Senior Technical Writer
Core
Creating and modifying technical documents for instruments, automation, test platforms, and products, including service procedures, user manuals, SOPs, and study protocols.
Role type
Senior Technical Writer (Regulated Medical Devices)
Builds
Service procedures, user and service manuals, training materials, SOPs, study protocols, reports, and customer notifications for cancer detection and treatment instruments.
Domain
Biotechnology / Medical Devices / Oncology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Technical writing in engineering/biotech, regulated document control, equipment/hardware documentation, project management, cross-functional collaboration, graphic creation, regulatory compliance (ISO 21 CFR 820)
Preferred skills
Oracle Cloud PLM familiarity, ISO 13485 compliance authoring
Technologies
Microsoft Office, Oracle Cloud PLM
Responsibilities
Manage documentation projects and host meetings with SMEs; mentor other technical writers; create educational materials and workshops; partner with cross-functional teams to understand product and audience needs; lead pre-review of drafts and reconcile comments; write and edit procedural and explanatory content; create graphics to support written content.
Seniority
Senior, hands-on IC
