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Validation Engineer Biomedical Jobs in Denton, TX

Agiliti

Biomedical Technician

Dallas, TX · On-site

$25 - $33.25/hr

An associate degree in electronics, mechanical engineering, or biomedical equipment technology ... Must hold a current, valid, and unrestricted driver's license. Must have a safe driving record ...

Stryker

Quality Engineering Intern

Flower Mound, TX · On-site

$35/hr

... validation including customer interaction. As Homer Stryker pointed out, "Ifyour toolsdon'twork ... Majors Targeted: Systems Engineer, Biomedical Eng, Software Eng, Electrical / Hardware Eng ...

Stryker

Quality Engineering Intern

Flower Mound, TX · On-site

$15 - $19.50/hr

... validation including customer interaction. As Homer Stryker pointed out, "If your tools don't work ... Majors Targeted: Systems Engineer, Biomedical Eng, Software Eng, Electrical / Hardware Eng ...

Stryker

Quality Engineering Intern

Flower Mound, TX · On-site

$15.25 - $20/hr

... validation including customer interaction. As Homer Stryker pointed out, "If your tools don't work ... Majors Targeted: Systems Engineer, Biomedical Eng, Software Eng, Electrical / Hardware Eng ...

Stryker

Quality Engineering Intern

Flower Mound, TX

$15 - $19.50/hr

... validation including customer interaction. As Homer Stryker pointed out, "If your tools don't work ... Majors Targeted: Systems Engineer, Biomedical Eng, Software Eng, Electrical / Hardware Eng ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

$75K - $90K/yr

Execute on the design, development, verification, and validation of new products, ensuring ... S. degree in Mechanical Engineering, Biomedical Engineering, or related field. * Minimum 5 years of ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site +1

$75K - $90K/yr

Execute on the design, development, verification, and validation of new products, ensuring ... S. degree in Mechanical Engineering, Biomedical Engineering, or related field. * Minimum 5 years of ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

Execute on the design, development, verification, and validation of new products, ensuring ... S. degree in Mechanical Engineering, Biomedical Engineering, or related field. * Minimum 5 years of ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

Execute on the design, development, verification, and validation of new products, ensuring ... S. degree in Mechanical Engineering, Biomedical Engineering, or related field. * Minimum 5 years of ...

Wolters Kluwer

Forward Deployed Engineer

Coppell, TX · Remote

Build, Integrate, and Validate * Design, code, integrate, test, and deploy prototypes and product ... Bachelor's degree in computer science, Software Engineering, Biomedical Informatics, Data Science ...

Wolters Kluwer

Forward Deployed Engineer

Coppell, TX · Remote

Build, Integrate, and Validate * Design, code, integrate, test, and deploy prototypes and product ... Bachelor's degree in computer science, Software Engineering, Biomedical Informatics, Data Science ...

Wolters Kluwer

Forward Deployed Engineer

Coppell, TX · Remote

Build, Integrate, and Validate * Design, code, integrate, test, and deploy prototypes and product ... Bachelor's degree in computer science, Software Engineering, Biomedical Informatics, Data Science ...

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All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Denton, TX

Validation Engineer Biomedical information

See Denton, TX salary details

$21

$48

$73

How much do validation engineer biomedical jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for validation engineer biomedical in Denton, TX is $48.75, according to ZipRecruiter salary data. Most workers in this role earn between $36.97 and $59.28 per hour, depending on experience, location, and employer.

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Denton, TX?

For Validation Engineer Biomedical jobs in Denton, TX, the most frequently searched job titles are:

What job categories do people searching Validation Engineer Biomedical jobs in Denton, TX look for?

The top searched job categories for Validation Engineer Biomedical jobs in Denton, TX are:

What cities near Denton, TX are hiring for Validation Engineer Biomedical jobs?

Cities near Denton, TX with the most Validation Engineer Biomedical job openings:

Validation Engineer Biomedical jobs near you
Infographic showing various Validation Engineer Biomedical job openings in Denton, TX as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 80% In-person, and 20% Hybrid job distribution, with an average salary of $101,405 per year, or $48.8 per hour.

Entry Level Validation Engineer

Barry-Wehmiller

Fort Worth, TX • On-site

$75K - $90K/yr

Full-time

Posted 6 days ago

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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