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 c GMP 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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