Technical Writer – GMP & Validation Documentation

NATOLI ENGINEERING CO INC; Missouri; On-site; USD 65,000 - 95,000; Full time

Job summary

NATOLI ENGINEERING CO INC is seeking an experienced technical writer to document highly technical content across software, engineering, and manufacturing domains. You will translate complex information into clear, user-friendly material and maintain standardized reference documentation.

Responsibilities include writing SOPs, validation protocols, and data templates, while collaborating with Engineering, QC, and Production to improve processes. 2–4 years of relevant experience is preferred.

Qualifications

• Bachelor’s degree in a relevant technical field; 2–4 years of writing experience.
• Ability to learn complex topics quickly and translate them for varied audiences.
• Experience writing documentation for multiple audiences and engineering teams.
• Superb written and verbal communication with high attention to detail.
• Experience collaborating with engineering to improve UX and create visuals.

Responsibilities

• Research, outline, write, and edit new and existing content with input from multiple departments.
• Independently gather information from subject matter experts to develop manuals and specs.
• Develop and maintain information architecture templates for easy data migration.
• Write SOPs, validation protocols, and related QA/Manufacturing documentation.
• Collaborate with Engineering, Customer Service, and Quality to improve processes.

Skills

Technical writing

Documentation

Content development

Editing

Communication skills

Cross-department collaboration

Education

Bachelor's degree in relevant technical field

Tools

XML tools

Job description

NATOLI ENGINEERING CO INC is seeking an experienced technical writer to document highly technical content across software, engineering, and manufacturing domains. You will translate complex information into clear, user-friendly material and maintain standardized reference documentation.

Responsibilities include writing SOPs, validation protocols, and data templates, while collaborating with Engineering, QC, and Production to improve processes. 2–4 years of relevant experience is preferred.