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Computer Systems Validation Jobs in Dublin, CA (NOW HIRING)

Jobtailor

Senior Systems Validation Engineer

San Jose, CA · On-site

$140 - $210/hr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Information Systems, or a related field * 8+ years of experience in systems validation, firmware validation, or ...

Supermicro

Sr. Systems Validation Engineer

San Jose, CA · On-site

$130K - $165K/yr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Information Systems, or a related field. * 8+ years of experience in systems validation, firmware validation, or ...

Supermicro

Sr. Systems Validation Engineer

San Jose, CA · On-site

$130K - $165K/yr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Information Systems, or a related field. * 8+ years of experience in systems validation, firmware validation, or ...

Jobtailor

System Validation Engineer

San Jose, CA · On-site

$120 - $180/hr

Bachelor's degree in Computer Engineering, Computer Science, Electrical Engineering, Information Systems, or a related field. * 3+ years of experience in systems validation, firmware validation, or ...

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Computer Systems Validation information

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How much do computer systems validation jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for computer systems validation in Dublin, CA is $61.17, according to ZipRecruiter salary data. Most workers in this role earn between $47.12 and $72.55 per hour, depending on experience, location, and employer.

What is computer systems validation?

Computer systems validation (CSV) is the process of ensuring that computer-based systems used in regulated industries, like pharmaceuticals and biotechnology, perform their intended functions consistently and reliably. This process involves documenting and testing systems to confirm they meet regulatory requirements, such as those set by the FDA. The goal is to ensure data integrity, product quality, and patient safety by minimizing the risk of system errors or failures. CSV typically includes activities like risk assessment, test planning, execution, and maintaining thorough records for audits.

What are the key skills and qualifications needed to thrive in computer systems validation, and why are they important?

To thrive in Computer Systems Validation, you need a solid understanding of regulatory requirements (such as FDA or EMA guidelines), software development life cycles, and risk management, often supported by a degree in life sciences, IT, or engineering. Experience with validation frameworks, documentation tools, and systems like GAMP 5 and knowledge of 21 CFR Part 11 compliance are typically required. Attention to detail, strong analytical thinking, and effective communication set professionals apart in this role. These skills and qualifications ensure validated systems are compliant, reliable, and support organizational quality and regulatory objectives.

What are some common challenges faced in a computer systems validation role, and how can they be addressed?

Professionals in Computer Systems Validation often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for multiple systems, and coordinating with cross-functional teams. Staying updated through regular training and industry resources helps address compliance changes. Clear communication and collaboration with IT, Quality Assurance, and business stakeholders are essential for efficient validation processes. Utilizing validation lifecycle management tools and standardized templates can also streamline documentation and reduce errors.

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

AspectComputer Systems ValidationQuality Assurance Specialist
CertificationsGAMP, CSV-specific trainingISO 9001, Six Sigma
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, service sectors
Primary FocusEnsuring computer systems meet regulatory standardsEnsuring overall product/service quality
Common UsageValidation of software, hardware in complianceProcess audits, quality improvement

Computer Systems Validation and Quality Assurance Specialist roles overlap in ensuring compliance and quality. However, CSV focuses specifically on validating computer systems to meet regulatory standards, especially in pharma and biotech industries. Quality Assurance Specialists have a broader scope, overseeing overall quality processes across various sectors. Both roles require similar certifications and work environments but differ in their primary objectives and specific tasks.

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

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

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

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

Computer Systems Validation jobs near you
Infographic showing various Computer Systems Validation job openings in Dublin, CA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $127,241 per year, or $61.2 per hour.

Manager, Computer Systems Validation (CSV)

Corcept Therapeutics

Redwood City, CA • On-site

$160K - $189K/yr

Full-time

Posted 20 days ago

Job description

The Manager, Computer Systems Validation (CSV) will be a core member of the Quality Systems Technology team and responsible for the implementation, management, ongoing support and review of Corcept's internal GXP validated systems. This individual will ensure IT Quality and Risk Management standards are defined, understood, designed into work activity, and achieved. This position will manage day-to-day operations for IT Compliance and Risk Management, working closely with key stakeholders from business teams, particularly QA, heavily guiding business teams on validation principles and requirements throughout the system lifecycle. This role will ensure compliance risks are identified, mitigated, and managed appropriately.

Responsibilities:

  • Provide assessment/review/oversight for Enterprise / GXP computer systems validation (focus on Pharmaceutical Systems)  
  • Experienced in developing validation strategies and authoring validation documents such as validation master plans, data migration plans, protocols, reports, discrepancies    
  • Ensure compliance and the validated state of all GXP systems 
  • Provide validation guidance on data migration activities as needed
  • Provide IT assessment and approval for GXP computer system changes
  •  Develop and support testing of proposed changes in system development environments
  • Experience in authoring and managing documents such as change control, Risk Assessments, Validation Plans, User Requirements Specifications, Functional Specifications, qualification protocols (IQ/OQ/PQ), Traceability Matrix, system procedures, deviations and CAPAs
  • Coordinate and support vendor support release activities 
  • Support and provide guidance to cross-functional groups with GXP system implementation projects and ongoing validation needs including system enhancements, releases and revalidation
  • Responsible to manage external CSV consultants in CSV projects 
  • Responsible as interface between IT and QA 

Preferred Education and Experience:

  • 8+ years' experience in QA or Validation performing protocol review and approval associated with the implementation and maintenance of computerized systems in pharma/biotech environment 
  • Solid knowledge of industry standards related to computerized systems and Electronic Records/Electronic Signatures; 21 CFR Part 210, 211& 11, Annex 11, GAMP5, ICH Q9, Data Integrity, CSA 

Skills, Qualifications, or Technical Proficiencies:

  • Thorough understanding of validation/qualification and concepts as it applies to pharmaceutical quality systems 
  • Excellent communication skills with the ability to effectively communicate across organizational levels and functions 
  • Proficiency with Veeva QualityDocs / QMS and ComplianceWire 
  • Experience with CTMS and Regulatory systems  
  • Ability to manage external software and consultant vendors 

The pay range that the Company reasonably expects to pay for this headquarters-based position is $160,600 - $189,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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