A bio pharmaceutical company in Waterford is seeking a Qualification Engineer to support the site requalification program.
The role involves coordinating periodic qualification studies, ensuring compliance with cGMP standards, and providing technical guidance on validation requirements.
Ideal candidates will have a relevant degree and 3-5 years of experience in the healthcare manufacturing sector, with knowledge of quality management systems.
This position offers a critical opportunity to ensure ongoing validation and compliance at the facility.
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