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Senior qa lead — cgmp

Athlone
Tandem Project Management Ltd.
Posted: 9 January
Offer description

A biopharmaceutical company headquartered in Athlone is seeking a Senior QA Specialist to oversee quality assurance activities for commercial and clinical products.
The successful candidate will have at least 7 years of relevant experience in the pharma industry, strong knowledge of c GMP regulations, and experience with new product introductions.
This role requires technical oversight and the ability to engage in continuous improvement initiatives while ensuring compliance with regulatory standards.
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