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Medical Device Engineer Jobs in Arizona (NOW HIRING)

QA/QC Engineer II

Phoenix, AZ · On-site

$71K - $92K/yr

The Quality Assurance Engineer has the responsibilities to coordinate and perform quality assurance and product development activities according to medical device regulations of 21 CFR 820 and/or ISO ...

QA/QC Engineer II

Phoenix, AZ · On-site

$71K - $92K/yr

The Quality Assurance Engineer has the responsibilities to coordinate and perform quality assurance and product development activities according to medical device regulations of 21 CFR 820 and/or ISO ...

Directs the engineering teams and activities for new product introduction, commercial and clinical ... In addition, the role provides leadership and direction for all Medical Device performance related ...

Senior Software Engineer

Scottsdale, AZ · On-site

$123K - $163K/yr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Directs the engineering teams and activities for new product introduction, commercial and clinical ... In addition, the role provides leadership and direction for all Medical Device performance related ...

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Directs the engineering teams and activities for new product introduction, commercial and clinical ... In addition, the role provides leadership and direction for all Medical Device performance related ...

Senior Software Engineer

Scottsdale, AZ · On-site

$123K - $162K/yr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Senior Software Engineer

Scottsdale, AZ · On-site

$123K - $163K/yr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Quality Engineer

Scottsdale, AZ · On-site

$70K - $90K/yr

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device components. In addition, this person will ...

Quality Engineer

Scottsdale, AZ · On-site

$70K - $90K/yr

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device components. In addition, this person will ...

Quality Engineer

Scottsdale, AZ

$72K - $93K/yr

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device components. In addition, this person will ...

Sr Hardware Engineer

Arizona City, AZ · On-site

$116.60 - $194.40/hr

Meet the Team Join a diverse and dynamic team of operations and engineers dedicated to delivering high-quality medical device products to patients around the world. Our team focuses on packaging ...

Showing results 21-40

Medical Device Engineer information

See Arizona salary details

$19

$46

$90

How much do medical device engineer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for medical device engineer in Arizona is $46.44, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $55.58 per hour, depending on experience, location, and employer.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

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

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

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

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

What cities in Arizona are hiring for Medical Device Engineer jobs?

Cities in Arizona with the most Medical Device Engineer job openings:

Infographic showing various Medical Device Engineer job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $96,601 per year, or $46.4 per hour.

Sr. R&D Engineer- Relocation Assistance Provided

Innovative Health

Scottsdale, AZ • On-site

$105K - $144K/yr

Full-time

Posted 11 days ago


Job description

The Senior R&D Engineer role is responsible for designing, developing, validating, and implementing various methods and processes, leading and assisting in projects to introduce new products into production. This role is expected to bring unique perspectives and creative solutions to challenges faced during reverse engineering and reprocessing technique development.

Essential Duties and Responsibilities:

• Assist and/or lead in development of new medical device platforms complying with design control process including applicable FDA and ISO requirements.

• Develop, write, and execute test methods.

• Train manufacturing/QC personnel as needed on test methods or manufacturing processes.

• Generate formal test protocols and reports.

• Execute test protocols and conduct bench testing. Document test results per GDP, ISO, and FDA requirements.

• Coordinate and oversee test sample builds. Assist with test sample builds as required.

• Use Solidworks to design test fixtures and devices. (if applicable)

• Design and fabricate test fixtures, tooling and equipment. (if applicable)

• Work with purchasing department to specify and procure capital equipment.

• Serve as a cross-functional team member for various project-related activities.

• Assist or lead process improvement projects to reduce costs.

• Assist with DFMEA and PFMEA risk assessments.

• Compile project status updates and present to senior management.

• Comply with company policies and procedures.

• Maintain project schedule and deliver projects on time.

• Focus on delivering products to support the R&D project pipeline.

• Provide technical leadership to junior engineers and technicians.

Clinical Support Responsibilities:

• Attend clinical cases for learning, device launch, and troubleshooting.

• Interact with clinicians and field personnel to understand clinical needs and provide technical support.

• Develop and maintain a deep understanding of medical device reprocessing techniques, including cleaning, sterilization, and biocompatibility requirements.

• Develop and maintain relationships with key opinion leaders and clinical partners.

Medical Device Reprocessing Responsibilities:

• Develop and optimize reprocessing methods for single-use medical devices.

• Conduct performance, biocompatibility and sterilization testing on reprocessed devices.

• Ensure compliance with all regulatory requirements for medical device reprocessing.

• Participate in cross-functional teams to introduce reprocessed devices into production.

Supervisory Responsibilities:

· Provide mentoring and guidance to other R&D team members, as well as supervise and manage the work of junior engineers.

Education, Qualifications and Skills:

· Minimum education: Bachelor's degree in engineering discipline (or equivalent experience)

· Minimum experience: 7-12 years of experience

· Strong background in R&D with experience in electromechanical medical devices.

· Experience with various types of medical device design verification testing in accordance with FDA regulations: device functional performance, biocompatibility, sterilization, packaging, transportation simulation, real-time and accelerated aging, etc.

· Excellent technical writing skills and substantial experience writing test plans, protocols, and reports.

· Excellent problem-solving skills as well as keen analytical abilities.

· Knowledge of Design Controls, Risk Management, Statistics, Engineering Principles, Test Method Development, Test Method Validation (Gage R&R), and Design Verification / Validation.

· Proficiency in CAD design and drafting (SolidWorks) a plus.

· Ability to work in a fast-paced, collaborative team environment.

· Strong hands-on prototyping skills.

· Self-starter and highly motivated.

· Ability to have fun by motivating and encouraging other team members.