... 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 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 ...
... 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 ...
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 ...
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 ...
Photonics Validation Engineer
Sunnyvale, CA · On-site
$170K - $250K/yr
Perform failure analysis efforts - root-causing device and system failures across optical ... Comprehensive medical, dental, and vision coverage * 401(k) retirement plan * Flexible vacation and ...
Photonics Validation Engineer
Sunnyvale, CA · On-site
$170K - $250K/yr
Perform failure analysis efforts - root-causing device and system failures across optical ... Comprehensive medical, dental, and vision coverage * 401(k) retirement plan * Flexible vacation and ...
Strong understanding of medical device product development and design control principles. * Excellent verbal and written communication skills, with the ability to train and support engineers at all ...
Quick apply
Strong understanding of medical device product development and design control principles. * Excellent verbal and written communication skills, with the ability to train and support engineers at all ...
Silicon Validation Engineer 5
$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
$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 ...
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 ...
Validation Engineer 1 as 100% Remote
Sunnyvale, CA · Remote
$74/hr
Validation Engineer 1 Location: 100% Remote Duration: 03 Months Pay Rate: $60.00 - $74.00/- on W2 ... Medical Device/Pharma/Life Sciences) with a focus on GxP systems. Preferred Skills and Experience ...
Quick apply
Validation Engineer 1 as 100% Remote
Sunnyvale, CA · Remote
$74/hr
Validation Engineer 1 Location: 100% Remote Duration: 03 Months Pay Rate: $60.00 - $74.00/- on W2 ... Medical Device/Pharma/Life Sciences) with a focus on GxP systems. Preferred Skills and Experience ...
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 · On-site
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 · On-site
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 sterilization standards, such as ISO 11135 and ISO 11137. • Excellent verbal and written communication, teamwork, and interpersonal skills to work across multiple constituents. • ...
... medical device sterilization standards, such as ISO 11135 and ISO 11137. • Excellent verbal and written communication, teamwork, and interpersonal skills to work across multiple constituents. • ...
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 ...
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 ...
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 Aug 8, 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.
Are medical device validation engineers in demand?
Medical device validation engineers are in high demand due to the increasing regulation and complexity of medical devices. They play a critical role in ensuring compliance with standards like ISO 13485 and FDA requirements, and their expertise in validation, testing, and quality assurance is sought after in the healthcare industry.
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?
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 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 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
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