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Medical Device Validation Engineer Jobs in Houston, TX

The Validation Engineer II will build and execute a periodic review program for our validated ... medical conditions), sexualorientation, gender identity or expression, national origin, ancestry ...

The Validation Engineer II will build and execute a periodic review program for our validated ... medical conditions), sexual orientation, gender identity or expression, national origin, ancestry ...

Senior Process Engineer

Stafford, TX · On-site

$80 - $100/hr

... validation, and sustainment of manufacturing processes supporting medical device products. This ... The Senior Manufacturing Engineer plays a critical role in driving integration projects ...

... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ... As a team of remarkably diverse engineers, we recognize that what we are really engineering is a ...

As an FPGA Engineer in our Oil & Gas division, you will develop high-reliability digital systems ... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ...

... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ... As a team of remarkably diverse engineers, we recognize that what we are really engineering is a ...

... are, medical devices, rail and semiconductor industries. We are looking for humble geniuses, who ... As a team of remarkably diverse engineers, we recognize that what we are really engineering is a ...

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

A Houston-based professional engineering firm is seeking a Principal Embedded Firmware Engineer to ... medical device firmware. This role focuses on Class I, II, and III medical devices, including ...

Principal Embedded Firmware Engineer

Houston, TX · On-site

$98K - $134K/yr

A Houston-based professional engineering firm is seeking a Principal Embedded Firmware Engineer to ... medical device firmware. This role focuses on Class I, II, and III medical devices, including ...

Senior Process Engineer

Stafford, TX · On-site

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development, optimization, validation, and sustainment of manufacturing processes supporting medical device products.

Senior Process Engineer

Stafford, TX · On-site

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development, optimization, validation, and sustainment of manufacturing processes supporting medical device products.

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Medical Device Validation Engineer information

See Houston, TX salary details

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$49

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How much do medical device validation engineer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for medical device validation engineer in Houston, TX is $49.65, according to ZipRecruiter salary data. Most workers in this role earn between $37.64 and $60.38 per hour, depending on experience, location, and employer.

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 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 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 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 popular job titles related to Medical Device Validation Engineer jobs in Houston, TX?

For Medical Device Validation Engineer jobs in Houston, TX, the most frequently searched job titles are:

What job categories do people searching Medical Device Validation Engineer jobs in Houston, TX look for?

The top searched job categories for Medical Device Validation Engineer jobs in Houston, TX are:

What cities near Houston, TX are hiring for Medical Device Validation Engineer jobs?

Cities near Houston, TX with the most Medical Device Validation Engineer job openings:

Infographic showing various Medical Device Validation Engineer job openings in Houston, TX as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $103,282 per year, or $49.7 per hour.

Validation Engineer II

Immatics NV

Houston, TX • On-site

Full-time

Medical, Dental, Vision

Posted 24 days ago


Job description

JoinImmaticsandshape thefuture ofcancerimmunotherapy; one patient at atime!

Immaticsis committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting ofPRAME, a target expressed in more than 50 cancers. Ourcutting-edgescience and robust clinical pipeline form the broadestPRAMEfranchise with the mostPRAMEindications and modalities, spanning TCR T-cell therapies and TCRbispecifics.

Why Join Us?

  • Innovative Environment:Helptopioneeradvancementsincancer immunotherapy.

  • Collaborative Culture:Be part ofa diverse team dedicated to yourprofessionalgrowth.

  • Global Impact:Contribute to therapiesthatmakealastingimpactonpatientsglobally.

Role Overview

We are seeking a Validation Engineer II to lead the implementation of new systems through the validation process and ensure all validation deliverables and regulations have been met. The Validation Engineer II will build and execute a periodic review program for our validated systems.

Schedule: 8:00 AM - 5:00 PM; Monday to Friday; On-site
Reports to:Senior Director, Enterprise Applications
Location: 13203Murphy Road Suite 100 Stafford, TX 77477

Basic Qualifications:

  • Bachelor's degree in Science, Engineering or a related major.Education in Biotechnology or a related major preferred

  • 5+ years experience in the pharmaceutical or biotech industry

PreferredQualifications:

  • Experience working within a GxP regulated manufacturing or laboratory environment.

  • An understanding of good documentation practices and data integrity principles.

  • Demonstrated understanding of 21 CFR Part 11, 21 CFR Part 210, 21 CFR Part 211, GAMP 5 and USP

  • Experience in writing and reviewing deviations and CAPAs, investigations leading to change controls

In thisrole youwill:

  • Draft validation documents including validation plans, user requirements specification (URS), risk assessments, configuration specification documents, installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) protocols, trace matrix and summary reports.

  • Execute test scripts from IQ/OQ/PQ protocols using good documentation practices and provide appropriate supporting evidence.

  • Create and manage project timelines and deliverables.

  • Monitor and review Quality Management Systems (CAPA, Change Controls, Deviations) and Batch Record Issuance procedures to ensure and maintain compliance with corporate and regulatory agency requirements.

  • Contribute to the writing, coordination, review, and approval of Quality Events when needed.

  • Coordinate, support, and investigate Corrective and Preventive Actions (CAPAs).

  • Draft SOPs and work instructions for system operation, maintenance, and cleaning.

  • Assist in Change Control process from initiation, revision of documents and processes up to training and implementation.

  • Assist in preparing QMS training materials and perform training as required.

  • Support cross-functional groups for QMS functions and projects not limited to Computer Systems Validation, Equipment Maintenance, Manufacturing, Quality Control, New Hire Onboarding, external and internal audits as needed.

  • Perform periodic reviews, requalifications and remediations for systems throughout the system lifecycle.

What do we offer?

AtImmatics, we believe in investing in our team's health,safetyand well-being.Here'swhat you can expectif youjoinImmatics

Comprehensive Benefits:

  • Competitive rates forHealth, Dental, and Vision Insurance

  • 4 weeksofvacation,grantedup front each year and prorated for firstand lastyearofemployment.

  • 12 company paid holidays

  • 7daysof sick time

  • 100%employer-paidlifeinsuranceup toat 1x annual salary, up to one hundred thousand dollars

  • 100%employer-paidshort-andlong-Termdisabilitycoverage

  • 401(k)withimmediateeligibilityandcompany match. The company will match100% of your contributions upto3% of yourbase salaryfor the first two yearsof employment, 4% foryears 2-3 of employment, and up to5%of your salaryfrom the fourth year onward of continued employment.

  • Partiallypaidparentalleavefor eligible employees.

  • Additionalvoluntaryemployee-paidbenefitsandservices,includingaccident,hospitalindemnity,andcriticalillnessinsurance,as well asidentitytheftprotectionandpetinsurance.

Equal Employment Opportunity

We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law.

Reasonable Accommodations

We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us atRecruitingUS@immatics.com.

Work Authorization

Applicants mustbe authorized towork in the United States without the need for current or future sponsorship.

Pre-Employment Requirements

Employment is contingent upon successful completion of a background check, referencechecksand pre-employment drug screening, wherepermittedby applicable law. For certain roles,additionalscreenings such as a credit check or motor vehicle record review may berequired, where job-related and consistent with business necessity.