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Medical Device Quality Control 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

Associate degree or technical certification in Manufacturing, Quality, Engineering Technology, or related field * 2+ years of experience in quality control, inspection, or metrology (medical device ...

Quality Engineer

Longview, TX · On-site

$64K - $82K/yr

Ensure the quality management system meets the company's medical device expectations and goals ... Maintains document control systems, ensuring accuracy, organization, accessibility, and compliance ...

Quality Engineer

Longview, TX · On-site

$64K - $82K/yr

... the company's medical device expectations and goals. § Formulate and maintain accurate ... Maintains document control systems, ensuring accuracy, organization, accessibility, and compliance ...

... the company's medical device expectations and goals. § Formulate and maintain accurate ... Maintains document control systems, ensuring accuracy, organization, accessibility, and compliance ...

Compensation: 20-25/hr Summary We're working with a growing medical device manufacturer looking to add a QA Inspector focused on incoming quality control. This role supports inspection of raw ...

... Medical is quality driven, surgeon inspired, and innovative medical device company. We have a ... Astura's QC Inspector will perform various inspection techniques of medical devices. This position ...

Company Profile Astura Medical is quality driven, surgeon inspired, and innovative medical device ... Astura's QC Inspector will perform various inspection techniques of medical devices. This position ...

... Medical is quality driven, surgeon inspired, and innovative medical device company. We have a ... Astura's QC Inspector will perform various inspection techniques of medical devices. This position ...

The Quality Control (QC) Scientist II will support the development of, and maintain, key elements ... At least 5 years of experience in a laboratory setting, preferably within a medical device ISO ...

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Medical Device Quality Control information

See Texas salary details

$10

$20

$31

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

As of Aug 21, 2026, the average hourly pay for medical device quality control in Texas is $20.01, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $22.40 per hour, depending on experience, location, and employer.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

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

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

Infographic showing various Medical Device Quality Control 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 $41,615 per year, or $20 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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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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