annual budget cycle, quarterly forecast and capital budget submissions
to achieve corporate deadlines and ensure divisional targets are met
and for planning, Monitoring and Controlling site spending - driving
the competitive agenda on site.

You must have prior knowledge and experience of Pharmaceutical
Facility/ Building/Utilities systems, in order to be considered for
this position.

Further Responsibilities Include:

* Support a suite team during a commissioning and qualification
program, incorporating Electrical and Instrumentation scope into the
overall project scope.

* Liaise with the various stakeholders on the C&Q team and the
overall project to ensure clear communication between all parties.

* 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.

* 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 connection dwgs 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.

* To ensure all specifications are adhered to at W2.

* To signoff documents at W2 & W3.

* To input and confirm before MC that all punch list category items
are closed.

* Provide coordination expertise during C&Q activities as needed.

* Assist in the coordinating of C&Q start-up activities , punch
list follow-up.

* Liaise with the various stakeholders on the overall project to
ensure clear communication between all parties.

* 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.

* Maintain a clean and safe working environment by enforcing
procedures, policies, and regulations.

Requirements

* Minimum of 4 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 control systems and automation.

* Working knowledge of C&Q documentation required for cGMP project
delivery.

* Working knowledge of word processing, spreadsheets, database
management software, CAD software, and PCs.

Please press apply now to submit your application. Alternatively, if
you would like further information on this position or other positions
win a similar sector, please feel free to contact our Shaunna Doherty
on (phone number removed) for a confidential conversation.

We are an equal opportunities Business. We welcome applications from
all suitably qualified candidates regardless of their race, sex,
disability, religion/belief, sexual orientation or age.

Each company within the Planet Equity Group is a "data controller".
This means that we are responsible for deciding how we hold and use
personal information about you in line with GDPR guidelines. Full
details regarding how we hold your data is available within our
Privacy Notice accessible Position: Commissioning & Qualification Engineer (C&Q / E&I)

We are one of the largest, best known Pharmaceutical companies in the
industry and our products are known globally.

We are looking to recruit a Project Engineer with prior experience of
Commissioning & Qualifying electrical and instrumentation equipment to
join us on an initial **Apply on the website** month contract.

You will be responsible for the Commissioning & Qualification
(C&Q) of E&I activities and assisting the lead in the
construction/FAT quality, aspects of the Suite scope and will
coordinate activities between Design, Construction, Process, Technical
Operations, C&Q, IPT and Maintenance.

You will hold responsibility for coordinating the preparation of the
annual budget cycle, quarterly forecast and capital budget submissions
to achieve corporate deadlines and ensure divisional targets are met
and for planning, Monitoring and Controlling site spending - driving
the competitive agenda on site.

You must have prior knowledge and experience of Pharmaceutical
Facility/ Building/Utilities systems, in order to be considered for
this position.

Further Responsibilities Include:

* Support a suite team during a commissioning and qualification
program, incorporating Electrical and Instrumentation scope into the
overall project scope.

* Liaise with the various stakeholders on the C&Q team and the
overall project to ensure clear communication between all parties.

* 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.

* 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 connection dwgs 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.

* To ensure all specifications are adhered to at W2.

* To signoff documents at W2 & W3.

* To input and confirm before MC that all punch list category items
are closed.

* Provide coordination expertise during C&Q activities as needed.

* Assist in the coordinating of C&Q start-up activities , punch
list follow-up.

* Liaise with the various stakeholders on the overall project to
ensure clear communication between all parties.

* 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.

* Maintain a clean and safe working environment by enforcing
procedures, policies, and regulations.

Requirements

* Minimum of 4 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 control systems and automation.

* Working knowledge of C&Q documentation required for cGMP project
delivery.

* Working knowledge of word processing, spreadsheets, database
management software, CAD software, and PCs.

Please press apply now to submit your application. Alternatively, if
you would like further information on this position or other positions
win a similar sector, please feel free to contact our Shaunna Doherty
on (phone number removed) for a confidential conversation.

We are an equal opportunities Business. We welcome applications from
all suitably qualified candidates regardless of their race, sex,
disability, religion/belief, sexual orientation or age.

Each company within the Planet Equity Group is a "data controller".
This means that we are responsible for deciding how we hold and use
personal information about you in line with GDPR guidelines. Full
details regarding how we hold your data is available within our
Privacy Notice accessible

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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