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Computer System Validation Manager Jobs in Piscataway, NJ

CYNET SYSTEMS

Validation Lead

Raritan, NJ · On-site

$50 - $55/hr

Strong Computer System Validation (CSV) expertise, especially within acquisition, divestiture, and ... Manage end-to-end processes from inventory and assessments to remediations and final dispositions.

Catapult

Senior Validation Manager

Princeton, NJ · On-site

... laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic ... Manage multiple validation projects simultaneously, plan, coordinate and track the progress of the ...

Catapult

Senior Validation Manager

Princeton, NJ · On-site

... laboratory instrument, computer system, cleaning, and manufacturing processes in an aseptic ... Manage multiple validation projects simultaneously, plan, coordinate and track the progress of the ...

Deloitte

System Test and Validation Lead

Morristown, NJ · On-site +1

This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

This role supports system validation strategy, audit readiness, CAPA management, and risk-based ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

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Computer System Validation Manager information

See Piscataway, NJ salary details

$48.4K

$107.4K

$163.5K

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

As of Aug 31, 2026, the average yearly pay for computer system validation manager in Piscataway, NJ is $107,407.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,900.00 and $134,500.00 per year, depending on experience, location, and employer.

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 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 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 are popular job titles related to Computer System Validation Manager jobs in Piscataway, NJ?

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

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

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

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

Computer System Validation Manager jobs near you
Infographic showing various Computer System Validation Manager job openings in Piscataway, NJ as of August 2026, with employment types broken down into 87% Full Time, 11% Part Time, and 2% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $107,407 per year, or $51.6 per hour.

Computer System Validation Lead

iTvorks,Inc

Princeton, NJ • On-site

Contractor

Re-posted yesterday

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.

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