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CQV Lead

  1. West Coast
Seattle
  1. Contract
Competitive
  1. CAPEX Projects
33419

This vacancy has now expired

CQV Lead - Pharmaceuticals - Seattle - 12-Month Contract 

Our client, a global biotechnology organisation, is recruiting for a CQV Lead to join their capital project in the Seattle. This new build facility will house a therapeutic protein production plant, and we are looking for a CQV Lead to help expand our client's biotech operations throughout the US. As the CQV Lead you will be responsible for implementing all safety requirements for a new build facility.


Responsibilities:
  • CQV Lead will be initially responsible for review of all Design deliverables including Drawings, Datasheets, specifications and Engineering Lists.
  • Point CQV person for Vendor review for all assigned Packages.
  • Lead CQV review, aligning with Transition Group in relation to review and approval of all Turnover Packages, both Vendor and Contractor Packages.
  • Liaise with CQV PM and Lead Scheduler in relation to schedule creation and management for all assigned Systems, ensuring all correct predecessors and successors are in place.
  • Lead CQV Interface with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all assigned systems.
  • Liaise with all Project Groups (Design/CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all assigned 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/SLIA/Test Matrices/Risk Assessments/QA Vendor Assessments/FAT/SAT/CTP/IOQ Protocols.
  • Lead execution of all CQV deliverables; FAT/SAT/CTP/IOQ
  • Generate and ensure timely approval of all Commissioning and IOQ Final Reports.

Requirements:
  • Experience as a CQV Lead on projects worth over $100million
  • 5 years CQV Lead experience
  • 8 years experience within a LifeSciences environment.

If this role is of interest to you, please apply now! 

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