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Csv Validation Jobs (NOW HIRING)

Intellectt INC

Validation Engineer

New York, NY · On-site

New York Summary: Seeking a Validation Engineer with strong experience in analytical instruments and CSA/CSV to support GMP operations in biologics / cell & gene therapy environments. Key ...

Moriah Engineering

PR · On-site

$90K - $118K/yr

CSV Leadto oversee the validation of major capital automation projects. The ideal candidate will have extensive expertise in validation and compliance, computer system validation (CSV), and ...

Validation & Engineering Group, Inc

PR

$57K - $58K/yr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Associate CSV - Periodic Review Scientist Position Summary The Associate CSV Periodic Review ...

Westbourne IT Global Services

GLIMS

Foster City, CA

$20 - $30/mo

Knowledge of GMP, CSV, validation, and data integrity principles. * Experience with incident management, change control, and documentation. * Ability to troubleshoot application and workflow issues.

Evotecgroup

IT CSV Engineer

Redmond, WA

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to : Senior Manager/Group Leader, CSV ... Lead validation efforts for Manufacturing (MFG), Quality Control (QC), enterprise, and PP&D systems ...

KBI Biopharma, Inc.

CSV Specialist II

Durham, NC · On-site

Responsible for supporting all aspects of the Computer Systems Validation (CSV) Lifecycle for the Validation Department to ensure all systems are in a qualified state suitable for the intended use.

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How much do csv validation jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for csv validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Csv Validation position, and why are they important?

To excel in CSV Validation, a strong background in life sciences, engineering, or a related technical discipline is essential, along with knowledge of computer system validation regulations and best practices. Familiarity with FDA 21 CFR Part 11, GAMP guidelines, and validation software tools is highly valued, and certifications such as PMP or CISA can be beneficial. Attention to detail, analytical thinking, and effective communication skills help professionals manage documentation and collaborate with cross-functional teams. These abilities ensure that systems in regulated environments are compliant, reliable, and meet industry standards for quality and data integrity.

What are the typical daily responsibilities of a CSV Validation professional?

CSV (Computer System Validation) Validation professionals are responsible for planning, executing, and documenting validation activities for computerized systems used in regulated industries like pharmaceuticals and biotechnology. Their daily tasks include reviewing system requirements, developing validation protocols, conducting risk assessments, performing validation testing, and documenting results in accordance with regulatory standards. They regularly collaborate with IT, quality assurance, and business stakeholders to ensure systems are compliant and audit-ready. Staying organized and detail-oriented is crucial, as each step must be carefully documented and verified for compliance. This role is dynamic and requires balancing technical tasks with frequent cross-functional communication.

What is a CSV Validation job?

A CSV Validation job involves verifying the accuracy, consistency, and integrity of data within CSV files. This role ensures that the data conforms to predefined formats, standards, and business rules. It often includes checking for missing values, incorrect data types, and formatting errors to prevent issues in data processing. Professionals in this role may use scripts, validation tools, or manual reviews to ensure data quality and compliance.

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Csv Validation jobs near you
Infographic showing various Csv Validation job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Senior CSV / Lab Instrument Validation Consultant

Senior CSV / Lab Instrument Validation Consultant

AdeptSource

Foster City, CA

Other

Posted 18 days ago

Job description

Sr. CSV / Lab Instrument Validation Specialist
Type of role:Contract
Duration:12-36+ months
Hourly pay rate:DOE (C2C, W2, or 1099 permissible)
Location:South San Francisco Bay Area (Remote during COVID)
Our customer is seeking a Senior CSV / Lab Instrument Validation Engineer who is well versed in laboratory Instrument processes within a Pharmaceutical environment.Must havehands experience onLab Instrument Qualification. You will be primarily responsible for planning, leading, and executing validation efforts for standalone Lab Instrument Software systems.
Must have strong experience in the following:
  • Responsible for performing validation of Laboratory Instrumentation by following approved standard operating procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements.
  • Responsible for the mapping and bringing consistency to the instrument lifecycle globally, from supporting purchase to instrument validation to decommissioning documentation.
  • Plan, lead, and execute the standardizing of validation efforts for standalone Lab Instrument Software systems.
  • Responsible for developing and executing on validation plans according to approved procedures, collation of test results, and organizes data packages and maintains all documentation pertaining to validation.
  • Ability to compile and analyze validation data, prepare reports and makes recommendations for changes and/or improvements.
  • Well versed in Laboratory Instrument process, ability to provide guidance to management on what improvements need to be made. (Essential for this role)
  • May also investigate and trouble-shoot problems which occur, and determine solutions.
  • Support change management and manage existing lab systems.
  • Participates on cross-functional project teams with the support of Development, Quality, and other groups
  • Familiar with FDA guidelines for Instrument and Software validation.
  • Experience must come from a pharmaceutical, biotech industry with direct knowledge of FDA regulations including 21CFR Part 11.
  • Self-motivated, good communication, technical writing, presentation skills, detail oriented, analytical, and a team player.

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