CSV Engineer
Somerset, NJ · On-site
Required : • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline • 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences ...
CSV Engineer
Somerset, NJ · On-site
Required : • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline • 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences ...
(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
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(Sr.) Validation Engineer
$80K - $120K/yr
Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.
Candidates with a strong understanding of computer system validation, quality management systems, and FDA regulations are encouraged to apply. On-site Contract Pay rate: DoE Primary Responsibilities:
Quick apply
Candidates with a strong understanding of computer system validation, quality management systems, and FDA regulations are encouraged to apply. On-site Contract Pay rate: DoE Primary Responsibilities:
CSV Consultant
Raritan, NJ · On-site
$48 - $53/hr
Pay Range: $48hr - $53hr Requirement/Must Have: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and ...
New
CSV Consultant
Raritan, NJ · On-site
$48 - $53/hr
Pay Range: $48hr - $53hr Requirement/Must Have: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and ...
New
Lab Computing Support Specialist
Rahway, NJ · On-site
$90K - $109K/yr
Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements. * Coordinate with vendors for system ...
Lab Computing Support Specialist
Rahway, NJ · On-site
$90K - $109K/yr
Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements. * Coordinate with vendors for system ...
Lab Computing Support Specialist
Rahway, NJ · On-site
$90K - $109K/yr
Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements. * Coordinate with vendors for system ...
Lab Computing Support Specialist
Rahway, NJ · On-site
$90K - $109K/yr
Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements. * Coordinate with vendors for system ...
CSV Consultant
Raritan, NJ · On-site
$48 - $53/hr
Pay Range: $48hr - $53hr Requirement/Must Have: * 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and ...
New
Quick apply
CSV Consultant
Raritan, NJ · On-site
$48 - $53/hr
Pay Range: $48hr - $53hr Requirement/Must Have: * 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and ...
New
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
$142.40 - $224.10/hr
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification, and computer system validation activities, and quality system compliance to ...
New
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
$142.40 - $224.10/hr
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification, and computer system validation activities, and quality system compliance to ...
New
We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Description : WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS.
We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Description : WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS.
Jr. Validation Engineer/QA Analyst/ Jr. QA Tester
Brooklyn, NY · On-site
$55K - $58K/yr
We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Description : WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS.
Jr. Validation Engineer/QA Analyst/ Jr. QA Tester
Brooklyn, NY · On-site
$55K - $58K/yr
We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. Description : WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS.
Familiarity with Pharmaceutical Development IT. * Experience with Computer Systems Validation, working knowledge of 21 CFR Part 11. * Experience with LIMS systems. * Experience with MODA is a plus.
Familiarity with Pharmaceutical Development IT. * Experience with Computer Systems Validation, working knowledge of 21 CFR Part 11. * Experience with LIMS systems. * Experience with MODA is a plus.
Candidates with a strong understanding of computer system validation, quality management systems, and FDA regulations are encouraged to apply. On-site Contract Pay rate: DoE Primary Responsibilities:
Quick apply
Candidates with a strong understanding of computer system validation, quality management systems, and FDA regulations are encouraged to apply. On-site Contract Pay rate: DoE Primary Responsibilities:
QA Manager
Harrison, NJ · On-site
Responsible to support to Computer system validation of Quality control applications. * Review of regulatory inspections observations to perform gap assessment and implementation of corrective ...
QA Manager
Harrison, NJ · On-site
Responsible to support to Computer system validation of Quality control applications. * Review of regulatory inspections observations to perform gap assessment and implementation of corrective ...
Validation Lab Manager
$124K - $182K/yr
About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System ... Experience within a computer hardware environment is preferred. * Fundamental understanding of ...
Validation Lab Manager
$124K - $182K/yr
About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System ... Experience within a computer hardware environment is preferred. * Fundamental understanding of ...
Validation Lab Manager
Secaucus, NJ · On-site
$124K - $182K/yr
About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System ... Experience within a computer hardware environment is preferred. * Fundamental understanding of ...
Validation Lab Manager
Secaucus, NJ · On-site
$124K - $182K/yr
About the Role The Validation Lab Manager will manage a team of technicians supporting ZT System ... Experience within a computer hardware environment is preferred. * Fundamental understanding of ...
Understanding of working in a regulated environment, or understanding of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation ...
Understanding of working in a regulated environment, or understanding of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation ...
Engineering Specialist
Millburn, NJ · On-site
... Computer System Validation (CSV) activities. Required Skills & Tools: • Experience with CSV and commissioning activities. • Strong knowledge of deviation investigation and documentation. • ...
Engineering Specialist
Millburn, NJ · On-site
... Computer System Validation (CSV) activities. Required Skills & Tools: • Experience with CSV and commissioning activities. • Strong knowledge of deviation investigation and documentation. • ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
$142.40 - $224.10/hr
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Associate Director, Metrologist and Compliance Lead, Medical Devices and Combination Products
Rahway, NJ · On-site
$142.40 - $224.10/hr
This role is responsible for maintaining laboratory measurement systems, calibration programs, equipment qualification and computer system validation activities, and quality system compliance to ...
