Sr. Technical Writer
Core
Creating and modifying technical documents for medical instruments, automation, and test platforms, 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, and reports for Abbott Cancer Diagnostics instruments and test platforms.
Domain
Healthcare / Medical Devices / Biotechnology
Required skills
Technical writing in engineering/biotech, regulated document control, equipment/hardware documentation, project management, cross-functional collaboration, technical editing, graphic creation, regulatory compliance knowledge
Preferred skills
ISO 13485 and 21 CFR 820 compliance, Oracle Cloud PLM familiarity
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 documentation needs; lead pre-reviews and reconcile comments for accuracy; create graphics and illustrations to support content; write and edit procedural instructions for complex processes.
Seniority
Senior, hands-on IC with mentorship responsibilities
