C&Q Engineer Downstream

Limerick  ‐ Onsite
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Description

Role - Commissioning & Qualification Engineer - Downstream
Type - initially 12 month contract
Location - Co. Limerick

One of our key clients, a global leader within bio-pharmaceuticals, is looking for a number of C&Q Engineers with experience of Downstream.

Key Responsibilities:

  • System P&ID walk down with construction prior to handover. Categorisation of punch list items & tracking to completion. Acceptance of system at mechanical completion (M/C).
  • Generate method statements, risk assessments & permit preparation for responsible areas from M/C to handover to site operations.
  • Pre-start safety checks, lockout & tag out & ensuring timely loop checking post-handover.
  • Co-ordinate and supervise third party vendors during SAT execution. Review and approve SAT protocols.
  • Generation, review and approval of commissioning protocols.
  • Execution of the system commissioning protocols, Installation & Operation Qualification protocols, Process Qualification protocols (where applicable) following GDP guidelines.
  • Ensure non-conformances & deviations are minimised and closed out with Engineering and QA Validation in a timely fashion.
  • Ensuring that punch list items are documented, tracked, expedited and resolved by system handover to site operations.
  • Attend daily communication meetings with area lead and report progress.
  • May supervise mechanical, electrical, and automation contractors.
  • Assists in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents.
  • Maintain a clean and safe working environment by enforcing procedures, policies, and regulations.

Key Requirements:

  • BSc/BEng or higher in chemical/biochemical or mechanical engineering
  • Advanced knowledge of cGMPs and sanitary equipment operating requirements.
  • Working knowledge of process control systems and automation. Allen Bradley PLC experience beneficial.
  • Advanced knowledge of C&Q documentation required for cGMP process equipment.
  • Substantial knowledge of clean room operation & function and of biopharmaceutical equipment.
  • Strong written and oral communication skills.
  • Ability to understand project plans and schedules.
  • Working knowledge of word processing, spreadsheets, database management software, CAD software, and PCs.
  • Direct experience with biopharmaceutical utilities and process equipment
Start date
2015-03-16
Duration
Initially 12 month contract
From
Quanta Consultancy Services
Published at
03.10.2015
Project ID:
994631
Contract type
Freelance
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