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Computer System Validation Engineer Jobs in San Francisco, CA

Validation Engineer I

San Francisco, CA ยท Remote

$20 - $23/hr

Support the planning, development, and implementation of computer systems validation documentation ... Bachelor's degree in related engineering discipline. * This is an entry-level position. Prior ...

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Work directly with hardware and software engineering teams to communicate system behavior ... Must hold a valid Driver's License in the state of residence. * Clean driving record: No ...

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Work directly with hardware and software engineering teams to communicate system behavior ... Must hold a valid Driver's License in the state of residence. * Clean driving record: No ...

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Computer System Validation Engineer information

See San Francisco, CA salary details

$34

$61

$89

How much do computer system validation engineer jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for computer system validation engineer in San Francisco, CA is $61.03, according to ZipRecruiter salary data. Most workers in this role earn between $45.87 and $75.91 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a computer system validation engineer?

To thrive as a Computer System Validation Engineer, you need a solid background in computer science or engineering, knowledge of regulatory requirements (such as FDA or GxP), and experience in validation processes. Familiarity with validation tools, quality management systems, and documentation software is typically required, along with certifications like ISPE or ASQ being beneficial. Strong attention to detail, analytical thinking, and effective communication are essential soft skills for coordinating teams and ensuring compliance. These skills and qualities are crucial to ensure that computer systems meet regulatory standards, maintain data integrity, and support business operations in regulated industries.

What are some common challenges faced by computer system validation engineers in regulated industries?

Computer System Validation Engineers often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and ensuring timely validation while coordinating with cross-functional teams. Balancing strict compliance with project deadlines can be demanding, especially when systems are complex or legacy infrastructure is involved. Additionally, effective communication with IT, QA, and business stakeholders is essential to address issues quickly and maintain validation standards.

What is the difference between Computer System Validation Engineer vs Quality Assurance Specialist?

AspectComputer System Validation EngineerQuality Assurance Specialist
CertificationsGAMP, GxP validation certificationsISO, Six Sigma, GMP certifications
Work EnvironmentPharmaceutical, biotech, medical device industriesManufacturing, software, healthcare sectors
Primary FocusValidating computer systems and software complianceEnsuring overall quality and process improvements

The Computer System Validation Engineer primarily focuses on validating computer systems to meet regulatory standards, ensuring software compliance in regulated industries. In contrast, the Quality Assurance Specialist oversees broader quality processes, including audits and process improvements. Both roles require knowledge of industry regulations but differ in scope and specific responsibilities.

Are computer system validation engineers in demand?

Computer System Validation Engineers are in demand due to the increasing regulation of pharmaceutical, biotech, and medical device industries that require compliant validation of computer systems. They often need skills in validation protocols, GxP regulations, and validation tools, making their expertise valuable in ensuring quality and compliance in regulated environments.

Do computer system validation engineers make good money?

Computer System Validation Engineers typically earn competitive salaries that vary by experience, location, and industry. They often have specialized skills in validation protocols, regulatory compliance, and validation tools, which can contribute to higher earning potential. Certification and experience in regulated environments like pharmaceuticals or biotech can also impact salary levels.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital field in regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It involves skills in validation protocols, documentation, and tools like GxP regulations and audit readiness, making it a stable and in-demand career path for those with technical and regulatory knowledge.

What does a computer system validation engineer do?

A computer system validation engineer ensures that computer systems used in regulated industries, such as pharmaceuticals or biotech, meet required standards for quality and compliance. They develop validation protocols, perform testing, document results, and ensure systems function correctly and securely, often using tools like GxP guidelines and validation software. Their work helps ensure data integrity and regulatory compliance throughout the system lifecycle.

What are popular job titles related to Computer System Validation Engineer jobs in San Francisco, CA?

For Computer System Validation Engineer jobs in San Francisco, CA, the most frequently searched job titles are:

What job categories do people searching Computer System Validation Engineer jobs in San Francisco, CA look for?

The top searched job categories for Computer System Validation Engineer jobs in San Francisco, CA are:

What cities near San Francisco, CA are hiring for Computer System Validation Engineer jobs?

Cities near San Francisco, CA with the most Computer System Validation Engineer job openings:

Infographic showing various Computer System Validation Engineer job openings in San Francisco, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $126,945 per year, or $61 per hour.

CSV Consultant (Computer System Validation)

Stark Pharma Solutions Inc

Redwood City, CA โ€ข On-site

Contractor

Re-posted 15 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