Job Description:
We are seeking a skilled Process Engineer to join our team on an exciting CapEx project in Dublin. As a Process Engineer, you will play a key role in the successful delivery of a new state-of-the-art facility.
Key Responsibilities:
* 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.
* 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.
* Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
* 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.
* Participate in construction system completion walkdowns.
* Perform shakedown and commissioning and qualification of systems.
Requirements:
* B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
* Extensive 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.
* Extensive Clean in Place (CIP) experience.
About This Opportunity:
This is a fantastic opportunity to work with an established market leader within their niche field. You will be part of a dynamic team delivering a cutting-edge project in a high-tech environment.