ZipRecruiter

Log In

1

Quality Engineer Medical Devices Jobs in Arizona

W. L. Gore & Associates, Inc.

Quality Engineer

Flagstaff, AZ · On-site

$65K - $84K/yr

Quality Engineer Req Id: 2015 State/Province: Arizona Business: Gore Medical Products Category ... You will be critical in ensuring medical devices are safe, effective, and meet user needs and ...

W. L. Gore & Associates, Inc.

Quality Engineer

Phoenix, AZ · On-site

$73K - $94K/yr

Quality Engineer Req Id: 1994 State/Province: Arizona Business: Gore Medical Products Category ... You will be critical in ensuring medical devices are safe, effective, and meet user needs and ...

Ralliant

Quality Engineer

Chandler, AZ · On-site

$70K - $91K/yr

Quality Engineer (Supplier Quality Focus) Location: Chandler, Arizona Reports To: Director of ... From concept to demonstration to delivery, we provide leading-edge energetic materials, devices and ...

Integrated Magnetics

Quality Engineer

Tucson, AZ · On-site

$61K - $80K/yr

The Quality Engineer will be responsible for developing, implementing, and maintaining quality ... medical industries. Key responsibilities include performing audits and inspections, analyzing ...

Corning

Quality Engineer

Glendale, AZ · On-site

$80K - $110K/yr

... devices. Position Summary The Quality Engineer is a key technical contributor responsible for ... Our health and well-being benefits include medical, dental, vision, paid parental leave, family ...

Integrated Magnetics

Quality Engineer

Tucson, AZ · On-site

$61K - $80K/yr

The Quality Engineer will be responsible for developing, implementing, and maintaining quality ... medical industries. Key responsibilities include performing audits and inspections, analyzing ...

Corning

Quality Engineer

Glendale, AZ · On-site

$80K - $110K/yr

... devices. Position Summary The Quality Engineer is a key technical contributor responsible for ... Our health and well-being benefits include medical, dental, vision, paid parental leave, family ...

Corning

Quality Engineer

Glendale, AZ

$80K - $110K/yr

... devices. Position Summary The Quality Engineer is a key technical contributor responsible for ... Our health and well-being benefits include medical, dental, vision, paid parental leave, family ...

iTech US, Inc.

Quality Engineer

Phoenix, AZ · On-site

$71K - $92K/yr

Job Title: Quality Engineer Location: Phoenix Arizona 12+ Months Must have Skills: Gen AI Assisted Development, Prompt Engineering, REST Assured, Selenium, Web Service / API Testing Position ...

Quest Global

Aftermarket Quality Engineer

Phoenix, AZ · On-site

$70K - $80K/yr

... 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 ...

Tekberry

Quality Engineer

Gilbert, AZ · On-site

$22 - $33/hr

Quality Engineer Pay Rate: $22 - $33/hour (DOE) Employment Type: Contract Schedule: M-F 7:30am-5pm Location: Gilbert, AZ 85233 (100% Onsite) Tekberry is seeking experienced Quality Engineer to ...

KBR

Quality Engineer

Phoenix, AZ · On-site

$71K - $92K/yr

Quality Engineer BELONG. CONNECT. GROW. with KBR. Around here, we define the future. We are a ... with company match, medical, dental, vision, life insurance, AD&D, flexible spending account ...

Rogers Corporation

Quality Engineer

Chandler, AZ · On-site

$70K - $90K/yr

Review and approve various quality documentation. * Support qualification of new product, processes ... devices, transportation interiors, industrial equipment and performance apparel, wireless ...

NextDeavor Inc.

Quality Engineer

Glendale, AZ · On-site

$90K - $94K/yr

Quality Engineer Full-time Glendale, AZ, US Exclusive confidential search -- details shared with qualified applicants. Benefits You'll Love * Salary range: $90,000 - $94,000/year * Bonus opportunity ...

Belcan

Quality Engineer

Prescott, AZ · On-site

$42 - $52/hr

Quality Engineer Locations: Prescott, AZ 86305 Area Code: 928, 480 Pay Rate: $42.00 to $52.00 per hour, based on experience, qualifications, and level of responsibility Shift: 1st Shift Employment ...

next page

Showing results 1-20

All JobsQuality Engineer Medical Devices JobsQuality Engineer Medical Devices Jobs in Arizona

Quality Engineer Medical Devices information

See Arizona salary details

$41.9K

$78.3K

$110.9K

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

As of Sep 3, 2026, the average yearly pay for quality engineer medical devices in Arizona is $78,315.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,100.00 and $86,700.00 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 Arizona?

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

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

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

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

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

Quality Engineer Medical Devices jobs near you
Infographic showing various Quality Engineer Medical Devices job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $78,315 per year, or $37.7 per hour.

