A leading company in the medical device sector located in Sligo is looking for a QA Validation Engineer to spearhead the site validation program ensuring compliance with FDA, EU cGMP, and GAMP standards.
The role involves coordinating validation activities for equipment, utilities, processes, and software, while also driving continuous improvement initiatives and supporting broader quality assurance efforts.
Candidates should have a qualification in engineering or a scientific discipline along with extensive experience in validation and regulatory compliance.
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