Validation Manager
Hercules, CA · On-site
... 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 ...
Hercules, CA · On-site
... 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 ...
Hercules, CA · On-site
... 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 ...
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
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
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 ...
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 ...
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 ...
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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 ...
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 ...
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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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 ...
... 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 ...
Be Seen First
Milpitas, CA · On-site
$26/hr
Collaborate with engineers, technicians, quality personnel, and production staff to resolve ... Medical device manufacturing experience. * Experience working with optical, fluidic, electronic, or ...
New
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Be Seen First
Milpitas, CA · On-site
$26/hr
Collaborate with engineers, technicians, quality personnel, and production staff to resolve ... Medical device manufacturing experience. * Experience working with optical, fluidic, electronic, or ...
New
Deliver results from various device testing domains, including functional, performance, new feature ... related medical conditions), sexual orientation, gender, gender identity, gender expression ...
Deliver results from various device testing domains, including functional, performance, new feature ... related medical conditions), sexual orientation, gender, gender identity, gender expression ...
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 ...
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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 ...
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 ...
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 ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer * San Jose, CA, USA * Full-time * Department ... Help set up FPGA/Emulation platform and device modeling * Help set up FPGA/Emulation debugging ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer * San Jose, CA, USA * Full-time * Department ... Help set up FPGA/Emulation platform and device modeling * Help set up FPGA/Emulation debugging ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer Location: San Jose, CA, USA Duration: Full-time OR C2H ... Help set up FPGA/Emulation platform and device modeling * Help set up FPGA/Emulation debugging ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer Location: San Jose, CA, USA Duration: Full-time OR C2H ... Help set up FPGA/Emulation platform and device modeling * Help set up FPGA/Emulation debugging ...
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 ...
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 ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer · San Jose, CA, USA · Full-time · Department ... KEY RESPONSIBILITIES · Help set up FPGA/Emulation platform and device modeling · Help set up FPGA ...
$152K - $195K/yr
Senior FPGA/Emulation Validation Engineer · San Jose, CA, USA · Full-time · Department ... KEY RESPONSIBILITIES · Help set up FPGA/Emulation platform and device modeling · Help set up FPGA ...
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 ...
$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
| 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.
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.
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
BS/MS in an Engineering discipline or Physical Sciences
Thanks
Warm Regards
Harshad
732-429-1922
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.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996