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CQV Lead

  1. Denmark
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
09-05-2023
31049
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CQV Lead – Pharmaceuticals – 12 Month Contract - Denmark

Reporting into the CQV Program Manager, this individual will be responsible for the delivery of the CQV activities on a complex QC Lab and Warehouse expansion project.

The Warehouse and QC lab will be delivered to support a large-scale Biopharmaceutical expansion program currently being executed on site.

CQV Lead Responsibilities:
  • Lead the Commissioning, Qualification and Validation of QC Lab and Warehouse systems
  • Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
  • Conduct FAT/SAT activities aligned to the current equipment vendor during installation and readiness.
  • Liaise with all Project Groups to ensure all Systems are managed appropriately for the Project Lifecycle.
  • Liaise with CQV Document Generation Lead in relation to generation and approval of assessments, reviews and protocols
  • Support execution of all LSCC CQV deliverables; IOQ, field execution
  • Generate and ensure timely approval of all Commissioning and IOQ Final Reports.
 About you:
  • 10 years’ experience including experience with design and construction projects for QC Lab / Warehouse facilities. 
  • Experience with complex projects.
  • Experience within generation of VPPs, risk assessments, and qualification protocols.
  • Previous experience of delivering FAT/SAT activities.
  • Strong leadership and communication skills
  • Computer skills (Spreadsheets, Word Processing, Visio, Microsoft Project
Are you a good fit for this CQV Lead? Apply now!

The candidate must have the rights to work in the location stated in the job advert.

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