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 ...
Rahway, NJ · On-site
$180 - $230/hr
Bachelor's Degree in computer science, math or science with a minimum of 10 year's experience working in relevant field for associated (System Validation, Quality Assurance, Testing Lead or related ...
Rahway, NJ · On-site
$180 - $230/hr
Bachelor's Degree in computer science, math or science with a minimum of 10 year's experience working in relevant field for associated (System Validation, Quality Assurance, Testing Lead or related ...
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
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 ...
Morristown, 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 ...
Morristown, 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 ...
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 ...
Morristown, 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 ...
Morristown, 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 ...
Morristown, 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 ...
Morristown, 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 ...
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
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
Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements.Prepare, review ...
New
Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements.Prepare, review ...
New
Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements. * Prepare ...
New
Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements. * Prepare ...
New
$10.81 - $17.83
2% of jobs
$17.83 - $24.84
9% of jobs
$24.84 - $31.86
1% of jobs
$31.86 - $38.87
4% of jobs
$43.13 is the 25th percentile. Wages below this are outliers.
$38.87 - $45.88
15% of jobs
$45.88 - $52.90
9% of jobs
The median wage is $58.74 / hr.
$52.90 - $59.91
13% of jobs
$65.50 is the 75th percentile. Wages above this are outliers.
$59.91 - $66.93
29% of jobs
$66.93 - $73.94
12% of jobs
$73.94 - $80.96
2% of jobs
$80.96 - $87.97
5% of jobs
$10
$55
$87
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 Bridgewater, NJ, the most frequently searched job titles are:
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