Manufacturing Technical Writer II

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

Job Title: Manufacturing Technical Writer II

Pay Rate: $40 - $44.02/Hr

Duration: 12 months

Location: Walpole, MA

This position is for the Healthcare Diagnostic division.

We are looking for a Manufacturing Technical Writer II. The primary role of this individual is to produce compliant, high-quality documentation. This role encompasses the support and coordination of writing, editing, and/or processing compliant documents and procedures in Manufacturing. The core competencies that are essential to success are attention to detail and organization. Critical thinking, with a solid understanding of quality implications, is necessary in managing document writing efficiently and compliantly. Communication is needed to maintain visibility of the documents and progress of the product/project.

• Write, edit, and/or process compliant Quality System documents and procedures, including manufacturing work instructions, manufacturing 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 specific products or processes to write and/or edit documents and/or procedures.
• Support documentation needs for manufacturing-related projects, e.g., process scale-ups.
• Gather and apply feedback to improve documents and/or procedures.
• Communicate status and meet project timelines and deadlines.
• Provide training support for the document change process.

Requirements:

• Strong verbal and written communication skills and organization
• 3-5 years of technical writing experience
• A high level of attention to detail
• Strong organizational skills
• Ability to work independently to create and report on plans/projects to complete multiple documents and/or projects in a timely manner
• Ability to present complex data in clear, concise text
• Ability to meet deadlines and work independently
• Proficient with Microsoft Office products, including Word, Excel, and PowerPoint