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Quality Engineer Medical Device Jobs in Texas (NOW HIRING)

Medical Device Quality Engineer

Austin, TX · On-site

$71K - $92K/yr

Medical Device Quality Engineer Reports To : Sr. Manager, Quality Engineering Location: Austin, TX Business Unit Description : As a member of the Quality Assurance team, you will support activities ...

New

Quality Engineer

Longview, TX

$64K - $82K/yr

Are you and experienced quality engineer who would like to work for a global supplier of medical ... Ensure the quality management system meets the company's medical device expectations and goals.

Quality Engineer

Longview, TX · On-site

$64K - $82K/yr

... medical device expectations and goals. § Formulate and maintain accurate documentation to meet all quality system and medical device expectations. § Lead and manage direct and indirect reports ...

... medical device expectations and goals. § Formulate and maintain accurate documentation to meet all quality system and medical device expectations. § Lead and manage direct and indirect reports ...

Quality Engineer

El Paso, TX · On-site

$34 - $35/hr

Medical Device Manufacturing domain Location: El Paso, TX 79912 Duration: 12 months (Possibility of extension 2nd shift - Schedule (desirable): Mon-Fri 3:00pm-12:00am Onsite Role Interviews - video ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Knowledge and experience with software as a medical device. * Independently plan, develop, maintain ... ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt/Black Belt, or equivalent certification.

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Minimum of four (4) years of experience in Engineering or Quality Engineering within the medical device, pharmaceutical, or equivalent industry if holding a Bachelor's degree * Minimum of two (2) ...

New

Staff Quality Engineer

Austin, TX · On-site

$110 - $150/hr

Position Summary. The Staff Quality Engineer will support the development, and maintain key ... Ensures manufacturing and testing of medical device IVDs is performed in accordance with Nuclein ...

New

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

Knowledge and experience with software as a medical device. * Independently plan, develop,maintain ... ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt/Black Belt, or equivalent certification.

Staff Quality Engineer

Austin, TX · On-site

$120 - $180/hr

Position Summary. The Staff Quality Engineer will support the development, and maintain key ... Ensures manufacturing and testing of medical device IVDs is performed in accordance with Nuclein ...

New

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Quality Engineer Medical Device information

See Texas salary details

$19

$34

$65

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

As of Aug 21, 2026, the average hourly pay for quality engineer medical device in Texas is $34.21, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $42.79 per hour, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that medical devices meet all regulatory standards and quality requirements. They develop and implement quality assurance processes, perform risk assessments, and conduct inspections and audits to make sure products are safe and effective. Quality Engineers also collaborate with design, manufacturing, and regulatory teams to resolve quality issues and improve product reliability. Their work is crucial for maintaining compliance with standards such as ISO 13485 and FDA regulations.

What are the key skills and qualifications needed to thrive as a quality engineer in the medical device industry?

To thrive as a Quality Engineer in the medical device industry, you need a strong background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and engineering principles, often supported by a relevant engineering degree. Familiarity with quality management systems (QMS), risk analysis tools (like FMEA), and certifications such as CQE (Certified Quality Engineer) are typically required. Attention to detail, problem-solving, and effective communication are critical soft skills for collaborating with cross-functional teams and ensuring product safety. These skills and qualifications are vital to maintain regulatory compliance, uphold product quality, and protect patient safety in a highly regulated environment.

How does a quality engineer in the medical device industry typically collaborate with cross-functional teams to ensure product compliance?

Quality Engineers in the medical device sector work closely with cross-functional teams such as design, manufacturing, regulatory affairs, and supply chain. They participate in design reviews, risk assessments, and process validations to ensure that products meet both internal quality standards and external regulatory requirements (such as FDA or ISO 13485). Regular collaboration involves reviewing documentation, addressing non-conformances, and implementing corrective actions. This teamwork is critical to proactively identify potential issues and maintain continuous product quality throughout the development and production lifecycle.

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

AspectQuality Engineer Medical DeviceQuality Assurance Specialist Medical Device
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, Six Sigma, ASQ certifications
Work EnvironmentDesign, development, manufacturing, and process improvementAuditing, compliance, documentation, and process verification
Employer & Industry UsageMedical device manufacturers, R&D labsMedical device companies, regulatory agencies, consulting firms

While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Texas?

The most popular types of Quality Engineer Medical Device jobs in Texas are:

What job categories do people searching Quality Engineer Medical Device jobs in Texas look for?

The top searched job categories for Quality Engineer Medical Device jobs in Texas are:

What cities in Texas are hiring for Quality Engineer Medical Device jobs?

Cities in Texas with the most Quality Engineer Medical Device job openings:

Infographic showing various Quality Engineer Medical Device job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $71,164 per year, or $34.2 per hour.

