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Validation Engineer Jobs in California (NOW HIRING)

Validation Engineer Location: Carlsbad, CA Job Summary: We are seeking a Validation Engineer with 2-5 years of validation experience in a regulated medical device, pharmaceutical, or life sciences ...

The Validation Engineer will be responsible for the following. * Develop, approve, and execute process validation studies and protocols for cell and gene therapy manufacturing. * Design and develop ...

Validation Engineer Location: San Diego, CA Duration: Longterm Job Summary: A Validation Engineer to lead and support quality-related validation activities within the Quality Management System. The ...

We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area contract development and manufacturing organization. Salary: $100-115k+/year depending on experience ...

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Validation Engineer II Location: Carlsbad, CA Type: W2 Contract Industry: Medical Devices / Healthcare We are actively hiring a Validation Engineer II in the Medical Devices / Healthcare industry.

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 IV Location: Santa Clara, CA Duration: Long-Term Role Overview: Looking for a Senior Test Method Validation Engineer to support product development for advanced medical device ...

Validation Engineer

Vista, CA ยท On-site

$103K - $142K/yr

A brief overview The Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of ...

Validation Engineer

Vista, CA ยท On-site

$103K - $142K/yr

A brief overview The Quality Engineer (QE) / Validation fulfills a critical role in GMP operations, supporting cleaning validation activities for API and PMO manufacturing, and the qualification of ...

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

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Validation Engineer information

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$22

$51

$77

How much do validation engineer jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for validation engineer 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 Is a Validation Engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

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

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges Validation Engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.
What are the most commonly searched types of Validation Engineer jobs in California? The most popular types of Validation Engineer jobs in California are:
What job categories do people searching Validation Engineer jobs in California look for? The top searched job categories for Validation Engineer jobs in California are:
What cities in California are hiring for Validation Engineer jobs? Cities in California with the most Validation Engineer job openings:
Infographic showing various Validation Engineer job openings in California as of July 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.
Validation Engineer

Validation Engineer

Intellectt INC

Carlsbad, CA โ€ข On-site

Contractor

Posted 10 days ago


Job description

Job Title: Validation Engineer

Location: Carlsbad, CA
ย 

Job Summary:

We are seeking a Validation Engineer with 2โ€“5 years of validation experience in a regulated medical device, pharmaceutical, or life sciences environment. The ideal candidate will develop and execute validation activities for manufacturing processes, equipment, and systems while ensuring compliance with FDA regulations, GMP, and internal quality standards.

Key Responsibilities:

  • Create, execute, and maintain validation protocols, reports, and related documentation.
  • Develop and manage Validation Master Plans (VMPs) for new and existing products.
  • Perform process, equipment, system, and software validation activities.
  • Review and assess change control documentation for validation impact.
  • Analyze validation results and prepare final validation reports.
  • Support internal and external audits by providing validation documentation and technical expertise.
  • Track validation project progress and ensure timely completion.
  • Collaborate with Manufacturing, Quality, Engineering, and Regulatory teams.
  • Mentor junior engineers and provide technical guidance when required.

Required Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related field (Master's preferred).
  • 2โ€“5 years of validation experience in Medical Devices, Pharmaceuticals, or Life Sciences.
  • Experience with process, equipment, and system validation.
  • Knowledge of FDA regulations, GMP, Quality Systems, and Design Control.
  • Experience with Validation Master Plans (VMP), IQ/OQ/PQ, Change Control, and Validation Documentation.
  • Strong technical writing, analytical, and problem-solving skills.
  • Excellent communication and cross-functional collaboration skills.