Job Title: C&Q Engineer
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We are an established market leader within our niche field, seeking a highly skilled C&Q Engineer to work on an exciting capex project in Ireland.
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Your role will be to support the project between the A&E firm and onsite for the development of the C&Q package of documentation, as well as the installation/commissioning and qualification of process equipment and utilities within the project scope.
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The job holder will provide technical expertise to ensure that systems, equipment, and processes are designed, installed, commissioned, and qualified to agreed specifications.
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Essential Duties and Responsibilities:
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1. Participate in design document reviews to ensure quality aspects are included in design.
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2. Attend Factory Acceptance Testing (FAT) and execute agreed testing protocols, signing off on permission to ship forms.
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3. Generate CQV documents at project level and for specific equipment/systems, liaising with Quality, Engineering, and CQV to align on critical parameters and document content.
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4. Track and confirm closure of action items identified through FAT, HAZOP, Design Qualification, and other reviews.
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5. Maintain a strong interface with Automation and Engineering teams to ensure information flow meets their needs, resolving issues as they arise.
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6. Participate in construction system completion walkdowns.
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7. Perform shakedown and commissioning/qualification of systems.
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Requirements:
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* Bachelor's degree in engineering discipline, particularly mechanical or process engineering.
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* Minimum 4 years' experience from biotechnology/pharmaceutical GMP manufacturing/CQV environment.
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* Demonstrated ability to work independently and proactively respond to business needs.
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* Excellent interpersonal and communication skills.
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* Familiarity with Delta-V & Navis Works is advantageous.
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If you are a motivated and experienced professional looking for a new challenge, please apply today.