ZipRecruiter

Log In

1

Computer System Validation Manager Jobs in Linden, NJ

TriOptus LLC

Engineering Specialist

Millburn, NJ · On-site

... • Support basic Computer System Validation (CSV) activities. Required Skills & Tools: • ... Management System), if applicable. • Experience using Kneat is preferred.

TriOptus LLC

Business or Systems Analyst

Warren, NJ · On-site

Provide updates to management through established mechanisms. * Actively participate in all phases ... Computer troubleshooting: 6 to 10 years * GXP System Validation/21CFR Part 11: 6 to 10 years

previous page

Showing results 41-60

All JobsComputer System Validation JobsComputer System Validation Manager JobsComputer System Validation Manager Jobs in Linden, NJ

Computer System Validation Manager information

See Linden, NJ salary details

$49.1K

$108.9K

$165.8K

How much do computer system validation manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for computer system validation manager in Linden, NJ is $108,917.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $136,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a computer system validation manager, and why are they important?

To thrive as a Computer System Validation Manager, you need expertise in computer system validation regulations (such as GxP, FDA 21 CFR Part 11), strong project management skills, and a background in life sciences or IT. Familiarity with validation lifecycle documentation tools, quality management systems (QMS), and compliance software is often required, along with relevant certifications like PMP or CSV-related credentials. Exceptional attention to detail, analytical thinking, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring regulatory compliance. These skills and qualifications are vital to ensure validated systems meet regulatory standards, minimize compliance risks, and support organizational quality objectives.

What are some common challenges a computer system validation manager faces during system implementation projects?

A Computer System Validation Manager often encounters challenges such as aligning validation activities with evolving regulatory requirements, managing tight project timelines, and coordinating between multiple stakeholders like IT, Quality Assurance, and business users. Ensuring thorough documentation and traceability, while adapting to technology updates or scope changes, can also be demanding. Proactive communication and strong project management skills are essential to mitigate risks and ensure successful, compliant system implementations.

What does a computer system validation manager do?

A Computer System Validation Manager is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals or biotechnology, meet all required compliance standards. They oversee the planning, execution, and documentation of validation activities to ensure systems are reliable, accurate, and secure. Their duties include managing validation projects, writing protocols, coordinating with IT and quality assurance teams, and ensuring adherence to regulations like FDA 21 CFR Part 11. This role is critical for maintaining product quality and regulatory compliance.

What is the difference between Computer System Validation Manager vs Computer System Validation Specialist?

AspectComputer System Validation ManagerComputer System Validation Specialist
CertificationsGAMP, CQE, CSQEGAMP, CQE, CSQE
Work EnvironmentManagement, oversight, strategic planningExecution, testing, documentation
Industry UsagePharmaceutical, biotech, regulated industriesPharmaceutical, biotech, regulated industries
Primary FocusLeading validation projects, team coordinationPerforming validation activities, testing

The main difference between a Computer System Validation Manager and a Computer System Validation Specialist lies in their roles. The manager oversees validation projects, manages teams, and ensures compliance, while the specialist executes validation tasks and documents testing procedures. Both roles require similar certifications and are vital in regulated industries like pharmaceuticals and biotech.

What job categories do people searching Computer System Validation Manager jobs in Linden, NJ look for? The top searched job categories for Computer System Validation Manager jobs in Linden, NJ are:
What cities near Linden, NJ are hiring for Computer System Validation Manager jobs? Cities near Linden, NJ with the most Computer System Validation Manager job openings:
Computer System Validation Manager jobs near you

Lab Computing Support Specialist

Cognizant Technology Solutions

Rahway, NJ • On-site

$90K - $109K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Cognizant rating

