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Medical Product Verification Engineer Jobs (NOW HIRING)

Join our Product Verification Engineering team and play a key role in ensuring the quality ... Medical device testing experience preferred * Azure DevOps/TFS experience is a plus * Preferred ...

Senior Verification Engineer

Boston, MA · On-site

$90K - $165K/yr

A Verification Engineer is a technical position responsible for testing and verification of ... Ensure that FDA-regulated medical products are tested in adherence to the applicable standards ...

New

A Verification Engineer is a technical position responsible for testing and verification of ... Ensure that FDA-regulated medical products are tested in adherence to the applicable standards ...

Senior Verification Engineer

Boston, MA · On-site

$90K - $165K/yr

... medical products are tested in adherence to the applicable standards, regulations (ISO 13485, IEC 62304) and best practices. · Manage relationships with clients · Contributing to the continuous ...

Our portfolio of automation solutions help manufacturers to develop and deliver products quickly ... Teradyne offers a variety of robust health and well-being benefit programs, including medical ...

... medical products are tested in adherence to the applicable standards, regulations (ISO 13485, IEC 62304) and best practices. • Manage relationships with clients • Contributing to the continuous ...

Verification Engineer

Huntsville, AL · On-site

$129K/yr

Verification Engineer Reference: 23-022 Job Type: Full-time Job Status: Interviewing Date Posted ... Once planned, we ensure the sub products (GFC, GCN, GSS, IDT) are properly decomposed. We utilize ...

Verification Engineer

Johns Creek, GA · Hybrid

$126K/yr

Role Overview We are seeking an experienced Verification Engineer to design and develop system-level UVM testbenches for advanced memory and interconnect products, including DDR5 DIMMs, Power ...

Design Verification Engineer

Austin, TX · On-site

$134K - $164K/yr

Design Verification Engineer ID: 1063 Location: Austin, TX More about this job > Description Design ... products for vision processing, aerospace FPGAs, medical electronics, RISC-V based SoC, ARM based ...

Role Overview We are seeking a highly capable Formal Verification Engineer to join our core product ... Unlimited PTO and full benefits (medical, vision, dental, 401k). * Two engineering-centric offices ...

AMS Verification Engineer

Richardson, TX · On-site +1

$122K/yr

... medical, and defense applications. You will develop verification plans, build and debug mixed ... Support design reviews, silicon readiness, bring-up planning, and product delivery What We're ...

Design Verification Engineer

Austin, TX · On-site

$134K - $164K/yr

Design Verification Engineer ID: 1058 Location: Austin, TX More about this job > Description Design ... products for vision processing, aerospace FPGAs, medical electronics, RISC-V based SoC, ARM based ...

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Medical Product Verification Engineer information

See salary details

$80K

$142.6K

$203.5K

How much do medical product verification engineer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for medical product verification engineer in the United States is $142,619.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What does a medical product verification engineer do?

A Medical Product Verification Engineer is responsible for testing and evaluating medical devices to ensure they meet regulatory standards, safety requirements, and design specifications. They develop and execute test plans, analyze data, and document results to verify that products perform as intended. This role often involves collaborating with design, quality, and regulatory teams to address any issues found during verification. Their work is critical in ensuring that medical products are safe and effective before reaching the market.

What are the key skills and qualifications needed to thrive as a medical product verification engineer, and why are they important?

To thrive as a Medical Product Verification Engineer, you need a strong background in biomedical engineering or a related field, with expertise in product testing, quality assurance, and regulatory standards. Familiarity with tools such as verification protocols, test automation software, and compliance with FDA or ISO 13485 regulations is essential. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These skills and qualities ensure medical products are safe, effective, and meet rigorous regulatory requirements, directly impacting patient outcomes and company reputation.

What are some common challenges faced by medical product verification engineers during product testing, and how can they be addressed?

Medical Product Verification Engineers often encounter challenges such as ensuring test protocols comply with strict regulatory standards and managing tight project timelines. Variability in device performance and unexpected test failures can also occur, requiring quick problem-solving and collaboration with design and quality teams. Addressing these challenges involves maintaining clear documentation, participating in cross-functional meetings, and staying updated on regulatory changes to ensure testing processes remain compliant and efficient.

What is the difference between Medical Product Verification Engineer vs Medical Device Quality Assurance Specialist?

