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Gmp qa specialist – pharma/med devices (batch review)

Cork
Uniting Holding
Posted: 5 March
Offer description

A leading automation firm in Cork is seeking a QA Specialist to ensure compliance with GMP documentation for FDA-regulated customers.
The ideal candidate will have a relevant qualification and 2-3 years of experience in a QA role within the pharmaceutical sector.
Responsibilities include supporting quality assurance in packaging, conducting batch record reviews, and collaborating with cross-functional teams.
Join us for personal and professional growth opportunities in a diverse and inclusive workplace.
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