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Csv Validation Engineer Jobs in California (NOW HIRING)

Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation ... CSV Engineer • Ensuring compliance with validation and regulatory standards Qualifications

Paid Time Off The Senior Validation Engineer - CSV at Lonza will be responsible for leading and executing validation activities for manufacturing processes, equipment, computerized systems, and ...

Paid Time Off The Senior Validation Engineer - CSV at Lonza will be responsible for leading and executing validation activities for manufacturing processes, equipment, computerized systems, and ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical ... Advanced validation expertise in equipment, computerized systems (CSV), analytical methods, and ...

CSV Engineer

Costa Mesa, CA · On-site

$55 - $60/hr

CSV Engineer Costa Mesa, CA or Seattle, WA(On-site) Visa: USC, GC & H4 EAD Key Responsibilities ... Generate and review validation reports and Validation Summary Reports (VSRs). * Author and maintain ...

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Csv Validation Engineer information

See California salary details

$23

$51

$85

How much do csv validation engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for csv validation engineer in California is $51.03, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $61.59 per hour, depending on experience, location, and employer.

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

To thrive as a CSV (Computer System Validation) Validation Engineer, you need expertise in validation methodologies, regulatory compliance (such as FDA 21 CFR Part 11), and a background in life sciences or engineering. Familiarity with validation tools, documentation systems, and quality management software is typically required, along with knowledge of industry standards like GAMP 5. Strong attention to detail, analytical thinking, and effective communication skills set outstanding candidates apart. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support safe, compliant operations in regulated environments.

What is a CSV validation engineer?

CSV Validation Engineers are professionals responsible for ensuring that computerized systems used in regulated industries, such as pharmaceuticals or biotechnology, comply with industry standards and regulations. CSV stands for Computer System Validation, which involves testing and documenting that systems function as intended and meet regulatory requirements for data integrity and security. These engineers typically create validation protocols, perform risk assessments, and support audits. Their work is crucial to ensure that electronic records and processes are reliable, traceable, and meet legal and industry guidelines.

What are some common challenges faced by a CSV validation engineer when working with cross-functional teams?

As a CSV Validation Engineer, one common challenge is ensuring clear communication and understanding between IT, QA, and business process teams regarding regulatory requirements and validation protocols. Misalignment on validation deliverables or timelines can occur, especially when teams have differing priorities or levels of familiarity with compliance frameworks. Proactively facilitating discussions, clarifying documentation, and providing training on Computer System Validation standards can help bridge gaps and keep projects on track.

What is the difference between Csv Validation Engineer vs Data Quality Analyst?

AspectCsv Validation EngineerData Quality Analyst
Required CredentialsBachelor's in Computer Science, Data Management, or related field; familiarity with data validation toolsBachelor's in Data Science, Statistics, or related; certifications like CDMP are common
Work EnvironmentData teams, software development, quality assuranceData analysis, reporting, data governance teams
Industry UsageTech, finance, healthcare, where data validation is criticalBusiness intelligence, analytics, data management sectors

The Csv Validation Engineer primarily focuses on validating and ensuring the accuracy of CSV data files through automated tools and scripts. In contrast, the Data Quality Analyst evaluates overall data quality, identifies issues, and implements data governance practices. Both roles require strong analytical skills and familiarity with data management, but their core responsibilities differ in scope and focus.

What are popular job titles related to Csv Validation Engineer jobs in California? For Csv Validation Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Csv Validation Engineer jobs in California look for? The top searched job categories for Csv Validation Engineer jobs in California are:
What cities in California are hiring for Csv Validation Engineer jobs? Cities in California with the most Csv Validation Engineer job openings:
Infographic showing various Csv Validation Engineer job openings in California as of August 2026, with employment types broken down into 88% Full Time, 5% Part Time, 2% Temporary, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $106,135 per year, or $51 per hour.

CSV Validation & Testing Lead - Life Sciences

Katalyst CRO

San Diego, CA • On-site

Full-time

Re-posted 29 days ago


Job description

Job Summary:
Katalyst CRO is a company focused on providing validation and testing services within the Life Sciences sector. They are seeking a CSV Validation & Testing Lead to ensure system integrity, data accuracy, and regulatory compliance for Poseida integration initiatives, while supporting validation activities across various platforms.
Responsibilities:
• Validation & Testing
• Design, develop, and execute validation strategies, test plans, and test cases
• Perform functional, integration, and data validation testing for enterprise systems
• Validate Tableau reporting outputs and eArchive system integrations
• Verify metadata accuracy and completeness during QMS migration activities
• Ensure archival integrity, traceability, and compliance of migrated records
• Compliance & Data Integrity
• Support CSV (Computer System Validation) activities and documentation
• Ensure compliance with ALCOA+ data integrity principles and regulatory standards
• Assist in validation lifecycle activities including execution evidence and defect tracking
• Collaborate with QA and compliance teams to address validation findings and remediation activities
• Coordination & Reporting
• Work closely with business, QA, and technical teams during testing and validation cycles
• Prepare validation summaries, execution reports, and compliance documentation
• Support issue resolution, retesting, and final sign-off activities
• Validation strategy and test plans
• Test execution and defect reports
• Data and metadata validation reports
• Archival verification documentation
• Final validation summary reports
Qualifications:
Required:
• 10+ years of experience in validation and testing within Life Sciences or regulated environments
• Strong experience in Clinical Data Validation and QMS validation processes
• Experience supporting CSV activities and regulatory compliance initiatives
• Knowledge of ALCOA+ principles, data integrity standards, and validation methodologies
• Hands-on experience validating Tableau reports and archival/eArchive systems
• Strong analytical, documentation, and stakeholder communication skills
• Experience with QMS migration and metadata validation
• Familiarity with Life Sciences compliance standards and GxP environments
• Exposure to enterprise archival systems and regulatory audit support
Company:
Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is headquartered in South Plainfield, USA, with a team of 51-200 employees. The company is currently Growth Stage.