Technical Writer

Advantage Technical; Minneapolis (MN); Hybrid; USD 70,000 - 90,000; Part time

Benefits offered by this job

401(k)

Vision insurance

Medical insurance

Job summary

A leading technical services firm is looking for a Technical Writer II specializing in labeling projects. This mid-senior level role entails planning, managing, and directing the creation of product literature and labeling. Ideal candidates will possess over 4 years of experience in a regulated industry, preferably in medical devices, and have specific labeling experience. The position offers a hybrid work arrangement, with competitive benefits including medical and vision insurance.

Qualifications

• 4+ years of experience in a regulated industry.
• Medical device industry experience.
• 2+ years of labeling experience.

Responsibilities

• Coordinate all product labeling deliverables.
• Manage creation and revision of labeling deliverables.
• Communicate project status, risks, and successes.
• Lead cross‑functional teams through labeling content development.
• Coordinate desktop publishing and artwork generation.

Skills

Labeling experience

Strong proficiency with Adobe Creative Suite

Proficiency with MS Office

Proficiency with MS Project

Job description

Technical Writer II – Labeling Project Specialist

Work Arrangement: Hybrid (3 days onsite per week)

Candidate Requirement: Local candidates only

Position Overview

The Labeling Project Specialist (LPS) is responsible for planning, managing, and directing the creation and revision of product literature and labeling. This role serves as the primary point of contact and subject matter expert for all labeling-related activities. The LPS works closely with cross‑functional project teams to ensure labeling content is accurate, compliant, high‑quality, and delivered on schedule.

Key Responsibilities

Labeling Development & Coordination

• Coordinate all product labeling deliverables, including labels, IFUs/DFUs, carton and pouch artwork, and related materials.
• Manage creation and revision of labeling deliverables from project initiation through completion.
• Assess project scope and collaborate with project management and team members to develop labeling plans and secure resources.
• Develop schedules, establish milestones, and ensure on‑time delivery of all labeling components.
• Communicate project status, risks, and successes to project and functional leadership.

Cross‑Functional Collaboration & Content Management

• Monitor dependencies across functions and address issues that may impact schedule or quality.
• Lead cross‑functional teams through labeling content development, including drafting, collecting inputs, revising content, and tracking changes.
• Promote consistency across labeling content and ensure alignment with regulatory and quality requirements.
• Facilitate team reviews to ensure labeling is accurate, complete, compliant, and customer‑focused.

Publishing, Release & Compliance

• Coordinate desktop publishing and artwork generation.
• Manage implementation and release activities for labeling deliverables.
• Oversee content changes and mitigate schedule impacts by ensuring accuracy and completeness.
• Implement labeling through the organization’s Document Control System.
• Apply expertise in labeling procedures, requirements, and quality systems to ensure error‑free deliverables.
• Identify opportunities for continuous improvement and drive innovation in labeling processes.

Qualifications

• 4+ years of experience in a regulated industry
• Medical device industry experience
• 2+ years of labeling experience

Preferred Qualifications

• Direct labeling or technical writing experience
• Experience with medical electrical equipment or capital equipment
• Strong proficiency with Adobe Creative Suite
• Proficiency with MS Office and MS Project

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Writing/Editing

Industries

Medical Equipment Manufacturing

Benefits

• 401(k)
• Vision insurance
• Medical insurance