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CQV Engineer Clean Utilities
Employer undisclosedRole managed by a recruiter
Commissioning and qualification engineer for clean utilities in a biopharma facility
CQV interface with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all systems.
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.
Generate and ensure timely approval of all Commissioning and IOQ Final Reports.
Liaise with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/SLIA/Test Matrices/Risk Assessments/QA Ven. or Assessments/FAT/SAT/CTP/IOQ Protocols
Lead execution of all LSCC CQV deliverables; IOQ, field execution
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.
Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
What you bring
clean utilities
biopharma design
microsoft project
complex projects
leadership
problem solving
Experience within Clean Utilities such as clean steam, clean water, purified water, WFI (Water for injection).
Requires extensive experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
Ability to keep work pace and meet deadlines. Good organising and planning skills.
Proven success working well in a team environment with flexibility to react to changing business needs.
Experience with complex projects and working in or around operating facilities.
Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project)
Strong leadership and communication skills. Problem solver with a focus on achievement of overall project goals.
Demonstrated proficiency communicating and collaborating at a variety of levels with customers, local vendors, equipment suppliers and operations staff.
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