MEP Turnover Engineer

Overview

MEP Turnover Engineer - Germany, Frankfurt - 12 Months Initial Contract. Are you a MEP Turnover Engineer looking for your next contract role? This is a fantastic opportunity 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, and Semiconductor 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 turnover, this is a timely opportunity 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.

Qualifications / 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!

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Engineering and Information Technology

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