Senior Medical Device Technical Writer — End-User Manuals

Techlink Systems Inc.; Saint Paul (MN); On-site; USD 70,000 - 100,000; Full time

Job summary

Techlink Systems Inc. is seeking a Technical Writer for on-site in St. Paul, MN.

The role focuses on researching, writing, and editing technical documentation for new and sustaining products, while collaborating with cross-functional teams to collect inputs for IFUs and ensuring compliance with regulatory labeling requirements. The ideal candidate has 2–6 years of end-user technical writing experience in the medical device or high-tech space, plus experience with content management systems and

Qualifications

• Bachelor's degree in a relevant technical discipline (e.g., engineering, sciences, English) or equivalent.
• 2–6+ years as a technical writer in medical device/high-tech environments.

Responsibilities

• Research, write, edit technical documentation for new and sustaining product development projects.
• Collaborate with engineering, marketing, regulatory, and clinical teams to gather inputs for IFUs.
• Follow internal processes and procedures.
• Understand and comply with medical device regulatory requirements related to labeling.
• Experience releasing documentation in a Document Control system.

Skills

Attention to detail

Self-starter

Content management

Project coordination

Team collaboration

Education

Bachelor’s Degree

Tools

Document Control System

Content Management System

Job description

Techlink Systems Inc. is seeking a Technical Writer for on-site in St. Paul, MN.

The role focuses on researching, writing, and editing technical documentation for new and sustaining products, while collaborating with cross-functional teams to collect inputs for IFUs and ensuring compliance with regulatory labeling requirements. The ideal candidate has 2–6 years of end-user technical writing experience in the medical device or high-tech space, plus experience with content management systems and