Job Details: C&Q Project Manager


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
C&Q Project Manager
Pharmaceutical

This position will report to the GES C&Q Leam EMEA as part of a
multi-disciplinary team responsible for commissioning & qualification
activities on a multi-product facility

Responsibilities:

* Project manage the day-to-day C&Q activities of the C&Q team

* Liaise with Project Controls function

* Support all suite teams during a C&Q program

* Assist the C&Q technical lead in the planning and tracking of
activities

* Actively support Last Planner System activities

* Review and input into deliverables such as technical requirement
specifications and vendor turnover documentation

* Participate in C&Q deliverables (system impact assessment, critical
component impact assessments, system boundary drawings, requirement
traceability matrix)

* Manage generation & execution of C&Q documentation (FAT, SAT, IOC,
IQ etc.)

* Monitor and report on approval of C&Q documentation

* Monitor and report review of CCRs and TOPs

* Participate in C&Q change controls, drive closure in a timely manner

* Support system P&ID walkdown with construction prior to handover

* Support review on all isometrics, weld logs, weld qualifications,
3rd party inspections, material of construction and redlining exercise

* Facilitate/expedite mechanical completion in conjunction with
construction team

* Pre-start up safety checks, LOTO & ensure loop checking and
calibrations

* Assist in investigation of process equipment, utility systems,
control system anomalies & safety incidents

Qualifications, Experience & Skills:

* Bachelor of Engineering / Science degree in Technical discipline

* Minimum 5 years&#**Apply on the website**; experience in
commissioning +/or validation of USP/DSP/Facilities/Utilities systems

* Previous experience in the pharmaceutical industry is essential

* Technical knowledge of black & clean utilities systems & equipment
and biotechnology processes

* Experience as a C&Q Lead / Project Manager on a major capital
project

* Working knowledge of process control systems and automation. DeltaV,
syringe & vial line experience beneficial

* Knowledge of C&Q documentation required for cGMP process equipment Pharmaceutical

This position will report to the GES C&Q Leam EMEA as part of a
multi-disciplinary team responsible for commissioning & qualification
activities on a multi-product facility

Responsibilities:

* Project manage the day-to-day C&Q activities of the C&Q team

* Liaise with Project Controls function

* Support all suite teams during a C&Q program

* Assist the C&Q technical lead in the planning and tracking of
activities

* Actively support Last Planner System activities

* Review and input into deliverables such as technical requirement
specifications and vendor turnover documentation

* Participate in C&Q deliverables (system impact assessment, critical
component impact assessments, system boundary drawings, requirement
traceability matrix)

* Manage generation & execution of C&Q documentation (FAT, SAT, IOC,
IQ etc.)

* Monitor and report on approval of C&Q documentation

* Monitor and report review of CCRs and TOPs

* Participate in C&Q change controls, drive closure in a timely manner

* Support system P&ID walkdown with construction prior to handover

* Support review on all isometrics, weld logs, weld qualifications,
3rd party inspections, material of construction and redlining exercise

* Facilitate/expedite mechanical completion in conjunction with
construction team

* Pre-start up safety checks, LOTO & ensure loop checking and
calibrations

* Assist in investigation of process equipment, utility systems,
control system anomalies & safety incidents

Qualifications, Experience & Skills:

* Bachelor of Engineering / Science degree in Technical discipline

* Minimum 5 years&#**Apply on the website**; experience in
commissioning +/or validation of USP/DSP/Facilities/Utilities systems

* Previous experience in the pharmaceutical industry is essential

* Technical knowledge of black & clean utilities systems & equipment
and biotechnology processes

* Experience as a C&Q Lead / Project Manager on a major capital
project

* Working knowledge of process control systems and automation. DeltaV,
syringe & vial line experience beneficial

* Knowledge of C&Q documentation required for cGMP process equipment

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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