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Validation Associate Jobs in California (NOW HIRING)

As a Qualiy Validation Associate you will work as part of cross-functional teams providing quality oversight, review, and approval of validation deliverables and change controls to ensure that ...

New

Senior Engineer, Process Validation

Sunnyvale, CA · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

Senior Engineer, Process Validation

Sunnyvale, CA · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Mentor junior validation associates in Process Validation, cGMP regulations, and principles of Quality by Design The essential requirements of the job include: * Bachelor or master degree in ...

Excellent employment opportunity for a Validation Engineer in the Fremont, CA area. * Manage and participate actively in all phases of qualification/validation for QC systems such as QC analytical ...

Validation Engineer

Vista, CA

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Work and communicate with different associates within the company to ensure timely completion of ... Experience with validation / monitoring of critical pharmaceutical utility systems, including ...

Validation Engineer

Vista, CA · On-site

$103K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Work and communicate with different associates within the company to ensure timely completion of ... Experience with validation / monitoring of critical pharmaceutical utility systems, including ...

Validation Engineer I

Irvine, CA · Hybrid

$60K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Associate's and/or Bachelor's degree in Science or Engineering * Minimum 0 - 2 years of previous ... validation documents, IOQ/PQ protocols, and final reports * An understanding of basic cGMP ...

Validation Engineer I

Irvine, CA · On-site

$60K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Associate's and/or Bachelor's degree in Science or Engineering * Minimum 0 - 2 years of previous ... validation documents, IOQ/PQ protocols, and final reports * An understanding of basic cGMP ...

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Validation Associate information

See California salary details

$22

$51

$77

How much do validation associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for validation associate in California is $51.32, according to ZipRecruiter salary data. Most workers in this role earn between $38.89 and $62.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a validation associate, and why are they important?

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What is a validation associate?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

How does a validation associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.

What are the most commonly searched types of Validation jobs in California?

The most popular types of Validation jobs in California are:

What job categories do people searching Validation Associate jobs in California look for?

The top searched job categories for Validation Associate jobs in California are:

What cities in California are hiring for Validation Associate jobs?

Cities in California with the most Validation Associate job openings:

Infographic showing various Validation Associate job openings in California as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 2% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Qualiy Validation Associate

Randstad

Thousand Oaks, CA

$60 - $74.20/hr

Full-time

Posted 2 days ago

New


Job description

As a Qualiy Validation Associate you will work as part of cross-functional teams providing quality oversight, review, and approval of validation deliverables and change controls to ensure that products and processes meet appropriate regulatory agency validation requirements, internal company standards and current industry practices. This position will typically focus on disciplines related to facilities, utilities, equipment, instruments, process qualification, cleaning, computer systems validation and data integrity.

salary: $60 - $74.2 per hour
shift: First
work hours: 8 AM - 4 PM
education: Bachelors

Responsibilities

  • Responsible for reviewing validation documents, against Standard Operating Procedures (SOPs) for accuracy and compliance with procedures, based on regulatory requirements and internal guidelines.
  • Review from a quality perspective the validation documentation required to assure the proper development of a project and support regulatory submissions.
  • Responsible for reviewing Validation Master Plans, Design Qualification, Installation Qualification, Operational Qualification, Performance Qualification, Computer System Validation, and Validation Maintenance packages in accordance with existing procedures. Reviews deliverables for compliance with existing requirements. Approves documentation related to system decommissioning.
  • Provide validation expertise and support for the development (or modification phases) of manufacturing facility, utilities, systems, process and information and Computerized System; address, include and implement all the applicable QA requirements.
  • Participate in the risk assessment related to the project.
  • Assure requirements traceability throughout the whole project life cycle.
  • Provide support in all quality-related issues, including GMP regulations
  • Maintain project metrics to communicate risk trends and implementation readiness to support project timelines and commercial readiness
  • May perform other duties as assigned.
The essential functions of this role include:
  • working in a smoke free environment
  • wearing steel toe shoes

  • Skills
  • Quality Assurance
  • Quality Control
  • SOP
  • GMP
  • Validations
  • Technical writing
  • Veeva

  • Qualifications
  • Years of experience: 5 years
  • Experience level: Experienced

  • Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


    Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
    This posting is open for thirty (30) days.
    Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
    Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
    We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.