Technical Writer - On-site
Core
Develop and maintain Instructions for Use (IFU), manuals, and technical documentation for regulated cranial and spinal medical devices.
Role type
Technical Writer (Regulated Medical Devices)
Builds
Product documentation for neurosurgical and spinal procedure devices
Domain
Healthcare / Medical Devices
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Technical writing, Adobe FrameMaker, Structured Authoring, XML, Content Management Systems, Adobe Acrobat, vector graphics, HTML, document publishing
Preferred skills
Medical device industry experience, regulated industry experience, Vasont CMS, online help systems, translation project management
Responsibilities
Develop and update IFU, manuals, and technical bulletins; Gather technical content from cross-functional teams; Create documentation using Adobe FrameMaker and structured authoring tools; Manage document version control and release processes; Coordinate translation projects; Review and edit documentation for accuracy and compliance; Support continuous improvement of documentation workflows.
Seniority
Mid-level, hands-on IC
