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Commissioning & Qualification Manager

  1. France
Paris
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
37588
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Commissioning & Qualification Manager - France, Paris - 12 Months Contract

Do you want to work at a leading global pharmaceutical manufacturer? If so, this is the assignment for you!

Our global client with manufacturing facilities in France, is currently investing significantly in their manufacturing programme. This state-of-the-art facility houses high-technology and next-generation processes to produce OTC and Oral Care Products that are distributed throughout the Globe. As such, they are looking for a Commissioning & Qualification Manager to join their Paris based project.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:
  • Lead and coordinate commissioning activities for clean utilities, black utilities, HVAC, process equipment and other GMP systems
  • Interface with client stakeholders, EPCM partners, and quality/engineering teams
  • Supervise and review commissioning documentation (checklists, protocols, reports, punchlists)
  • Manage system readiness, FAT/SAT follow-up, and ensure proper handover to qualification
  • Troubleshoot on-site issues and drive pragmatic resolution
  • Contribute to project planning and scheduling of commissioning scope
Desirable Experience:
  • Solid experience in commissioning management within GMP-regulated Life Sciences/Pharma facilities
  • Strong understanding of the CQV lifecycle and cross-functional project execution
  • Comfortable navigating technical documentation (P&IDs, datasheets, URS, etc.)
  • Fluent in French (mandatory); professional English required
  • Proven leadership on-site and ability to work in a dynamic, multi-disciplinary environment
If this role is of interest to you, please apply now!

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