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Computer System Validation Jobs in Bridgewater, NJ

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Validation Lead

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.

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Computer System Validation information

See Bridgewater, NJ salary details

$10

$55

$87

How much do computer system validation jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for computer system validation in Bridgewater, NJ is $55.53, according to ZipRecruiter salary data. Most workers in this role earn between $42.74 and $65.87 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 job?

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 the Computer System Validation position, 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 is the work of computer system validation?

Computer System Validation (CSV) is the process of ensuring that computer systems used in regulated environments function correctly and comply with industry standards. It involves documenting and testing software, hardware, and related processes to verify they meet specified requirements, often using validation protocols and tools. CSV is essential in industries like pharmaceuticals and healthcare to ensure data integrity and regulatory compliance.

What degree is best for cis jobs?

For Computer System Validation (CSV) roles, a bachelor's degree in computer science, information technology, life sciences, or engineering is typically preferred. Relevant certifications such as GxP or validation-specific training can enhance job prospects, and strong knowledge of regulatory requirements like FDA or EMA guidelines is beneficial.

What is the salary of SoC validation engineer?

The salary of a SoC validation engineer typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. Professionals in this role often have skills in hardware description languages and verification tools, which can influence compensation.
What are popular job titles related to Computer System Validation jobs in Bridgewater, NJ? For Computer System Validation jobs in Bridgewater, NJ, the most frequently searched job titles are:
What job categories do people searching Computer System Validation jobs in Bridgewater, NJ look for? The top searched job categories for Computer System Validation jobs in Bridgewater, NJ are:
What cities near Bridgewater, NJ are hiring for Computer System Validation jobs? Cities near Bridgewater, NJ with the most Computer System Validation job openings:
Infographic showing various Computer System Validation job openings in Bridgewater, NJ as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $115,494 per year, or $55.5 per hour.

Computer System Validation Lead

iTvorks,Inc

Princeton, NJ • On-site

Contractor

Posted 25 days ago


Job description

Company Description
iTvorks provides answers to enterprises in a wide range of business sectors such as medical, real estate, and finance among others. We have reliably helped many organizations see their visions come to life by entirely managing the lifecycles of their products, infrastructure and applications.
Job Description
Candidate needs to work from our Client site Based in Foster City CA.
  • 21 CFR Part 210 / 211
  • GAMP 5 Risk-Based validation / ICH Q9 hands-on implementation knowledge
  • Manufacturing, Distribution process and procedure
  • Experience in managing large implementations/upgrade project
  • Strong knowledge on change management procedure & process; Should have handled more than 20+ change requests
  • Hands-on knowledge of Deviation and CAPA Management
  • Leading and managing testing and validation activities in synchronization with project scope, schedule, and objective
  • Must possess formal training/certification on Testing & Validation
  • Excellent communication skills
  • Excellent technical writing skills
  • Should be able to work independently with minimum supervision

Should have worked in cross-functional environments and comfortable to liaison with business
Qualifications
Below applications Experience Must.
  • SAP
  • Oracle EBS
  • LIMS
  • VEEVA or Salesforce

Additional Information
All your information will be kept confidential according to EEO guidelines.