Sr. Technical Writer
Abbott · Madison
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Senior Technical Writer at Abbott responsible for creating and maintaining technical documentation for diagnostic instruments, automation systems, and test platforms. The role involves managing documentation projects, mentoring junior writers, and collaborating with cross-functional teams including regulatory, quality, and engineering to ensure accurate, compliant, and user-focused materials.
What they're looking for
- Bachelor's degree in Biotechnology, Engineering, Technical Communications, or equivalent field; or High School Diploma/GED with 4+ years relevant experience
- 7+ years technical writing experience in engineering or biotechnology field
- 3+ years experience in regulated document control environment
- 2+ years equipment or hardware technical writing experience
- Proficiency in Microsoft Office programs
- Authorization to work in United States without sponsorship
- Experience authoring documents compliant with ISO 13485 and 21 CFR 820 regulations (preferred)
What you'll be doing
- Manage documentation projects by coordinating meetings with regulatory, quality, and subject matter experts
- Create and evolve technical documents including service procedures, SOPs, user manuals, and training materials
- Mentor other technical writers and provide editorial feedback on documentation quality
- Partner with cross-functional teams across Abbott Cancer Diagnostics to understand product requirements and documentation gaps
- Develop educational materials and host workshops for internal departments
Privacy & handoff
This role links to Abbott's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.