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Computer Systems Validation Jobs in Atlanta, GA (NOW HIRING)

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

New

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

New

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

New

The role demands deep technical expertise across the full validation lifecycle - including URS development, FAT/SAT execution, and Computer System Validation (CSV) - as well as hands-on experience ...

Systems Administrator

Decatur, GA · On-site

$61K - $98K/yr

Supports development and implementation of new technology; researches and evaluates computer ... Must possess and maintain a valid Georgia driver's license.

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Computer Systems Validation information

See Atlanta, GA salary details

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$52

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How much do computer systems validation jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for computer systems validation in Atlanta, GA is $52.24, according to ZipRecruiter salary data. Most workers in this role earn between $40.24 and $61.97 per hour, depending on experience, location, and employer.

What is the work of computer system validation?

Computer Systems 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 helps maintain data integrity, quality, and regulatory compliance in industries like pharmaceuticals and healthcare.

What is the salary of a CSV engineer?

A Computer Systems Validation (CSV) engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Certifications in validation or quality assurance and proficiency with regulatory standards like FDA or GxP can influence compensation levels.

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

To thrive in Computer Systems Validation, you need a solid understanding of regulatory requirements (such as FDA or EMA guidelines), software development life cycles, and risk management, often supported by a degree in life sciences, IT, or engineering. Experience with validation frameworks, documentation tools, and systems like GAMP 5 and knowledge of 21 CFR Part 11 compliance are typically required. Attention to detail, strong analytical thinking, and effective communication set professionals apart in this role. These skills and qualifications ensure validated systems are compliant, reliable, and support organizational quality and regulatory objectives.

Is computer system validation a good field?

Computer Systems Validation (CSV) is a vital role in regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It involves skills in validation protocols, documentation, and understanding regulatory requirements such as FDA or EMA guidelines. The field offers steady employment opportunities, especially for professionals with certifications like GAMP or 21 CFR Part 11 knowledge.

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

AspectComputer Systems ValidationQuality Assurance Specialist
CertificationsGAMP, CSV-specific trainingISO 9001, Six Sigma
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, service sectors
Primary FocusEnsuring computer systems meet regulatory standardsEnsuring overall product/service quality
Common UsageValidation of software, hardware in complianceProcess audits, quality improvement

Computer Systems Validation and Quality Assurance Specialist roles overlap in ensuring compliance and quality. However, CSV focuses specifically on validating computer systems to meet regulatory standards, especially in pharma and biotech industries. Quality Assurance Specialists have a broader scope, overseeing overall quality processes across various sectors. Both roles require similar certifications and work environments but differ in their primary objectives and specific tasks.

What is computer systems validation?

Computer systems validation (CSV) is the process of ensuring that computer-based systems used in regulated industries, like pharmaceuticals and biotechnology, perform their intended functions consistently and reliably. This process involves documenting and testing systems to confirm they meet regulatory requirements, such as those set by the FDA. The goal is to ensure data integrity, product quality, and patient safety by minimizing the risk of system errors or failures. CSV typically includes activities like risk assessment, test planning, execution, and maintaining thorough records for audits.

What is the salary of SoC validation engineer?

The salary of a SoC validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Professionals in this role often have skills in hardware description languages and verification tools such as SystemVerilog and UVM.

What are some common challenges faced in a Computer Systems Validation (CSV) role, and how can they be addressed?

Professionals in Computer Systems Validation often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and coordinating with cross-functional teams. Staying updated through regular training and industry resources helps address compliance changes. Clear communication and collaboration with IT, Quality Assurance, and business stakeholders are essential for efficient validation processes. Utilizing validation lifecycle management tools and standardized templates can also streamline documentation and reduce errors.
What are popular job titles related to Computer Systems Validation jobs in Atlanta, GA? For Computer Systems Validation jobs in Atlanta, GA, the most frequently searched job titles are:
What cities near Atlanta, GA are hiring for Computer Systems Validation jobs? Cities near Atlanta, GA with the most Computer Systems Validation job openings:
Infographic showing various Computer Systems Validation job openings in Atlanta, GA as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $108,651 per year, or $52.2 per hour.

Computer Systems Validation (CSV) IT Engineer (IT Support Specialist)

corbion

Tucker, GA

$96K - $115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago


Job description

At Corbion, we exist to champion preservation in all its forms, preserving food and food production, health, and our planet.

The CSV IT Engineer is responsible for ensuring that computerized systems used in Corbion-regulated environments comply with applicable Good Manufacturing Practice (GMP) regulations, data integrity standards, and validation requirements. In this role, you will  support the validation lifecycle of GxP systems, including infrastructure, applications, cloud environments, manufacturing systems, laboratory systems, and quality systems.

You will be a part of the global Corbion IT organization as a full-time onsite position, based in Tucker, Georgia.  Works closely with Regional & Global IT, Quality Assurance (QA), Manufacturing, Engineering, Automation, and business stakeholders to ensure systems are implemented, maintained, and operated in compliance with FDA and other Corbion regulatory expectations.

This position is critical in maintaining validated states for computerized systems and ensuring compliance with regulations of: 21 CFR Part 11, GAMP 5, ALCOA+ Data Integrity principles, FDA GMP requirements, Corbion Service Management SLA and quality standards.

