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Computer Systems Validation Jobs in California (NOW HIRING)

Basic experience with equipment cleaning and computer systems validation methodologies is a plus. * Experience in electronic validation systems is preferred but not required. * Openness to learning ...

Basic experience with equipment cleaning and computer systems validation methodologies is a plus. * Experience in electronic validation systems is preferred but not required. * Openness to learning ...

Computer Systems Analyst III

Ridgecrest, CA · On-site

$27.63 - $34.54/hr

Must possess a valid, state-issued driver's license. * Requires competence in all phases of systems analysis techniques, concepts, methods, and knowledge of available system software, computer ...

Computer Systems Analyst III

Ridgecrest, CA · On-site

$27.63 - $34.54/hr

Must possess a valid, state-issued driver's license. * Requires competence in all phases of systems analysis techniques, concepts, methods, and knowledge of available system software, computer ...

Computer Systems Analyst III

Ridgecrest, CA · On-site

$27.63 - $34.54/hr

Must possess a valid, state-issued driver's license. * Requires competence in all phases of systems analysis techniques, concepts, methods, and knowledge of available system software, computer ...

$130K - $209K/yr

Lead investigation and review deviation investigations related to manufacturing process equipment, utilities, automation, computer systems, validation, and laboratory instruments. * Provide ...

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Come join R&D Lab in Super Micro Computer. We strive to ensure the product quality and reliability ... Experience in server systems, personal computers, IOT and embedded systems preferred. * At least 2 ...

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Supermicro Computer is currently looking for talented System Validation Engineer to partner with Hardware Designing team to validate in-house servers and workstation platforms, troubleshoot and ...

Showing results 41-60

Computer Systems Validation information

See California salary details

$10

$53

$84

How much do computer systems validation jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for computer systems 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 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 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 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 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 are popular job titles related to Computer Systems Validation jobs in California? For Computer Systems Validation jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Computer Systems Validation jobs? Cities in California with the most Computer Systems Validation job openings:
Infographic showing various Computer Systems Validation job openings in California as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 10% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $111,503 per year, or $53.6 per hour.

Engineer, Validation

Herbalife

Lake Forest, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago


Job description

Join an award-winning team at one of Orange County's Top Workplaces! Herbalife at Lake Forest has been recognized by the OC Register for our exceptional workplace culture, and we're looking for a dedicated Engineer, Validation to help us maintain our world-class standards.

ROLE AT A GLANCE: 

This is your opportunity to play a critical role in ensuring the products that improve millions of lives around the world are manufactured with the highest level of quality, safety, and integrity.

The Validation Engineer is responsible for all equipment and process validation activities at Herbalife Innovation and Manufacturing site, with primary focus at the Lake Forest location. Execution of validation activities is done to state and federal regulatory requirements, Herbalife and/or other applicable regulations and standards. The Validation Engineer supports all projects required for the expansion and improvement of operations at the production facility and coordinates all validation activities and projects with departmental managers.

The person in this role will be working around ingredients such as powder, milk, soy, & gluten.

In this role, you will be empowered to take ownership, drive meaningful improvements, and be recognized as a trusted technical authority across the organization

HOW YOU’LL MAKE AN IMPACT: 

Every validation you complete helps ensure that a product meeting the highest quality standards reaches someone who depends on it. Here's how you'll do that day to day:

  • Facilitates validation/qualification projects (planning, scheduling, execution, project reports, etc.).
  • Creates validation protocols and summary reports in compliance with Herbalife standards and/or government regulations. This includes investigating and resolving protocol deviations in a timely manner.
  • Coordinates change control and equipment-related changes (this includes providing assessment and feedback regarding change requests for equipment, facility, process modifications, etc.).
  • Maintains SOPs related to validation/qualification (i.e. validation master plans, validation templates) and update them, as required, to meet current standards.
  • Acts as back-up for management of the Global Environmental Monitoring (EM) program, which includes acting as an administrator for the associated Vaisala viewLinc application and working with temperature & humidity data loggers.
  • Additional duties as assigned.

TEAM DYNAMICS:  

You'll be joining a collaborative, passionate team that values expertise, mutual respect, and a shared drive to get it right. Your voice matters here — your insights and technical recommendations will directly shape how we operate.

  • Be able to work effectively with interdisciplinary departments to meet project deadlines and serve as a validation authority consulting with Engineering, Operations, and Quality.

LEADERSHIP AND SUPERVISORY RESPONSIBILITIES: 

Not applicable for this position.

Your technical expertise directly supports the team who help make our amazing products.


Experience

We're looking for someone who brings real-world GMP expertise and is ready to make an immediate impact:

  • 3-5 years of validation/qualification and process engineering experience in a GMP environment.
  • 5+ years of experience in Good Manufacturing Practices and Good Documentation Practices.
  • Experience in food, pharmaceutical and/or medical device process development.

QUALIFICATIONS FOR SUCCESS: 

Education

  • Bachelor of Science in Chemistry or field of Engineering 

Skills/Certifications 

  • Strong technical writing skills. Detailed knowledge of grammar, spelling, punctuation, and the fundamentals of technical GMP documentation.
  • Strong mechanical aptitude and process knowledge. Ability to work independently with minimal supervision.
  • Knowledge of PLC and automated controls qualification.
  • Knowledge of qualification fundamentals and requirements for powder and liquid handling, processing, and packaging.
  • Basic experience with equipment cleaning and computer systems validation methodologies is a plus.
  • Experience in electronic validation systems is preferred but not required.
  • Openness to learning skills outside of validation but is required for the expansion and improvement of operations at the production facility.

Ready to bring your validation expertise to a company with real global impact? Apply today and become part of the Herbalife team.

#LI-NP1


Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.