We are seeking a highly skilled and experienced C&Q Engineer to join our project in Dublin on an initial 12-month contract.
C&Q Engineer Job Description
As a key member of our team, you will participate in design document reviews to ensure quality aspects are included in design. You will also attend FAT and execute agreed testing protocols, sign off on permission to ship forms, and 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.
* You will be responsible for tracking and confirming closure of action items identified through FAT, HAZOP, Design Qualification and other reviews.
You will need:
* A degree in engineering discipline, with particular emphasis on 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.
* Familiarity with Delta-V & Navis Works is an advantage.
This role requires a high level of technical expertise, attention to detail, and excellent problem-solving skills. If you have the required experience and skills, please submit your application.