Sterile Equipment Validation Engineer (CQV)

Asset Recruitment is currently looking for a CQV Engineer to join a leading global pharmaceutical company in Connacht, Ireland. This role involves validating equipment for sterile injectable manufacturing and ensuring compliance with industry standards.

The successful candidate will have a Bachelor's or Master's in Engineering or Science, and at least 4-5 years' experience in validation processes, particularly in sterile environments. The role supports regulatory compliance and requires strong analytical and communication skills.