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Computer System Validation Jobs in Frisco, TX (NOW HIRING)

Ankura

Model Validation Director

Dallas, TX · On-site +1

The Model Validation Director is expected to lead and execute model validation testing processes on ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

Texas Instruments

Validation Engineer NCG

Dallas, TX · On-site

As a validation engineer, you play a vital role in assuring the quality and performance of TI ... Ability to quickly ramp on new systems and processes * Demonstrated strong interpersonal ...

Texas Instruments

Validation Engineer NCG

Dallas, TX · On-site

As a validation engineer, you play a vital role in assuring the quality and performance of TI ... Ability to quickly ramp on new systems and processes * Demonstrated strong interpersonal ...

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Computer System Validation information

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How much do computer system validation jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for computer system validation in Frisco, TX is $50.84, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $60.29 per hour, depending on experience, location, and employer.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What is the salary of computer system validation?

The salary for a Computer System Validation specialist typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Certifications such as GAMP or CSV training can influence earning potential, and roles often require knowledge of regulatory standards like FDA or ISO.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What is the work of computer system validation?

Computer System Validation (CSV) is the process of ensuring that computer systems used in regulated environments function correctly and comply with industry standards. It involves documenting and testing software, hardware, and related processes to verify they meet specified requirements, often using validation protocols and tools. CSV is essential in industries like pharmaceuticals and healthcare to ensure data integrity and compliance with regulations such as FDA or GMP.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It often requires knowledge of regulatory guidelines, validation protocols, and tools like GxP and 21 CFR Part 11. The field offers steady demand, opportunities for certification, and roles in quality assurance and compliance management.

Is CSV a skill?

In the context of Computer System Validation, CSV refers to Computer System Validation itself, which is a process rather than a skill. However, skills related to CSV include understanding validation protocols, regulatory requirements, and proficiency with validation tools and documentation. These skills are essential for professionals performing CSV tasks in regulated industries like pharmaceuticals and biotech.
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Computer System Validation jobs near you
Validation Engineer

Validation Engineer

Paper Converting Machine

Fort Worth, TX • On-site

Full-time

Posted 22 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:

Validation Engineer (Design Group)

Who You'll Work With

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class engineer and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.

When you join Design Group as a Validation Engineer, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world's leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.

What You'll Do

You'll work individually and in teams to support capital projects, remediation efforts, and change management for our clients. You will assist in the development of new programs, best practices, and program implementation for some of industry's biggest names and many technology-driven companies entering into commercial manufacturing.

  • Deliver Commissioning and Qualification (C&Q) solutions and services for client facility, utility, process, and equipment
  • Develop and execute a variety of validation and FDA compliance related documents/protocols
  • Author specifications, assessments, and test protocols across a diverse Life Science market comprised of Pharmaceuticals, Biotechnology, Cell & Gene Therapy, and Medical Device clients
  • Assist in the development and implementation of Quality Management System (QMS) procedures, in harmony with regulatory standards such as ICH Q1, CFR 21 Part 210 and 211, CFR 21 Part 820, ICH Q8, ICH Q9, and ICH Q10, and 21 CFR Part 11.
  • Collaborate with teams to perform investigations, diagnose problems, and troubleshoot validation issues
  • Prepare written validation reports with high level of detail and organization
  • Communicate with project stakeholders the progress relative to plan
  • Manage project deliverables to agreed schedule and scope
  • Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team.

What You'll Bring

  • A passion for a career in the Life Science industry
  • Excellent communication and interpersonal skills and ability to interact with all levels of management, clients, and vendors A passion for a career in the Life Science industry
  • Excellent communication and interpersonal skills and ability to interact with all levels of management, clients, and vendors
  • Bachelor's degree in Bioengineering, Biomedical Engineering, Chemical Engineering, or similar technical degree preferred.
  • Project experience in a cGMP manufacturing environment such as pharmaceutical, biotech, or medical device facility
  • Project Experience with authoring and executing validation protocols of automation/computerized systems, QC Laboratory equipment, packaging systems, and/or utilities and facilities is desired
  • Proficient computer skills (Microsoft Office, Microsoft Project, & AutoCAD)
  • Proficient with written and verbal technical communication including generating reports and conducting group presentations.
  • Willing and able to travel as necessary for project requirements to include but not be limited to: project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.

Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.


 

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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