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Computer System Validation Jobs in New York (NOW HIRING)

Noblesoft Technologies

CSV Engineer

Raritan, NJ · On-site

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)

Tempus, Inc.

Senior Quality Engineer

Manhattan, NY · On-site

$100 - $150/hr

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and computer systems against user, functional and regulatory requirements.****Responsibilities:

Katalyst CRO

CSV Engineer

Somerset, NJ · On-site

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 ...

Katalyst CRO

CSV Engineer

Somerset, NJ · On-site

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 ...

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Computer System Validation information

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How much do computer system validation jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for computer system validation in New York is $59.43, according to ZipRecruiter salary data. Most workers in this role earn between $45.77 and $70.48 per hour, depending on experience, location, and employer.

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.

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.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It offers opportunities for professionals with skills in validation protocols, regulatory requirements, and tools like GxP and 21 CFR Part 11. The field provides steady employment, career growth, and the chance to work on critical quality assurance processes.

What are the most commonly searched types of Computer System Validation jobs in New York?

The most popular types of Computer System Validation jobs in New York are:

What are popular job titles related to Computer System Validation jobs in New York?

For Computer System Validation jobs in New York, the most frequently searched job titles are:

What job categories do people searching Computer System Validation jobs in New York look for?

The top searched job categories for Computer System Validation jobs in New York are:

Computer System Validation jobs near you
Infographic showing various Computer System Validation job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $123,607 per year, or $59.4 per hour.

Sr. Analyst IT Validation - Remote

Unicon Pharma Inc.

Stamford, CT • On-site

Full-time

Re-posted 9 days ago

Job description

Job Title:  Sr. Analyst, IT Validation Services

Department: Information Technology

Length of Assignment: 12 Months

Work Location: Remote

Working days and Hours: Monday – Friday 35 hours (9AM-5PM)

Primary Responsibilities

  • Creation, review, approval, and DMS processing of Computer System Lifecycle deliverables for Projects and Change Controls:
  • Validation Plans/Summary Reports
  • Risk Assessments
  • User Requirements
  • Specifications
  • Test Plans

Test Scripts: IQ, OQ or PQ

  • Assess and implement the most effective validation strategy for each activity.
  • Oversee test execution for cross-functional teams, including training, tracking, and reviews.
  • Build strong relationships with business counterparts to understand processes and requirements, ensuring delivery of compliant computer system solutions.
  • Work effectively with IT colleagues to ensure compliance with validation processes and proper documentation.
  • Collaborate with Information System Quality Assurance (ISQA) to ensure compliance on all projects, procedures and audits related to Information Technology.

Education and Experience Requirements

  • BS/Equivalent Training/Certification and minimum of 5 years of relevant experience in computer systems validation, change management and systems development life cycle methodologies.

Necessary Knowledge, Skills, and Abilities

  • Expertise in Computer System Validation (CSV), Systems Development Life Cycle (SDLC) methodologies and CSV regulations, standards, and best practices
  • Working knowledge of Computer Software Assurance (CSA) guidance and its applicability.
  • Excellent written and verbal communication skills with a focus on Good Documentation Practices (GDP).

Technical knowledge of the following computer systems and software (at a minimum):

  • MS software packages such as Outlook, Word, Excel, PowerPoint and MS Project
  • SAP, LIMS, or other Manufacturing, Distribution and Laboratory systems
  • Veeva Vault
  • ServiceNow
  • Robust knowledge and understanding of pharmaceutical manufacturing, packaging, operations, quality, and supply chain processes and related systems.
  • Working knowledge of project management principles, and ability to operate under tight timelines, within budget and to specified quality and compliance goals.
  • Solid relationship and conflict management skills, and ability to navigate complex, fast-moving, business environments in a self-directed manner.

Supervisory Responsibilities (if applicable):

  • There are no supervisory responsibilities expected in this position.