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Computer System Validation Jobs in New York (NOW HIRING)

ClifyX

Computer system Validation Tester

Somerset, NJ · On-site

ClifyX is seeking a Computer System Validation Tester to ensure compliance with industry standards in computerized systems validation. The role involves performing risk assessments, drafting ...

CYNET SYSTEMS

Validation Lead

Raritan, NJ · On-site

$50 - $55/hr

Strong Computer System Validation (CSV) expertise, especially within acquisition, divestiture, and separation contexts. * Experience in writing and executing documentation for all aspects of ...

Deloitte

System Test and Validation Lead

Jericho, NY · On-site +1

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 ...

Deloitte

System Test and Validation Lead

Stamford, CT · On-site +1

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 ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

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 ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

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 ...

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Computer System Validation information

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How much do computer system validation jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for computer system validation in New York is $59.43, according to ZipRecruiter salary data. Most workers in this role earn between $45.77 and $70.48 per hour, depending on experience, location, and employer.

What is a computer system validation?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What are the key skills and qualifications needed to thrive in computer system validation, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What are some typical challenges faced in computer system validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are the most commonly searched types of Computer System Validation jobs in New York?

The most popular types of Computer System Validation jobs in New York are:

What are popular job titles related to Computer System Validation jobs in New York?

For Computer System Validation jobs in New York, the most frequently searched job titles are:

What job categories do people searching Computer System Validation jobs in New York look for?

The top searched job categories for Computer System Validation jobs in New York are:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in New York 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, 2% Hybrid, and 7% Remote job distribution, with an average salary of $123,607 per year, or $59.4 per hour.

Computer system Validation Tester

ClifyX

Somerset, NJ • On-site

Full-time

Re-posted 16 days ago

Job description

Job Summary:
ClifyX is seeking a Computer System Validation Tester to ensure compliance with industry standards in computerized systems validation. The role involves performing risk assessments, drafting necessary documentation, and providing training related to validation processes.
Responsibilities:
• Ensure compliance to industry standards like GAMP5, FDA 21 CFR Part 11 on electronic records, electronic signatures etc.
• Define Risk based strategies for validation of computerized systems and author/review end-to-end Computerized Systems Validation documentation in accordance with Computerized Systems Validation Master Plan
• Perform system risk assessments, systems gap analysis, review and approve action plans to ensure compliance during and after the system validation
• Draft SOPs, writing scripts for IQ, OQ, PQ and handling CSV
• Help, guide and direct the project manager during the system implementation and validation process, and ensure compliance with corporate policies and procedures.
• Provide training related to computerized systems validation, quality and compliance to users and appropriate personnel
• Experience in Internal Audit, External Audit. Face regulatory, customer, IT Quality System related inspections for all computerized systems
• Responsible for review & verification of Corrective Action Plan for audits
• Perform periodic review/monitoring of computer systems implemented
• Proven experience in developing Master Validation Plan, validation scripts, Validation reports, all documentations required during CSV Implementation Process
Qualifications:
Required:
• Computer System Validation
• Life cycle
• Process Validation
• Risk Assessment
• FDA standards
• Test Planning
• Corrective Action Plan
• 8+ years of experience in CSV Implementation with MES/ SCADA experience
• Ensure compliance to industry standards like GAMP5, FDA 21 CFR Part 11 on electronic records, electronic signatures etc.
• Define Risk based strategies for validation of computerized systems and author/review end-to-end Computerized Systems Validation documentation in accordance with Computerized Systems Validation Master Plan
• Perform system risk assessments, systems gap analysis, review and approve action plans to ensure compliance during and after the system validation
• Draft SOPs, writing scripts for IQ, OQ, PQ and handling CSV
• Help, guide and direct the project manager during the system implementation and validation process, and ensure compliance with corporate policies and procedures.
• Provide training related to computerized systems validation, quality and compliance to users and appropriate personnel
• Experience in Internal Audit, External Audit. Face regulatory, customer, IT Quality System related inspections for all computerized systems
• Responsible for review & verification of Corrective Action Plan for audits
• Perform periodic review/monitoring of computer systems implemented
• Proven experience in developing Master Validation Plan, validation scripts, Validation reports, all documentations required during CSV Implementation Process
Preferred:
• Project Management skills and Team handling
Company:
ClifyX provides innovative business solutions which satisfy requirements for mission-critical reliability, scalability, interoperations. Founded in 1998, the company is headquartered in South Plainfield, USA, with a team of 501-1000 employees. The company is currently Late Stage.
ClifyX logo

About ClifyX

Sourced by ZipRecruiter

ClifyX is a well-established player in the IT Services sector that specializes in providing result-oriented technological solutions to a wide range of industrial verticals. Based in South Plainfield, New Jersey, ClifyX offers a comprehensive selection of IT services that include project staffing, application development, professional consulting, and other IT-based solutions. While the company's website, clifyx.com, does not divulge the exact founding date, it is clear that ClifyX has grown into a renowned name within their domain, thanks to their unwavering commitment to innovative practices. The company's mission statement revolves around harnessing the power of technology to assist their clientele in steering their respective businesses towards success.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

Year founded

1998

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