C&Q Engineers

Overview

Engineer to lead CQV activities for a new state‑of‑the‑art pharma manufacturing facility in Dublin.

Key Responsibilities

• fat testing
• action tracking
• design review
• hazop review
• cqv documentation

Tasks

-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. -Participate in design document reviews and ensure that quality aspects are included in design. -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.

Requirements

• gmp manufacturing
• delta-v
• navis works
• b.sc
• mechanical
• communication

What You Bring

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

People Also Searched For

About Qcs Staffing

-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.

Sector Specialisms