Computer System Validation information
See Woodbridge, NJ salary details
$10.68 - $17.61
2% of jobs
$17.61 - $24.54
9% of jobs
$24.54 - $31.46
1% of jobs
$31.46 - $38.39
4% of jobs
$42.60 is the 25th percentile. Wages below this are outliers.
$38.39 - $45.32
15% of jobs
$45.32 - $52.25
9% of jobs
The median wage is $58.02 / hr.
$52.25 - $59.18
13% of jobs
$64.69 is the 75th percentile. Wages above this are outliers.
$59.18 - $66.10
29% of jobs
$66.10 - $73.03
12% of jobs
$73.03 - $79.96
2% of jobs
$79.96 - $86.89
5% of jobs
$10
$54
$86
How much do computer system validation jobs pay per hour?
As of Aug 7, 2026, the average hourly pay for computer system validation in Woodbridge, NJ is $54.84, according to ZipRecruiter salary data. Most workers in this role earn between $42.21 and $65.05 per hour, depending on experience, location, and employer.
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.
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.
Is computer system validation a good field?
Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring software and systems meet compliance standards such as GxP. It involves documentation, testing, and validation of computer systems, often requiring knowledge of regulatory requirements and validation tools. The field offers stable employment opportunities and career growth for professionals with technical skills and certifications like GAMP or 21 CFR Part 11 compliance.
What job categories do people searching Computer System Validation jobs in Woodbridge, NJ look for? The top searched job categories for Computer System Validation jobs in Woodbridge, NJ are:
What cities near Woodbridge, NJ are hiring for Computer System Validation jobs? Cities near Woodbridge, NJ with the most Computer System Validation job openings:
Full-time
Re-posted 16 days ago
Job description
Job Summary:
Katalyst CRO is a company focused on providing services in the life sciences sector, and they are seeking an IT CSV Validation Engineer. This role is responsible for authoring and executing validation test scripts for regulated systems, ensuring compliance with regulatory requirements and data integrity standards in GxP environments.
Responsibilities:
• Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems
• Support validation activities for ERP Master Data Governance processes, ensuring data accuracy, integrity, and compliance
• Perform validation of Data Lake platforms and associated system interfaces, including data ingestion, transformation, and reporting layers
• Collaborate with cross-functional teams (IT, QA, Business, Data Engineering) to define validation scope, risk assessments, and acceptance criteria
• Ensure compliance with GxP, 21 CFR Part 11, and data integrity requirements throughout the system lifecycle
• Support deviation investigations, CAPAs, and change control activities related to validated systems
• Maintain validation documentation including Validation Plans, Risk Assessments, Traceability Matrices, and Summary Reports
Qualifications:
Required:
• Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline
• 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences environments
• Strong experience with test script authoring and execution for GxP systems
• Experience supporting Master Data Governance processes
• Experience validating Data Lake environments and system interfaces
• Strong understanding of GxP, 21 CFR Part 11, and data integrity principles
• Ability to work independently and manage multiple validation activities with minimal oversight
Preferred:
• SAP experience preferred but not required
• Snowflake experience preferred
• Familiarity with AI/advanced data platforms is a plus
• Experience with validation management tools such as Val Genesis is a plus
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.
Katalyst CRO is a company focused on providing services in the life sciences sector, and they are seeking an IT CSV Validation Engineer. This role is responsible for authoring and executing validation test scripts for regulated systems, ensuring compliance with regulatory requirements and data integrity standards in GxP environments.
Responsibilities:
• Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems
• Support validation activities for ERP Master Data Governance processes, ensuring data accuracy, integrity, and compliance
• Perform validation of Data Lake platforms and associated system interfaces, including data ingestion, transformation, and reporting layers
• Collaborate with cross-functional teams (IT, QA, Business, Data Engineering) to define validation scope, risk assessments, and acceptance criteria
• Ensure compliance with GxP, 21 CFR Part 11, and data integrity requirements throughout the system lifecycle
• Support deviation investigations, CAPAs, and change control activities related to validated systems
• Maintain validation documentation including Validation Plans, Risk Assessments, Traceability Matrices, and Summary Reports
Qualifications:
Required:
• Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline
• 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences environments
• Strong experience with test script authoring and execution for GxP systems
• Experience supporting Master Data Governance processes
• Experience validating Data Lake environments and system interfaces
• Strong understanding of GxP, 21 CFR Part 11, and data integrity principles
• Ability to work independently and manage multiple validation activities with minimal oversight
Preferred:
• SAP experience preferred but not required
• Snowflake experience preferred
• Familiarity with AI/advanced data platforms is a plus
• Experience with validation management tools such as Val Genesis is a plus
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.