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Home Based Manufacturing Technical Writer Jobs (NOW HIRING)

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Position may be hybrid for 4 days in office and one day at home. Preferred * Prior experience in a ... We manufacture bio-based polymers with a goal of replacing single-use petroleum-based plastics. Our ...

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Technical Writer

Henderson, NV · On-site

$30 - $33/hr

Whether your background is in technical writing, quality systems, quality control, quality ... Translate complex manufacturing processes into clear, user-friendly documentation * Observe ...

We're looking for a skilled Technical Writer who can transform complex engineering and ... Primarily office-based with regular visits to climate-controlled manufacturing and production areas

Talk to warehouse, supply chain, manufacturing, and SAP teams to understand how they do their work ... Update documents based on feedback from managers and subject matter experts. * Help prepare ...

Collaborate with Quality Engineers, Manufacturing Engineers, and Operations to identify critical-to ... Job Type & Location This is a Contract position based out of Saint Paul, MN. Pay and Benefits The ...

Technical Writer

Hammond, IN · On-site

$32 - $36/hr

Position Overview A manufacturing organization in the East Canton, OH area is seeking a Technical ... for extension based on business needs. Key Responsibilities * Develop, draft, edit, and format ...

Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract Compensation: $32.00 - $38.00 per hour Work Model: Onsite - onsite Hours: 40.0 hours per week Responsibilities:

Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract Compensation: $32.00 - $38.00 per hour Work Model: Onsite - onsite Hours: 40.0 hours per week Responsibilities:

Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract Compensation: $32.00 - $38.00 per hour Work Model: Onsite - onsite Hours: 40.0 hours per week Responsibilities:

Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract Compensation: $32.00 - $38.00 per hour Work Model: Onsite - onsite Hours: 40.0 hours per week Responsibilities:

Technical Writer, Manufacturing Location: Cudahy, WI Type: Long-term Contract Compensation: $32.00 - $38.00 per hour Work Model: Onsite - onsite Hours: 40.0 hours per week Responsibilities:

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How much do home based manufacturing technical writer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for home based manufacturing technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is a home based manufacturing technical writer?

Home Based Manufacturing Technical Writers are professionals who create technical documents, manuals, and guides related to manufacturing processes, equipment, and products, all while working remotely from their homes. They translate complex technical information into clear, user-friendly documentation for engineers, production teams, and end users. These writers often collaborate with subject matter experts remotely to ensure accuracy and clarity in their materials. Their work helps improve safety, efficiency, and understanding within manufacturing environments. The flexibility of working from home allows them to serve clients or employers across various regions and industries.

What skills and qualifications are needed to thrive as a home based manufacturing technical writer?

To thrive as a Home Based Manufacturing Technical Writer, you need strong technical writing ability, knowledge of manufacturing processes, and often a degree in engineering, technical communication, or a related field. Familiarity with documentation tools like Adobe FrameMaker, Microsoft Word, and content management systems, as well as experience with CAD or product lifecycle management software, is common. Exceptional attention to detail, the ability to explain complex concepts clearly, and strong self-motivation are standout soft skills for this remote role. These skills ensure you can produce accurate, user-friendly documentation that supports safe and efficient manufacturing operations from a home office.

How does a home based manufacturing technical writer typically collaborate with remote engineering and production teams?

As a Home Based Manufacturing Technical Writer, you’ll frequently communicate with engineers, product managers, and production staff through virtual meetings, email, and collaboration platforms. You’ll review technical documents, clarify complex processes, and request additional information to ensure accuracy in manuals and SOPs. Building strong remote relationships is critical, as you’ll often rely on detailed descriptions, annotated diagrams, and screen-sharing sessions to gather the information needed for clear, compliant documentation.
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Infographic showing various Home Based Manufacturing Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Manufacturing Technical Writer

