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Csv Validation Jobs (NOW HIRING)

Intellectt INC

CSV Engineer

Social Circle, GA · On-site

Longterm Job Summary The CSV Engineer supports validation activities for computerized systems used in pharmaceutical/biopharmaceutical manufacturing. The role focuses on ensuring systems, equipment ...

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How much do csv validation jobs pay per hour?

As of Jul 12, 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 July 2026, with employment types broken down into 2% As Needed, 85% Full Time, 3% Part Time, 1% Temporary, and 9% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Senior Quality Validation & Compliance Manager

IT Minds LLC

San Diego, CA • On-site

Other

Posted 25 days ago

Job description

Job Title: Senior Quality Validation & Compliance Manager

Location: Remote / Hybrid / Onsite

Duration: Long-Term Contract

Position Overview

We are seeking a highly experienced Senior Quality Validation & Compliance Manager to lead Quality Systems, Validation, Computer System Validation (CSV), Regulatory Compliance, and GxP initiatives within regulated Pharmaceutical, Biotechnology, Medical Device, and Life Sciences environments.

The ideal candidate will possess extensive experience managing Quality Management Systems (QMS), validation programs, regulatory inspections, audit readiness, data integrity initiatives, and compliance activities while ensuring adherence to FDA, EMA, MHRA, ICH, GAMP 5, and global GxP requirements.

This role will serve as a key quality leader supporting Quality Assurance, Validation, Regulatory Affairs, Manufacturing, Engineering, Laboratory Operations, and IT organizations.

Key Responsibilities

  • Lead and maintain enterprise Quality Management Systems (QMS) programs.
  • Provide oversight of Validation Lifecycle Management activities including Process Validation, Equipment Qualification, Cleaning Validation, Analytical Method Validation, and Computer System Validation (CSV).
  • Develop, review, and approve validation documentation including Validation Plans, Risk Assessments, IQ/OQ/PQ Protocols, Traceability Matrices, Validation Reports, SOPs, and Quality Records.
  • Ensure compliance with GMP, GLP, Google Cloud Platform, GVP, 21 CFR Part 11, Annex 11, GAMP 5, Data Integrity, and global regulatory requirements.
  • Lead quality investigations, deviations, CAPAs, change controls, non-conformances, and remediation activities.
  • Support FDA, EMA, MHRA, ISO, and customer inspections and audits.
  • Drive inspection readiness programs and regulatory compliance initiatives.
  • Partner with cross-functional teams including Quality Assurance, Regulatory Affairs, Validation, Manufacturing, Engineering, Laboratory Operations, and IT.
  • Conduct risk assessments and implement risk-based validation approaches.
  • Lead continuous improvement initiatives to strengthen quality and compliance processes.
  • Mentor and provide leadership to quality, validation, and compliance teams.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, Chemistry, or related field.
  • 10+ years of Quality Assurance, Validation, Compliance, or Regulatory experience within Pharmaceutical, Biotechnology, Medical Device, or Life Sciences industries.
  • 5+ years of leadership experience managing Quality, Validation, or Compliance programs.
  • Strong experience supporting regulated GxP environments.

Mandatory Experience

  • Quality Management Systems (QMS)
  • Computer System Validation (CSV)
  • Process Validation
  • Equipment Qualification (IQ/OQ/PQ)
  • GMP / cGMP Compliance
  • GxP Compliance (GMP, GLP, Google Cloud Platform)
  • CAPA Management
  • Deviation Investigations
  • Change Control
  • Risk Assessments
  • Audit Management
  • Inspection Readiness
  • Regulatory Compliance
  • Data Integrity (ALCOA+)
  • Validation Lifecycle Management

Regulatory & Compliance Expertise

Strong knowledge of:

  • FDA Regulations
  • 21 CFR Part 11
  • 21 CFR Parts 210, 211, and 820
  • EU Annex 11
  • GAMP 5
  • ICH Guidelines
  • ISO 13485
  • Data Integrity Requirements
  • ALCOA+ Principles
  • GMP, GLP, Google Cloud Platform, and GxP Regulations

Preferred Systems Experience

Experience supporting and validating one or more of the following systems:

  • TrackWise
  • Veeva
  • LabWare LIMS
  • Empower
  • SAP
  • MasterControl
  • ETQ
  • ComplianceWire
  • DeltaV
  • MES
  • SCADA
  • Quality Management Platforms

Preferred Industry Experience

  • Pharmaceutical Manufacturing
  • Biotechnology
  • Biologics
  • Cell & Gene Therapy
  • Medical Devices
  • Combination Products
  • Laboratory Informatics
  • Global Quality & Compliance Programs

Preferred Certifications

  • ASQ Certified Quality Engineer (CQE)
  • ASQ Certified Quality Auditor (CQA)
  • PMP Certification
  • Lean Six Sigma Green Belt or Black Belt
  • ISO Lead Auditor Certification

Top Mandatory Skills

Quality Assurance | QMS | CSV | Validation | GxP | GMP | Regulatory Compliance | CAPA | Deviations | Change Control | Audit Readiness | Data Integrity | Risk Assessments | IQ/OQ/PQ | FDA Compliance | GAMP 5

Best Regards,

Satya Satish J | Technical Recruiter | IT Minds LLC |

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