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Csv Validation Jobs in San Ramon, CA (NOW HIRING)

PSC Biotech

SAP CSV Lead

San Francisco, CA · Remote

$40 - $53/hr

Your Role We are seeking an experienced SAP CSV Lead to provide strategic leadership and oversight ... Provide validation leadership throughout SAP S/4HANA implementations, enhancements, upgrades, and ...

PSC Biotech

Validation Engineer I

San Francisco, CA · Remote

$20 - $23/hr

Initiate and oversee system CSV associated change control requests and associated validation documentation. * Identify and troubleshoot any potential risks and effectively implement required ...

Tempus

Senior Quality Engineer

Redwood City, CA · On-site +1

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and computer systems against user, functional and regulatory requirements. Responsibilities: * Support ...

Cerus

IT Portfolio & Project Manager

Concord, CA · Hybrid

$108K - $127K/yr

Computer System Validation (CSV) and Regulatory Compliance * Coordinate and support Computer System Validation (CSV) activities, including validation planning, execution, and documentation, in ...

Siri InfoSolutions Inc

RF Test Engineer

Fremont, CA · On-site

... CSV and dashboard/reporting tools such as Tableau. Preferred Skills: Prior experience supporting Customer or similar high-compliance product validation environments. Experience in conducted RF ...

Cerus

IT Portfolio & Project Manager

Concord, CA · On-site

$108K - $127K/yr

Computer System Validation (CSV) and Regulatory Compliance * Coordinate and support Computer System Validation (CSV) activities, including validation planning, execution, and documentation, in ...

Revance

Associate Director, IT R&D

Newark, CA · On-site

The individual will manage a team of validation engineers and system administrators while ... Provide strategic direction for the IT R&D lab systems and CSV process improvement programs. * Own ...

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All JobsCsv Validation JobsCsv Validation Jobs in San Ramon, CA

Csv Validation information

See San Ramon, CA salary details

$25

$58

$87

How much do csv validation jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for csv validation in San Ramon, CA is $58.11, according to ZipRecruiter salary data. Most workers in this role earn between $44.04 and $70.67 per hour, depending on experience, location, and employer.

What is a csv validation?

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.

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 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 popular job titles related to Csv Validation jobs in San Ramon, CA?

For Csv Validation jobs in San Ramon, CA, the most frequently searched job titles are:

What cities near San Ramon, CA are hiring for Csv Validation jobs?

Cities near San Ramon, CA with the most Csv Validation job openings:

Csv Validation jobs near you
Infographic showing various Csv Validation job openings in San Ramon, CA as of August 2026, with employment types broken down into 1% As Needed, 89% Full Time, 5% Part Time, and 5% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $120,862 per year, or $58.1 per hour.

CSV Consultant (Computer System Validation)

Stark Pharma Solutions Inc

Redwood City, CA • On-site

Contractor

Re-posted 7 days ago

Job description

Job Title: CSV Consultant (Computer Systems Validation)

Location: Redwood City, CA

Type: Contract

Job Summary

We are seeking an experienced CSV Consultant to support validation activities across multiple GxP-regulated systems within a pharmaceutical environment. This role will focus on computer systems validation, revalidation efforts, data migration activities, and documentation management for critical business and quality systems.

The ideal candidate will have strong experience with validated systems, change control processes, and regulatory compliance in GMP/GxP environments.

Key Responsibilities

  • Lead and support validation activities for GxP-regulated systems including:
  • SAS Studio
  • Veeva Quality Docs
  • CTMS
  • TraceLink
  • Argus
  • Support system revalidation and data migration projects to ensure compliance and data integrity
  • Develop, review, and execute validation documentation including:
  • Validation Plans
  • User Requirements Specifications (URS)
  • Risk Assessments
  • IQ/OQ/PQ protocols
  • Traceability Matrices
  • Summary Reports
  • Create and support User Acceptance Testing (UAT) scripts and execution activities
  • Manage change control documentation and support deviation resolution activities
  • Ensure validation activities align with FDA, GAMP5, and GxP compliance requirements
  • Collaborate with IT, Quality, Clinical, and Business stakeholders to support validated system implementations and updates
  • Maintain accurate and compliant documentation throughout the system lifecycle

Required Qualifications

  • Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related field
  • 5+ years of experience in Computer Systems Validation (CSV) within pharmaceutical or biotech environments
  • Hands-on experience validating GxP systems and supporting regulated system implementations
  • Strong knowledge of FDA 21 CFR Part 11, GAMP5, and GxP requirements
  • Experience with validation documentation, UAT execution, and change control processes
  • Familiarity with systems such as SAS Studio, Veeva, CTMS, TraceLink, or Argus
  • Strong analytical, documentation, and communication skills