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Medical Device Validation Engineer Jobs in Arizona

Intellectt INC

The Automation Validation Engineer will be responsible for validating automation systems and ensuring compliance with regulatory and industry standards within a medical device environment. Key ...

RD Partners

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

R&D Partners is seeking to hire a Validation Engineer in Tucson, AZ . Your main responsibilities as ... medical device companies. R&D Partners is an equal-opportunity employer. Company Description R&D ...

CREXENDO, INC

Software Validation Engineer

Tempe, AZ · On-site

Crexendo Software Validation Engineer You will be part of a team working on Crexendo's (NASDAQ ... Crexendo offers a comprehensive benefits package including; equity, medical, vision, dental ...

Three Point Solutions

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Principal R&D Engineer Client: Medical Device Manufacturing Company Duration: 8.5 Months ... Lead the development, validation, and optimization of medical device manufacturing processes.

Aptyx

Quality Manager- MED DEVICE ISO13485

Tempe, AZ · On-site

The Quality Manager will lead a team of quality engineers and inspectors, partner closely with ... Ensure all Device History Records (DHRs), Device Master Records (DMRs), and validation ...

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Medical Device Validation Engineer information

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?

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.
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Medical Device Validation Engineer jobs near you
Infographic showing various Medical Device Validation Engineer job openings in Arizona as of July 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 100% In-person job distribution.
Automation Validation Engineer

Automation Validation Engineer

Intellectt INC

On-site

Contractor

Posted yesterday

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for an Automation Validation Engineer based in Arizona with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Job Title: Automation Validation Engineer
Location: Arizona
Job Summary:
The Automation Validation Engineer will be responsible for validating automation systems and ensuring compliance with regulatory and industry standards within a medical device environment.

Key Responsibilities:

  • Validate automation systems (MES, SCADA, PLC, HMI)
  • Develop and execute validation protocols, test scripts, and reports
  • Ensure compliance with FDA regulations and GAMP standards
  • Troubleshoot and resolve automation system issues
  • Collaborate with manufacturing, quality, and engineering teams
  • Maintain accurate validation documentation

Requirements:

  • 5+ years of automation validation experience (medical device preferred)
  • Strong knowledge of MES, SCADA, PLC, and HMI systems
  • Experience with validation protocols and regulatory standards (FDA, GAMP)
  • Bachelor’s degree in Electrical Engineering, Computer Science, or related field
  • Strong analytical, problem-solving, and communication skills

Preferred:

  • Experience with ISO 13485 and 21 CFR Part 11
  • Background in medical device manufacturing and quality systems

Thanks & Regards,
Vyshnavi Thuraka
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999- Ext: 225