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Computer Systems Validation Jobs in New Jersey (NOW HIRING)

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 ...

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 ...

CSV Consultant

Raritan, NJ ยท 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 ...

CSV Lead

Raritan, NJ ยท On-site

Advanced knowledge of Computer Systems Validation (CSV). * Strong understanding of GXP, 21 CFR Part 11, EU GMP Annex 11, GAMP 5, and Data Integrity. * Hands-on experience with risk-based validation ...

Showing results 41-60

Computer Systems Validation information

See New Jersey salary details

$10

$55

$87

How much do computer systems validation jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for computer systems validation in New Jersey is $55.15, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $65.38 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 New Jersey?

For Computer Systems Validation jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Computer Systems Validation jobs in New Jersey look for?

The top searched job categories for Computer Systems Validation jobs in New Jersey are:

What cities in New Jersey are hiring for Computer Systems Validation jobs?

Cities in New Jersey with the most Computer Systems Validation job openings:

Infographic showing various Computer Systems Validation job openings in New Jersey as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $114,704 per year, or $55.1 per hour.

Specialist, Metrology and Validation (On-site)

MSD

Rahway, NJ โ€ข On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago


Job description

Job Description

The Pharmaceutical Analysis & Digital Technologies (PADT) Analytical Capabilities & Operations (ACO) department of our Research and Development Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility.

The Metrology and Validation Specialist will work as part of the integrated US Metrology and Validation team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and supports the onboarding, qualification, validation, and routine maintenance of analytical equipment and instrumentation within a GMP environment.

The key responsibilities of this role will include:

  • Partner with scientific teams across DSCS to drive compliance and operational excellence.

  • Onboard, qualify, and maintain laboratory equipment and instrumentation in both GMP and non-GMP environment.

  • Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements.

  • Prepare, review, and approve documentation such as master inventory lists, qualification documentation, calibration documentation, computer system inventories.

  • Support internal and external quality audits and maintain laboratory state of permanent inspection readiness.

  • Author or contribute to Standard Operating Procedures (SOP).

  • Originate and own Investigations and Change Management records.

  • Collaborate with cross-functional teams to deliver department level prioritiesand initiatives.

The successful candidate must function both independently and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. Strong communications skills and eagerness to adapt and learn are essential attributes. As a member of our team, you will be joining scientific and technical problem solvers who are dedicated to creating the life-changing medicines of tomorrow.

Education Minimum Requirements (standard for each level)

  • Bachelor's degree, or higher, in analytical chemistry or related field with 3+ years relevant industry experience.

Required Experience and Skills

  • A strong team player with the ability to work both independently and cross-functionally to deliver on complex objectives.

  • Proven track record of strong technical and innovative problem solving.

  • Desire and ability to learn new concepts outside of core expertise and training.

  • Excellent verbal and written communication skills, demonstrated creativity, and strong interpersonal skills.

  • Related industry experience with metrology and equipment maintenance and calibration.

  • Experience working within a GMP environment.

  • Understanding of GMP policies and procedures.

Preferred Experience and Skills

While not required, experience in one or more of the following areas is beneficial.

  • Demonstrated commitment to multiculturalism and inclusion.

  • Experience leading a team for a common goal.

  • Experience in Auditing and Compliance within pharmaceutical industry, including change management and deviation management.

  • Experience supporting internal and external quality audits.

  • Experience in Instrument commissioning, qualification, and validation (CQV).

  • Experience in instrument computer system validation.

  • Experience with IT, computerized systems, software and applications, including Secure Desktop.

  • Experience with developing tools (e.g., Power Apps) or utilizing AI.

ARD

EligibleforRP

Required Skills:

Analytical Instrumentation, Analytical Laboratory Equipment, Calibration Procedures, Change Controls, Computer System Validation (CSV), Data Analysis, Equipment Calibrations, Equipment Maintenance, Equipment Qualification, GMP Environments, Laboratory Instrumentation, Metrology, Regulatory Compliance, Technical Writing, Validation Activities

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$96,200.00 - $151,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

09/5/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.