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Quality Engineer Medical Device Jobs in Texas (NOW HIRING)

HotRun Inc.

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.

HotRun Inc.

Quality Engineer

Longview, TX

$90K - $115K/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 ...

HotRun Inc.

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 ...

ALOIS LLC

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 ...

Enovis

Sr. Quality Engineer

Austin, TX · On-site

$87K - $118K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

Nuclein,-LL

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

Enovis

Sr. Quality Engineer

Austin, TX

$87K - $118K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

Nuclein, LLC.

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

Cedarparktexasedc

Sr. Quality Engineer

Austin, TX · On-site

$120 - $180/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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.

New

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Quest Medical, Inc.

Quality Engineer

Allen, TX · On-site

$67K - $86K/yr

  • Retirement

  • PTO

Provide quality engineering support to engineering project teams associated with new product ... A minimum of 5 years' experience in the medical device manufacturing industry is preferred.

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Quality Engineer Medical Device information

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$19

$34

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

As of Aug 19, 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.

More about Quality Engineer Medical Device jobs

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 are popular job titles related to Quality Engineer Medical Device jobs in Texas?

For Quality Engineer Medical Device jobs in Texas, the most frequently searched job titles 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:

Quality Engineer Medical Device jobs near you
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.

Quality Engineer - Post Market

Argon Medical Devices Inc

Athens, TX • On-site

$85 - $125/hr

Other

Posted 21 hours ago

Posted today

Argon Medical Devices rating

6.5

Company rating: 6.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

Job description

Company Overview:

Argon Medical is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compasses which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day.

ARGON MEDICAL DEVICES IS NOT LEVERAGING SEARCH FIRMS

Position Overview:

The Quality Engineer (Post-Market) - Complaints Investigator is responsible for investigating product complaints, evaluating product performance and safety issues, and supporting post-market quality activities to ensure compliance with applicable regulatory requirements and internal procedures. This role provides quality engineering support for complaint handling, post-market surveillance, risk management, regulatory reporting, and continuous improvement initiatives to ensure product quality, patient safety, and regulatory compliance throughout the product lifecycle.

What you will do:

Primary Duties

  • Lead complaint evaluations and investigations to determine product failure modes, identify root causes, assess patient and user impact, and ensure timely closure of complaint records.
  • Perform risk assessments associated with customer complaints, product performance issues, and adverse events to determine product safety impact and support risk management activities.
  • Analyze complaint, and post-market surveillance data to identify trends, emerging quality signals, and opportunities for product and process improvement.
  • Assess complaints for reportability and support regulatory reporting activities, including Medical Device Reporting (MDR), Vigilance Reporting, Field Actions, and other applicable global regulatory requirements.
  • Lead investigations of product nonconformances, quality issues, and product performance concerns identified through post-market monitoring activities.
  • Collaborate with cross-functional teams, including Regulatory Affairs, Medical Affairs, Manufacturing, Engineering, and Customer Service, to investigate and resolve product quality issues.
  • Initiate and support Corrective and Preventive Actions (CAPA), ensuring appropriate containment, root cause analysis, effectiveness verification, and documentation.
  • Maintain and support risk management activities by evaluating complaint trends and post-market data for potential impacts to product risk profiles, hazard analyses, and risk management files.
  • Ensure compliance with FDA Quality System Regulations (21 CFR Part 820), ISO 13485, ISO 14971, Medical Device Reporting (MDR), Medical Device Vigilance, and other applicable global regulations.

Travel 5-10% as required.

Skills for Success:
  • Bachelor's degree in engineering, Life Sciences, Quality, or related technical field required.
  • 3+ years of Quality Engineering, Complaint Investigation, Post-Market Surveillance, or Medical Device Quality Systems experience required.
  • Experience conducting complaint investigations, root cause analysis, and product performance evaluations required.
  • Strong knowledge of FDA Quality System Regulations, ISO 13485, ISO 14971, Medical Device Reporting (MDR), and post-market surveillance requirements required.
  • Experience with CAPA, nonconformance management, risk assessment, and quality system processes required.
  • Working knowledge of medical device adverse event reporting and regulatory compliance requirements are preferred.
  • Strong analytical, technical writing, problem-solving, and communication skills required.
  • Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or equivalent certification preferred.
  • Experience supporting regulatory inspections and third-party audits preferred.
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