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Computer System Validation Jobs in California (NOW HIRING)

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal SerDes IP. In this highly visible role, you will actively work within Analog-Mixed/Signal design team ...

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal SerDes IP. In this highly visible role, you will actively work within Analog-Mixed/Signal design team ...

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

$126K - $220K/yr

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal SerDes IP. In this highly visible role, you will actively work within Analog-Mixed/Signal design team ...

Apple

SerDes System Validation Engineer

Cupertino, CA

$181K - $318K/yr

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal SerDes IP. In this highly visible role, you will actively work within Analog-Mixed/Signal design team ...

PSC Biotech

LabWare Specialist

Thousand Oaks, CA

$85K - $115K/yr

Support Computer System Validation (CSV) activities for LabWare implementations and enhancements. * Author and/or contribute to validation deliverables. * Ensure full requirements-to-configuration ...

New

PSC Biotech

LabWare Specialist

Ventura, CA · On-site

Support Computer System Validation (CSV) activities for LabWare implementations and enhancements. * Author and/or contribute to validation deliverables. * Ensure full requirements-to-configuration ...

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Computer System Validation information

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$10

$53

$84

How much do computer system validation jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for computer system validation in California is $53.61, according to ZipRecruiter salary data. Most workers in this role earn between $41.30 and $63.56 per hour, depending on experience, location, and employer.

What are some typical challenges faced in Computer System Validation roles?

Professionals in Computer System Validation often encounter challenges such as keeping up with evolving regulatory requirements, ensuring complete and accurate documentation, and coordinating with cross-functional teams to implement validation protocols. Balancing thoroughness with project deadlines can also be demanding, as every validation step must stand up to external audits. However, these challenges provide valuable experience, strengthen project management abilities, and emphasize teamwork—key attributes that support career advancement into validation leadership or quality assurance roles.

What is a Computer System Validation job?

A Computer System Validation (CSV) job involves ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, meet compliance and regulatory requirements. CSV professionals develop and execute validation protocols to confirm that software, hardware, and processes function as intended and maintain data integrity. They work with quality assurance, IT, and regulatory teams to document compliance with standards like FDA 21 CFR Part 11 and GxP. This role is critical in maintaining system reliability, product quality, and patient safety.

What is the salary of computer system validation?

The salary for a Computer System Validation specialist typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Certifications such as GAMP or CSV training can influence earning potential, and roles often require knowledge of regulatory standards like FDA or ISO.

What are the key skills and qualifications needed to thrive in the Computer System Validation position, and why are they important?

To excel in Computer System Validation, candidates typically need a background in computer science, engineering, or life sciences, with expertise in validating software and systems in regulated environments such as pharmaceuticals or medical devices. Familiarity with tools like validation documentation software, GAMP 5 guidelines, FDA 21 CFR Part 11 regulations, and potentially certifications like CSV Professional or Six Sigma is highly valued. Strong attention to detail, analytical thinking, and effective communication skills help professionals work collaboratively and document findings precisely. These abilities ensure compliance, data integrity, and the reliability of computerized systems critical to safety and quality.

What is the work of computer system validation?

Computer System Validation (CSV) is the process of ensuring that computer systems used in regulated environments function correctly and comply with industry standards. It involves documenting and testing software, hardware, and related processes to verify they meet specified requirements, often using validation protocols and tools. CSV is essential in industries like pharmaceuticals and healthcare to ensure data integrity and compliance with regulations such as FDA or GMP.

Is computer system validation a good field?

Computer System Validation (CSV) is a vital part of regulated industries like pharmaceuticals and biotech, ensuring that computer systems meet quality and compliance standards. It often requires knowledge of regulatory guidelines, validation protocols, and tools like GxP and 21 CFR Part 11. The field offers steady demand, opportunities for certification, and roles in quality assurance and compliance management.

Is CSV a skill?

In the context of Computer System Validation, CSV refers to Computer System Validation itself, which is a process rather than a skill. However, skills related to CSV include understanding validation protocols, regulatory requirements, and proficiency with validation tools and documentation. These skills are essential for professionals performing CSV tasks in regulated industries like pharmaceuticals and biotech.
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Computer System Validation jobs near you
Senior Computer System Validation Consultant

Senior Computer System Validation Consultant

CYNET SYSTEMS

San Diego, CA • On-site

$23 - $28/hr

Contractor

Posted 7 hours ago

Job description

Job Overview:
 
Pay Range: $23.98hr - $28.98hr
  • The role involves leading computer system validation activities across the system lifecycle, ensuring regulatory compliance, data integrity, and quality governance in a biopharmaceutical environment, including validation planning, risk management, and audit readiness.