Medical Device Quality Engineer

Enovis

Austin, TX • On-site

$71K - $92K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New


Enovis rating

8.9

Company rating: 8.9 out of 10

Based on 24 frontline employees who took The Breakroom Quiz


Job description

Who We Are

ABOUT ENOVIS

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond.For more information about Enovis, please visit www.enovis.com.

What You'll Do

At Enovis we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence - with the goal of transforming medical technology as we know it.

Because that's how we change the lives of patients for the better. And that's how we create better together. Why work at Enovis? See for yourself.

As a key member of the Quality Team, you will support Enovis in helping drive the medical technology industry forward by supporting quality processes, patient safety, and compliance.

Job Title:

Medical Device Quality Engineer

Reports To:

Sr. Manager, Quality Engineering

Location:

Austin, TX

Business Unit Description:

As a member of the Quality Assurance team, you will support activities that help Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title/High Level Position Summary:

Utilizing foundational knowledge of engineering and problem-solving principles, this position is responsible for supporting quality assurance activities related to the implementation, maintenance, and improvement of procedures and work instructions to help ensure safety, quality, and compliance with Company standards and government regulations.

Essential Responsibilities:

  • Ensuringcompliance with internal and external specifications and standards, including GMP, ISO, FDA, andCMDR requirements.
  • Supporting evaluation of product quality issues that mayimpactdevice performance, patient safety, or regulatory compliance.
  • Supporting the evaluation of nonconforming material andassistingwith dispositions through cross-functional engineering review as part of the MRB.
  • Supporting updates or changes to quality standards, procedures, and work instructions.
  • Assistingwith process and equipment validations, including IQ/OQ/PQ documentation.
  • Supporting supplier quality activities, including review of incoming nonconformances, supplier corrective actions (SCARs),audits,and supplier performancemonitoring.
  • Performing trend analysis on production and quality data toidentifyimprovement opportunities.
  • Contributing toroot cause investigations using structured problem-solving methods.
  • Contributing to CAPA activities, including investigation, documentation, and effectiveness verification.
  • Partnering with Manufacturing and Operations to help address quality or compliance concerns.
  • Participatingin internal and external audits, including audit preparation, providing support during audits, andassistingwith closure of findings
  • Supporting specialprojects asassigned
Minimum Basic Qualifications:
  • Bachelor's degree in Engineering, Science, or related technical field and 0-2 years of experience, preferably in medical device manufacturing
  • Required knowledge of FDA/GMP, CMDR, MDD and ISO 13485 quality standards.
  • Basic understanding ofgooddocumentation practices,and quality best practices.
  • Demonstratedability to write clear, concise technical documentation.
  • Must be able to work 100% onsite at Austin manufacturing facility
  • Proficiency in MS Office Suite, including Excel, Word and PowerPoint
  • Must be able to lift 50 lbs.
  • Must be able to bend, twist, and lift overhead.

Desired Characteristics:

  • Internship, co-op, or prior experience in manufacturing, quality, engineering,ina regulatedindustrypreferred.
  • Exposure to manufacturingequipmenttransfers and validation activities, including IQ/OQ/PQ, preferred.
  • Background or coursework related to Medical Device, Pharmaceuticals,oranotherregulated industry preferred.
  • Basic knowledge of ISO 13485 quality standards preferred.
  • Basic familiarity with quality and problem-solving tools (e.g., DMAIC, FMEA, statistical analysis) preferred.
  • Basic knowledge of manufacturing processes preferred, including precision machining,finishing,inspection,product cleaning, and sterilization.
  • Basic knowledge ofGeometric Dimensioning & Tolerancing (GD&T)preferred.
  • Preferred exposure to the following software packages: SolidWorks, SolidWorksePDM, Oracle R12, and Agile PLM.
  • CQE, Lean, or Six Sigma exposure or certification preferred, but notrequired

Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.

"Creating better together". It's the Enovis purpose, and it's what drives us and empowers us every day on a global scale. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.

What does creating better together mean to us at Enovis? Discover the "why" behind our purpose, values and behaviors:

Our Enovis Purpose, Values and Behaviors on Vimeo

We offer a comprehensive benefits package that includes:

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Spending and Savings Accounts
  • 401(k) Plan
  • Vacation, Sick Leave, and Holidays
  • Income Protection Plans
  • Discounted Insurance Rates
  • Legal Services

Join us in creating better together.

EQUAL EMPLOYMENT OPPORTUNITY
Enovis provides equal employment opportunities based on merit, experience, and other work-related criteria without regard to race, color, ethnicity, religion, national origin, sex, age, pregnancy, disability, veteran status, or any other status protected by applicable law. We also strive to provide reasonable accommodation to employees' beliefs and practices that do not conflict with Enovis policies and applicable law. We value the unique contributions that every employee brings to their role with Enovis.


What Enovis employees say

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About ENOVIS

Sourced by ZipRecruiter

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Wilmington, DE, US

Year founded

1995

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