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Csv Validation Consultant Jobs (NOW HIRING)

Zifo

Principal CQV Consultant

Cary, NC · On-site

Advise and guide onsite/remote validation consultants on qualification strategy, deviations, test ... cleaning validation basics, utilities (WFI/PW/HVAC), and facility/equipment commissioning. * CSV ...

Alliance Biotech Solutions LLC

CSV Engineer

Raleigh, NC · On-site

Job Type Full-time Description The Senior Computer System Validation (CSV) Engineer is responsible ... consulting firm specializing in biopharmaceutical engineering and validation services. As industry ...

Alliance Biotech Solutions LLC

CSV Engineer

Raleigh, NC · On-site

The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of ... consulting firm specializing in biopharmaceutical engineering and validation services. As industry ...

Just - Evotec Biologics

IT CSV Engineer

Redmond, WA · On-site

$115K - $135K/yr

Ensure compliance and maintain the validated state of all GxP systems. * Manage external CSV consultants and oversee their contributions to CSV projects. * Serve as a subject matter expert (SME) for ...

Spruce Infotech

Validation Expert

Fort Worth, TX · On-site

... a consulting services organization and/or industry experience. * Understanding of key ... CSV related SOPs as necessary. * Work with project management to build an integrated project plan ...

Evotec

IT CSV Engineer

Redmond, WA · On-site

$115K - $135K/yr

Ensure compliance and maintain the validated state of all GxP systems. * Manage external CSV consultants and oversee their contributions to CSV projects. * Serve as a subject matter expert (SME) for ...

Evotecgroup

IT CSV Engineer

Redmond, WA

$115K - $135K/yr

Ensure compliance and maintain the validated state of all GxP systems. * Manage external CSV consultants and oversee their contributions to CSV projects. * Serve as a subject matter expert (SME) for ...

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Csv Validation Consultant information

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How much do csv validation consultant jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for csv validation consultant in the United States is $58.47, according to ZipRecruiter salary data. Most workers in this role earn between $51.44 and $65.14 per hour, depending on experience, location, and employer.

What does a CSV Validation Consultant do?

A CSV Validation Consultant specializes in ensuring that computer systems used in regulated industries, such as pharmaceuticals and healthcare, comply with regulatory requirements for data integrity, particularly those involving CSV (Computer System Validation) processes. They assess, document, and test systems that handle data in CSV format to ensure accuracy, reliability, and compliance with standards like FDA 21 CFR Part 11. Their role includes developing validation protocols, performing risk assessments, and supporting audits. They help organizations avoid costly compliance issues and ensure the integrity of electronic records.

What are the key skills and qualifications needed to thrive as a CSV Validation Consultant, and why are they important?

To thrive as a CSV Validation Consultant, you need expertise in computer system validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a background in life sciences or IT. Familiarity with validation documentation tools, risk assessment methodologies, and industry standards like GAMP 5 is typically required. Strong analytical skills, attention to detail, and effective communication are essential soft skills for managing complex validation projects and collaborating with cross-functional teams. These abilities ensure that computer systems are compliant, reliable, and meet quality standards critical to regulated industries.

What are some typical challenges a CSV Validation Consultant faces when working on multiple projects simultaneously?

CSV Validation Consultants often manage several validation projects at once, each with its own regulatory requirements and timelines. Balancing these can be challenging, as it requires excellent organizational skills, prioritization, and clear communication with stakeholders to ensure deliverables are met without compromising quality. Consultants must also stay updated on evolving compliance standards and collaborate closely with QA teams, IT, and system owners to address issues promptly and maintain documentation accuracy across all projects.

What is the difference between Csv Validation Consultant vs Data Analyst?

AspectCsv Validation ConsultantData Analyst
CertificationsData validation, quality assurance certificationsData analysis, statistical certifications
Work EnvironmentData validation projects, quality assurance teamsData interpretation, reporting, business insights
Industry UsageData management, compliance, data integrity rolesBusiness intelligence, market research, reporting

The Csv Validation Consultant primarily focuses on ensuring data accuracy and integrity through validation processes, often working within quality assurance teams. In contrast, a Data Analyst interprets data to generate insights and support decision-making. While both roles handle data, their core responsibilities and work environments differ significantly.

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Csv Validation Consultant jobs near you
Infographic showing various Csv Validation Consultant job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 6% Part Time, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $121,624 per year, or $58.5 per hour.

Manager, Computer Systems Validation (CSV)

Corcept Therapeutics

Redwood City, CA

$160K - $189K/yr

Full-time

Re-posted 16 hours ago

Job description

The Manager, Computer Systems Validation (CSV) will be a core member of the Quality Systems Technology team and responsible for the implementation, management, ongoing support and review of Corcept's internal GXP validated systems. This individual will ensure IT Quality and Risk Management standards are defined, understood, designed into work activity, and achieved. This position will manage day-to-day operations for IT Compliance and Risk Management, working closely with key stakeholders from business teams, particularly QA, heavily guiding business teams on validation principles and requirements throughout the system lifecycle. This role will ensure compliance risks are identified, mitigated, and managed appropriately.

Responsibilities:

  • Provide assessment/review/oversight for Enterprise / GXP computer systems validation (focus on Pharmaceutical Systems)  
  • Experienced in developing validation strategies and authoring validation documents such as validation master plans, data migration plans, protocols, reports, discrepancies    
  • Ensure compliance and the validated state of all GXP systems 
  • Provide validation guidance on data migration activities as needed
  • Provide IT assessment and approval for GXP computer system changes
  •  Develop and support testing of proposed changes in system development environments
  • Experience in authoring and managing documents such as change control, Risk Assessments, Validation Plans, User Requirements Specifications, Functional Specifications, qualification protocols (IQ/OQ/PQ), Traceability Matrix, system procedures, deviations and CAPAs
  • Coordinate and support vendor support release activities 
  • Support and provide guidance to cross-functional groups with GXP system implementation projects and ongoing validation needs including system enhancements, releases and revalidation
  • Responsible to manage external CSV consultants in CSV projects 
  • Responsible as interface between IT and QA 

Preferred Education and Experience:

  • 8+ years' experience in QA or Validation performing protocol review and approval associated with the implementation and maintenance of computerized systems in pharma/biotech environment 
  • Solid knowledge of industry standards related to computerized systems and Electronic Records/Electronic Signatures; 21 CFR Part 210, 211& 11, Annex 11, GAMP5, ICH Q9, Data Integrity, CSA 

Skills, Qualifications, or Technical Proficiencies:

  • Thorough understanding of validation/qualification and concepts as it applies to pharmaceutical quality systems 
  • Excellent communication skills with the ability to effectively communicate across organizational levels and functions 
  • Proficiency with Veeva QualityDocs / QMS and ComplianceWire 
  • Experience with CTMS and Regulatory systems  
  • Ability to manage external software and consultant vendors 

The pay range that the Company reasonably expects to pay for this headquarters-based position is $160,600 - $189,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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