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Computer System Validation Engineer Jobs in Georgia

You will ensure that manufacturing systems, equipment and processes are designed and delivered in ... Engineering, QA, or Manufacturing roles. * Hands-on experience during facility start-up ...

Lead Design Engineer

Duluth, GA ยท On-site

$94K - $124K/yr

Actively participate in system validation efforts, including preparation and execution of URS, FRS ... Bachelor's or Master's degree in Instrumentation & Control, Electronics, Computer Engineering , or ...

... programming languages such as Java, C, C# - Experience or exposure to systems administration - Must have legal authorization to work in the US. We do NOT sponsor any visas. - 4 year degree in ...

Software Engineer 1

Norcross, GA ยท On-site

$90 - $120/hr

Bachelor's degree in Electrical Engineering, Computer Engineering, Computer Science, or a related ... Proficiency in using oscilloscopes, logic analyzers, and diagnostic tools for system validation and ...

Showing results 41-60

Computer System Validation Engineer information

See Georgia salary details

$24

$43

$63

How much do computer system validation engineer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for computer system validation engineer in Georgia is $43.74, according to ZipRecruiter salary data. Most workers in this role earn between $32.88 and $54.38 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a computer system validation engineer?

To thrive as a Computer System Validation Engineer, you need a solid background in computer science or engineering, knowledge of regulatory requirements (such as FDA or GxP), and experience in validation processes. Familiarity with validation tools, quality management systems, and documentation software is typically required, along with certifications like ISPE or ASQ being beneficial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for coordinating teams and ensuring compliance. These skills and qualities are crucial to ensure that computer systems meet regulatory standards, maintain data integrity, and support business operations in regulated industries.

What are some common challenges faced by computer system validation engineers in regulated industries?

Computer System Validation Engineers often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and ensuring timely validation while coordinating with cross-functional teams. Balancing strict compliance with project deadlines can be demanding, especially when systems are complex or legacy infrastructure is involved. Additionally, effective communication with IT, QA, and business stakeholders is essential to address issues quickly and maintain validation standards.

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

AspectComputer System Validation EngineerQuality Assurance Specialist
CertificationsGAMP, GxP validation certificationsISO, Six Sigma, GMP certifications
Work EnvironmentPharmaceutical, biotech, medical device industriesManufacturing, software, healthcare sectors
Primary FocusValidating computer systems and software complianceEnsuring overall quality and process improvements

The Computer System Validation Engineer primarily focuses on validating computer systems to meet regulatory standards, ensuring software compliance in regulated industries. In contrast, the Quality Assurance Specialist oversees broader quality processes, including audits and process improvements. Both roles require knowledge of industry regulations but differ in scope and specific responsibilities.

Are computer system validation engineers in demand?

Computer System Validation Engineers are in demand due to the increasing regulation of pharmaceutical, biotech, and medical device industries that require compliant validation of computer systems. They often need skills in validation protocols, GxP regulations, and validation tools, making their expertise valuable in ensuring quality and compliance in regulated environments.

Do computer system validation engineers make good money?

Computer System Validation Engineers typically earn competitive salaries that vary by experience, location, and industry. They often have specialized skills in validation protocols, regulatory compliance, and validation tools, which can contribute to higher earning potential. Certification and experience in regulated environments like pharmaceuticals or biotech can also impact salary levels.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital field in regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It involves skills in validation protocols, documentation, and tools like GxP regulations and audit readiness, making it a stable and in-demand career path for those with technical and regulatory knowledge.

What does a computer system validation engineer do?

A computer system validation engineer ensures that computer systems used in regulated industries, such as pharmaceuticals or biotech, meet required standards for quality and compliance. They develop validation protocols, perform testing, document results, and ensure systems function correctly and securely, often using tools like GxP guidelines and validation software. Their work helps ensure data integrity and regulatory compliance throughout the system lifecycle.

What are popular job titles related to Computer System Validation Engineer jobs in Georgia?

For Computer System Validation Engineer jobs in Georgia, the most frequently searched job titles are:

What cities in Georgia are hiring for Computer System Validation Engineer jobs?

Cities in Georgia with the most Computer System Validation Engineer job openings:

Infographic showing various Computer System Validation Engineer job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,980 per year, or $43.7 per hour.

Qualification and Validation Lead (US)

UCB

Atlanta, GA โ€ข On-site

$148K - $194K/yr

Full-time

Re-posted 28 days ago


Job description

Make your mark for patients

UCB is embarking on one of the most significant investments in its history through the development of a new state-of-the-art biologics manufacturing campus in Georgia, USA.

Designed to power the future of biologics, this new facility will strengthen UCB's global manufacturing network, expand supply capabilities for future medicines, and support our long-term ambition of bringing innovative treatments to patients around the world. The project combines cutting-edge technology, sustainability, digital innovation, and operational excellence to create a future-ready manufacturing ecosystem.

As a true greenfield initiative, it offers a unique opportunity to help design, build, and launch a world-class biologics manufacturing facility from the ground up while working within a diverse international team spanning the United States and Europe.

We are looking for talented, curious and ambitious individuals who want to make a lasting impact and contribute to shaping the future of biologics manufacturing at UCB.

We are looking for a Qualification and Validation Lead who is collaborative, rigorous and proactive to join us in our Internal Manufacturing team. This position is based in Atlanta, Georgia and requires domestic & international travel.

About the role

This role is contributing to the design and delivery of a future-ready biologics manufacturing facility. You will ensure that manufacturing systems, equipment and processes are designed and delivered in compliance with regulatory and quality requirements. You will contribute to building a compliant and inspection-ready facility by integrating validation principles throughout the project lifecycle in a rapidly evolving project environment.

Who you'll work with

You will be working in a team that collaborates with manufacturing sites, quality experts and project stakeholders. The team focuses on ensuring compliance, alignment with regulatory expectations and readiness for inspections working across different time zones.

What you'll do

  • Develop, implement, and lead the overall Qualification and Validation strategy for the entire site, while ensuring its successful execution and ongoing compliance across all operations.
  • Define and represent qualification and validation requirements across the project.
  • Ensure compliance with regulatory and quality standards throughout design and delivery.
  • Review and assess technical documentation related to validation activities.
  • Contribute to inspection readiness and support audit and regulatory interactions.
  • Translate operational and regulatory expectations into project requirements.
  • Promote strong quality and compliance culture across stakeholders.

Interested? For this role we're looking for the following education, experience and skills

Mandatory requirements
  • Minimum 10 years of experience in qualification and validation activities within regulated environments (biopharma, pharmaceutical or similar), gained from Engineering, QA, or Manufacturing roles.
  • Hands-on experience during facility start-up / commissioning phases, with strong exposure to the transition from project delivery to routine manufacturing operations.
  • Experience in greenfield or brownfield projects.
  • Experience in biotech is mandatory.
  • In-depth knowledge of quality systems (GxP), including qualification and validation lifecycle (URS, risk assessments, IQ/OQ/PQ).
  • Demonstrated ability to autonomously author and review qualification and validation documentation (protocols, reports, strategies).
  • Minimum 5 years of experience in technology transfer and/or analytical method transfer within industrial manufacturing environments.
  • Strong understanding of manufacturing processes, with the ability to assess operational readiness and support ramp-up activities.
Strong plus
  • Background in production/manufacturing environments, with a solid understanding of shopfloor realities and constraints.
  • Experience working in multi-product facilities, with an understanding of associated challenges.

The reasonably anticipated salary range for this position is $148,000-194,300 per year.The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer.All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.


Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Employment Type: OTHER