Technical Writer – GMP/Regulated Documentation Lead

abbott; Alabama; On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott is seeking a Technical Writer to create and update manuals, SOPs, study protocols, and training materials for instruments and automation. You will work with SMEs across Regulatory, Quality, R&D, and other teams to ensure accuracy and clear instructions for users with varying expertise.

The role requires 3+ years of technical writing in a regulated setting, strong MS Office skills, and the ability to manage multiple projects on schedule.

Qualifications

• Associate degree or equivalent with 2+ years of relevant experience in lieu of degree.
• 3+ years of technical writing experience in engineering/biotech/software fields.
• Experience in a regulated document control environment.
• Proficient in MS Office applications including Word styles, PPT, Excel macros and pivot tables.
• Authorization to work in the United States without sponsorship.

Responsibilities

• Create and modify technical documents for instruments, automation, SOPs, study protocols, reports, and notifications.
• Collaborate with SMEs across multiple functions to ensure accuracy and clarity of procedures.
• Lead pre-review of drafts and reconcile SME comments for usability and compliance.
• Develop graphics/illustrations to support technical content and user understanding.
• Maintain documentation aligned with Quality Management System requirements.

Skills

Technical writing

Document control

MS Office

Education

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

Tools

Microsoft Word

PowerPoint

Excel macros

Pivot tables

Job description

Abbott is seeking a Technical Writer to create and update manuals, SOPs, study protocols, and training materials for instruments and automation. You will work with SMEs across Regulatory, Quality, R&D, and other teams to ensure accuracy and clear instructions for users with varying expertise.

The role requires 3+ years of technical writing in a regulated setting, strong MS Office skills, and the ability to manage multiple projects on schedule.