Requirement/Must Have:

  • Bachelor’s degree in Life Sciences or related discipline within the pharmaceutical/biotech industry.
  • Strong experience in CSV (Computer System Validation) and Quality Compliance.
  • Deep understanding of 21 CFR Part 11, GxP (211/820), GAMP 5, and EU Annex 11.
  • Strong knowledge of data integrity and validated systems in regulated environments.
  • Experience with quality management systems including Change Control, Deviations, CAPA, Document Control, Training, EDMS, and LMS.
  • Strong technical understanding of IT systems, networked applications, and infrastructure in regulated environments.
  • Proficiency in MS Excel, PowerPoint, and Word.
  • Strong communication, collaboration, and stakeholder management skills.

Experience:

  • Experience working in life sciences, biotech, or pharmaceutical environments.
  • Experience in validation lifecycle management and compliance oversight.
  • Experience supporting regulated GMP systems and audits.

Responsibilities:

  • Author, review, and approve validation deliverables including validation plans, risk assessments, URS, configuration specifications, test scripts (IQ/OQ/PQ), and validation summary reports.
  • Perform requalification and periodic reviews of existing computer systems.
  • Oversee system development lifecycle processes ensuring compliance across build, test, deploy, and maintenance phases.
  • Act as quality lead for project teams and guide validation and compliance activities.
  • Review and approve system lifecycle documentation to ensure SOP and regulatory compliance.
  • Support and lead internal and external audits and regulatory inspections.
  • Conduct risk assessments and escalate compliance or security issues as required.
  • Prepare compliance and validation status reports for management.
  • Perform gap assessments for legacy systems and integration readiness.
  • Advise teams on implementing security and compliance controls to ensure data integrity.
  • Promote teamwork and align daily activities with organizational quality goals.

Should Have:

  • Strong understanding of laboratory, manufacturing, and quality systems in GMP environments.
  • Experience with cell and gene therapy or pharmaceutical data systems preferred.
  • Strong knowledge of advanced quality systems and validation processes.

Skills:

  • Computer System Validation (CSV).
  • Regulatory compliance (21 CFR Part 11, GxP, GAMP 5, EU Annex 11).
  • Risk management and audit support.
  • Quality systems (CAPA, Change Control, Deviations, Document Control).
  • System lifecycle and validation documentation.
  • MS Office Suite (Excel, Word, PowerPoint).
  • Data integrity and regulated system compliance.

Qualification And Education:

  • Bachelor’s degree in Life Sciences or related field required.

Founded in 2010 and headquartered in the Washington, DC metro area, Cynet Systems Inc. is a leading staffing and recruiting powerhouse. Proudly recognized as a nationally and locally certified diversity firm, Cynet delivers agile, scalable talent solutions across industries. With an active footprint in all 50 U.S. states and Canada, we support thousands of consultants through our expansive, high-performing recruitment engine operating across North America and Asia—ensuring speed, quality, and consistency in every hire.
Cynet Systems logo

About Cynet Systems

Sourced by ZipRecruiter

Cynet Systems Inc is a staffing and recruiting corporation nestled in Ashburn, VA, USA. Established in 2010, the company operates within the Information Technology and Services sector, specializing in providing effective workforce solutions to different business needs, including IT consulting, direct hire, and contract staffing services. Through the years, Cynet Systems has built an impressive portfolio, going beyond borders and expanding its operations internationally in Canada and India. Rooted in its core values of teamwork, leadership, and commitment, Cynet Systems helps businesses unlock their full potential by providing versatile and competent professionals that perfectly align with their needs. Fueled by their unwavering mission to deliver top-tier talent to businesses worldwide, Cynet Systems garnered various recognitions including SIA's fastest-growing staffing firms and Best Place to Work in Virginia for 2019.

Industry

It services

Company size

501 - 1,000 Employees

Headquarters location

Sterling, VA, US

Year founded

2010

Social media

Twitter

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