... 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 ...
... 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 ...
Staff Compliance Validation Engineer
Brisbane, CA · On-site
$130K - $150K/yr
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
Staff Compliance Validation Engineer
Brisbane, CA · On-site
$130K - $150K/yr
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
... medical device, pharmaceutical, or biotechnology preferred). * Strong knowledge of validation ... across engineering and manufacturing teams. Preferred Qualifications: * Enterprise Architect
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 ...
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 ...
Quick apply
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 ...
Power Validation Engineer
Sunnyvale, CA · On-site
$100K - $130K/yr
Lead power validation of AI Glass products across all device use cases * Design, develop, and ... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ...
Quick apply
Power Validation Engineer
Sunnyvale, CA · On-site
$100K - $130K/yr
Lead power validation of AI Glass products across all device use cases * Design, develop, and ... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ...
Working remotely you will have direct interface with medical device engineering and purchasing ... personnel to identify opportunities for our key principle products and technologies. This will ...
Working remotely you will have direct interface with medical device engineering and purchasing ... personnel to identify opportunities for our key principle products and technologies. This will ...
Working remotely you will have direct interface with medical device engineering and purchasing ... personnel to identify opportunities for our key principle products and technologies. This will ...
Working remotely you will have direct interface with medical device engineering and purchasing ... personnel to identify opportunities for our key principle products and technologies. This will ...
... in medical device development. * Ensure adherence to regulatory standards (FDA, ISO 13485, IEC ... Creation and review of validation deliverables including but not limited to. Responsibilities:
... in medical device development. * Ensure adherence to regulatory standards (FDA, ISO 13485, IEC ... Creation and review of validation deliverables including but not limited to. Responsibilities:
... in medical device development. * Ensure adherence to regulatory standards (FDA, ISO 13485, IEC ... Creation and review of validation deliverables including but not limited to Requirement ...
... in medical device development. * Ensure adherence to regulatory standards (FDA, ISO 13485, IEC ... Creation and review of validation deliverables including but not limited to Requirement ...
Senior Mechanical Engineer (Medical Device)
San Jose, CA · On-site
$122K - $161K/yr
Senior Mechanical Engineer (Medical Device) Location: San Jose, CA Duration: 6-12 Months Contract ... Experience with FDA compliance, DFMEA, validation/testing Responsibilities: * Lead design of ...
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Senior Mechanical Engineer (Medical Device)
San Jose, CA · On-site
$122K - $161K/yr
Senior Mechanical Engineer (Medical Device) Location: San Jose, CA Duration: 6-12 Months Contract ... Experience with FDA compliance, DFMEA, validation/testing Responsibilities: * Lead design of ...
Abbott's Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role ...
Quick apply
Abbott's Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role ...
Be Seen First
Medical Device Sales Representative
San Francisco, CA · Remote
$80K/yr
Valid U.S. driver's license and acceptable driving record Job Summary: The District Sales Manager ... Prior medical device, technical product, or travel sales experience a plus. * Experience building ...
Quick apply
Be Seen First
Medical Device Sales Representative
San Francisco, CA · Remote
$80K/yr
Valid U.S. driver's license and acceptable driving record Job Summary: The District Sales Manager ... Prior medical device, technical product, or travel sales experience a plus. * Experience building ...
Medical Device R&D Engineer
$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
$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 ...
Silicon Validation Engineer 5
San Jose, CA · On-site
$175K - $219K/yr
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
Silicon Validation Engineer 5
San Jose, CA · On-site
$175K - $219K/yr
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
Product Validation Engineer
Livermore, CA · Hybrid
Excellent compensation including company paid medical premiums, generous retirement plan and other ... Validation Engineering is responsible for the testing, simulation, and evaluation of systems ...
Product Validation Engineer
Livermore, CA · Hybrid
Excellent compensation including company paid medical premiums, generous retirement plan and other ... Validation Engineering is responsible for the testing, simulation, and evaluation of systems ...
Silicon Validation Engineer 3
San Jose, CA · On-site
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
Silicon Validation Engineer 3
San Jose, CA · On-site
As a Silicon Design Validation engineer, you will have an opportunity to learn and train yourself ... Proficiency with bench equipment for device characterization such as BERT, VNA, Oscilloscopes ...
Product Validation Engineer
Livermore, CA · Hybrid
Excellent compensation including company paid medical premiums, generous retirement plan and other ... Validation Engineering is responsible for the testing, simulation, and evaluation of systems ...
Product Validation Engineer
Livermore, CA · Hybrid
Excellent compensation including company paid medical premiums, generous retirement plan and other ... Validation Engineering is responsible for the testing, simulation, and evaluation of systems ...
Medical Device Validation Engineer information
See San Ramon, CA salary details
$25.25 - $30.89
2% of jobs
$30.89 - $36.53
6% of jobs
$36.53 - $42.18
13% of jobs
$43.94 is the 25th percentile. Wages below this are outliers.
$42.18 - $47.82
13% of jobs
$47.82 - $53.46
11% of jobs
The median wage is $56.28 / hr.
$53.46 - $59.10
12% of jobs
$59.10 - $64.74
9% of jobs
$69.09 is the 75th percentile. Wages above this are outliers.
$64.74 - $70.38
13% of jobs
$70.38 - $76.02
13% of jobs
$76.02 - $81.66
6% of jobs
$81.66 - $87.31
3% of jobs
$25
$58
$87
How much do medical device validation engineer jobs pay per hour?
As of Jul 18, 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 reach or exceed a $500,000 annual salary, especially with experience, advanced skills, and leadership roles. Medical Device Validation Engineers typically earn less, but senior-level professionals with extensive expertise and certifications may approach high six-figure incomes in certain industries or companies.
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.
Are validation engineers in demand?
Validation engineers, including those in the medical device industry, are in high demand due to strict regulatory requirements and the need for quality assurance. Their skills in validation protocols, risk management, and compliance with standards like ISO 13485 and FDA regulations make them valuable in manufacturing and quality assurance roles across healthcare and biotech sectors.
Do validation engineers make good money?
Validation engineers, including those in the medical device industry, typically earn competitive salaries that vary based on experience, location, and certifications. They often require knowledge of regulatory standards and validation tools, which can influence compensation levels. Overall, validation engineering is considered a well-paying profession within engineering fields.
What is the difference between Medical Device Validation Engineer vs Quality Assurance Engineer?
| Aspect | Medical Device Validation Engineer | Quality Assurance Engineer |
|---|---|---|
| Credentials | Engineering degree, certifications like CQE or validation-specific training | Engineering or related degree, CQE or QA certifications |
| Work Environment | Design validation, process validation, testing labs | Audits, process improvements, compliance documentation |
| Industry Usage | Product development, validation phases in medical device manufacturing | Ensuring 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:
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 ManagerÂ
Location: Hercules, CA
Duration: Full timeÂ
Job Description
Lead Engineering Verification and Validation Activities managing a small contingent of validation engineers.Â
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 MeasuresÂ
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 ProjectsÂ
o Apply methodologies to drive reliability improvements
o Develop and execute reliability test methods
Support Change Control Process
Support Engineering Design Reviews
Required SkillsÂ
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 ExperienceÂ
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 AnalysisÂ
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
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