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Computer Systems Validation Jobs in Bridgewater, NJ

(Sr.) Validation Engineer

Pennington, NJ · On-site

$80K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support facility, utility, equipment, process, cleaning, and computer system validation (CSV) activities. * Support technology transfer and startup activities for new client manufacturing programs.

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 ...

CSV Consultant

Raritan, NJ · On-site

$48 - $53/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Experience in validating ERP/SAP/ MES Manufacturing applications * 3+ years' experience with System Development Lifecyle 7+ years' experience in Computer System Validation (Based on the role selected)

CSV Consultant

Raritan, NJ · On-site

$48 - $53/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

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 ...

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 ...

Technical Analyst / Project Manager

Princeton, NJ · On-site +1

$85K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Computer Systems and Technology: Strong knowledge of computer systems validation (SDLC methodologies) web/ETL technology, and cloud-based systems; and proficiency with computer skills including ...

Technical Analyst / Project Manager

Princeton, NJ · On-site +1

$85K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Computer Systems and Technology: Strong knowledge of computer systems validation (SDLC methodologies) web/ETL technology, and cloud-based systems; and proficiency with computer skills including ...

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

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

Lead Engineer

Summit, NJ

$108K - $143K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices * Knowledge of pharmaceutical, manufacturing and ...

Showing results 41-60

Computer Systems Validation information

See Bridgewater, NJ salary details

$10

$55

$87

How much do computer systems validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for computer systems 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 is computer systems validation?

Computer systems validation (CSV) is the process of ensuring that computer-based systems used in regulated industries, like pharmaceuticals and biotechnology, perform their intended functions consistently and reliably. This process involves documenting and testing systems to confirm they meet regulatory requirements, such as those set by the FDA. The goal is to ensure data integrity, product quality, and patient safety by minimizing the risk of system errors or failures. CSV typically includes activities like risk assessment, test planning, execution, and maintaining thorough records for audits.

What are the key skills and qualifications needed to thrive in computer systems validation, and why are they important?

To thrive in Computer Systems Validation, you need a solid understanding of regulatory requirements (such as FDA or EMA guidelines), software development life cycles, and risk management, often supported by a degree in life sciences, IT, or engineering. Experience with validation frameworks, documentation tools, and systems like GAMP 5 and knowledge of 21 CFR Part 11 compliance are typically required. Attention to detail, strong analytical thinking, and effective communication set professionals apart in this role. These skills and qualifications ensure validated systems are compliant, reliable, and support organizational quality and regulatory objectives.

What are some common challenges faced in a computer systems validation role, and how can they be addressed?

Professionals in Computer Systems Validation often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and coordinating with cross-functional teams. Staying updated through regular training and industry resources helps address compliance changes. Clear communication and collaboration with IT, Quality Assurance, and business stakeholders are essential for efficient validation processes. Utilizing validation lifecycle management tools and standardized templates can also streamline documentation and reduce errors.

What is the difference between Computer Systems Validation vs Quality Assurance Specialist?

AspectComputer Systems ValidationQuality Assurance Specialist
CertificationsGAMP, CSV-specific trainingISO 9001, Six Sigma
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, service sectors
Primary FocusEnsuring computer systems meet regulatory standardsEnsuring overall product/service quality
Common UsageValidation of software, hardware in complianceProcess audits, quality improvement

Computer Systems Validation and Quality Assurance Specialist roles overlap in ensuring compliance and quality. However, CSV focuses specifically on validating computer systems to meet regulatory standards, especially in pharma and biotech industries. Quality Assurance Specialists have a broader scope, overseeing overall quality processes across various sectors. Both roles require similar certifications and work environments but differ in their primary objectives and specific tasks.

What are popular job titles related to Computer Systems Validation jobs in Bridgewater, NJ?

For Computer Systems Validation jobs in Bridgewater, NJ, the most frequently searched job titles are:

What job categories do people searching Computer Systems Validation jobs in Bridgewater, NJ look for?

The top searched job categories for Computer Systems Validation jobs in Bridgewater, NJ are:

Infographic showing various Computer Systems Validation job openings in Bridgewater, NJ as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 11% Part Time, 5% Contract, and 1% Nights. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $115,494 per year, or $55.5 per hour.

Project Manager, Validation

Barry Wehmiller Group

East Brunswick, NJ • On-site

Full-time

Re-posted 13 days ago


Job description

About Us:

BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.


 

Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.


 

Job Description:

Project Manager, Validation

Who You'll Work With

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.

When you join Design Group as a Project Manager, Validation, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world's leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.

What You'll Do

You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.

  • Responsible for preparing, executing commissioning and qualification documents for a variety of utility, facility, and process equipment.
  • Lead and manage a diverse portfolio of validation projects simultaneously (equipment qualification, process validation, cleaning validation, system digitization, etc.)
  • Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.
  • Serve as the primary on-site point of contact and local engineering leader for major pharmaceutical manufacturing clients
  • Build and maintain strong relationships with client stakeholders across operations, quality, regulatory, and executive levels
  • Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team

What You'll Bring

  • Minimum 10+ years of demonstrated experience with validation of pharmaceutical or medical device processes and equipment
  • FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the Pharmaceutical Industry
  • Validation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desired
  • Excellent leadership skills including the ability to simultaneously organize, and successfully execute multiple project responsibilities
  • Candidates need to possess good communication and interpersonal skills and the ability to interact with all levels of management, clients, and vendors.
  • Strong computer skills are also required
  • Willing and able to travel as necessary for project requirements to include but not be limited to: project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.
  • Bachelor's degree in Chemical Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering or equivalent technical degree.

Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Sr. Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.

#LI-TH1

Feel like you're on the path to becoming a Project Manager, Validation but you're not quite there yet? We'd love to connect with you to see if we can take you from where you are today and grow you into a Design Group Engineering Consultant.


 

At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful work-therefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.


 

Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.


Company:

Design Group