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Computer System Validation Jobs in Princeton, NJ

WuXi Biologics

Senior Engineer l, Validation

Cranbury, NJ · On-site

$73K - $117K/yr

Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. * Experience in the qualification of biologics ...

Kashiv Biosciences LLC

Validation Engineer III

Piscataway, NJ · On-site

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Working knowledge of Computer Systems Validation lifecycle and documentation. * Proficient in Microsoft Word, Excel, and PowerPoint. * Must be able to work independently with adequate supervision ...

Kashiv BioSciences, LLC

Validation Engineer III

Piscataway, NJ · On-site

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Working knowledge of Computer Systems Validation lifecycle and documentation. * Proficient in Microsoft Word, Excel, and PowerPoint. * Must be able to work independently with adequate supervision ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

Validation activities include Facility/Clean rooms, manufacturing equipment, laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic environment. In this role, you ...

Uncountable

Validation Engineer

New York, NY · On-site

$70K - $80K/yr

Review system requirements, design specifications, and user stories to ensure they are testable and ... Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related field (or ...

GenScript/ProBio

Automation Engineer, GMP

Pennington, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Expertise in scientific / technical subject areas - Equipment Qualification, Computer System Validation, SCADA system architecture, Biotech Process Equipment/Systems. * Proficient in use of ...

Capgemini Engineering

POMS MES Techno-Functional SME

New York, NY · On-site

$73K - $174K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support Computer System Validation (CSV) activities throughout the system lifecycle. * Author, review, and maintain validation documentation including: * User Requirements Specifications (URS ...

U-Haul

Field Computer Specialist

New York, NY · On-site

$5.3K - $5.8K/mo

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The position requires a valid driver's license with a clean driving record. A company-provided van ... Security camera systems, DVR/NVRs, coax and IP, including wiring and camera installation ...

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All JobsComputer System Validation JobsComputer System Validation Jobs in Princeton, NJ

Computer System Validation information

See Princeton, NJ salary details

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How much do computer system validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for computer system validation in Princeton, NJ is $57.44, according to ZipRecruiter salary data. Most workers in this role earn between $44.23 and $68.12 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 are popular job titles related to Computer System Validation jobs in Princeton, NJ?

For Computer System Validation jobs in Princeton, NJ, the most frequently searched job titles are:

What job categories do people searching Computer System Validation jobs in Princeton, NJ look for?

The top searched job categories for Computer System Validation jobs in Princeton, NJ are:

What cities near Princeton, NJ are hiring for Computer System Validation jobs?

Cities near Princeton, NJ with the most Computer System Validation job openings:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in Princeton, NJ as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $119,474 per year, or $57.4 per hour.

Senior Engineer l, Validation

WuXi Biologics

Cranbury, NJ • On-site

$73K - $117K/yr

Full-time

Re-posted 19 days ago

Job description

Job Title - Senior Engineer l, Validation
Work Location - Cranbury NJ
Job Summary
The Validation Engineer supports the successful operation of facility, laboratory, cGMP Manufacturing and business functions at WuXi Biologics sitesthoughout the United States through interaction with internal customers and external service providers. The incumbent in this role, executes projects or programs put in place to address validation requirements and issues. This individual works independently or in teams under the direction of their management to complete assignments. Using solid analytical skills, the incumbent is able to complete their tasks and recognize problems and develop possible solutions of correction to recommend to management. This individual will participate in the work group on multi-disciplinary and cross-functional teams and uses established relationships to contribute to teams and stakeholders with fact-based, business value knowledge.
Job Responsibilities
  • Maintains all qualified equipment systems in compliance with policies, guidelines and procedures across multiple sites within the WuXi Biologics United States network, including, but not limited too; Cranbury (NJ), Robbinsville (NJ), and Wocester (MA)
  • Experience with specialized qualification/validation equipment; examples being: Kaye Validator (or similar), clamp meter, RTD probe, etc.
  • Supervise & trains junior personnel. commissioning/qualification/validation activities..
  • Contributes or initiates/authors change controls, validation plans, qualification protocols, associated reports and procedures.
  • Authors, reviews, and/or executes qualification and validation protocols.
  • Executes qualification and/or validation of equipment, process control systems validation (CSV), cleaning validation/verification, shipping validation, and process validation from implementation through to operational use or execution.
  • Performs periodic field review, and re-qualification of qualified systems
  • Participate with investigations into qualification failures, and assists with remediation plans including deviations and CAPAs associated with qualified/validated systems and equipment.
  • Contributes to reviews and/or revision of written procedures (SOP).
  • Assist or lead in equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.
  • Provides assistance to internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.
  • Supports facilities new construction and relocation projects.
  • Reviews calibration, qualification and validation documentation for accuracy, completeness and compliance to WuXi standards.
  • Promotes and provides excellent customer service and support
  • Maintains a positive relationship and work collaboratively with all the members of the Facility & Engineering Department and site customers while promoting a positive team environment.
  • Ensure equipment, facilities and programs are maintained in compliance.
  • Responsible to contribute in the preparation for regulatory inspection readiness, reugulatory audits, and initial/routine audits (internal and external by partners/potential partners).

Qualifications
  • BS in Engineering or Science related discipline or equivalent industry experience. preferred.
  • Minimum of 8 years' experience in FDA-regulated industry (or similar). with 3 years experience in commissioning, validation, and qualification.
  • Experience in risk mitigation, complex problem solving, and troubleshooting to achieve cGMP production operation success.
  • Excellent communications skills. Great team player and ability to collaborate with internal stakeholders, vendors and clients to achieve alignment and work effectively.
  • Must work in a self-motivated, highly flexible, well-organized and detailed-oriented style with requirement of some evening conference call time.
  • Must be able to wear appropriate PPE, ability to stand /Sit/walk for long periods of time, ability to Lift 50 lbs. occasionally.
  • Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
  • Experience in the qualification of biologics equipment a plus.
  • Strong written and verbal communication skills.
  • Experience writing, executing, and reviewing equipment qualification documents
  • Strong multi-tasking ability in conjunction with proven organizational skills. Ability to organize assigned tasks in a high paced environment and concurrently monitor

The anticipated salary range for this position is $73,000 - $117,000
The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.

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