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Biologics gmp documentation specialist

Limerick
ESS Ltd.
Posted: 7h ago
Offer description

A leading engineering firm in Ireland is seeking a Technical Writer responsible for managing documentation at a new biologics facility. The role involves creating and updating engineering documentation such as SOPs and SWIs, ensuring compliance with Good Documentation Practices. The ideal candidate should have 3-5 years of experience in technical writing within a GMP environment and possess strong communication skills. This role is critical for supporting the client through project handover and into production.
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