Technical Writer

Technical Writer – Ireland, Cork  – Initial 12-Month Contract – Life Sciences 

Are you interested in joining a world leading biopharmaceutical company, focused on developing advanced and innovative treatments for those suffering with rare diseases?

This is a fantastic opportunity to work in a state-of-the-art facility in Cork. You will be joining a leading Biopharmaceutical company who focus on a range of products which are life-changing for individuals.

Our client is currently seeking a Technical Writer.

What you’ll deliver:

• Lead and maintain the Biologics CoE documentation management strategy, ensuring compliance, inspection readiness, and operational effectiveness.
• Author, review, and approve GMP documentation including SOPs, Batch Process Documents (BPDs), work instructions, protocols, reports, and forms.
• Act as SME for Veeva QualityDocs and ComplianceWire, providing system support, guidance, and training to stakeholders.
• Collaborate with cross-functional SMEs to develop accurate, compliant documentation and support document lifecycle management, including change controls.

What’s required:

• Bachelor's degree in Science, Engineering, Biotechnology, Life Sciences, or a related discipline, or equivalent combination of education and relevant experience.
• Proven experience in technical writing, document control, or quality documentation within a regulated pharmaceutical, biotechnology, biologics, medical device, or related industry.
• Strong understanding of GMP, GxP, Data Integrity, ALCOA+ principles, and regulatory compliance requirements.
• Experience working with electronic Quality Management Systems (eQMS) and Learning Management Systems (LMS), preferably Veeva QualityDocs and ComplianceWire.

If this role is of interest, please apply now!
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