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Sr Validation Engineer Jobs in Riverside, CA (NOW HIRING)

Skylimit Systems

Sr. Project Engineer

Orange, CA

$140K - $160K/yr

This opportunity is ideal for an experienced Senior Project Engineer who enjoys owning complex ... Lead product qualification, validation, and manufacturing readiness activities * Collaborate with ...

HCLTech

Hardware Test Engineer

Irvine, CA · On-site

$59K/yr

HCLTech is looking for a Hardware Design & Validation Engineer (4-7 years) with expertise in board ... Throughout your time with us, we offer transparent communication with senior-level employees ...

Rivian

Senior Manager of Program Validation

Irvine, CA

$124K - $125K/yr

As Senior Manager, Vehicle Validation, you will lead the team responsible for vehicle-level ... Bachelor's degree in Engineering or a related technical field, or equivalent combination of ...

Rivian

Senior Manager of Program Validation

Irvine, CA · On-site

$124K - $125K/yr

As Senior Manager, Vehicle Validation, you will lead the team responsible for vehicle-level ... Bachelor's degree in Engineering or a related technical field, or equivalent combination of ...

ADP, Inc.

Senior Automation Developer

Santa Ana, CA · On-site

$146 - $183/hr

Senior Automation Developer Regular Full-Time Technical Santa Ana, CA, US Salary Range: $146,336.00 ... output validation). Engineering Excellence & Governance * Owns the full automation lifecycle ...

New

Jacobs Management Group

Senior Process Engineer

Corona, CA · On-site

$107K - $138K/yr

Senior Process Engineer My client, a leader in medical-grade extrusion manufacturing, is hiring a ... Own validation and qualification (IQ/OQ/PQ) protocols * Partner with maintenance on root cause ...

Masimo Corporation

Sr Engineer III, Algorithm

Irvine, CA · On-site

$150 - $185/hr

The Senior Engineer III, Algorithms leads the design, development, validation, and optimization of advanced biomedical signal processing algorithms supporting Masimo's noninvasive monitoring ...

Masimo

Sr Engineer III, Algorithm

Irvine, CA

$150K - $185K/yr

The Senior Engineer III, Algorithms leads the design, development, validation, and optimization of advanced biomedical signal processing algorithms supporting Masimo's noninvasive monitoring ...

Masimo

Sr Engineer III, Algorithm

Irvine, CA · On-site

$150K - $185K/yr

The Senior Engineer III, Algorithms leads the design, development, validation, and optimization of advanced biomedical signal processing algorithms supporting Masimo's noninvasive monitoring ...

TP-Link Systems Inc.

Senior Hardware Engineer

Irvine, CA · On-site

$118K - $158K/yr

Define and execute hardware validation plans, including functional testing, power validation ... senior engineer or technical lead role. * Experience in consumer networking, wireless router ...

TP-Link Systems Inc.

Senior Hardware Engineer

Irvine, CA

$118K - $158K/yr

Define and execute hardware validation plans, including functional testing, power validation ... senior engineer or technical lead role. * Experience in consumer networking, wireless router ...

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Showing results 21-40

All JobsSr Validation Engineer JobsSr Validation Engineer Jobs in Riverside, CA

Sr Validation Engineer information

See Riverside, CA salary details

$36

$67

$103

How much do sr validation engineer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for sr validation engineer in Riverside, CA is $67.58, according to ZipRecruiter salary data. Most workers in this role earn between $53.94 and $76.73 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

What are the key skills and qualifications needed to thrive as a Sr validation engineer?

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What are some common challenges a Sr validation engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

What are popular job titles related to Sr Validation Engineer jobs in Riverside, CA?

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

What job categories do people searching Sr Validation Engineer jobs in Riverside, CA look for?

The top searched job categories for Sr Validation Engineer jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Sr Validation Engineer jobs?

Cities near Riverside, CA with the most Sr Validation Engineer job openings:

Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in Riverside, CA as of August 2026, with employment types broken down into 88% Full Time, 8% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $140,556 per year, or $67.6 per hour.

Senior Designer - Design Verification & Validation

Stark Pharma Solutions Inc

Irvine, CA • On-site

Contractor

Posted 29 days ago

Job description

Position: Senior Designer – Design Verification & Validation
Location: California
Duration: Long Term

Job Overview

We are seeking an experienced Senior Designer – Design Verification & Validation to support design verification, equipment qualification, documentation, and manufacturing process improvement activities in a medical device manufacturing environment. The ideal candidate will have experience with SolidWorks, Windchill, validation documentation, and cross-functional project support.

Key Responsibilities

  • Support equipment qualification activities including IQ, OQ, and TMV.
  • Create, update, and execute validation and test protocols.
  • Develop and revise engineering drawings using SolidWorks.
  • Manage document creation, updates, and release through Windchill.
  • Support equipment software validation and prepare validation requirements.
  • Create and maintain PFMEA, process instructions, and technical documentation.
  • Perform GD&T drawing reviews and support design verification activities.
  • Develop DOE (Design of Experiments) for process characterization.
  • Create and release project deliverables, design specifications, and material specifications.
  • Support manufacturing activities, supplier transfers, equipment repairs, and continuous process improvements.

Required Qualifications

  • 5–8 years of experience in design verification, validation, or medical device product development.
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related discipline.
  • Strong experience with SolidWorks and Windchill PLM.
  • Hands-on experience with IQ/OQ/TMV, design verification, and validation documentation.
  • Knowledge of GD&T, PFMEA, and DOE methodologies.
  • Experience supporting manufacturing, engineering change documentation, and cross-functional projects.
  • Strong technical documentation, problem-solving, and project management skills.
  • Experience in a regulated medical device manufacturing environment is preferred.