Overview
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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Writing/Editing and Project Management
Industries
Medical Equipment Manufacturing
Writing and Editing
Manufacturing
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