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Manufacturing Technical Writer Jobs in Texas (NOW HIRING)

Saronic

Technical Writer, Manufacturing

Austin, TX · On-site

$65 - $90/hr

Job Overview: Saronic seeks a Technical Writer to create clear, concise, and comprehensive ... Familiarity with referencing design engineering drawings and the manufacturing lifecycle * Track ...

Umicore

Intern - Technical Writer

Pasadena, TX · On-site

Develop, revise, and standardize Standard Operating Procedures (SOPs) for manufacturing and ... English or Professional Writing with technical writing experience * Minimum GPA of 3.0 preferred.

Umicore

Intern - Technical Writer

Pasadena, TX

Develop, revise, and standardize Standard Operating Procedures (SOPs) for manufacturing and ... English or Professional Writing with technical writing experience * Minimum GPA of 3.0 preferred.

Bedrock

SCM Technical Writer

Houston, TX · On-site

$35 - $75/hr

SCM Technical Writer - Contingent Labor Summary of the Position: Technical writer to develop high ... and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to ...

ASR International Corporation

Senior Technical Writer

TX · On-site +1

$90K - $110K/yr

This role supports technical writing, product research, data validation, Item Purchase Description ... Perform market research to identify current manufacturer part number references and supplier ...

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Manufacturing Technical Writer information

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How much do manufacturing technical writer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for manufacturing technical writer in Texas is $36.28, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $43.89 per hour, depending on experience, location, and employer.

What is a manufacturing technical writer?

A Manufacturing Technical Writer creates clear and concise documentation for manufacturing processes, equipment, and standards. They develop user manuals, work instructions, and technical guides to ensure accurate production and compliance. Their role involves collaborating with engineers, operators, and quality teams to translate complex technical details into understandable content. Strong writing, technical expertise, and attention to detail are essential for success in this role.

What are the typical daily responsibilities of a manufacturing technical writer?

As a Manufacturing Technical Writer, your daily responsibilities typically include researching complex machinery or production processes, creating and updating instruction manuals, standard operating procedures, and safety documentation. You will frequently collaborate with engineers, production managers, and quality assurance teams to gather accurate information and ensure documentation reflects current practices. Reviewing and testing documents for clarity and usability, maintaining version control, and complying with industry or regulatory standards are also central to the role. This position requires a proactive approach to communication and a commitment to continuous improvement in documentation practices.

What are the key skills and qualifications needed to thrive in the manufacturing technical writer position, and why are they important?

A Manufacturing Technical Writer should possess strong writing, editing, and document management skills, often supported by a degree in technical communication, engineering, or a related field. Familiarity with authoring tools such as Adobe FrameMaker, MadCap Flare, and knowledge of Document Control Systems (DCS) or Product Lifecycle Management (PLM) are commonly required, along with certifications like CPTC. Excellent communication, attention to detail, and the ability to quickly grasp complex manufacturing processes make candidates stand out. These competencies ensure technical documentation is accurate, clear, and effectively supports safe and efficient manufacturing operations.

Are manufacturing technical writers still in demand?

Manufacturing technical writers are still in demand as companies require clear documentation for complex machinery, processes, and safety procedures. They often work closely with engineers and use tools like Adobe FrameMaker or MadCap Flare, with demand driven by manufacturing industry growth and technological advancements.

What are the most commonly searched types of Manufacturing Technical Writer jobs in Texas?

The most popular types of Manufacturing Technical Writer jobs in Texas are:

What are popular job titles related to Manufacturing Technical Writer jobs in Texas?

For Manufacturing Technical Writer jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Manufacturing Technical Writer jobs in Texas look for?

The top searched job categories for Manufacturing Technical Writer jobs in Texas are:

Manufacturing Technical Writer jobs near you
Infographic showing various Manufacturing Technical Writer job openings in Texas as of August 2026, with employment types broken down into 5% Internship, 81% Full Time, and 14% Contract. Highlights an 82% In-person, 6% Hybrid, and 12% Remote job distribution, with an average salary of $75,465 per year, or $36.3 per hour.

Manufacturing Technical Writer

Confluent Medical Technologies

Austin, TX • On-site

Full-time

Posted 12 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.

Apply