Technical Writer

Role overview

This position is for a Technical Writer focused on the medical device sector. The role centers on producing precise, easy-to-follow, and regulation-aligned documentation that supports the design, use, and ongoing upkeep of medical devices. You will turn technical and regulatory material into clear language suitable for end users, healthcare professionals, and regulatory stakeholders.

What you will do

• Create and maintain essential documentation such as user manuals, package inserts, technical guides, and related device materials.
• Partner with product management, R&D, regulatory affairs, quality assurance, and other teams to collect accurate input and confirm technical details.
• Make sure all documentation complies with applicable medical device rules and standards, including FDA and other regulatory requirements where relevant.
• Revise and refresh content as products evolve, regulations change, or user feedback highlights improvements.
• Review documentation carefully to maintain high standards of accuracy, consistency, and overall quality.

Experience and qualifications

The role calls for at least 5 years of technical writing experience, ideally in the medical device, pharmaceutical, or broader regulated healthcare environment. Strong editing, proofreading, and audience-aware writing skills are important, along with a solid grasp of medical device terminology, design, and function. Candidates should also be comfortable working across teams, paying close attention to detail, and using documentation tools such as Microsoft Word, Adobe Acrobat, and XML editors.

Additional information

This is a full-time, onsite position based in Bray, County Wicklow, Ireland.