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CQV Engineer

  1. France
Toulouse
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
15-05-2024
34200
CQV Engineer - Pharmaceuticals - France - 6-Month Contract 

Are you looking for your next contract, and fancy the opportunity to work in the beautiful Toulouse? Our client, a global biotechnology organisation, are recruiting for a CQV Engineer to join their team in the construction of their new biopharmaceutical production plant. This new build facility will be vital vehicle in helping our client continue global access to life changing therapeutics.


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.
  • 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 systems within the fill finish building
  • 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 Ven. or Assessments/FAT/SAT/CTP/IOQ Protocols
  • Lead execution of all CQV deliverables; IOQ, field execution
  • Run Weekly CQV Meeting and ensure updates are provided to Weekly CQV Meeting.
  • Generate and ensure timely approval of all Commissioning and IOQ Final Reports.
 
Requirements:
  • Minimum of 5 years’ experience including experince with expansion projects.
  • Experience working with process equipment including; filtration systems, chromatography equipment and consumables, bioreactors, cell culture systems, mixing systems, bioprocessing containers, sterilisers, centrifuges, incubators, biosafety cabinets,.
  • Experience with complex projects and working in or around operating facilities.
  • Experience within process equipment within the pharmaceutical / biotech industries
  • Ability to keep work pace and meet deadlines. Good organising and planning skills.
  • Demonstrated proficiency communicating and collaborating at a variety of levels with customers, local 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)


If this role is of interest to you, please apply now! 
 
 #LI-CO1


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