Medical Device Technical Writer - Hybrid (4 Onsite Days)

Lancesoft; Minneapolis (MN); Hybrid; USD 70,000 - 100,000; Full time

Job summary

Lancesoft is seeking a Technical Writer for its Minneapolis, MN site to support the production of customer-facing product documentation for medical device labeling and instructions for use (IFUs). You will work with cross-functional teams to ensure content accuracy and regulatory compliance across multiple projects.

The role emphasizes quality, organized project management, and the ability to handle complex documentation within a regulated environment.

Qualifications

• Must-have: Quality/Compliance mindset and strong technical writing/documentation skills.

Responsibilities

• Develop labeling products and associated documentation, including prototyping, editing, formatting, and coordinating reviews and approvals.
• Collaborate with colleagues and cross-functional partners to ensure accuracy and quality of labeling content.
• Management of multiple projects and priorities while meeting expected timelines.
• Revise, edit, and format legacy product documentation such as user guides, service manuals, instructions for use (IFUs).
• Ensure labeling compliance with regulatory/QSR requirements and EU MDR where applicable.

Skills

Quality/Compliance Mindset

Technical Writing/Documentation

Job description

Lancesoft is seeking a Technical Writer for its Minneapolis, MN site to support the production of customer-facing product documentation for medical device labeling and instructions for use (IFUs). You will work with cross-functional teams to ensure content accuracy and regulatory compliance across multiple projects.

The role emphasizes quality, organized project management, and the ability to handle complex documentation within a regulated environment.