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MEP Turnover Engineer

  1. Germany, Frankfurt
Frankfurt ( Oder)
  1. Contract
Competitive
  1. Data Centres
37644
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MEP Turnover Engineer - Germany, Frankfurt - 12 Months Initial Contract 

Are you a MEP Turnover Engineer looking for your next contract role? We have a fantastic opportunity for you to join our valued client in Frankfurt on an initial 12 month contract.

Experienced at delivering highly efficient projects for state-of-the-art Data Centres, Pharma, Semi- Conductor infrastructures around the world, our client is a global leader in design, engineering and delivery of facilities for high tech industries. This is your chance to join an innovative, market leading data centre company as their newest MEP Turnover Engineer . With growth plans to almost double their already huge turnover, there could not be a better time to join!

Responsibilities:
  • System Ownership: Understand the scope, boundaries, and turnover requirements of assigned MEP systems.
  • Turnover Dossier Compilation: Prepare and compile system-specific turnover packages, including test packs, certifications, as-built drawings, and quality records.
  • Walkdowns & Punch List Management: Conduct system walkdowns with contractors, commissioning teams, and client reps. Record and expedite closure of punch items.
  • Documentation Control: Ensure all documentation is accurate, complete, and compliant with pharmaceutical QA/QC standards.
  • Interface Coordination: Liaise with construction, QA/QC, commissioning, and validation teams to align turnover milestones with project timelines.
  • Progress Reporting: Attend daily turnover meetings and provide updates on system readiness, documentation status, and outstanding issues.
  • Regulatory Compliance: Ensure all turnover activities meet GMP, FDA, and MHRA requirements where applicable.
Requirements:
  • System Ownership: Understand the scope, boundaries, and turnover requirements of assigned MEP systems.
  • Turnover Dossier Compilation: Prepare and compile system-specific turnover packages, including test packs, certifications, as-built drawings, and quality records.
  • Walkdowns & Punch List Management: Conduct system walkdowns with contractors, commissioning teams, and client reps. Record and expedite closure of punch items.
  • Documentation Control: Ensure all documentation is accurate, complete, and compliant with pharmaceutical QA/QC standards.
  • Interface Coordination: Liaise with construction, QA/QC, commissioning, and validation teams to align turnover milestones with project timelines.
  • Progress Reporting: Attend daily turnover meetings and provide updates on system readiness, documentation status, and outstanding issues.
If this role is of interest to you, please apply now!

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