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From Home Computer System Validation Jobs in Bloomfield, NJ

Jobtailor

Director, Business System Validation

Rahway, NJ · On-site

$180 - $230/hr

Bachelor's Degree in computer science, math or science with a minimum of 10 year's experience working in relevant field for associated (System Validation, Quality Assurance, Testing Lead or related ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

New York, NY · On-site +1

... from complexity and accelerate their path to value creation. Qualifications Required ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

MSD

Specialist, Metrology and Validation (On-site)

Rahway, NJ

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Participate in laboratory computer system validation activities associated with new or upgraded ... from search firms for employment opportunities. All CVs / resumes submitted by search firms to any ...

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All JobsComputer System Validation JobsFrom Home Computer System Validation JobsFrom Home Computer System Validation Jobs in Bloomfield, NJ

From Home Computer System Validation information

See Bloomfield, NJ salary details

$10

$55

$88

How much do from home computer system validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for from home computer system validation in Bloomfield, NJ is $55.60, according to ZipRecruiter salary data. Most workers in this role earn between $42.84 and $65.96 per hour, depending on experience, location, and employer.

Is computer system validation a good field?

Computer system validation is a specialized field within quality assurance and regulatory compliance, primarily in industries like pharmaceuticals and healthcare. It involves ensuring that computer systems meet regulatory standards through documentation, testing, and validation protocols, often requiring knowledge of GxP regulations and validation tools. The field offers steady demand and opportunities for certification and skill development.

What is the difference between From Home Computer System Validation vs From Home Quality Assurance Specialist?

AspectFrom Home Computer System ValidationFrom Home Quality Assurance Specialist
CertificationsGxP validation, 21 CFR Part 11ISO 9001, QA certifications
Work EnvironmentPrimarily remote, focused on system testing and validationRemote or onsite, focused on process audits and compliance
Industry UsagePharmaceutical, biotech, healthcareManufacturing, software, healthcare
Job FocusEnsuring computer systems meet regulatory standardsEnsuring overall quality processes and compliance

From Home Computer System Validation primarily involves verifying that computer systems meet regulatory standards, especially in healthcare and biotech industries. In contrast, From Home Quality Assurance Specialist focuses on broader quality processes and compliance across various industries. Both roles may be remote and require similar certifications, but their core responsibilities differ in scope and focus.

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From Home Computer System Validation jobs near you

Computer System Validation (CSV) Engineer

Kashiv BioSciences, LLC

Piscataway, NJ

Full-time

Re-posted 14 days ago

Job description

Description


Position Type: Full-time Employee (FTE)

Location: Piscataway, NJ (onsite - physical presence required)

Reports To: Sr. Director of IT

Work Authorization: Must be authorized to work in the U.S. without sponsorship, now or in the future


Position Summary


We are seeking an experienced CSV Engineer to support validation activities across a broad portfolio of regulated systems, including laboratory instrumentation, engineering and manufacturing equipment, and enterprise platforms. This role serves as a liaison across Quality, IT, Laboratory, and Manufacturing functions, ensuring systems are validated and maintained in compliance with 21 CFR Part 11, GxP, and EMA requirements.


Essential Duties & Responsibilities

  • Plan, author, and execute validation deliverables (VP, URS, FS, DS, IQ/OQ/PQ, Traceability Matrix, Validation Summary Reports) across assigned systems
  • Support CSV activities across lab instruments (HPLC, GC, spectrophotometers, balances, etc.), engineering and manufacturing equipment, and enterprise systems including Caliber LIMS, SAP, and BMRAM
  • Partner with system owners, QA, and IT to maintain systems in a validated state through change control and periodic review
  • Execute risk assessments and data integrity assessments aligned with ALCOA+ principles
  • Support audits, inspections, CAPA investigations, and deviations related to computerized systems
  • Collaborating with senior validation leads and SMEs to drive consistent practices across sites

Requirements

Position Requirements and Qualifications

  • Bachelor's degree in Life Sciences, Engineering, or IT; OR equivalent laboratory experience in a life sciences environment
  • Minimum 5 years of CSV experience in a GxP-regulated environment
  • Working knowledge of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Hands-on experience authoring and executing IQ/OQ/PQ protocols
  • Experience validating at least two of: laboratory instruments, engineering/manufacturing equipment, LIMS, SAP, or CMMS/calibration platforms (e.g., BMRAM)

Experience:  

  • Minimum 5 years of CSV experience in a GxP-regulated environment
  • Working knowledge of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Hands-on experience authoring and executing IQ/OQ/PQ protocols
  • Experience validating at least two of: laboratory instruments, engineering/manufacturing equipment, LIMS, SAP, or CMMS/calibration platforms (e.g., BMRAM)

Specialized Knowledge and Skills: 

  • Familiarity with GAMP 5 principles and risk-based validation
  • Exposure to Caliber LIMS
  • Exposure to SAP (QM, MM, PP) in a GxP context
  • Experience with BMRAM or equivalent CMMS/calibration systems
  • Prior experience acting as a liaison across IT, Quality, Lab, and Manufacturing teams

Work Environment & Physical Demands:

  • This is an on-site position
  • Must be able to work extended hours or weekend hours, as may be required.

Noise:

  • No extraordinary noise levels.

Standing/Lifting:

  • Very unlikely, but can be able to lift at least 20 lbs.

Visual:

  • No extraordinary requirements.

Stress:

  • High-paced demanding environment to meet ambitious project goals.

Travel:

  • Moderate domestic travel may be required.

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