Technical Writer — GMP/Regulated Lab Documentation

Thornton Tomasetti; Madison (WI); On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott is seeking a skilled Technical Writer to develop and maintain manuals, SOPs, test protocols, and training materials for instruments and automation. The role involves collaborating with SMEs across Regulatory, Quality, R&D, and Operations to ensure accurate and actionable documentation for complex processes.

You will write, revise, and illustrate technical content, stay updated on product changes, and deliver high-quality documents that meet standards for a global healthcare leader.

Qualifications

• Associate degree in Biotechnology, Engineering, Technical Communications, or related field is required.
• 3+ years of technical writing experience in engineering/biotech/software fields.
• Experience in a regulated document control environment.
• Proficient with Microsoft Office applications (Word, PowerPoint, Excel).

Responsibilities

• Create and modify technical documents for instruments and automation (service manuals, SOPs, study protocols).
• Collaborate with SMEs to ensure accuracy and usability of documentation.
• Present information clearly with graphics to aid user understanding.
• Manage document projects with internal departments and meet deadlines.
• Maintain current knowledge of product developments and documentation requirements.

Skills

Technical writing

Time management

Documentation clarity

Education

Associate degree in Biotechnology, Engineering, Technical Communications, or related field

High school diploma with 2+ years related experience

Tools

Microsoft Office (Word, PowerPoint, Excel)

Job description

Abbott is seeking a skilled Technical Writer to develop and maintain manuals, SOPs, test protocols, and training materials for instruments and automation. The role involves collaborating with SMEs across Regulatory, Quality, R&D, and Operations to ensure accurate and actionable documentation for complex processes.

You will write, revise, and illustrate technical content, stay updated on product changes, and deliver high-quality documents that meet standards for a global healthcare leader.