Technical Writer

A fantastic opportunity to work in a state-of-the-art facility in Cork. You will be joining a PPQ campaign for a new life saving biologic drug in 2020. To ensure success, you will be an addition to a team of Biopharmaceutical professionals which will all contribute to meeting company, industry and regulatory goals and standards. 


We are looking for a Technical Writer who has strong experience in authoring GMP documentation. This position is an initial 6-month contract with a possibility of extension. It could be a fantastic steppingstone for somebody with 2-3 years’ experience looking to move into a QA/Validation role within pharma/biopharma projects upon completion. 


This role will consist of collaborating with various SME’s and departments to draft, author and approve GMP documents. Once these have been approved, it will be your duty to load them onto the document management software – TrackWise.


Technical Writer experience/qualifications:

• Must have 2+ years’ experience in authoring SOP’s and GMP documents
• Good technical knowledge/understanding within a pharma/biopharma manufacturing site
• Strong knowledge of TrackWise
• Excellent communication skills and highly organised
• Previous experience of a PPQ campaign would be beneficial
• Available to start in September

This is the perfect opportunity for a Technical Writer to work on an impressive site and take the next step in their career!



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