Manufacturing Technical Writer II: Quality Docs & Process

Infosoft Inc.; Walpole (MA); On-site; USD 55,000 - 61,000; Part time

Job summary

Infosoft Inc. in Walpole, MA is seeking a Manufacturing Technical Writer II to produce compliant, high-quality documentation within the Healthcare Diagnostics division. The role focuses on writing, editing, and processing manufacturing-related documents and procedures.

Candidates should have 3–5 years of technical writing experience, strong attention to detail, and be proficient with Microsoft Office. You will collaborate with Manufacturing, Quality, Engineering, and Technical teams to meet

Qualifications

• 3–5 years of technical writing experience.
• Strong verbal and written communication skills.
• High level of attention to detail.
• Strong organizational skills.
• Ability to work independently to create and report on plans/projects.
• Ability to present complex data in clear, concise text.
• Proficient with Microsoft Office products including Word, Excel, and PowerPoint.

Responsibilities

• Write, edit and process compliant Quality System documents and procedures, including manufacturing work instructions, forms, guidance procedures, and risk files.
• Create and/or edit flow charts, diagrams and other visual aids.
• Collaborate with Manufacturing, Quality, Engineering, and Technical organizations to learn about products or processes to write/edit documents and procedures.
• Support documentation needs for manufacturing-related projects, e.g., process scale-ups.
• Gather and apply feedback to improve documents and procedures.
• Communicate status and meet project timelines and deadlines.
• Provide training support for the document change process.

Skills

Technical writing

Attention to detail

Organization

Independent work

Verbal and written communication

Microsoft Office

Process documentation

Tools

Microsoft Word

Excel

PowerPoint

Job description

Infosoft Inc. in Walpole, MA is seeking a Manufacturing Technical Writer II to produce compliant, high-quality documentation within the Healthcare Diagnostics division. The role focuses on writing, editing, and processing manufacturing-related documents and procedures.

Candidates should have 3–5 years of technical writing experience, strong attention to detail, and be proficient with Microsoft Office. You will collaborate with Manufacturing, Quality, Engineering, and Technical teams to meet