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