AspectMedical Product Verification EngineerMedical Device Quality Assurance Specialist
CredentialsBachelor's in Engineering, certifications in verification/validationBachelor's in Life Sciences or Engineering, certifications in QA
Work EnvironmentDesign labs, testing facilities, R&D departmentsManufacturing sites, quality control labs, compliance offices
Employer & Industry UsageMedical device companies, biotech firmsMedical device manufacturers, healthcare companies
Common Search & ComparisonYesYes

Medical Product Verification Engineers focus on testing and validating medical devices to ensure they meet specifications, working closely with R&D teams. Medical Device Quality Assurance Specialists concentrate on maintaining quality standards, compliance, and regulatory requirements throughout manufacturing. Both roles are essential in the medical device industry but differ in their primary focus and responsibilities.

What are popular job titles related to Medical Product Verification Engineer jobs?

For Medical Product Verification Engineer jobs, the most frequently searched job titles are:

Infographic showing various Medical Product Verification Engineer job openings in the United States as of September 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $142,619 per year, or $68.6 per hour.

Product Verification Engineer

Palo Alto, CA • On-site

$115K - $159K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Key responsibilities

  • Write and execute testing cases, including UI automated tests, for radiotherapy systems.

  • Perform automation software testing, develop and modify test plans, and analyze test results.

  • Coordinate test efforts, document defects, and ensure quality system integration in verification and validation environments.


Job description

## Product Verification EngineerApplyremote type: Hybridlocations: PAO H 3120time type: Full timeposted on: Posted 8 Days Agojob requisition id: R-29238Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.In this new role, you will be part of our Product Verification Engineering team. You will be responsible for writing and executing testing cases and doing UI automated tests using our in-house developed python testing framework to test our latest radiotherapy systems. We closely collaborate with other engineering locations of Varian, mainly at our R&D sites in Budapest, Hungary, Baden, Switzerland and Palo Alto, United States.**Description*** Performs automation software testing using systematic tests to develop, apply, and maintain quality standards for treatment delivery products.* Develops, modifies, and executes automation software test plans.* Helps manage and drive test schedule and related activities.* Performs hands-on installation and configuration of Hardware and Software components for verification and validation test environments.* Executes test cases in an efficient and timely manner.* Identifies and clearly documents encountered software defects.* Works closely with other testers and developers to coordinate test efforts and to resolve issues.* Maintains documentation of test results to assist in debugging and modification of software.* Analyzes test results to ensure existing functionality and recommends corrective actions.* Consults with development engineers in resolution of problems.* Ensures quality system integration into the overall function of scientific computation, data acquisition, and processing.* Analyses and reviews product specifications (e.g product requirement, system, functional, and design specifications) to ensure product quality, safety, reliability, and testability.* Perform product testing independently in test labs and test cell environments.* Travels to off-site test locations (Varian company offices or hospitals, located domestically or internationally) occasionally and performs product testing.**Minimum Required Skills and Knowledge*** Strong programming skills, preferably in python and experience working with .NET framework.* Ability to demonstrate solid Object-Oriented Programming knowledge.* Proficiency in TFS (Azure) is a plus.* Professional work experience in testing of software.* Experience with Medical device testing in software/hardware integration is highly desired.* Strong knowledge of software testing methodology, industry standard testing, and bug tracking tools.* Good written and verbal communication (English), and strong interpersonal skills.* Ability to work on assigned tasks under tight time constraints.* Ability to do computer tasks with minimal supervision.* Solid understanding of software development life cycle.* Can travel to off-site test locations (domestic and international) and perform product testing.* Experience in a clinical radiation oncology environment and working knowledge of Varian products (Treatment Planning, information systems, treatment delivery systems) are highly desired.**Typical Education and Experience*** Bachelors degree in Computer Science (or a related technical field) and 5+ years of related working experience* Or Masters Degree in Computer Science (or a related technical field) with 3+ years of related working experience.**Who we are**: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.**How we work:** When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.To find out more about Siemens Healthineers businesses, please visit our company page here.The base pay range for this position is:$115,980 - $159,478Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance.The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time.**Equal Employment Opportunity Statement:** Siemens Healthineers is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.**EEO is the Law:** Applicants and employees are protected under Federal law from discrimination. To learn more, click here.**Reasonable Accommodations:** Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at peopleconnectvendorsnam.func@siemens-healthineers.com. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.**California Privacy Notice:** California residents have the right to receive additional notices about their personal information. To learn more, click here.**Export Control:** “A successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”**Data Privacy:** We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.**Beware of Job Scams:** Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.**To all recruitment agencies:** Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.We are a team of 72,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what’s possible in healthcare to help improve people’s lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways. #J-18808-Ljbffr