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Computer Validation Jobs in Cupertino, CA (NOW HIRING)

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Computer Validation information

See Cupertino, CA salary details

$13

$67

$106

How much do computer validation jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for computer validation in Cupertino, CA is $67.02, according to ZipRecruiter salary data. Most workers in this role earn between $51.59 and $79.47 per hour, depending on experience, location, and employer.

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

AspectComputer ValidationQuality Assurance Specialist
Required CredentialsGxP, 21 CFR Part 11, validation certificationsISO standards, QA certifications, GxP knowledge
Work EnvironmentPharmaceutical, biotech, regulated industriesManufacturing, healthcare, regulated industries
Employer & Industry UsageRegulated industries requiring validated systemsEnsuring quality compliance across processes

Computer Validation focuses on verifying that computer systems meet regulatory requirements and function correctly, primarily in regulated industries. Quality Assurance Specialists oversee overall quality processes, ensuring compliance and standards across various operations. While both roles require knowledge of GxP and industry regulations, Computer Validation is more technical and system-specific, whereas QA Specialists have a broader scope in quality management.

Is computer validation a good field?

Computer validation is a specialized field within quality assurance and regulatory compliance, focusing on ensuring that computerized systems meet industry standards such as 21 CFR Part 11. It often requires knowledge of validation protocols, testing, and documentation, and can offer stable employment opportunities in regulated industries like pharmaceuticals and biotech. The field values certifications and technical skills, making it suitable for professionals interested in compliance, quality systems, and technology validation.

What job categories do people searching Computer Validation jobs in Cupertino, CA look for?

The top searched job categories for Computer Validation jobs in Cupertino, CA are:

What cities near Cupertino, CA are hiring for Computer Validation jobs?

Cities near Cupertino, CA with the most Computer Validation job openings:

Computer Validation jobs near you

CSV Consultant (Computer System Validation)

Redwood City, CA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

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