Job Description
Seeking a C&Q Engineer to lead the development of C&Q documentation and installation/commissioning for a large-scale Cell Culture facility in Dublin, Ireland. The role requires technical expertise to ensure systems, equipment, and processes meet agreed specifications. The successful candidate will have a B.Sc/B.Eng degree in mechanical or process engineering, with 4+ years of experience in biotechnology or pharmaceutical GMP manufacturing/CQV environment. Key responsibilities include participating in design document reviews, attending FAT and execution of testing protocols, generating CQV documents, and maintaining a strong interface with automation and engineering teams. The ideal candidate will have excellent interpersonal and communication skills, with experience in Delta-V and Navis Works an advantage. This is an 11-month fixed-term contract with a hybrid working model.