Key Responsibilities

  • Provide daily IT operations support, including end-user support, desktop deployments, service management activities, and general IT support across Company locations.
  • Lead and execute the full Computer System Validation (CSV) lifecycle for GxP-regulated computerized systems, ensuring systems remain in a validated state through implementation, operation, maintenance, periodic review, and retirement.
  • Develop, execute, and maintain validation documentation, including validation plans, risk assessments, traceability matrices, test protocols/scripts, validation summary reports, and validation records.
  • Validate and support regulated systems, including SCADA/HMI systems, historian platforms, laboratory systems (LIMS), cloud-based GxP applications, and related infrastructure.
  • Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, ALCOA+ Data Integrity principles, GMP requirements, and Company quality standards.
  • Perform risk assessments using GAMP 5 methodologies and evaluate system security, audit trails, electronic signatures, user access controls, and data integrity controls.
  • Manage validation impacts associated with system changes, including change controls, regression testing, requalification activities, deviations, CAPAs, and remediation efforts.
  • Coordinate validation activities and deliverables with vendors, third-party integrators, and internal stakeholders.
  • Support regulatory inspections, customer audits, and internal compliance reviews, including addressing audit findings and implementing corrective actions.
  • Support disaster recovery, backup validation, and business continuity testing to ensure compliance and operational readiness.
  • Partner with Quality Assurance, Manufacturing, Engineering, Automation, Infrastructure, Cybersecurity, and business teams to ensure compliant system implementation and operation.
  • Provide compliance and validation guidance during system implementations, upgrades, and enhancements.
  • Train end users on validated procedures, compliance requirements, and data integrity expectations.
  • Monitor GMP systems, backups, and data integrity controls while supporting ongoing system maintenance, upgrades, and continuous improvement initiatives.

Required Qualifications

  • Associate's degree in Computer Science, Engineering, Biotechnology, Pharmaceutical Sciences, Automation Engineering, or related discipline.
  • 5+ years in IT Infrastructure and pharmaceutical, biotechnology, medical device, or regulated healthcare environments.
  • Extensive experience and proven track record of CSV lifecycle management, GMP environments, and regulatory audits.
  • Technical Skills Validation & Compliance: GAMP 5, FDA 21 CFR Part 11, Annex 11, and Data Integrity principles
  • IT & Infrastructure experience: VMware, Veeam Backups and Replication, Microsoft End User Computing, Windows Server, Active Directory, SQL/Postgres databases, Cloud technologies, and Cisco LAN and Wireless proven skills.
  • Preferred Certifications: VMware VCP-DCV + VCP-VCF, Veeam Certified Engineer VMCE, Microsoft MCP, ITIL, Cisco LAN and WLAN technologies, and ISPE GAMP Certification.
  • Excellent technical writing and  detail-oriented mindset .
  • Analytical problem-solving.
  • Exceptional communication skills, 
  • Excellent time management and prioritization

Our offer 

The anticipated compensation range for this position is $96,000 to $115,000. The final pay offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and years of experience within the job, the type years of and experience within the industry, education, etc. Please note, Corbion is a multi-state employer and this pay scale may not reflect positions that work in other states or locations. In addition to the base compensation, we offer the following benefits*:

  • Bonus potential
  • Paid time off, including company holidays
  • 401K with company match
  • Medical, dental, vision and basic life insurance coverage are offered to employees and eligible dependents (provided they meet eligibility requirements)
  • Flexible spending accounts
  • Education assistance
  • Short- and long- term disability
  • Employee Assistance Program (EAP)
  • Lifestyle and wellness benefits

 

*Please note, this is intended to provide a general description of benefits and other compensation and is not a substitute for applicable plan documents or company policies. Eligibility requirements for these benefits will be controlled by applicable plan documents.

About Corbion

Corbion is a sustainable ingredients company dedicated to preserving what matters, including food and food production, health, and the planet. We specialize in lactic acid, lactic acid derivatives, food preservation solutions, functional blends, and algae ingredients, using our deep application and product knowledge to propel nature’s ingenuity through science. With more than a century of experience, we continue working side-by-side with our customers to make our cutting-edge technologies work for them. Leveraging our advanced capabilities in fermentation and preservation technology, we help customers differentiate their products in diverse markets ranging from food and animal nutrition to home & personal care, pharmaceuticals, electronics, medical devices, and bioplastics. In 2025, Corbion generated annual sales of € 1,267.4 million with a workforce of 2,408 FTEs. Corbion is listed on Euronext Amsterdam. For more information:  www.corbion.com

Corbion is an equal opportunity employer and committed to a diverse workplace.  All applicants will be considered equally without regard to race, color, ethnicity, veteran status, religion, national origin, marital status, political affiliation, age, sex, sexual orientation, handicapping condition, membership in an organization or any other non-merit factors.

Corbion provides reasonable accommodation to applicants.

EOE/M/F/Vet/Disabled

Corbion does not accept unsolicited resumes from individual recruiters or third party recruiting agencies in response to job postings. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers. All candidates must be submitted by approved Corbion vendors who have been expressly requested to make a submission by our Talent Acquisition team for a specific job opening. No placement fees will be paid to any firm unless such a request has been made by the Corbion Talent Acquisition team and such candidate was submitted to the Corbion Talent Acquisition Team.