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Computer System Validation Csv Jobs in Illinois (NOW HIRING)

Required * 7+ years of experience in Software Quality Assurance and Computer System Validation within regulated environments. * Hands-on experience authoring and executing SDLC validation ...

Required * 7+ years of experience in Software Quality Assurance and Computer System Validation within regulated environments. * Hands-on experience authoring and executing SDLC validation ...

Application Administrator

Chicago, IL · On-site

$90 - $120/hr

Contribute and support computer system validation projects, including application change control as required by GxP, Southern Research policies and procedures. * Draft CSV documentation as needed ...

Jr QA Tester

Sibley, IL · On-site

$55K - $58K/yr

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title ...

Jr QA Tester

Sibley, IL · On-site

$55K - $58K/yr

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title ...

JR QA TESTER

Evanston, IL · On-site

$55K - $58K/yr

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title ...

JR QA TESTER

Evanston, IL · On-site

$55K - $58K/yr

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. RELOCATION IS A MUST AND 4 WEEKS MANDATORY IN-PERSON TRAINING IN RESTON, VA Title ...

Ensure systems follow a compliant CSV / CSA (Computer Software Assurance) approach based on system risk and intended use. * Review and approve validation deliverables, including URS, risk assessments ...

Ensure systems follow a compliant CSV / CSA (Computer Software Assurance) approach based on system risk and intended use. * Review and approve validation deliverables, including URS, risk assessments ...

Responsibilities: - Develop and maintain MPCS system validation plans aligned with program gateway ... Electrical Engineering, Computer Engineering, Systems Engineering, Mechanical Engineering, or ...

Responsible for managing the development and the execution of qualifications, validations, re-qualifications and re-validations for process and laboratory equipment, computer systems, utilities ...

Bachelor's degree in Electrical Engineering, Computer Engineering, Systems Engineering, or a related field. * 3-4 years of experience in systems engineering and validation, preferably in the ...

Responsible for managing the development and the execution of qualifications, validations, re-qualifications and re-validations for process and laboratory equipment, computer systems, utilities ...

Bachelor's degree in Electrical Engineering, Computer Engineering, Systems Engineering, or a related field. * 3-4 years of experience in systems engineering and validation, preferably in the ...

Showing results 41-60

Computer System Validation Csv information

See Illinois salary details

$28

$50

$73

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

As of Sep 7, 2026, the average hourly pay for computer system validation csv in Illinois is $50.20, according to ZipRecruiter salary data. Most workers in this role earn between $37.74 and $62.40 per hour, depending on experience, location, and employer.

What is a computer system validation CSV?

A Computer System Validation (CSV) job involves ensuring that computerized systems used in regulated industries, such as pharmaceuticals and medical devices, comply with industry standards and regulatory requirements (e.g., FDA 21 CFR Part 11, GxP). CSV professionals develop validation protocols, conduct testing, and document system performance to ensure data integrity, reliability, and compliance. Their role is critical in maintaining system quality and avoiding regulatory risks.

What are the key skills and qualifications needed to thrive in computer system validation CSV?

To thrive as a Computer System Validation (CSV) professional, you need a solid understanding of computer science, regulatory compliance (such as FDA 21 CFR Part 11), and validation methodology, often supported by a degree in a scientific or technical field. Familiarity with documentation tools, validation protocols, and quality management systems, as well as certifications like PMP or Six Sigma, is highly beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills enable effective cross-functional collaboration. Mastering these skills ensures accurate validation processes, regulatory compliance, and smooth project execution in highly regulated environments.

What are some typical challenges faced by computer system validation CSV professionals and how are they addressed?

Computer System Validation (CSV) professionals often encounter challenges such as keeping up with evolving regulations, managing complex documentation requirements, and ensuring robust communication between IT, quality assurance, and business teams. Navigating system upgrades while maintaining compliance with strict regulatory standards requires careful planning and thorough risk assessment. Successful candidates address these challenges by staying current with industry guidance, utilizing validation templates and checklists, and fostering strong teamwork across various departments. Building collaborative relationships and maintaining meticulous records help ensure both audit readiness and smooth project completion.

Is computer system validation a good field?

Computer System Validation (CSV) is a specialized field within regulated industries like pharmaceuticals and biotech, focusing on ensuring software and systems meet compliance standards such as GxP. It offers opportunities for professionals with skills in quality assurance, validation protocols, and regulatory requirements, often requiring certifications like GAMP or 21 CFR Part 11 knowledge. The field provides stable employment with growth potential, especially as compliance regulations become more stringent.

What are the most commonly searched types of Computer System Validation Csv jobs in Illinois?

The most popular types of Computer System Validation Csv jobs in Illinois are:

What are popular job titles related to Computer System Validation Csv jobs in Illinois?

For Computer System Validation Csv jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Csv jobs in Illinois look for?

The top searched job categories for Computer System Validation Csv jobs in Illinois are:

Infographic showing various Computer System Validation Csv job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $104,410 per year, or $50.2 per hour.

Senior SQA Engineer

3B Staffing LLC

Chicago, IL • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Skill Matrix :

  • 7+ years of SDLC experience in the Pharmaceutical and Medical Device industries.
  • 7+ years of Software Quality Assurance and Computer System Validation experience.
  • Hands on experience in validation plans, FMEA, requirements, IQ/OQ/PQ, traceability matrices, system releases.
  • Experience reviewing and approving validation documentation, CAPAs, change controls, and defect management processes.
  • Strong knowledge of GxP regulations, validation principles, risk management methodologies.
  • Experience with automated testing tools and platforms (JIRA, Confluence, HP ALM, Tosca, QTest, M-Files or similar systems).
  • Experience with AWS, Databricks, GitHub, or CI/CD tools is preferred.

Required

  • 7+ years of experience in Software Quality Assurance and Computer System Validation within regulated environments.
  • Hands-on experience authoring and executing SDLC validation deliverables (e.g., validation plans, FMEA, requirements, IQ/OQ/PQ, traceability matrices, system releases).
  • Strong knowledge of GxP regulations, validation principles, risk management methodologies, and industry best practices.
  • Demonstrated experience reviewing and approving validation documentation, CAPAs, change controls, and defect management processes.
  • Familiarity with both Waterfall and Agile software development methodologies.
  • Experience with automated testing tools and platforms.
  • Proficiency with tools such as JIRA, Confluence, HP ALM, Tosca, QTest, M-Files, or similar systems (experience with AWS, Databricks, GitHub, or CI/CD tools is a plus).
  • Strong communication and interpersonal skills with the ability to effectively influence stakeholders, provide regulatory guidance, and operate independently in a cross-functional environment.

Responsibilities:

  • Lead and execute software validation activities across the SDLC, including development, review, and approval of deliverables such as validation plans, FMEA/risk assessments, requirements, IQ/OQ/PQ, traceability matrices, and system releases.
  • Perform independent SQA review and approval of SDLC documentation to ensure compliance with GxP regulations, internal procedures, and industry standards.
  • Ensure all IT validation packages are inspection-ready and maintain a continuous state of audit compliance.
  • Collaborate cross-functionally with IT, development teams, and business SMEs to support validation efforts and ensure alignment with business and regulatory requirements.
  • Review and provide quality oversight for CAPAs, change controls, and software defects, ensuring appropriate validation impact assessment and resolution.
  • Contribute to validation strategy development and continuous improvement initiatives for regulated IT systems and processes.
  • Support implementation and validation of automated testing frameworks and tools to enhance efficiency and quality of software validation activities.