7.4

Company rating: 7.4 out of 10

Based on 85 frontline employees who took The Breakroom Quiz

52nd of 72 rated business consultants

Job description

"Please note, this role is not able to offer visa transfer or sponsorship now or in the future."
As a Lab Computing Support Specialist, you will make an impact by ensuring the reliability, compliance, and operational excellence of laboratory systems that support research, quality, and manufacturing activities within a regulated Life Sciences environment. You will be a valued member of the Laboratory Informatics and IT team and work collaboratively with laboratory scientists, quality assurance, validation, infrastructure, application support, and business stakeholders to maintain compliant and efficient laboratory operations.
In this role, you will:
  • Manage the lifecycle of laboratory systems, including implementation, validation, maintenance, upgrades, patching, backup, archival, and decommissioning activities.
  • Provide technical support for laboratory software systems, instrument integration platforms, and analytical instruments while troubleshooting software, hardware, and connectivity issues.
  • Partner with laboratory, QA, and IT teams to ensure compliance with GxP, GLP, GMP, Computer System Validation (CSV), and data integrity requirements.
  • Coordinate with vendors for system installations, maintenance, upgrades, issue resolution, and service management while ensuring compliance with regulatory and operational requirements.
  • Support audits, inspections, change management, deviation management, CAPA activities, documentation updates, and continuous improvement initiatives across laboratory systems.

Work model
At Cognizant, we strive to provide flexibility wherever possible, and we are here to support a healthy work-life balance through our various well-being programs. Based on this role's business requirements, this is an onsite position requiring 5 days per week in a client office in West Point, Pennsylvania.
The working arrangements for this role are accurate as of the date of posting. This may change based on the project you're engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations.
What you need to have to be considered
  • Bachelor's degree in Life Sciences, Information Technology, Engineering, Computer Science, or a related discipline.
  • Experience supporting laboratory systems within pharmaceutical, biotechnology, or other regulated Life Sciences environments.
  • Strong understanding of GxP, GLP, GMP, data integrity principles, and regulatory requirements.
  • Hands-on experience with Computer System Validation (CSV), SDLC, and validation lifecycle activities.
  • Experience supporting laboratory software applications, analytical instruments, and instrument integration platforms.
  • Knowledge of laboratory workflows and familiarity with analytical instruments such as HPLC, GC, spectrophotometers, or similar laboratory technologies.
  • Experience with user administration, backup and recovery processes, software upgrades, patch management, and system maintenance activities.
  • Working knowledge of ticketing and service management tools such as ServiceNow, Remedy, or similar platforms.
  • Experience with deviation management, change control, CAPA processes, and audit support activities.
  • Strong troubleshooting, communication, technical documentation, and stakeholder management skills.

These will help you stand out
  • Experience supporting regulated laboratory environments within pharmaceutical research, development, manufacturing, or quality operations.
  • Knowledge of Computer System Validation deliverables and regulatory frameworks including FDA 21 CFR Part 11, GAMP 5, and CSV best practices.
  • Experience supporting laboratory system onboarding, offboarding, configuration management, and data archival processes.
  • Experience participating in regulatory inspections, audit readiness activities, and remediation programs.
  • Familiarity with Jira, ServiceNow, or other IT service management and workflow platforms.
  • Experience working within Agile delivery environments.
  • Exposure to automation, AI-enabled support solutions, or digital transformation initiatives in laboratory operations.

We're excited to meet people who share our mission and can make an impact in a variety of ways. Don't hesitate to apply, even if you only meet the minimum requirements listed. Think about your transferable experiences and unique skills that make you stand out as someone who can bring new and exciting things to this role.
Salary and Other Compensation:
Applications will be accepted until August 18th, 2026.
The annual salary for this position is between $90,000 - $109,000 depending on experience and other qualifications of the successful candidate.
This position is also eligible for Cognizant's discretionary annual incentive program, based on performance and subject to the terms of Cognizant's applicable plans.
Benefits: Cognizant offers the following benefits for this position, subject to applicable eligibility requirements:
  • Medical/Dental/Vision/Life Insurance
  • Paid holidays plus Paid Time Off
  • 401(k) plan and contributions
  • Long-term/Short-term Disability
  • Paid Parental Leave
  • Employee Stock Purchase Plan

Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.
About Cognizant:
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, bridging the gap between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization's unique context into technology systems that amplify human potential, drive tangible outcomes and keep global enterprises ahead in a fast-changing world. See how at cognizant.ai or @cognizant.
Additional employment information
Compensation information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law.
Applicants may be required to attend interviews in person or by video conference. In addition, candidates may be required to present their current state or government issued ID during each interview.
Cognizant is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
If you have a disability that requires reasonable accommodation to search for a job opening or submit an application, please email [email protected] for roles based in the Americas or [email protected] for roles based in India.

What Cognizant employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply