Technical Writer

GxP Recruitment; Galway; On-site; EUR 40,000 - 60,000; Full time

Job summary

A recruitment agency is seeking a Technical Writer for the medical device industry. The role involves creating clear and regulatory-compliant documentation, such as user manuals and guides. The ideal candidate will have excellent writing skills, familiarity with medical device regulations, and the ability to collaborate with various teams. Strong attention to detail and experience with documentation software are essential for success in this position.

Qualifications

• Ability to adapt writing style to different audiences.
• Experience with regulatory standards in medical devices.

Responsibilities

• Producing user manuals and technical guides.
• Working with cross-functional teams to gather information.
• Ensuring compliance with regulations.
• Updating documentation based on feedback.
• Maintaining quality and accuracy through review processes.

Skills

Excellent writing, editing, and proofreading skills

Understanding of medical device terminology

Familiarity with relevant regulations

Strong communication and interpersonal skills

Meticulous attention to detail

Experience with documentation software

Tools

Microsoft Word

Adobe Acrobat

XML editors

Job description

Technical writer

A Technical Writer in the medical device industry is crucial for creating clear, accurate, and regulatory-compliant documentation that supports the development, use, and maintenance of medical devices. They translate complex technical information into easily understandable language for various audiences, including users, healthcare professionals, and regulatory bodies.

Key Responsibilities:

• Producing user manuals, package inserts, technical guides, and other documentation related to medical devices.
• Working closely with cross-functional teams (e.g., product management, R&D, regulatory affairs, quality assurance) to gather information and ensure accuracy.
• Ensuring all documentation adheres to relevant regulations and standards, such as those set by the FDA or other regulatory bodies.
• Maintaining and updating documentation to reflect product changes, new regulations, or user feedback.
• Ensuring the quality and accuracy of all technical documentation, often through rigorous review and testing processes.

Skills and Qualifications:

• Excellent writing, editing, and proofreading skills, with the ability to adapt writing style to different audiences.
• Understanding of medical device terminology, design, and functionality.
• Familiarity with relevant regulations and standards for medical devices.
• Strong communication and interpersonal skills to work effectively with various teams.
• Meticulous attention to detail to ensure accuracy and consistency in documentation.
• Experience with relevant software for documentation creation and management (e.g., Microsoft Word, Adobe Acrobat, XML editors).