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Computer Validation Jobs in Texas (NOW HIRING)

SoC Validation Engineer

Austin, TX

$171.60K - $302.20K/yr

Computer architectures (cache, memory hierarchy, data pipelines) and logic design. Experience with ... validation software engineering or related field Pay & Benefits At Apple, base pay is one part of ...

SoC Validation Engineer

Austin, TX

$171.60K - $302.20K/yr

Computer architectures (cache, memory hierarchy, data pipelines) and logic design. Experience with ... validation software engineering or related field Pay & Benefits At Apple, base pay is one part of ...

SoC Validation Engineer

Austin, TX

$171.60K - $302.20K/yr

Computer architectures (cache, memory hierarchy, data pipelines) and logic design. Experience with ... validation software engineering or related field Pay & Benefits At Apple, base pay is one part of ...

SoC Validation Engineer

Austin, TX

$147.40K - $272.10K/yr

Computer architectures (cache, memory hierarchy, data pipelines) and logic design. Experience with ... validation software engineering or related field Pay & Benefits At Apple, base pay is one part of ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsExperience with assembly programming (ARM ISA is a plus)Knowledge of ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsExperience with assembly programming (ARM ISA is a plus)Knowledge of ...

You will be part of a team responsible for the functional validation of our CPUs, with the aim of ... Computer Engineering Understanding of CPU architecture including instruction sets, pipelines ...

You will be part of a team responsible for the functional validation of our CPUs, with the aim of ... Computer Engineering Understanding of CPU architecture including instruction sets, pipelines ...

You will be part of a team responsible for the functional validation of our CPUs, with the aim of ... Computer Engineering Understanding of CPU architecture including instruction sets, pipelines ...

You will be part of a team responsible for the functional validation of our CPUs, with the aim of ... Computer Engineering Understanding of CPU architecture including instruction sets, pipelines ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsExperience with assembly programming (ARM ISA is a plus)Knowledge of ...

You will be part of a team responsible for the functional validation of our CPUs, with the aim of ... Computer Engineering Understanding of CPU architecture including instruction sets, pipelines ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsUnderstanding of low-level software, firmware and device driversExperience ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsUnderstanding of low-level software, firmware and device driversExperience ...

... Computer EngineeringUnderstanding of CPU architecture including instruction sets, pipelines, caches, and memory subsystemsExperience with assembly programming (ARM ISA is a plus)Knowledge of ...

Bachelor's degree in electrical/computer engineering or computer science and 6+ years of experience ... Emulation * Chip logical validation concepts and methodologies Job Type:Experienced Hire Shift:

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Computer Validation information

See Texas salary details

$9

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How much do computer validation jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for computer validation in Texas is $50.61, according to ZipRecruiter salary data. Most workers in this role earn between $38.99 and $60.00 per hour, depending on experience, location, and employer.

What is the difference between Computer Validation vs Quality Assurance Specialist?

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

What cities in Texas are hiring for Computer Validation jobs? Cities in Texas with the most Computer Validation job openings:
Infographic showing various Computer Validation job openings in Texas as of May 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $105,261 per year, or $50.6 per hour.

Head of QA Operations - Cell Therapy

Lonza

Houston, TX

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago


Lonza rating

8.1

Company rating: 8.1 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

33rd of 71 rated pharmaceutical


Job description

Head of Quality Assurance Ops - Cell Therapy

Location: This is an on-site position located in Pearland, TX

The purpose of this role is to oversee all aspects of quality assurance operations for the Lonza Houston cell therapy asset, ensuring that the quality systems and controls meet Lonza global standards and regulatory requirements.

What you will get:

A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus.

  • Medical, dental and vision insurance.

  • 401(k) matching plan.

  • Life insurance, as well as short-term and long-term disability insurance.

  • Employee assistance programs.

  • Paid time off (PTO).

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.

What you will do:

  • Develops and implements the overall quality strategy for the facility.

  • Manages QA Ops budget and resources to maximize efficiency and maintain quality/compliance at high levels.

  • Develops, directs, and maintains quality systems in support of CT manufacturing in a manner consistent with global quality systems, Lonza Corporate requirements and standards and current regulatory requirements, (primarily US FDA and European requirements) and others as needed.

  • Interfaces with site QA functions to support or develop appropriateinterfaces with the site-based QA systems.

  • Develop working relationships with other site functions for support of equipment, facility, utility, cleaning services and computer
    validation/qualification.

  • Oversees all aspects of QA operations within the facility, including but not limited to executed batch record review, on the floor QA support, deviation investigations, change controls, Quality Agreements, and SOP and master batch record review.

  • For significant issues, interfaces with customers and internal groups for resolution of quality issues. Develops good working relationships with clients and ensures appropriate and timely responses to client inquiries.

  • Has decision-making authority for any Quality issues; informs Site Quality Head of critical issues in a timely manner.

  • Builds and maintains expertise in the QA Ops teams, including
    development of staff.

  • Applies aseptic manufacturing experience, including aseptic process validation, to ensure that CT/GT operations meet customer and regulatory expectations and requirements for aseptic manufacturing at all phases of product development.

What we are looking for:

  • 10+ years' experience Biopharmaceutical manufacturing experience and/or quality operations or quality systems working in a GMP environment.

  • 5+ years' management of Quality Assurance staff.

  • 5+ years' aseptic processing experience.

  • Experience with regulations (US, EU and other).

About Lonza:

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.


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