We are seeking an experienced
Technical Writer
to join a
medical devices
company, based in Dublin, creating clear, user-friendly documentation for medical devices, operator manuals, and technical content supporting software solutions and GUIs.
12-month contract
initially, with a strong likelihood of extension
Up to
€60/hour
DOE
Responsibilities
* Develop and edit medical device labelling content, including user manuals and device labels.
* Collaborate across functions (Regulatory, Quality, Clinical, Engineering, Commercial, Human Factors) to ensure clarity, compliance, and completeness.
* Translate complex technical information into accessible, end-user-friendly content.
* Extract key details from engineering documentation and create clinical instructions.
* Ensure compliance with EU and US medical device labelling regulations and standards.
* Research and prepare updates for manuals, bulletins, and other documents.
* Review and edit content created by others.
* Maintain documentation accuracy with product updates and support translations.
* Follow established processes to ensure compliant and timely output.
Requirements
* 5+ years' experience as a Technical Writer, ideally in medical devices
.
* Strong writing and editing skills with attention to detail.
* Proven knowledge of US/EU medical device labelling standards.
* Proficiency with common writing tools (Adobe Creative Suite, MS Office).
* QMS knowledge beneficial; MasterControl experience is a plus.
* Strong problem-solving and collaboration skills.
* Ability to work in a fast-paced, dynamic environment.
If this sounds like a role that you would be interested in discussing further, please apply today