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Gmp/mes technical writer for start-up pharma

Limerick
Milestone
Technical writer
Posted: 21 December
Offer description

A consultancy firm in County Limerick is seeking an experienced Technical Writer to support a pharmaceutical client. The ideal candidate will possess over 3 years of Technical Writing experience, specifically with MES documentation in GMP environments. Responsibilities include authoring and reviewing GMP documentation, supporting compliance initiatives, and ensuring documentation is audit-ready. This is a contract position targeting candidates with strong stakeholder engagement skills and experience in start-up facilities.
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