Confluent Medical Technologies

Austin, TX • On-site

Full-time

Posted 9 days ago


Job description

Job Description:
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.
We are looking for a Manufacturing Technical Writer to join our team in Austin, TX. As a uniquely qualified candidate, you will:
The Manufacturing Technical Writer is responsible for developing, revising, and maintaining clear, consistent, and technically accurate documentation that supports engineering, manufacturing, quality, and product lifecycle activities for medical device products and processes.
This role works closely with Process Development Engineering, Quality, Operations, and Supply Chain to translate engineering knowledge, process requirements, and quality system inputs into controlled documentation. The Technical Writer will draft a substantial portion of a broad range of documents-including work instructions, inspection procedures, purchasing specifications, protocols, reports, ERP part-creation documentation, and risk documentation-so that engineers can efficiently complete the final technical details before approval.
A key focus of the role is creating work instructions that can be effectively transferred and implemented by production personnel at Confluent manufacturing locations, including Costa Rica. The Technical Writer will also help establish consistent standards, templates, terminology, and practices for manufacturing documentation across the organization.
Key Responsibilities
  • Shadow engineers and technicians during development and pilot builds to capture manufacturing processes and create clear, accurate work instructions.
  • Develop documentation from direct observation, engineering inputs, drawings, specifications, build notes, design outputs, test data, supplier information, ERP requirements, risk-management inputs, and draft procedures.
  • Review, simplify, and standardize engineer-generated work instructions to improve clarity, consistency, and usability for production operators.
  • Create, revise, and standardize inspection procedures, purchasing specifications, protocols, technical reports, manufacturing work instructions, and other controlled documentation required to support product development, production, and quality activities
  • Support part creation and related documentation in the ERP system by gathering required information, preparing draft records or supporting documentation, and coordinating review with Engineering, Quality, Supply Chain, and Operations.
  • Transform complex or text-heavy procedures into clear, visual, step-by-step instructions using photographs, diagrams, tables, pictograms, and other operator-friendly formats.
  • Apply plain-language, controlled-language, and user-centered principles to improve comprehension, reduce ambiguity, and support manufacturing personnel with varying levels of technical experience and English proficiency.
  • Develop documentation that supports effective manufacturing and process transfer from U.S. development sites to production operations, including Confluent's Costa Rica site.
  • Collaborate with Engineering, Quality, Operations, and Training to verify technical accuracy and ensure documentation reflects approved manufacturing processes.
  • Ensure documentation complies with applicable Quality Management System, document control, regulatory, ERP, purchasing, inspection, validation, and risk-management requirements.
  • Identify gaps, inconsistencies, and ambiguity in manufacturing documentation and work with subject-matter experts to resolve them.
  • Route completed documents through Confluent's Quality Management System and document-control workflows, coordinating approvals, resolving review comments, and ensuring final records are released appropriately.
  • Help establish and continuously improve documentation templates, terminology, visual standards, style guidelines, and workflows.
  • Provide guidance to engineers and other subject-matter experts on effective manufacturing documentation practices.
  • Perform other related duties as assigned.

Required Qualifications
  • Bachelor's degree in Technical Writing, Communications, Engineering, Manufacturing, or a related field, or equivalent relevant experience.
  • 3-5+ years of technical writing experience in manufacturing, medical devices, life sciences, or another regulated environment.
  • Demonstrated experience creating or maintaining controlled technical documentation such as manufacturing work instructions, SOPs, inspection procedures, specifications, protocols, reports, risk documentation, or similar records.
  • Ability to understand technical processes and translate complex engineering information into clear, concise, operator-ready instructions.
  • Experience working directly with engineers, technicians, operators, and other technical subject-matter experts.
  • Familiarity with Quality Management Systems, document control, approval routing, revision-controlled documentation, and cross-functional technical review processes.
  • Strong written, verbal, visual communication, and cross-functional collaboration skills.
  • Ability to independently manage multiple documentation projects and priorities.
  • Ability to gather incomplete or preliminary technical inputs, organize them into structured drafts, and work with engineers to finalize technical details

Preferred Qualifications
  • Experience in medical device manufacturing and FDA- and/or ISO-regulated environments.
  • Experience supporting new product introduction, design transfer, manufacturing transfer, or process validation.
  • Experience with ERP part setup, item master data, bills of material, purchasing specifications, supplier documentation, inspection planning, or related product lifecycle documentation.
  • Experience developing visual work instructions for manufacturing personnel or audiences with varying English proficiency.
  • Spanish-language proficiency and/or experience supporting manufacturing operations in Costa Rica or Latin America.
  • Willingness to travel up to 25% on occasion, including Costa Rica, to support project work
  • Proficiency with Microsoft Word, graphics/image-editing tools, and electronic document management systems.

Core Competencies
  • Ability to translate engineering complexity into manufacturing simplicity
  • Strong attention to technical accuracy, completeness, and documentation traceability
  • Operator-centered communication
  • Manufacturing and process orientation
  • Cross-functional collaboration
  • Ability to drive document drafts through review, approval, and release workflows
  • Quality and regulatory awareness
  • Visual communication
  • Continuous-improvement mindset

We regret that we are unable to sponsor employment visas or consider individuals on time-limited visa status for this position.
Confluent Medical Technologies is an equal opportunity employer.
Only qualified candidates will be contacted.