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Validation Jobs in Georgia (NOW HIRING)

Senior System Validation Engineer

Johns Creek, GA · Hybrid

$96K - $132K/yr

Senior System Validation Engineer This exciting role will be responsible for validating high-speed memory buffer semiconductor products, developing automation scripts, and ensuring system compliance ...

Architecting scalable hardware validation frameworks and establishing a dedicated testing lab requires deep technical execution across low-level Linux, embedded electronics, and cloud interfaces. You ...

DRG Clinical Validation Lead DRG Clinical Validation Lead Anticipated End Date: 8/28/2026 Virtual: This role enables associates to work virtually full-time, with the exception of required in-person ...

Responsibilities - Leading data validation and risk management initiatives to support client objectives - Utilizing advanced analytics techniques to extract insights from complex datasets ...

Security Officer Identity Validation Allied Universal ® , North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working ...

DRG Clinical Validation Lead Anticipated End Date: 8/28/2026 Virtual: This role enables associates to work virtually full-time, with the exception of required in-person training sessions, providing ...

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Director & Summary The Opportunity As a Data Validation Risk Director, within our Risk & Regulatory practice, you will ...

Showing results 41-60

Validation information

See Georgia salary details

$19

$43

$65

How much do validation jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for validation in Georgia is $43.90, according to ZipRecruiter salary data. Most workers in this role earn between $33.27 and $53.37 per hour, depending on experience, location, and employer.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Georgia? The most popular types of Validation jobs in Georgia are:
What cities in Georgia are hiring for Validation jobs? Cities in Georgia with the most Validation job openings:
Infographic showing various Validation job openings in Georgia as of August 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $91,322 per year, or $43.9 per hour.

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

Corbion

Tucker, GA • On-site

$96K - $115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 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.