Quality Engineer

W. L. Gore & Associates, Inc.

Flagstaff, AZ • On-site

$65K - $84K/yr

Full-time

Re-posted 4 days ago

W. L. Gore & Associates rating

8.9

Company rating: 8.9 out of 10

Based on 80 frontline employees who took The Breakroom Quiz

8th of 545 rated manufacturers

Job description

Quality Engineer
Req Id: 2015
State/Province: Arizona
Business: Gore Medical Products
Category: Engineering, Scientists & Technicians
Sub-Category: Engineering
Work Arrangement: Hybrid
Posting Start Date: 7/29/26
Posting End Date: 10/30/26
About the Role
We are looking for experienced (minimum of 3 years) or senior (minimum of 5 years) Design Assurance Engineers/Product Quality Engineers to join our New Product Development (NPD) team. In this role, you will apply your technical capabilities and problem-solving skills to define product requirements, facilitate risk management activities, develop test methods, and evaluate product performance and safety to support new medical device development. This is a hands-on engineering role embedded in product development projects, working cross-functionally to address technical uncertainties and execute design control processes. You will be critical in ensuring medical devices are safe, effective, and meet user needs and intended uses across diverse clinical environments.
This role requires the ability to independently manage work, apply risk-based thinking, and navigate ambiguity while collaborating across functions and maintaining communication with leadership.
These positions are based at our facility in Flagstaff, AZ.
Responsibilities
  • Promote an inclusive and healthy environment in alignment with the Gore Culture
  • Plan and execute design assurance / product quality engineering work in collaboration with technical leadership and cross-functional partners to support new product development
  • Apply design control processes throughout product development to ensure products meet user needs, intended use, and performance expectations
  • Develop and refine user needs, design inputs, and design outputs, ensuring product requirements are clear, measurable, testable and traceable to support effective verification, validation, and evaluation of product performance
  • Develop, improve, and validate test methods used to evaluate product or process performance, including supporting creation of new methods as required for product development
  • Plan, support, and execute design verification and design validation activities to ensure product safety, effectiveness, and performance across intended use conditions
  • Identify, evaluate, and mitigate product risks throughout development, including application of design and usability risk management approaches (e.g., dFMEA, uFMEA)
  • Lead technical investigations and problem-solving efforts to address product or process issues, resolve technical uncertainties, and improve product performance
  • Ensure design control documentation and traceability meet Design History File (DHF) expectations, including linkage across user needs, design inputs, design outputs, risk controls, and verification/validation activities
  • Document and communicate technical plans, experimental results, and conclusions in alignment with quality system and regulatory requirements

Required Qualifications
  • For an Experienced engineering position, a Bachelor's Degree in Engineering, Science or Technical Field with solid knowledge of engineering fundamentals and a minimum of 3 years of applied experience OR a Master's degree with a minimum of 2 years in applied experience
  • For a Senior engineering position, a Bachelor's Degree in Engineering, Science or Technical Field with solid knowledge of engineering fundamentals and a minimum of 5 years of applied experience OR a Master's degree with a minimum of 4 years in applied experience
  • Demonstrated experience identifying, evaluating, and mitigating product or process risks using structured risk management approaches
  • Demonstrated experience working within a regulated quality system (QMS), with exposure to areas such as design controls, investigations, or corrective and preventive action processes
  • Demonstrated experience developing, executing, or improving test methods used to evaluate product or process performance
  • Demonstrated ability to interpret, evaluate, and apply technical requirements, specifications, and acceptance criteria to support engineering decisions and evaluation of product performance (Demonstrated experience with bidirectional traceability - maintaining links from user need, system, subsystem and test, with full audit history)
  • Demonstrated ability to analyze technical data and apply statistical methods to characterize product or process performance and support engineering decisions
  • Demonstrated understanding of sampling plans and data-based decision making in a regulated environment
  • Demonstrated ability to solve technical problems and make informed engineering decisions
  • Demonstrated ability to work independently and collaborate effectively across functions to resolve technical challenges and drive work to completion
  • Strong written and verbal communication skills, including ability to clearly document technical rationale, results, and conclusions
  • Ability to travel up to 10%

Desired Qualifications
  • For an Experienced engineering position, a Bachelor's Degree in Engineering, Science or Technical Field with solid knowledge of engineering fundamentals and a minimum of 5 years of applied experience OR a Master's degree with a minimum of 4 years in applied experience
  • For a Senior engineering position, a Bachelor's Degree in Engineering, Science or Technical Field with solid knowledge of engineering fundamentals and minimum 7 years of applied experience OR a Master's degree with a minimum of 6 years in applied experience
  • Familiarity with medical device quality system and regulatory expectations, including FDA 21 CFR 820 / QMSR, ISO 13485, ISO 14971, and design control requirements.
  • Relevant engineering experience in the medical device industry, including familiarity with applicable regulatory standards and quality system expectations
  • Experience with design controls, risk management, and requirements management within new product development (NPD) environments

What We Offer
Our success is based on the capability and creativity of our Associates, and we are proud to offer a comprehensive and competitive total rewards program that supports your everyday and helps you build your tomorrow.
We provide benefits that offer choice and flexibility and promote overall well-being. And in keeping with our belief that every Associate should share in the collective success of the enterprise; we provide a distinctive Associate Stock Ownership Plan in each country as well as potential opportunities for "profit-sharing". Learn more at gore.com/careers/benefits
Gore is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, national origin, ancestry, age, status as a qualified individual with a disability, genetic information, pregnancy status, medical condition, marital status, sexual orientation, status as a protected veteran, gender identity and expression, and any other characteristic protected by applicable laws and regulations.
Gore is committed to a drug-free workplace. All employment is contingent upon successful completion of drug and background screening. Gore will consider qualified applicants with criminal histories, e.g., arrest and conviction records, in a manner consistent with the requirements of applicable laws.
Gore requires all applicants to be eligible to work within the United States. Gore generally will not sponsor visas unless otherwise noted on the position description.
Information at a Glance

What W. L. Gore & Associates employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply