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Validation Engineer Jobs in California (NOW HIRING)

Cryoport Systems, LLC

Validation Engineer

Irvine, CA · On-site

$108 - $132/hr

Position Summary The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature ...

Cryoport

Validation Engineer

Irvine, CA · On-site

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

The Validation Engineer - Consulting Services will support the Consulting Services team's offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply ...

Semtech

Silicon Validation Engineer

San Diego, CA · On-site

The Validation Engineer is responsible for pre- and post-silicon validation of mixed-signal integrated circuits (ICs). Pre-silicon responsibilities include hardware emulation, FPGA prototyping, lab ...

Supermicro

Application Validation Engineer

San Jose, CA · On-site

$89K - $115K/yr

Supermicro is looking for an Application Validation Engineer with GPU knowledge and testing experience to take ownership in motherboard, system, and add-on-card testing. The individual will work with ...

GILLIG

Product Validation Engineer

Livermore, CA · On-site

Validation Engineering is responsible for the testing, simulation, and evaluation of systems, components and vehicle platforms for GILLIG's continuously evolving product line. It is instrumental in ...

Conductor

Link Validation Engineer

San Francisco, CA · On-site

$110 - $160/hr

We're looking for link validation engineers to help with DVT and bringup of the core optical link and PHY. Ideal Background: Ideal candidates for this role should have: * Hands-on experience with the ...

Semtech

Silicon Validation Engineer

San Diego, CA · On-site

The Silicon Validation Engineer will create test plans, runand analyzelab measurements, author characterization reports, and contribute to overall verification coverage closure. The role requires ...

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How much do validation engineer jobs pay per hour?

As of Sep 5, 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 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 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.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
More about Validation Engineer jobs

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

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

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

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

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Cities in California with the most Validation Engineer job openings:

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

Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in California as of August 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $106,736 per year, or $51.3 per hour.

Validation Engineer

Cryoport Systems, LLC

Irvine, CA • On-site

$108 - $132/hr

Other

Medical, Retirement

Posted 17 days ago

Job description

Position Summary

The Validation Engineer - Consulting Services will support the Consulting Services team’s offerings around shipper, packaging, and shipping lane qualifications across temperature sensitive supply chains. This is a client‑facing role within the Cryoport Systems Consulting Services department that is responsible for engaging in client discussions, performing qualifications, and developing technical reports.

Primary Responsibilities
  • Participate and oversee internal Consulting Services qualification processes including development of validation procedures.
  • Perform internal validations by developing validation protocols and reports, preparing equipment, and documenting & analyzing test results.
  • Support project creations for shipping lane qualifications, packaging configurations, systemized operational qualifications (physical and/or thermal performance testing), and shipping feasibility studies.
  • Manage qualification activities for Consulting Services’ client‑related projects.
  • Work as a team with all Consulting Services team members.
  • Engage with clients presenting validation plans in client collaboration meetings.
  • Develop and customize customer‑centric quality‑driven protocols.
  • Assist with coordination between external third‑party testing laboratories to ensure protocol execution, timelines, and quality metrics are achieved.
  • Evaluate, document, and articulate client‑specific results utilizing strong communication skills.
  • Assist in optimizing existing protocols, processes, and reporting for all validation activities.
  • Engage in continuous process improvement areas within Cryoport Systems Consulting Services.
  • Support cross‑organizational departments as needed.
Competencies & Personal Attributes
  • Professional with high attention to detail who focuses on client success.
  • Strong communication skills – written and verbal.
  • Analytical thinker with proficiency in math, statistics, and data analysis applications.
  • Strong organizational skills to manage multiple projects within overlapping timeframes.
  • Team player with ability to manage internal and external teams to achieve deliverables.
  • Self‑motivated with initiative to self‑learn to fill in knowledge gaps and expand contributions.
Qualifications and Education Requirements
  • BA/BS degree (in Life Sciences/Biopharma or a related healthcare field is highly preferred but not required).
  • 2+ years of experience in Biopharmaceuticals, Medical Device Industry (specifically Cell & Gene Therapies is highly preferred).
  • 2+ Years of Experience in writing professional documentation with customer‑facing materials.
  • Preferred experience with ISO, IATA, ASTM and ISTA standards relating to the pharmaceutical supply chain.
  • Preferred experience with Equipment and Process Validation using DQ, IQ, OQ, and PQ.
  • Knowledge of cGMP requirements, FDA and ICH guidelines is highly preferred.
  • Experience using Excel, creating pivot tables, graphs and customer digestible and meaningful visual and tabular analytics.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Teams).
  • Project Management skills/training is desirable.
Preferred Skills
  • Understanding of Cold Chain and temperature‑sensitive logistics, Packaging testing and qualification (GDP).
  • Good Distribution Practices (USP 36 – Chapter 1079, Good Storage and Distribution Practices for Drug Products).
  • ISO 21973 Biotechnology General requirements for transportation of cells for therapeutic use.
  • 21CFR Part 210 cGMP in Manufacturing, Processing, Packing, or Holding of Drugs.
  • 21CFR Part 211 cGMP for Finished Pharmaceuticals.
Compensation

Up to $120,000 depending on experience + bonus, stock, 401k match, benefits, etc.

Benefits

Health insurance, a 401K with company match, and stock equity (Nasdaq: CYRX).

Equal Opportunity Employer

Cryoport Systems is an Equal Opportunity Employer offering competitive compensation with a generous benefits package that includes health insurance, a 401K with company match and stock equity.

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