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Medical Device Validation Engineer Jobs in San Ramon, CA

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Develop test methods, protocols, and reports for: * concept evaluations * verification & validation ... engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on ...

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Develop test methods, protocols, and reports for: * concept evaluations * verification & validation ... engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on ...

Be Seen First

Collaborate with engineers, technicians, quality personnel, and production staff to resolve ... Medical device manufacturing experience. * Experience working with optical, fluidic, electronic, or ...

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Deliver results from various device testing domains, including functional, performance, new feature ... related medical conditions), sexual orientation, gender, gender identity, gender expression ...

Product Validation Engineer

Sunnyvale, CA · On-site

$118K - $170K/yr

... various device testing domains, including functional, performance, new feature, and regression ... medical conditions), sexual orientation, gender identity, gender expression, age, status as a ...

Develop test methods, protocols, and reports for: * concept evaluations * verification & validation ... engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on ...

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Showing results 1-20

Medical Device Validation Engineer information

See San Ramon, CA salary details

$25

$58

$87

How much do medical device validation engineer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for medical device validation engineer in San Ramon, CA is $58.11, according to ZipRecruiter salary data. Most workers in this role earn between $44.04 and $70.67 per hour, depending on experience, location, and employer.

What are some common challenges faced by Medical Device Validation Engineers during the validation process?

Medical Device Validation Engineers often encounter challenges such as ensuring compliance with evolving regulatory standards, managing tight project timelines, and coordinating cross-functional teams. Additionally, they must address unexpected technical issues that arise during testing and validation, and meticulously document results to meet quality and audit requirements. Effective communication and adaptability are crucial for successfully navigating these challenges and delivering safe, effective medical devices.

What does a Medical Device Validation Engineer do?

A Medical Device Validation Engineer is responsible for ensuring that medical devices meet regulatory and quality standards before they reach the market. They design and execute tests to validate that products perform as intended, documenting procedures and results to comply with industry regulations such as FDA and ISO guidelines. Their work involves collaborating with design, manufacturing, and quality assurance teams to identify risks and verify that devices are safe and effective for use. This role is crucial for patient safety and for a company's ability to market medical products globally.

What engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. Achieving this level typically requires extensive experience, advanced skills, and sometimes leadership roles or working in high-paying industries.

How much does a validation engineer make at Pfizer?

A validation engineer at Pfizer typically earns between $70,000 and $100,000 annually, depending on experience, location, and certifications. Salaries may also include benefits such as health insurance and bonuses, with some roles requiring knowledge of validation protocols and regulatory standards.

Do validation engineers make good money?

Validation engineers, including those in the medical device industry, typically earn competitive salaries that reflect their specialized skills in quality assurance, regulatory compliance, and testing. Salaries vary based on experience, location, and certifications such as GxP or ISO standards, but generally offer strong compensation compared to many entry-level roles. The profession often includes benefits like healthcare and opportunities for career advancement.

What engineers make $300,000 a year?

Senior medical device validation engineers with extensive experience, specialized skills in quality assurance, and certifications such as ISO 13485 can reach annual salaries of $300,000 or more. These roles often require advanced knowledge of regulatory standards, validation processes, and proficiency with testing tools in highly regulated environments.

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

AspectMedical Device Validation EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like CQE or validation-specific trainingEngineering or related degree, CQE or QA certifications
Work EnvironmentDesign validation, process validation, testing labsAudits, process improvements, compliance documentation
Industry UsageProduct development, validation phases in medical device manufacturingEnsuring overall product quality, compliance, and process control

The Medical Device Validation Engineer focuses on validating medical devices through testing and process validation, ensuring products meet regulatory standards. In contrast, the Quality Assurance Engineer oversees overall quality systems, audits, and compliance processes. Both roles require similar certifications and work within the medical device industry, but their core responsibilities differ in scope and focus.

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

To thrive as a Medical Device Validation Engineer, you need a strong background in biomedical engineering or a related field, with expertise in validation protocols, regulatory compliance, and risk analysis. Familiarity with technical standards such as ISO 13485, FDA 21 CFR Part 820, and tools like statistical analysis software and validation management systems is essential. Attention to detail, problem-solving abilities, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills are crucial to guarantee that medical devices meet regulatory requirements, function safely, and reach the market efficiently.
What are popular job titles related to Medical Device Validation Engineer jobs in San Ramon, CA? For Medical Device Validation Engineer jobs in San Ramon, CA, the most frequently searched job titles are:
What job categories do people searching Medical Device Validation Engineer jobs in San Ramon, CA look for? The top searched job categories for Medical Device Validation Engineer jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Medical Device Validation Engineer jobs? Cities near San Ramon, CA with the most Medical Device Validation Engineer job openings:
Validation Manager

Full-time

Posted 25 days ago


Job description

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Position: Validation Manager 

Location: Hercules, CA

Duration: Full time 

Job Description

Lead Engineering Verification and Validation Activities managing a small contingent of validation engineers. 

Serve as Subject Matter Expert (SME) for all verification and validation activities

Develop and oversee verification protocols to verify engineering specifications

Develop and oversee validation protocols to validate customer requirements

Analyze verification and validation test data

Document test protocols and reports

Support Root Cause Analyses and Develop Corrective Measures 

o Conduct root cause analysis using test data and/or field failure data

o Develop and verify/validate effective countermeasures against root cause(s) of failure

Support Reliability Improvement Projects 

o Apply methodologies to drive reliability improvements

o Develop and execute reliability test methods

Support Change Control Process

Support Engineering Design Reviews

Required Skills 

An understanding/working knowledge of Fluidics/Filling Operations, Automation, Robotics, Cold Storage, Packaging, and site validation. DI Water Systems

Highly proficient in the use of MS Office Suite (Word, Excel, Power-point, Project)

Proficient in the use of Minitab and/or other statistical analysis software

Excellent written and verbal communication skills

Ability to work effectively in teams - cross-functionally and within engineering

Ability to multitask effectively and efficiently

Ability to work effectively with general direction

Highly capable of independent and critical thought and action


Required Experience 

BS/MS in an Engineering discipline or Physical Sciences

Six Sigma Green Belt (preferred)

Test Implementation, Verification & Validation, and Risk Assessment

Root Cause Analysis, Development of Corrective Actions

Hands on application of Statistical Analysis 

Working knowledge of FDA regulatory requirements and all internal quality standards

5-7 years of experience in medical device validation/FDA regulated industry.

3-5 years of management leadership experience

Project planning skills



Qualifications

BS/MS in an Engineering discipline or Physical Sciences

Additional Information

Thanks

Warm Regards

Harshad

732-429-1922


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996