Technical Writer

GForce Life Sciences • Contract • St Paul, MN, US • 9h ago

6-month Contract

Onsite in St. Paul, MN

Must be able to work on a W2

What You’ll Do

Research, write, and edit technical documentation supporting product development initiatives
Collaborate with engineering, marketing, regulatory affairs, clinical, and other partners to gather inputs and align content for IFUs
Follow internal documentation processes and procedures
Ensure labeling content aligns with medical device regulatory requirements
Prepare and release documentation through a document control system
Manage multiple documentation projects in a fast-paced, changing environment with high attention to detail

Qualifications

Bachelor’s degree in a relevant discipline (e.g., Communications, Science, English) or equivalent
2–6+ years of progressively responsible technical writing experience in a medical or high-technology environment (biotech preferred)
Current or recent medical device or pharma industry experience (including 2–6 years in medical devices)
Direct end-user writing experience (e.g., clinician and/or patient manuals)
Experience working in a content management system (required)
Familiarity releasing documentation in a document control system
Strong technical aptitude and ability to learn new tools quickly
Content management expertise beyond baseline requirements is a plus