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Validation Engineer Iii Jobs in California (NOW HIRING)

Validation Engineer III

Riverside, CA ยท On-site

$110K - $130K/yr

Validation Engineer III Location: Riverside, CA Salary Range: $110,000 - $130,000 Position Summary The Validation Engineer III will be responsible for planning, executing, and managing test and ...

The Validation Engineer will be responsible for the following. * Develop, approve, and execute ... Chemical engineers preferred, with a minimum of three (3) years relevant experience. * Experience ...

Silicon Validation Engineer

Sunnyvale, CA ยท On-site

$65 - $70/hr

One of our Direct Client looking for Cobol Developer Job Details: Job Title: Silicon System ... Hands-on experience in bring-up and validation of complex SoCs. 3+ years of embedded systems or ...

Fremont, CA Contract Duration: 3-24 months Rate: Negotiable Responsibilities: * Excellent employment opportunity for a Validation Engineer in the Fremont, CA area. * Manage and participate actively ...

Bachelor's degree in Engineering, Information Technology, or a related field. * 3-5+ years of experience in SAP validation or ERP system validation. * Ability to translate business and technical ...

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Validation Engineer Iii information

See California salary details

$22

$51

$77

How much do validation engineer iii jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for validation engineer iii 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 roles and responsibilities of a Validation Engineer III?

A Validation Engineer III is responsible for ensuring that products, processes, and systems meet regulatory and company standards for quality and safety. This role typically involves planning and executing validation tests, writing protocols and reports, analyzing data, and troubleshooting validation issues. Validation Engineer IIIs often lead validation projects, mentor junior staff, and work closely with cross-functional teams in industries like pharmaceuticals, biotechnology, or manufacturing. They ensure compliance with regulatory requirements such as FDA, GMP, or ISO standards. Strong analytical, documentation, and project management skills are important for success in this position.

What skills and qualifications are needed to thrive as a Validation Engineer III?

To excel as a Validation Engineer III, you need a strong background in engineering or life sciences, extensive knowledge of validation protocols, and experience in regulated industries such as pharmaceuticals or medical devices. Familiarity with technical tools like validation lifecycle management software, statistical analysis packages, and regulatory standards (e.g., FDA, GMP) is typically required, along with relevant certifications such as Six Sigma or CQE. Critical thinking, attention to detail, and effective communication are crucial soft skills for documenting processes and collaborating with cross-functional teams. These competencies ensure compliance, product quality, and the successful execution of complex validation projects.

What are common challenges faced by a Validation Engineer III, and how can they be addressed?

As a Validation Engineer III, one common challenge is coordinating among cross-functional teams such as manufacturing, quality, and regulatory departments to ensure validation activities meet strict compliance standards and timelines. Managing multiple projects simultaneously while adhering to evolving regulatory requirements can also be demanding. Strong project management, effective communication, and staying updated on industry guidelines help address these challenges and ensure successful validation outcomes.

What is the difference between Validation Engineer Iii vs Validation Engineer Ii?

AspectValidation Engineer IiiValidation Engineer Ii
Required CertificationsGMP, GxP, or industry-specific validation certificationsGMP, GxP, or industry-specific validation certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingPharmaceutical, biotech, or medical device manufacturing
Experience LevelAdvanced, with 3+ years of validation experienceIntermediate, with 1-3 years of validation experience
Job ResponsibilitiesLeading validation projects, complex troubleshooting, mentoringSupporting validation activities, executing protocols

The Validation Engineer Iii typically has more experience and handles complex validation projects, often leading initiatives and mentoring junior staff. In contrast, Validation Engineer Ii focuses on supporting validation tasks and executing protocols under supervision. Both roles are common in regulated industries like pharmaceuticals and biotech, with the Iii level requiring more expertise and responsibility.

What are popular job titles related to Validation Engineer Iii jobs in California?

For Validation Engineer Iii jobs in California, the most frequently searched job titles are:

Infographic showing various Validation Engineer Iii job openings in California as of August 2026, with employment types broken down into 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Validation Engineer - III

Santa Monica, CA โ€ข On-site

Contractor

Re-posted 16 days ago


Job description

Santa Monica, CA
Contract Duration: 6-18 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Validation Engineer III in the Santa Monica, CA area.
  • Responsible for performing the validation of computer systems.
  • This includes developing validation master plans with minimum supervision, preparing protocols independently, analyzing test results, and preparing technical reports.
  • Contributes directly to the completion of validation projects through the development of validation schedules, master plans, validation protocols and reports for systems that may be complex in nature, to support clinical and commercial manufacturing.
  • Coordinates validation activities with, and seeks team supports from, Validation, Development, Manufacturing, Engineering, Quality, third Parties, and other groups on validation projects to ensure validation projects are carried out on time and on budget.
  • Coordinates the activities of assigned validation and contract personnel and ensures the quality of completed work.
  • Reviews protocols, reports and data tables generated by peers and contract personnel.
  • Represents the department on cross-functional project teams.
  • As required, assists in preparation of regulatory submissions and presents validations in respective SME areas to regulatory authorities during routine internal and pre-approval inspections.

Experience:

  • Bachelor's Degree and 1-2 years of related experience