CQV Engineer

Northern Ireland
30 Nov 2017
08 Dec 2017
Contract Type
Full Time
Role and responsibilities:
  • Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all Systems, ensuring all correct predecessors and successors are in place.
  • Liaise with CQV start-up team in relation to punch list closure both pre-mechanical completion and during the CQV execution phase.
  • Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
  • Lead CQV interface with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all LSCC systems.
  • Liaise with all Project Groups (Design/CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all Systems are managed appropriately for the Project Lifecycle.
  • Liaise with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/SLIA/Test Matrices/Risk Assessments/QA Vendor Assessments/FAT/SAT/CTP/IOQ Protocols.
  • Execution of all LSCC CQV deliverables; IOQ, field execution.
  • Ensure timely approval of all Commissioning and IOQ Final Reports.
  • Minimum of 5 years’ experience including experience with design and construction projects for biopharmaceutical / pharmaceutical manufacturing facilities.
  • Experience with complex projects and working in or around operating facilities.
  • Ability to keep work pace and meet deadlines. Good organizing and planning skills.
  • Demonstrated proficiency communicating and collaborating on a variety of levels with customers, vendors, equipment suppliers and operations staff.
  • Proven success working well in a team environment with flexibility to react to changing business needs.
  • Strong leadership and communication skills. Problem solver with a focus on achievement of overall project goals.
  • Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project).

This job was originally posted as www.totaljobs.com/job/77586311