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Computer Validation Jobs in Santa Clara, CA (NOW HIRING)

Collabera

Validation Engineer

Milpitas, CA · On-site

Must be computer literate, and detail/quality oriented. Will be trained to perform validation and prepare protocols in one or more of the following areas: facilities, utilities, equipment, computer ...

PlusAI

Perception Validation Engineer

Santa Clara, CA

$140K - $170K/yr

As a Perception Validation Engineer , you will be responsible for defining, developing, and ... Bachelor's or Master's degree in Computer Science, Robotics, Electrical Engineering, Aerospace ...

New

PlusAI

Perception Validation Engineer

Santa Clara, CA

$140K - $170K/yr

As a Perception Validation Engineer , you will be responsible for defining, developing, and ... Bachelor's or Master's degree in Computer Science, Robotics, Electrical Engineering, Aerospace ...

New

Google

TPU Validation Manager

Mountain View, CA · On-site

Bachelor's degree in Electrical Engineering, Computer Engineering, Computer Science, or a related field, or equivalent practical experience. * 8 years of experience in SoC validation. * 5 years of ...

PlusAI

Perception Validation Engineer

Santa Clara, CA · On-site

$140K - $170K/yr

As a Perception Validation Engineer , you will be responsible for defining, developing, and ... Bachelor's or Master's degree in Computer Science, Robotics, Electrical Engineering, Aerospace ...

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All JobsComputer Validation JobsComputer Validation Jobs in Santa Clara, CA

Computer Validation information

See Santa Clara, CA salary details

$12

$63

$101

How much do computer validation jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for computer validation in Santa Clara, CA is $63.79, according to ZipRecruiter salary data. Most workers in this role earn between $49.13 and $75.67 per hour, depending on experience, location, and employer.

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 with opportunities for certification and skill development. The field is considered important in industries like pharmaceuticals and biotech, where system integrity and data accuracy are critical.

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.

What are popular job titles related to Computer Validation jobs in Santa Clara, CA? For Computer Validation jobs in Santa Clara, CA, the most frequently searched job titles are:
What job categories do people searching Computer Validation jobs in Santa Clara, CA look for? The top searched job categories for Computer Validation jobs in Santa Clara, CA are:
What cities near Santa Clara, CA are hiring for Computer Validation jobs? Cities near Santa Clara, CA with the most Computer Validation job openings:
Computer Validation jobs near you
Infographic showing various Computer Validation job openings in Santa Clara, CA as of August 2026, with employment types broken down into 33% Full Time, 33% Part Time, and 34% Contract. Highlights an 100% In-person job distribution, with an average salary of $132,691 per year, or $63.8 per hour.

CSV Consultant (Computer System Validation)

Stark Pharma Solutions Inc

Redwood City, CA • On-site

Contractor

Re-posted 25 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