C&Q Engineer – Ireland - Contract
We are seeking an experienced C&Q Engineer to join our team in Ireland for a capex project.
Key Responsibilities:
* Support the development of the C&Q package of documentation and installation/commissioning/qualification of process equipment and utilities.
* Provide technical expertise to ensure systems, equipment, and processes meet agreed specifications.
Essential Duties and Responsibilities:
1. Participate in design document reviews and ensure 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, liaising 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 Automation and Engineering teams to ensure information flow meets their needs, 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 is an advantage.