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Platform Validation Engineer Jobs in California (NOW HIRING)

With our expansive platform of management solutions and decades of temperature-controlled supply ... POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ...

Validation Engineer III

Riverside, CA · On-site

$110K - $130K/yr

Validation Engineer III Location: Riverside, CA Salary Range: $110,000 - $130,000 Position Summary ... platform. This role will ensure that all vehicle systems, mechanical, electrical, and software ...

Validation Engineer 4

San Jose, CA · On-site

$82 - $87/hr

Requires experience and demonstrated technical expertise in the development & execution of platform ... engineers and technicians in the planning, test, & debug processor validation. Nice to Have: * An ...

Validation Engineer 4

Folsom, CA · On-site

$65 - $70/hr

Platform level electrical characterization experience with processor I/O interfaces is preferred ... experienced engineers and technicians in planning, testing, & debugging processor validation.

These platforms and their associated product candidates are designed to be more effective ... The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and ...

Validation Engineer 4

San Jose, CA · On-site

$82 - $87/hr

Requires experience and demonstrated technical expertise in the development & execution of platform ... engineers and technicians in the planning, test, & debug processor validation. Nice to Have: * An ...

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 ...

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 ...

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 ...

This includes working with emulation platforms, proto-ICs, validation boards, FW and SW to bring an ... in C/C++ programming • Demonstrated strong analytical and problem-solving skills Ability to ...

ASIC Validation Engineer

Saratoga, CA · On-site

$185K - $250K/yr

Collaborate with board design and test engineering teams on validation platforms, sockets, and ... characterization boards. Qualifications * B.S. or M.S. in Electrical Engineering, Computer ...

This includes working with emulation platforms, proto-ICs, validation boards, FW and SW to bring an ... in C/C++ programming • Demonstrated strong analytical and problem-solving skills Ability to ...

Showing results 41-60

Platform Validation Engineer information

See California salary details

$22

$51

$77

How much do platform validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for platform 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 platform validation engineer?

Platform Validation Engineers are professionals responsible for testing and validating hardware and software platforms to ensure they function correctly, meet design specifications, and are compatible with other system components. They work closely with design, development, and quality assurance teams to create and execute test plans, identify issues, and help resolve them before products reach customers. Their work is crucial in industries like semiconductors, computing, and embedded systems, where platform reliability and interoperability are essential.

What are some common challenges platform validation engineers face when testing new hardware platforms?

Platform Validation Engineers often encounter challenges such as debugging complex hardware-software interactions, ensuring compatibility across a wide range of system configurations, and reproducing intermittent issues under different workloads. Collaboration with cross-functional teams—including hardware designers, firmware developers, and software engineers—is essential for troubleshooting and root-cause analysis. Staying adaptable and maintaining clear documentation helps manage these challenges and ensures timely delivery of reliable, validated platforms.

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

To thrive as a Platform Validation Engineer, you need strong knowledge of system architecture, hardware and software integration, and testing methodologies, typically supported by a degree in electrical engineering, computer engineering, or a related field. Familiarity with validation tools like oscilloscopes, logic analyzers, scripting languages (Python, Perl), and experience with industry standards (such as PCIe, USB, or BIOS/UEFI) are commonly required. Analytical thinking, problem-solving, and effective communication are vital soft skills for diagnosing issues and collaborating with cross-functional teams. These skills ensure robust platform performance, timely bug detection, and successful product launches.

What is the difference between Platform Validation Engineer vs Hardware Validation Engineer?

AspectPlatform Validation EngineerHardware Validation Engineer
Required CredentialsBachelor's in Engineering, certifications in testing or validationBachelor's in Electrical, Mechanical, or related Engineering, certifications in hardware testing
Work EnvironmentTechnology companies, software and hardware integration labsManufacturing facilities, hardware testing labs
Industry UsageTech, consumer electronics, embedded systemsElectronics, automotive, aerospace
Common Search/ComparisonYesYes

The Platform Validation Engineer primarily focuses on testing and validating software and hardware platforms to ensure compatibility and performance, often working in integrated environments. In contrast, the Hardware Validation Engineer concentrates on testing physical hardware components for durability, functionality, and compliance. Both roles require engineering backgrounds and certifications, but their focus areas and work environments differ, catering to different stages of product development.

What cities in California are hiring for Platform Validation Engineer jobs?

Cities in California with the most Platform Validation Engineer job openings:

Validation Engineer

Irvine, CA • On-site

Cryoport, Inc.
1 - 5K employees

Full-time

Medical, Retirement

Re-posted 16 days ago


Job description

Cryoport Systems is a comprehensive supply chain partner for the life sciences industry, delivering specialized solutions to meet the challenges of the biopharmaceutical, cell and gene therapy, reproductive medicine, and animal health markets. Our offerings span logistics, BioServices and biostorage, cryopreservation, and consulting, ensuring the highest standards of quality and reliability for sensitive materials. With our expansive platform of management solutions and decades of temperature-controlled supply chain expertise, Cryoport Systems helps Enable the Outcome™ by supporting certainty and precision in the supply chain, whether advancing groundbreaking therapies, supporting families on their reproductive journeys, or enhancing animal health programs.
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 (include but are not limited to):
• Participate and oversee internal Consulting Services qualification processes including:
  • Assist in the development of validation procedures.
  • Perform internal validations including 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' 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.
  • Assists 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 utilized 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 ñ written and verbal.
• Analytical thinker with proficient skills 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, Power Point, 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.
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 (Nasdaq: CYRX).