C&Q Engineers at Qcs Staffing in Dublin, County Dublin, Ireland | Kablio

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C&Q Engineers

Employer undisclosedRole managed by a recruiter

C&Q Engineer for pharma CapEx project, handling design, testing, and CQV docs.

6 days ago ago

Experienced (8-12 years), Expert & Leadership (13+ years)

Contractor

Dublin, County Dublin, Ireland

Onsite

Your recruiting firm

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Founded with the aim of providing top-tier staffing solutions for diverse sectors.
Focus on long-term partnerships with clients, ensuring the right talent for specialized roles.
Expert in recruiting for both large-scale projects and niche, high-demand sectors.
Has become a trusted partner in sectors such as Industrial, Energy, and Infrastructure.
Notable for a rapid response to market demands and changing industry trends.
Experience in delivering recruitment services for large infrastructure and energy projects.
Specializes in sourcing skilled professionals for both permanent and temporary roles.
Recognized for working on complex and large-scale projects with a diverse client base.

About the client

About the client

Information not given or found

Role

Description

cqv docs

design review

fat execution

ship signoff

action tracking

hazop review

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.
Participate in design document reviews and ensure that quality aspects are included in design.
Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.

Requirements

initiative

engineering degree

delta-v

navis works

gmp

communication

Demonstrated ability to work on own initiative and proactively respond to business needs.
B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
Familiar with Delta-V & Navis Works an advantage.
Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
Excellent interpersonal and communication skills.

Benefits

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Training + Development

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Interview process

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Visa Sponsorship

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Security clearance

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