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Medical Device Product Development Engineer Jobs in Arizona

Erbe USA Incorporated

Sr. R&D Engineer

Tempe, AZ · On-site

$101K - $139K/yr

As a senior member of the Engineering team, responsibilities will include leading New Product ... At least 7 years' experience in medical device R&D, product development, design controls, or other ...

Gn

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Ziehm Orthoscan

Senior Software Engineer

Scottsdale, AZ

$123K - $163K/yr

As a Senior Software Engineer, you will be developing primarily C++ applications for medical ... product development environments. * Knowledge of DICOM and IEC62304 Medical Device Software ...

Orthoscan, Inc.

Senior Software Engineer

Scottsdale, AZ · On-site

$120 - $170/hr

As a Senior Software Engineer, you will be developing primarily C++ applications for medical ... product development environments. * Knowledge of DICOM and IEC 62304 Medical Device Software ...

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All JobsMedical Device Product Development Engineer JobsMedical Device Product Development Engineer Jobs in Arizona

Medical Device Product Development Engineer information

See Arizona salary details

$36.8K

$81.9K

$123.5K

How much do medical device product development engineer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical device product development engineer in Arizona is $81,898.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,100.00 and $93,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device product development engineer?

To thrive as a Medical Device Product Development Engineer, you need a strong background in biomedical, mechanical, or electrical engineering, along with knowledge of FDA regulations and product development processes. Familiarity with CAD software, prototyping tools, risk management systems, and regulatory standards such as ISO 13485 is typically required. Creativity, problem-solving, and effective teamwork are essential soft skills that drive innovation and ensure project success. These skills and qualifications are crucial for developing safe, effective medical devices that meet strict regulatory requirements and address real-world healthcare needs.

What are some common challenges medical device product development engineers face when working on new product designs?

Medical Device Product Development Engineers often navigate strict regulatory requirements and rigorous testing protocols to ensure product safety and compliance. Balancing innovative design with manufacturability and cost constraints can be challenging, as can coordinating input from cross-functional teams such as clinical, regulatory, and manufacturing. Additionally, managing project timelines while accommodating iterative design changes based on feedback or testing results requires strong organizational and communication skills.

What does a medical device product development engineer do?

A Medical Device Product Development Engineer is responsible for designing, developing, and testing medical devices to ensure they are safe, effective, and compliant with regulatory standards. They work closely with cross-functional teams, including quality assurance, regulatory affairs, and manufacturing, to take products from concept through to production. Their tasks often include prototyping, risk assessment, documentation, and troubleshooting any issues that arise during the development process. Additionally, they must stay updated on industry standards and regulations to ensure that products meet all necessary requirements for market approval.

What is the difference between Medical Device Product Development Engineer vs Quality Assurance Engineer?

AspectMedical Device Product Development EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like PMP or Six Sigma often preferredEngineering or science degree, certifications like CQE or ISO auditor training
Work EnvironmentDesign labs, R&D departments, cross-functional teamsManufacturing facilities, quality control labs, compliance departments
Industry UsageInvolved in designing and developing new medical devicesEnsures products meet quality standards and regulatory requirements

While both roles are essential in the medical device industry, the Medical Device Product Development Engineer focuses on creating and improving devices, whereas the Quality Assurance Engineer ensures these devices meet safety and quality standards. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Medical Device Product Development Engineer jobs in Arizona?

For Medical Device Product Development Engineer jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Medical Device Product Development Engineer jobs in Arizona look for?

The top searched job categories for Medical Device Product Development Engineer jobs in Arizona are:

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

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

Medical Device Product Development Engineer jobs near you
Infographic showing various Medical Device Product Development 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 $81,898 per year, or $39.4 per hour.

Sr. R&D Engineer- Relocation Assistance Provided

Innovative Health LLC

Scottsdale, AZ • On-site

$101K - $139K/yr

Full-time

Posted 10 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.