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CQV Engineer

  1. France
Toulouse
  1. Contract
Competitive
  1. Life Sciences
38134
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CQV Engineer - France, Toulouse - 4 Months Initial Contract

Our client, a global biotechnology organisation, is recruiting for a CQV Engineer to join their capital project in Toulouse. This new build facility will house a therapeutic protein production plant, and we are looking for a CQV Engineer to help expand our client's biotech operations throughout Europe. As the CQV Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.

Responsibilities:
  • Prepare and review Test Matrices to ensure all requirements are captured, approved, and revision-controlled.
  • Coordinate with the Document Preparation Lead to manage deliverables and approvals via the Document Generation Tracker, including milestone tracking.
  • Lead Verification Design activities (EDR/DQ) and oversee vendor documentation review and approval.
  • Support protocol development (FAT, IV, SAT, FV) in collaboration with the Document Preparation Lead.
  • Engage with vendors to ensure GEP and GDP compliance for reusable test documentation.
  • Contribute meaningfully to CQV scheduling and milestone planning.
  • Support vendor/supplier Quality Audits as needed.
  • Coordinate EDMQ system use for protocol reviews and approvals; lead execution of IV deliverables (e.g. Walkdowns, Tag Verification, Loop Checks, STW, PSSR, DSTW).
  • Ensure timely closure of CQV Punchlist items.
  • Liaise with and apply the Engineering Change Management System (ECM).
  • Review and approve Vendor and Field Turnover Packages against VDR to meet system validation requirements.
  • Align qualification activities with project timelines and business priorities.
Reqirements:
  • Prepare CSR’s (Commissioning Summary Reports) for executed documentation.
  • Ensure all the requirements for the IOQ summary reports are available and the good engineering and documentation practices have been followed throughout. 
  • Review all vendor and site change controls for impact to the completed testing as required. 
  • Liaise with QA in close-out of all CQV deviations and exceptions 
  • Generate Project specific SOP's / other documentation as applicable 
  • Support CQV and QA programmes as required
If this role is of interest, please apply now!
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