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Quality Engineer Medical Devices Jobs in Tennessee

The Design Quality Engineer serves as the key resource for ensuring compliance to ISO, EU MDR, and FDA QSR requirements for Medical Devices. The Design Quality Engineer takes the lead with quality ...

Quality Engineer I

Morristown, TN

$63K - $81K/yr

What You'll Do As a Quality Engineer I , you will: * Facilitate and maintain validation project ... Background in nutritional products, medical devices, pharmaceuticals, or similar industries.

Sr Quality Engineer

Memphis, TN

$86K - $116K/yr

The Sr Quality Engineer provides quality engineering expertise to manufacturing, engineering ... governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR. * Strong working ...

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

The Sr Quality Engineer provides quality engineering expertise to manufacturing, engineering ... governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR. * Strong working ...

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

The Sr Quality Engineer provides quality engineering expertise to manufacturing, engineering ... governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR. * Strong working ...

Quality EngineerOverview We are seeking a Quality Engineer to support validation, quality systems ... Experience in medical devices, pharmaceuticals, diagnostics, nutritional products, or a similar ...

Quality EngineerOverview We are seeking a Quality Engineer to support validation, quality systems ... Experience in medical devices, pharmaceuticals, diagnostics, nutritional products, or a similar ...

Sr Quality Engineer

Memphis, TN · On-site

$90 - $120/hr

... governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR. * Strong working ... Previous Quality Engineering or Product Development experience and GD&T and electronics knowledge ...

Quality Engineer

Smithville, TN · On-site

$60K - $78K/yr

Quality Engineer Work Location: Smithville, TN 37166 Duration: Direct Hire/Fulltime Shift: 8am- 5pm; Monday- Friday Position Summary: The Quality Engineer is responsible for supporting manufacturing ...

Quality Engineer

Shelbyville, TN · On-site

$61K - $79K/yr

Quality Engineer Location : Shelbyville Overview of Role: The Quality Engineer is the primary onsite Quality representative at the Tennessee manufacturing facility, responsible for ensuring process ...

Quality Engineer

Nashville, TN · On-site

$69K - $89K/yr

Engineer 1 -Quality Engineer Asurion is the global leader in technology support and protection. Innovation and dedication to delighting customers have made it the preferred provider of technology ...

New

Quality Engineer

Shelbyville, TN · On-site

$61K - $79K/yr

Quality Engineer Location : Shelbyville Overview of Role: The Quality Engineer is the primary on-site Quality representative at the Tennessee manufacturing facility, responsible for ensuring process ...

Quality Engineer

Murfreesboro, TN · On-site

$64K - $83K/yr

Description The Quality Engineer is responsible for understanding customer quality related ... of medical parts. Duties and Responsibilities • Establish and participate in supplier ...

Quality Engineer

Knoxville, TN · On-site

$68K - $88K/yr

Type One Energy is seeking a Quality Engineer (QE) to coordinate with Engineering and associated support functions for design assurance, supplier quality, prototype quality, traceability ...

Quality Engineer

Murfreesboro, TN · On-site

$64K - $83K/yr

The Quality Engineer is responsible for understanding customer quality related requirements ... medical parts. Duties and Responsibilities Establish and participate in supplier qualification ...

Quality Engineer

Oak Ridge, TN · On-site

$68K - $88K/yr

Edgewater Technical Associates is seeking qualified candidates for a Quality Engineer opportunity ... We offer multiple individual and family benefit options including paid time off, medical, dental ...

Quality Engineer

Oak Ridge, TN · On-site

$68K - $88K/yr

Edgewater Technical Associates is seeking qualified candidates for a Quality Engineer opportunity ... We offer multiple individual and family benefit options including paid time off, medical, dental ...

Quality Engineer

Pulaski, TN · On-site

$70K - $91K/yr

Quality Engineer Specific Duties * The Quality Engineer Complies with all BOS, ISO/TS-16949 and Customer Specific requirements. * Understands Plant/Customer KPI's and works with team to meet and ...

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Showing results 1-20

Quality Engineer Medical Devices information

See Tennessee salary details

$40.8K

$76.3K

$108K

How much do quality engineer medical devices jobs pay per year?

As of Aug 29, 2026, the average yearly pay for quality engineer medical devices in Tennessee is $76,275.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,300.00 and $84,400.00 per year, 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 products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are popular job titles related to Quality Engineer Medical Devices jobs in Tennessee?

