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Sr. CSV/CSA/Validation Engineer

Katalyst Healthcares and Lifesciences

Raritan, New Jersey • Today

Full-time

Computer System Validation (CSV) Engineer

Spadtek Solutions LLC

Piscataway, New Jersey • 2d ago

Easy Apply

Full-time, Third Party

Depends on Experience

CSV Validation Lead

Nityo Infotech Corporation

Hybrid in Raritan, New Jersey • 10d ago

Easy Apply

Contract

Depends on Experience

Sr. Business Systems Analyst - Validation (CSA) Governance & Process Support

Arthrex

Remote • Today

Full-time

To define

CSV Validation Lead

Nityo Infotech Corporation

Hybrid in Raritan, New Jersey • 2d ago

Easy Apply

Contract

Depends on Experience

Computer System Validation (CSV) Quality Support Lead

Innova Solutions, Inc

Morristown, New Jersey • 5d ago

Easy Apply

Contract

Depends on Experience

Senior Engineer, Process Validation

Danaher Corporation

Remote • Today

Full-time

USD 100,000.00 - 130,000.00 per year

CSV Analyst / Validation Analyst | Raritan, NJ / New Brunswick, NJ| Contract

Healthcare Triangle Inc

Hybrid in Raritan, New Jersey • 3d ago

Easy Apply

Contract, Third Party

Depends on Experience

Computer System Validation (CSV) Consultants(Biotech Industry exp is must)(Only Visa Independent Candidate/W2)

SumasEdge Corporation

Piscataway, New Jersey • 2d ago

Easy Apply

Contract

Depends on Experience

CSV Consultant(Computer System Validation ? GenAI, Agentic , SAP

W3Global

Raritan, New Jersey • Today

Contract

USD45.0/HOURLY - USD52.0/HOURLY

Computer System Validation (CSV) Consultants

Resourcesys

Piscataway, New Jersey • 3d ago

Easy Apply

Contract

CSV/Validation Consultant

K-Tek Resourcing LLC

Raritan, New Jersey • 5d ago

Easy Apply

Contract, Third Party

Depends on Experience

Job Details

Skills

SaaS
PaaS
Cloud Computing
Computerized System Validation
Acquisition
Inventory
Business Systems
Pharmaceutics
Biotechnology
Medical Devices
GxP
Writing
Documentation
Regulatory Compliance
WIS
System Testing
Traceability Matrix
Specification Gathering
Test Methods
Test Plans
Acceptance Testing
Scripting
Supervision
Management

Summary

Roles & Responsibilities:

Need someone strong with GXP applications, saas/paas, infrastructure, quality, cloud concepts, cloud applications, etc.
In addition to validation and regulation experience, the resource should have the following experience:
Must be able to Independently support Business Separation activities for Large global & regional GxP Computerized systems. With minimal supervison.
Strong CSV Expertise, especially within Acquisition/Divestiture/Separation.
bility to manage end-end from Inventory, assessments, remediations to final dispositions;
Infrastructure Qualifications & Business Systems Validations 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources.
Specifically in the Pharmaceutical, biotechnology, or medical device industry.

Experience:

Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation;
Define and implement Risk based validation activities.
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, SOPs/WIs).
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, systems and UAT test scripts and Test procedures.

Skills.

bility to work as a team player, lead a team or accomplish tasks without supervision.
bility to work with remote teams and support several changes/projects simultaneously.
bility to provide Validation guidance, timely reviews, and escalations to management

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 45a14325d7d2fc197b51bfbd9a2d5c51
Posted 2 days ago

Fitment

Dice Job Match Score™

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Hybrid in Raritan, New Jersey

•

3d ago

Hi ,Greetings ! We do have opening for our client, Role : Validation AnalystLocation : Raritan, NJ / New Brunswick, NJ Duration : Long-term Contract Job Description : Candidates need to have hands-on experience in validating and implementing infrastructure systems and tools. e.g. aws, azure, JIRA, ServiceNow etc. Any experience with divestiture/separation a huge plus. e.g. Manufacturing site cutovers (infrastructure and applications), Must be able to work out of Raritan or New Brunswick Office

Easy Apply

Contract, Third Party

Depends on Experience

CSV Consultant(Computer System Validation ? GenAI, Agentic , SAP

Raritan, New Jersey

•

Today

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Contract

USD45.0/HOURLY - USD52.0/HOURLY

CSV Engineer

Raritan, New Jersey

•

Today

Summary : Roles & Responsibilities : Strong CSV and Quality expertise with ability to independently lead validation activities across the SDLC for GxP systems with minimal supervision. 7-10 years of relevant experience. Proven experience with Manufacturing, MES, and Data Platform Applications, including support for global and regional GxP computerized systems. Deep knowledge of GxP compliance, FDA/Global regulations, and Inspection Readiness. Expertise in validation documentation and deliverable

Full-time

Validation Lead

Hybrid in Raritan, New Jersey

•

12d ago

Role: Validation Lead Location: Raritan, NJ(Hybrid) Duration: 6+ Months Must Have - Computer System Validation Experience M&A related Data Migration and related infrastructure qualification in data Platform domain Job Description: Must be able to Independently support Business Separation activities for Large global & regional GxP Computerized systems. with minimal supervision.Recent experience with Acquisitions/Separations/Divestiture from J&J a huge plus.Strong CSV Expertise, especially withi

Easy Apply

Contract

Depends on Experience

Job Details

Skills

SaaS
PaaS
Cloud Computing
Computerized System Validation
Acquisition
Inventory
Business Systems
Pharmaceutics
Biotechnology
Medical Devices
GxP
Writing
Documentation
Regulatory Compliance
WIS
System Testing
Traceability Matrix
Specification Gathering
Test Methods
Test Plans
Acceptance Testing
Scripting
Supervision
Management

Summary

Roles & Responsibilities:

Need someone strong with GXP applications, saas/paas, infrastructure, quality, cloud concepts, cloud applications, etc.
In addition to validation and regulation experience, the resource should have the following experience:
Must be able to Independently support Business Separation activities for Large global & regional GxP Computerized systems. With minimal supervison.
Strong CSV Expertise, especially within Acquisition/Divestiture/Separation.
bility to manage end-end from Inventory, assessments, remediations to final dispositions;
Infrastructure Qualifications & Business Systems Validations 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources.
Specifically in the Pharmaceutical, biotechnology, or medical device industry.

Experience:

Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation;
Define and implement Risk based validation activities.
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, SOPs/WIs).
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, systems and UAT test scripts and Test procedures.

Skills.

bility to work as a team player, lead a team or accomplish tasks without supervision.
bility to work with remote teams and support several changes/projects simultaneously.
bility to provide Validation guidance, timely reviews, and escalations to management

Dice Id: 91116760
Position Id: 45a14325d7d2fc197b51bfbd9a2d5c51
Posted 2 days ago

Fitment

Dice Job Match Score™

🔢 Crunching numbers...

Create job alert

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Hybrid in Raritan, New Jersey

•

3d ago

Easy Apply

Contract, Third Party

Depends on Experience

CSV Consultant(Computer System Validation ? GenAI, Agentic , SAP

Raritan, New Jersey

•

Today

Contract

USD45.0/HOURLY - USD52.0/HOURLY

CSV Engineer

Raritan, New Jersey

•

Today

Full-time

Validation Lead

Hybrid in Raritan, New Jersey

•

12d ago

Easy Apply

Contract

Depends on Experience

Sr. CSV/CSA/Validation Engineer

Skills

Summary

Dice Job Match Score™

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Sr. CSV/CSA/Validation Engineer

Job Details

Skills

Summary

Dice Job Match Score™

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