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We wish to recruit an Upstream CQV Lead for a client based in Dublin

PM Group wish to recruit an Upstream CQV Lead for a client based in Dublin. 

Key Responsibilities

  • CQV Upstream Engineer for associated Upstream Building (Bioreactors, both seed and production, Centrifuges, Harvest), initially responsible for review of all design deliverables from designers including drawings, datasheets, specifications and engineering lists
  • Point CQV person for vendor review for all upstream vendor packages
  • Assist CQV SME for all upstream systems
  • Liaise with stakeholders in relation to construction readiness and a schedule for all upstream systems, perform and lead all field walkdowns for all upstream systems
  • Support CQV review, aligning with Transition Group in relation to review and approval of all turnover packages, both vendor and contractor packages within the building for upstream.
  • Liaise with CQV SWAT Team in relation to punchlist closure both pre-M/C and during the CQV execution phase for upstream systems within building
  • 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 for upstream equipment
  • Ensure commissioning readiness of all upstream systems to support equipment start-up and IOQ testing
  • Support CQV review on all isometrics, weld logs, weld qualifications, 3rd party inspections, material of construction and redlining exercise
  • Liaise with all project groups (Design/CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all upstream systems are managed appropriately for the entire project lifecycle
  • Liaise with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/Test Matrices/Risk Assessments/QA Vendor Assessments/FAT/SAT/CTP/IOQ Protocols
  • Support execution of all upstream CQV deliverables; FAT/SAT/CTP/IOQ
  • Support weekly CQV upstream meetings and ensure updates are provided to weekly CQV meeting
  • Generate and ensure timely approval of all commissioning and IOQ final reports for upstream equipment

Qualifications and Experience

  • Minimum 8 years CQV upstream experience on large scale projects
  • Working knowledge of ASTM E2500 / leveraging verification process
  • Experience with liaising with other departments and building PMs/leads  
  • Experience with design and construction projects for biopharmaceutical manufacturing facilities 
  • Experience in CQV Team
  • Experience with complex projects and working in or around operating facilities
  • Demonstrated proficiency communicating and collaborating at a variety of levels with customers, vendors, equipment suppliers and operations staff
  • Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)

Please Note

All CV’s are treated in the strictest confidence.
Recruitment agencies need not apply.

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Do you have what it takes ?

Upstream CQV Lead DU19142 - DU19142

Dublin, Ireland

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