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Validation Associate Jobs in California (NOW HIRING)

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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 Jun 14, 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.

How much does a validation specialist make in the US?

A validation specialist in the US typically earns between $60,000 and $85,000 annually, depending on experience, industry, and location. Entry-level roles may start around $50,000, while experienced professionals with certifications can earn over $100,000. Skills in quality assurance, regulatory compliance, and validation tools are often required for higher salaries.

What job makes $10,000 a month without a degree?

A Validation Associate typically does not earn $10,000 a month without a degree; such high earnings are uncommon for this role. Generally, jobs that can pay $10,000 monthly without a degree include specialized sales, real estate brokers, certain tech sales positions, or skilled trades with experience and commissions. These roles often require strong skills, certifications, or extensive experience rather than formal degrees.

Is QC a high paying job?

Quality Control (QC) roles, including validation associates, typically offer salaries that are average or slightly above average compared to other entry-level positions in manufacturing and healthcare industries. Compensation varies based on experience, location, and industry, with specialized skills and certifications potentially increasing earning potential.

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 are Validation Associates?

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.

Is Associate the lowest position?

In the role of Validation Associate, this position is typically an entry-level or early-career role within the validation or quality assurance departments. It is often the starting point before advancing to higher roles such as Senior Validation Associate or Validation Specialist, depending on the company's structure and experience required. The lowest position in a validation or quality team may vary by organization but often begins with entry-level titles like Validation Associate or Technician.

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 are popular job titles related to Validation Associate jobs in California? For Validation Associate jobs in California, the most frequently searched job titles 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:
Validation Engineer - Cold Storage & Analytical Equipment - (JP14626)

Validation Engineer - Cold Storage & Analytical Equipment - (JP14626)

3 Key Consulting

Thousand Oaks, CA

$45 - $55/hr

Other

Posted 7 days ago


Job description

Job Title: Validation Engineer - Cold Storage & Analytical Equipment - (JP14626)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Final Product Technologies Development
Duration: 12+ months (with likely extensions and/or conversion to permanent)
Posting Date: 10/10/25
Pay Rate: $45 - $55/hour W2
Notes: Only qualified candidates need apply. Fully onsite. Local candidates only
3 Key Consulting is hiring a Validation Engineer - Cold Storage & Analytical Equipment for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
We are looking for candidates with experience in:
  • Cold Storage Validation Experience
  • Analytical Equipment experience
  • Preferably Lab Ops/Equipment Background
  • Drafting Documents

Primarily responsible for ensuring adherence to computer validation standards and procedures for computer-related systems. Responsibilities include participation in system design, preparation of test protocols, analysis of test results and preparation of summaries. Provides guidance and sets standards in producing quality documentation, serves as the liaison between the IS and Quality functions, provides testing and IT compliance guidance, and provides timely and effective response and follow-through in the resolution of IT Quality/Project compliance issues.
Why is the Position Open?
Unplanned Project.
Top Must Have Skills:
  • Strong and clear communication skills
  • Paying attention to details
  • Drafting documentation
  • Nice to specifically have cold storage and computerized Analytical Equipment familiarity
  • Ability to switch on different project at the same time
  • Can work as a team player and independently

Day to Day Responsibilities:
This role is responsible for ensuring compliance with cold storage validations, computer validations for analytical laboratory instruments, and supporting ad hoc laboratory operations projects. Key duties include participating in system design, preparing and executing test protocols, analyzing results, and generating summary reports. The position provides guidance on IT compliance and quality documentation standards, serves as a liaison between laboratory, IS, and Quality functions, and ensures timely resolution of issues during installation and qualification activities. Success in this role requires strong communication and multitasking skills, the ability to follow established procedures, and the flexibility to work independently as well as within a team. Onsite presence is required.
Basic Qualifications:
Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experience
Employee Value Proposition:
Industry experience.
Red Flags:
  • Not local or able to be onsite
  • No experience with drafting documents or any type of general Lab Operations
  • Not able to work in a fast-faced environment

Interview process:
Interview with hiring Manager and team via MS Teams online
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.