C&Q Engineer

Dublin  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Description

A Consultancy working within the life science industry are seeking a commissioning and qualification engineer to be part of a multi-discipline team responsible for Commissioning & Qualification (C&Q) activities on site for with their existing Pharmaceutical clients.

Role Functions
  • Report to the Operations Director and/or the C&Q Manager/ Project Manager on the given project.
  • Coordinate & lead cross functional project teams for the Installation, Commissioning & Qualification based on planned timelines and scope.
  • Attend system walk downs in advance of achieving Construction/FAT handover of the utility generation / equipment.
  • Facilitate the completion of outstanding construction punch items through required safety procedures and permits.
  • Review all the appropriate installation and vendor documentation for completeness & ensure it reflect the System's as installed conditions.
  • Confirm the site installation is as per approved design specification and meet system I IQ requirements.
  • Facilitate/expedite Mechanical Completion in conjunction with the Construction team. (Liaise with construction contractors towards successful completion of Construction Turn Over Documentation).
  • Generate, execute and report all system test documentation (FAT/ SAT/Commissioning Test Protocols/IQ/OQ/PQ) for the project based on available approved client templates & design documentation.
  • Ensure all the safety documents, i.e. Method Statements, SPA, etc. are prepared and approved prior to the commencement of execution activities.
  • Coordinate local contractor company resources for all commissioning & qualification execution activities. Approve their relevant Method Statements, SPA & Permits-to-Work.
  • Ensure project change(s) are properly managed and effectively documented.


Role Function
  • Act as the technical liaison with System vendors for support and/or, on site attendance, as required, throughout the Commissioning & Qualification process.
  • Manage the site attendance for the vendors, contractors and specialist contractors.
  • Confirm all vendor documentation executions are compliant with GxP practices & the executed documentation is acceptable to support validation.


Role Responsibilities
  • Ensure that system delivery progresses in accordance with the approved project schedule.
  • Notify project management, in a timely manner, of all relevant issues which may impact on system progress.
  • Ability to work in construction project environment within Ireland and EU.
  • Coordinate with design and/or project teams to resolve any identified technical issues.
  • Organise/attend all coordination meetings necessary to progress the job. Possess good communication skills.
  • Ensure that all works carried out on your scope or responsibility by construction, commissioning and contract team members are performed in accordance with site safe working practices.
  • Ensure the cohesive operation of your cross-functional team and coordinate work for effective and efficient completion.


Requirements
  • Bachelor of Engineering or Science Degree in Engineering or Technology related discipline.
  • Minimum of 3-4 years' experience in commissioning and/or validation of clean and dirty utilities within Pharmaceutical industry.
  • Good knowledge of the Life Cycle Management Process on the qualification of regulated systems in the Life Sciences Industry.


For immediate consideration please apply below with an up to date CV.

Not sure yet? No CV ready? Give me a call on for more information on the company and role.
Start date
04/2016
From
Real Staffing
Published at
12.02.2016
Project ID:
1068237
Contract type
Permanent
To apply to this project you must log in.
Register