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Entry Level Document Composition Developer Jobs in Dallas, TX

Barry-Wehmiller

Entry Level Validation Engineer

Dallas, TX · On-site

$75K - $90K/yr

Prepare and execute FAT, SAT, IQ, and OQ documentation for equipment and automated systems ... engineering, or a related technical degree * Academic, co-op, internship, project, or entry-level ...

New

FiberLight LLC

Network Engineer I

Allen, TX · On-site

Follow process documents to configure network devices Help configure and troubleshoot basic routing ... Experience with Cisco, Juniper, or other network equipment is a plus. Entry-level certifications (e ...

JND Inc.

[Entry Level] Software Tester (2608-2)

Plano, TX · On-site

$28 - $32/hr

Detect, document, and track software defects and inconsistencies with clear, reproducible steps ... Great interpersonal and communication skills Our team of highly experienced developers offer a wide ...

JND

[Entry Level] Software Tester (2608-2)

Plano, TX · On-site

$28 - $32/hr

Detect, document, and track software defects and inconsistencies with clear, reproducible steps ... Great interpersonal and communication skills Our team of highly experienced developers offer a wide ...

FiberLight LLC

Network Engineer I

Allen, TX · On-site

... documents to configure network devices • Help configure and troubleshoot basic routing protocols ... telecommunications (internships or entry-level roles count). • Layer 1- Experience ...

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All JobsDocument Composition Developer JobsEntry Level Document Composition Developer JobsEntry Level Document Composition Developer Jobs in Dallas, TX

Entry Level Document Composition Developer information

See Dallas, TX salary details

$31.7K

$93.1K

$159.8K

How much do entry level document composition developer jobs pay per year?

As of Sep 3, 2026, the average yearly pay for entry level document composition developer in Dallas, TX is $93,135.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,300.00 and $100,400.00 per year, depending on experience, location, and employer.

What is the difference between Entry Level Document Composition Developer vs Entry Level Technical Writer?

AspectEntry Level Document Composition DeveloperEntry Level Technical Writer
CredentialsHigh school diploma or associate's; some roles prefer technical or writing coursesHigh school diploma; often prefers degrees in English, Communications, or related fields
Work EnvironmentOffice or remote; collaborates with developers and engineersOffice or remote; works closely with subject matter experts and editors
Industry UsageUsed in software, engineering, and technical fields for creating technical documentsCommon in technology, manufacturing, and scientific industries for user manuals and documentation

Both roles involve creating technical documents, but Entry Level Document Composition Developers often focus on formatting and assembling technical content, while Entry Level Technical Writers emphasize writing and editing original content. The roles overlap in skills and industry usage, but differ slightly in focus and responsibilities.

What are popular job titles related to Entry Level Document Composition Developer jobs in Dallas, TX?

For Entry Level Document Composition Developer jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Entry Level Document Composition Developer jobs in Dallas, TX look for?

The top searched job categories for Entry Level Document Composition Developer jobs in Dallas, TX are:

Entry Level Document Composition Developer jobs near you
Infographic showing various Entry Level Document Composition Developer job openings in Dallas, TX as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $93,135 per year, or $44.8 per hour.

Entry Level Validation Engineer

Barry-Wehmiller

Dallas, TX • On-site

$75K - $90K/yr

Full-time

Posted 2 days ago

New

Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Who You'll Work With

At Design Group,you'llcollaborate with experienced leaders, technical specialists, and subject matter experts to solve complex challenges for some of the world's leading companies.You'lljoin a growing team of more than 1,500 professionals across 45 U.S. offices whereyou'llbe empowered to make an impact, develop yourexpertise, and grow your career.

What You'll Do

In this role,you'llbe responsible forsupporting validation and regulatory compliance activities for pharmaceutical, medical device, and other life sciences projects.You'llwork closely with validation engineers, project teams, clients, vendors, and technical specialists to develop protocols, execute testing, investigate issues, and document results. This position playsan important rolein helping clientsdemonstratethat equipment, utilities, facilities, and automated systems meet quality and regulatory requirements while giving you hands-on experience invalidationengineering and project delivery.

  • Develop and execute validation and FDA compliance documents and protocols for pharmaceutical equipment and automated systems

  • Support manufacturing process design, facility development, and project execution activities

  • Prepare and execute FAT, SAT, IQ, and OQ documentation for equipment and automated systems

  • Assistwith development and execution of quality management system procedures and related compliance documentation

  • Apply applicable requirements from 21 CFR Parts 211 and 820 and ICH Q1, Q8, Q9, and Q10 to project deliverables

  • Conduct investigations and support troubleshooting of validation and compliance issues

  • Prepare clear written validation reports that document testing, results, deviations, and conclusions

  • Coordinate with clients, vendors, engineers, and project teams to support validation planning and execution

  • Support installation, start-up, commissioning, and site-based validation activities

  • Build technicalexpertisein life sciences validation, quality systems, documentation practices, and regulatory compliance

What You'll Bring

Qualifications

  • Bachelor of Science in bioengineering, biomedical engineering, chemical engineering, or a related technical degree

  • Academic, co-op, internship, project, or entry-level experience related to validation, quality, pharmaceutical manufacturing, medical devices, automation, utilities, facilities, or regulated environments

  • Proficiencyusing Microsoft Office and ability to prepare clear technical documentation

  • Ability to organize and execute multiple project responsibilities simultaneously

  • Ability to travel for project requirements, including installation and start-up activities, client and company meetings, trainings, seminars, forums, and conventions

Preferred Qualifications

  • Co-op or project experience with validation of automation, packaging equipment, utilities, or facilities

  • Co-op or project experience in pharmaceutical or medical device environments

  • Exposure to FAT, SAT, IQ, OQ, quality systems, FDA requirements, or technical report writing

Compensation

The approximate pay range for this position is$75,000-$90,000. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities, as well as geographic location of the position.


 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group

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