For Quality Engineer Medical Devices jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Quality Engineer Medical Devices jobs in Tennessee look for?

The top searched job categories for Quality Engineer Medical Devices jobs in Tennessee are:

What cities in Tennessee are hiring for Quality Engineer Medical Devices jobs?

Cities in Tennessee with the most Quality Engineer Medical Devices job openings:

Infographic showing various Quality Engineer Medical Devices job openings in Tennessee as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $76,275 per year, or $36.7 per hour.

Design Quality Engineer II

Memphis, TN • On-site


CONMED
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

7.9

Company rating: 7.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

Great coworkers

People enjoy working here

Good employer


Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 13 days ago


Job description

The Design Quality Engineer II is responsible for supporting all quality engineering activities to support the new product life cycle, from concept to commercialization, and sustaining activities. The Design Quality Engineer will serve as the quality engineering contact and be a key member of the cross-functional development and sustaining teams. The Design Quality Engineer serves as the key resource for ensuring compliance to ISO, EU MDR, and FDA QSR requirements for Medical Devices. The Design Quality Engineer takes the lead with quality initiatives with inter-organizational impact following QSR, CONMED Policies, standards and regulations. Works under direction from Quality Management.**This is an on-site role in Memphis, TN.** Key Duties and Responsibilities
  • Supports and provides direction to product development teams for the required quality deliverables.
  • Ensures that product design meets customer expectations, regulatory requirements, appropriate voluntary standards, and all corporate requirements. Shows focus toward continuous improvement.
  • Review, assess, and approve product design documentation to ensure compliance throughout product development cycle. Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.
  • Troubleshoot and direct the resolution of quality issues by fostering effective interdepartmental and cross-functional partnerships.
  • A relentless focus on the safety and the efficacy of the medical device.
  • Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.
  • Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.
  • Leads and provides support on risk management activities with a focus on clinician and patient safety.
  • Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.
  • Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.
  • Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.
  • Leads and provides support on risk management activities with a focus on clinician and patient safety.
  • Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.
  • Support sustaining activities such as complaint investigation and complaint trending. Monitor and analyze manufacturing and service trends. Perform Predicate Device reviews and surveillance reports. Able to perform data mining, analyze data and create trend reports.
  • Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management.
  • Investigates process and product issues identified through complaints and trend analysis of other conformance data. Works with other functional groups to resolve difficult quality problems on products, processes, or materials used in manufacturing operations.
  • Direct and facilitate investigations and the corresponding preventative actions and corrective actions that result from abnormal results, customer complaints, quality inquiries, and other quality performance indicators.
  • Travel Requirements (including international): 0-5%
  • Support internal and external audits. Provide support for audit preparation activities. Participate in the back-room as needed.
Minimum Requirements
  • B.S. degree in Engineering such as Electrical, Mechanical, or Biomedical Engineering and 2+ years of medical device experience (or equivalent work experience), or M.S. and 1+ years of medical device experience.
Preferred Requirements
  • Must be able to interpret and apply Quality Systems Regulations and ISO quality requirements and stay abreast of new industry standards and concepts.
  • Knowledge of design controls, 21 CFR 820, ISO 13485, ISO 14971, EU MDR, and applicable medical device regulations.
  • Must be capable to plan schedules and to manage multiple projects simultaneously.
  • Professional certifications (CQE, CQA, CMQ/OE, Lead Auditor) are desirable.
  • Design for Six Sigma training is desired along with knowledge of statistical methodologies.
  • Involvement in back-room support process during external audits and/or inspections.
  • Experience reviewing design verification and design validation protocols.
  • Excellent communication, problem solving, organizational, and interpersonal skills are required.
  • Strong technical writing skills.
  • Works independently with minimal direction or supervision.
  • Decision intelligence.
Physical Requirements
  • Ability to sit/stand for 8 hours.
  • Ability to sit at a computer terminal for an extended period.
ADA Disclosure:
  • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

*** This position is not eligible for employer based sponsorship. ***

Benefits:

CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.

  • Competitive compensation
  • Excellent healthcare including medical, dental, vision and prescription coverage
  • Short & long term disability plus life insurance -- cost paid fully by CONMED
  • Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period
  • Employee Stock Purchase Plan -- allows stock purchases at discounted price
  • Tuition assistance for undergraduate and graduate level courses

Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives!

CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.

Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-929-7176 option #5.



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