Medical Device Tech Writer — Clinician & Patient Manuals

Intellectt Inc; Saint Paul (MN); On-site; USD 55,000 - 62,000; Full time

Benefits offered by this job

Health Insurance (Medical, dental, and

Vision insurance

401(k) retirement plan

Paid Time Off (PTO)

Job summary

Intellectt Inc. is seeking a skilled technical writer in Minnesota to develop and maintain medical device documentation. You will write Instructions for Use, clinician manuals, and patient manuals, while ensuring compliance with labeling requirements.

Collaborate with Engineering, Regulatory Affairs, Marketing, and Clinical teams to release documents through content management and document control systems, managing multiple projects with accuracy and deadlines.

Qualifications

• Bachelor's degree in a relevant technical field, Communications, Science, or English.
• 2-6+ years of technical writing experience, including 2-6 years in the medical device industry.
• Current or recent medical device or pharmaceutical industry experience.
• Direct experience writing clinician and/or patient manuals.
• Experience with content management and document control systems.

Responsibilities

• Write, edit, and maintain technical documentation for medical device products.
• Develop Instructions for Use (IFUs), clinician manuals, and patient manuals.
• Collaborate with Engineering, Regulatory Affairs, Marketing, and Clinical teams.
• Ensure documentation complies with medical device labeling requirements.
• Release and maintain documents using document control and content management systems.
• Independently manage multiple projects while maintaining accuracy and meeting deadlines.

Skills

Technical writing

Content management

Document control

Project management

Education

Bachelor's degree

Tools

Content management systems

Document control systems

Job description

Intellectt Inc. is seeking a skilled technical writer in Minnesota to develop and maintain medical device documentation. You will write Instructions for Use, clinician manuals, and patient manuals, while ensuring compliance with labeling requirements.

Collaborate with Engineering, Regulatory Affairs, Marketing, and Clinical teams to release documents through content management and document control systems, managing multiple projects with accuracy and deadlines.