Technical Writer - GMP/ISO Documentation Specialist

Abbott Laboratories; Madison (WI); On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott Laboratories in Madison, WI is seeking an experienced Technical Writer to produce and revise documentation for instruments, automation, SOPs, study protocols, and training materials.

You will partner with SMEs across regulatory, quality, R&D, and operations to create clear, accurate content. The role requires strong English writing skills, detail orientation, and ability to work in a regulated environment with strict documentation controls. Travel up to 10% may be required.

Qualifications

• Associate degree or higher in a related field or high school diploma with 2+ years of relevant experience.
• 3+ years of technical writing in engineering, biotech, or software.
• Experience in a regulated document control environment.
• Authorization to work in the United States without sponsorship.
• Proficient with Microsoft Office applications and document formatting.

Responsibilities

• Collaborate with SMEs to create and evolve technical documentation.
• Write, revise, and edit procedures, SOPs, study protocols, and reports.
• Manage project schedules and meet deadlines.
• Reconcile SME comments to ensure accuracy and usability.
• Create graphics/illustrations to support written content.
• Ensure documents meet quality standards and reader comprehension.
• Travel up to 10% between Abbott locations.

Skills

Technical writing

Document control

MS Office

Regulatory compliance

English proficiency

Education

Associate degree (Biotech/Engineering/Technical Communications)

High school + 2+ years experience

Tools

Microsoft Word

PowerPoint

Excel

Job description

Abbott Laboratories in Madison, WI is seeking an experienced Technical Writer to produce and revise documentation for instruments, automation, SOPs, study protocols, and training materials.

You will partner with SMEs across regulatory, quality, R&D, and operations to create clear, accurate content. The role requires strong English writing skills, detail orientation, and ability to work in a regulated environment with strict documentation controls. Travel up to 10% may be required.