C&Q Engineer – Ireland - Contract
We are an established market leader in our niche field, and we have a fantastic opportunity for a C&Q Engineer to work on an exciting capex project in Ireland.
Your Role
You will support the project between the A&E firm and onsite for the development of the C&Q package of documentation and later the installation/commissioning and qualification of process equipment and utilities that are within the project scope.
As a C&Q Engineer, you will provide technical expertise to ensure that systems, equipment, and processes are designed, installed, commissioned, and qualified to the agreed specifications.
Essential Duties and Responsibilities:
1. Participate in design document reviews and ensure that quality aspects are included in design.
2. Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
3. Generate CQV documents at project level and for specific equipment/systems. Liaise with Quality, Engineering, and CQV to align on Critical parameters and document content.
4. Track and confirm closure of action items identified through FAT, HAZOP, Design Qualification, and other reviews.
5. Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.
6. Participate in construction system completion walkdowns.
7. Perform shakedown and commissioning and qualification of systems.
Requirements:
* B.Sc/B.Eng degree in engineering discipline, with particular emphasis mechanical or process engineering.
* Minimum of 4 years' experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
* Demonstrated ability to work on own initiative and proactively respond to business needs.
* Excellent interpersonal and communication skills.
* Familiar with Delta-V & Navis Works an advantage.