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C&Q Manager

  1. France
  1. Contract
Competitive
24505/EF
  1. Commisions, Qualification and Validation
Date Posted06 Mar 2020
I am currently recruiting for a C&Q Manager to work for our client based in the Paris area on their Cell and Gene Therapy project on an initial 12-month contract basis.
  • Responsible for leading and managing their own and any external partners to achieve the project objectives, budget, time schedule and functionality according to URS, GxP and HSE requirements
  • Supports the Project Manager to achieve project objectives regarding functionality, GxP and HSE compliance within approved scope, budget and time schedule
  • Supports the Project Manager to set-up the Commissioning & Qualification Engineering team with appropriate resources to meet project objectives
  • Directly reports major challenges to Project Manager
  • Oversees, plans, conducts and coordinates the Commissioning & Qualification works for all of the project scope, monitors the ongoing progress, including the coordination of the project with internal stakeholders, regulatory authorities and agencies
  • Establishes the Commissioning & Qualification project team organizational structure and modifies accordingly together with the Project Manager during the phases of project execution
  • Leads, coordinates and reviews the work of less experienced engineers and / or technical support personnel assigned to the project
  • Establishes and Implement the project Commissioning and Qualification strategy for all elements of the project including Building, Utilities and Process Equipment
  • Ensures the installation meets the user requirements, codes, standards, site procedures, maintenance requirements, regulatory and legal requirements and that the standard of workmanship is of the required quality
  • Ensures the implementation of all relevant requirements around issues such as safety, permits, environmental regulations and good manufacturing practices on responsible scope
  • Ensures readiness for inspections together with user quality organization
  • Responsible for formal hand over including documentation to the user organization
Skills Required:
  • Previous experience working as a C&Q Manager
  • Experience working on projects in Cell and Gene is preferred but the minimum is experience of Biological manufacturing operations
Desirable Skills:
  • French language skills would be beneficial but not essential
If this role is of interest, please apply now. 

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

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