Responsibilities: * pply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures, and training. * Ensure system validation aligns with Data ...
New
Responsibilities: * pply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures, and training. * Ensure system validation aligns with Data ...
New
Responsibilities: * pply quality standards and cGMP requirements to validate computer systems, including hardware, software, procedures, and training. * Ensure system validation aligns with Data ...
New
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge * Manufacturing, Distribution process and procedure * Experience in managing large implementations/upgrade project * Strong ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review * Execute risk assessments and data integrity assessments aligned with ALCOA ...
... Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and enterprise supply chain applications; strong knowledge of CSA ...
... Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on validation and deployment of SAP ERP, WMS, and enterprise supply chain applications; strong knowledge of CSA ...
Raritan, NJ · On-site
Retirement
PTO
The Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager is responsible for guiding and managing the project team throughout the building and execution of quality into enterprise ...
New
Raritan, NJ · On-site
Retirement
PTO
The Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager is responsible for guiding and managing the project team throughout the building and execution of quality into enterprise ...
New
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 ...
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 ...
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 ...
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 ...
Princeton, NJ · 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 ...
Princeton, NJ · 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 ...
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 ...
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 ...
Princeton, NJ · 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 ...
Princeton, NJ · 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 ...
Princeton, NJ · 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 ...
Princeton, NJ · 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 ...
Raritan, NJ · On-site
Retirement
PTO
The Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager is responsible for guiding and managing the project team throughout the building and execution of quality into enterprise ...
New
Raritan, NJ · On-site
Retirement
PTO
The Enterprise Quality R&D Clinical Computer System Validation (CSV) Manager is responsible for guiding and managing the project team throughout the building and execution of quality into enterprise ...
New
Somerville, NJ · On-site
$45 - $50/hr
Perform Computer System Validation (CSV) activities for SAP ERP, WMS, and enterprise applications. * Develop and execute validation documentation, including Validation Plans, Requirements, Test ...
Quick apply
Somerville, NJ · On-site
$45 - $50/hr
Perform Computer System Validation (CSV) activities for SAP ERP, WMS, and enterprise applications. * Develop and execute validation documentation, including Validation Plans, Requirements, Test ...
Raritan, NJ · On-site
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
Raritan, NJ · On-site
We are seeking an experienced CSV Consultant with expertise in Computer System Validation (CSV) , SAP ERP , and Generative AI/Agentic AI in a GxP-regulated environment . The ideal candidate will have ...
Raritan, NJ · On-site
Role - Validation Lead Location - Raritan, NJ (Hybrid) W2/C2C Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro ...
Raritan, NJ · On-site
Role - Validation Lead Location - Raritan, NJ (Hybrid) W2/C2C Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro ...
Raritan, NJ · On-site
$48 - $53/hr
Experience in the Pharmaceutical, biotechnology, or medical device industry. * 2+ years' experience with System Development Lifecycle. * 3+ years' experience in Computer System Validation.
Quick apply
Raritan, NJ · On-site
$48 - $53/hr
Experience in the Pharmaceutical, biotechnology, or medical device industry. * 2+ years' experience with System Development Lifecycle. * 3+ years' experience in Computer System Validation.
East Windsor, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
East Windsor, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Hightstown, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
Quick apply
Hightstown, NJ · On-site
Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site ...
$10.52 - $17.35
2% of jobs
$17.35 - $24.17
9% of jobs
$24.17 - $31
1% of jobs
$31 - $37.83
4% of jobs
$41.97 is the 25th percentile. Wages below this are outliers.
$37.83 - $44.65
15% of jobs
$44.65 - $51.48
9% of jobs
The median wage is $57.17 / hr.
$51.48 - $58.30
13% of jobs
$63.74 is the 75th percentile. Wages above this are outliers.
$58.30 - $65.13
29% of jobs
$65.13 - $71.96
12% of jobs
$71.96 - $78.78
2% of jobs
$78.78 - $85.61
5% of jobs
$10
$54
$85
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.
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.
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.
For Computer System Validation jobs in East Windsor, NJ, the most frequently searched job titles are:
Cities near East Windsor, NJ with the most Computer System Validation job openings:

Other
Posted 2 days ago
New