
Nityo Infotech Corporation
Hybrid in Raritan, New Jersey • 5d ago
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Contract
Depends on Experience
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Nityo Infotech Corporation
Hybrid in Raritan, New Jersey • 5d ago
Easy Apply
Contract
Depends on Experience


Nityo Infotech Corporation
Hybrid in Raritan, New Jersey • 4d ago
Easy Apply
Contract
Depends on Experience





K-Tek Resourcing LLC
Raritan, New Jersey • 4d ago
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Contract, Third Party
Depends on Experience

Role CSV Validation Lead
Location -Raritan, NJ(Hybrid)
Job Details:
5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation activities and 21 CFR remediation projects with knowledge of CSA, GAMP 5, 21 CFR Part 11, Annex 11, and audit/inspection readiness.
Experience in the Pharmaceutical, biotechnology, or medical device industry.
Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation.
Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports.
Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs.
Experience in QA Methodologies, designing, reviewing and approving Test Plans, System/UAT test scripts and Test procedures.
Strong verbal and written communication skills.
Ability to work as a team player, lead a team or accomplish tasks without supervision.
Ability to work with remote teams and support several changes/projects simultaneously.
Ability to provide Validation guidance, timely reviews, and escalations to TQ management
🔢 Crunching numbers...
Hybrid in Raritan, New Jersey
•
4d ago
Role CSV Validation Lead Location -Raritan, NJ(Hybrid) Job Details: 5+ years of Computer System Validation (CSV) experience in GxP-regulated environments, with hands-on experience in retro-validation activities and 21 CFR remediation projects with knowledge of CSA, GAMP 5, 21 CFR Part 11, Annex 11, and audit/inspection readiness. Experience in the Pharmaceutical, biotechnology, or medical device industry. Experience in FDA and/or Global regulated environment with good understanding of GxP standa
Easy Apply
Contract
Depends on Experience
Raritan, New Jersey
•
Today
CSV Lead, Hybrid We have an immediate need for an experienced CSV Lead with strong expertise in LIMS LabVantage, Computer System Validation (CSV), GxP standards, and risk-based validation to lead validation activities within a regulated Pharmaceutical or Biotechnology environment. This is a hybrid position based in Raritan, NJ for a candidate with deep experience in LIMS LabVantage, CSV, FDA/GxP regulated environments, GAMP, validation planning, requirements documentation, compliance/validation
Easy Apply
Contract
$50.00 - 55.00
Hybrid in Raritan, New Jersey
•
Today
About Us: CodeForce 360 is a trusted global IT talent partner helping Fortune 500 companies, system integrators, and enterprise organizations build high-performing technology teams. With over 16 years of industry expertise, we combine speed, precision, and market intelligence to deliver exceptional talent across today's most in-demand technologies. About the Job- We are looking for an experienced CSV Lead to join one of our enterprise client engagements. The ideal candidate should have st
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Third Party, Contract
$47 - $52
Hybrid in Raritan, New Jersey
•
20d ago
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 strong experience validating enterprise applications while ensuring compliance with FDA and global regulatory standards. Key Responsibilities: Perform Computer System Validation (CSV) activities for SAP ERP, WMS, and enterprise applications.Develop and execute validation documentation, including Valida
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Contract
45 - 50