Junior Technical Writer - Medical Device Documentation

FUJIFILM; Durham (NC); On-site; USD 65,000 - 80,000; Full time

Job summary

FUJIFILM Healthcare Americas Corporation is seeking a detail-oriented technical writer to design, develop, and maintain high-quality documentation for medical technology products. Familiarity with MadCap Flare is a plus.

You will collaborate across engineering, manufacturing, service, and projects to translate complex specs into clear manuals and procedures. Responsibilities include reviews for accuracy, records maintenance, and participating in standards improvements while ensuring FDA and ISO

Qualifications

• Bachelor's degree in English, Technical Communication, CS or related field.
• 0–2 years of technical writing experience preferred; internships or projects welcome.
• Basic understanding of technology, software development, or healthcare.
• Familiarity with desktop publishing tools such as MadCap Flare or RoboHelp is advantageous.
• Good verbal and written communication; team and independent work capability.
• Familiarity with Windows OS environment.

Responsibilities

• Develop and update technical documentation (manuals, online help, service/manufacturing guides).
• Collaborate with engineers, manufacturing, service and project teams to gather information.
• Translate technical specs into clear, user-friendly manuals and procedures.
• Support reviews for accuracy and usability under supervision.
• Maintain documentation records and assist with control/compliance processes.
• Participate in continuous improvement of documentation standards and tools.
• Ensure compliance with FDA and ISO 13485 requirements and other laws.

Skills

Technical writing

Team collaboration

Attention to detail

Verbal communication

Windows OS familiarity

Education

Bachelor's degree in English, Technical Communication, Computer Science, or related field

Tools

MadCap Flare

Adobe RoboHelp

Job description

FUJIFILM Healthcare Americas Corporation is seeking a detail-oriented technical writer to design, develop, and maintain high-quality documentation for medical technology products. Familiarity with MadCap Flare is a plus.

You will collaborate across engineering, manufacturing, service, and projects to translate complex specs into clear manuals and procedures. Responsibilities include reviews for accuracy, records maintenance, and participating in standards improvements while ensuring FDA and ISO