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Medical Device Product Development Jobs in Arizona

Orthoscan, Inc.

Senior Software Engineer

Scottsdale, AZ · On-site

$123K - $163K/yr

... product development environments. * Knowledge of DICOM and IEC62304 Medical Device Software, Software Life Cycle Processes (strongly preferred and highly valued for this role). Competencies:

Aptyx

Dip Mold Operator

Tempe, AZ · On-site

$16.50 - $19.75/hr

Job DescriptionProduction Operator - Stethoscope Manufacturing Position SummaryThe Production Operator is responsible for manufacturing, assembling, inspecting, testing, and packaging medical device ...

Aptyx

Dip Mold Operator

Tempe, AZ · On-site

$16 - $19.50/hr

Production Operator - Stethoscope Manufacturing Position Summary The Production Operator is responsible for manufacturing, assembling, inspecting, testing, and packaging medical device products ...

Crown Medical, Inc.

Medical Supply Sales Rep

Phoenix, AZ · On-site

$85K - $116K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Aptyx

Dip Mold Operator

Tempe, AZ

$16 - $19.50/hr

Production Operator - Stethoscope Manufacturing Position Summary The Production Operator is responsible for manufacturing, assembling, inspecting, testing, and packaging medical device products ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ · On-site

The Quality Assurance Engineer I supports quality assurance and product development activities in accordance with medical device regulations, including 21 CFR 820, the Medical Device Directive (MDD ...

New

Aptyx

Dip Mold Operator

Tempe, AZ · On-site

$16.50 - $19.75/hr

Production Operator - Stethoscope Manufacturing Position Summary The Production Operator is responsible for manufacturing, assembling, inspecting, testing, and packaging medical device products ...

Hanger, Inc.

QA/QC Engineer I

Phoenix, AZ · On-site

The Quality Assurance Engineer I supports quality assurance and product development activities in accordance with medical device regulations, including 21 CFR 820, the Medical Device Directive (MDD ...

New

medplast

Commercial Development Manager

Tempe, AZ · On-site

As Commercial Development Manager you will develop quotes for plastic parts and assemblies based on ... Ability to read and interpret product design drawings used within the medical device industry.

Innovative Health

Sr. R&D Engineer

Scottsdale, AZ

$105K - $144K/yr

... medical device reprocessing. · Participate in cross-functional teams to introduce reprocessed devices into production. Supervisory Responsibilities: · Provide mentoring and guidance to R&D team ...

Innovative Health LLC

Sr. R&D Engineer

Scottsdale, AZ · On-site

$101K - $139K/yr

... medical device reprocessing. • Participate in cross-functional teams to introduce reprocessed devices into production. Supervisory Responsibilities: • Provide mentoring and guidance to R&D team ...

Innovative Health LLC

Sr. R&D Engineer

Scottsdale, AZ · On-site

$101K - $139K/yr

... medical device reprocessing. · Participate in cross-functional teams to introduce reprocessed devices into production.Supervisory Responsibilities: · Provide mentoring and guidance to R&D team ...

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

Medical Device Product Development information

See Arizona salary details

$39.6K

$118.3K

$134.7K

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

As of Aug 23, 2026, the average yearly pay for medical device product development in Arizona is $118,338.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,700.00 and $133,300.00 per year, depending on experience, location, and employer.

What is a medical device product development?

A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.

What are some typical challenges faced in medical device product development roles?

Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.

What are the key skills and qualifications needed to thrive in medical device product development?

To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

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

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

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

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

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

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

Medical Device Product Development jobs near you
Infographic showing various Medical Device Product Development job openings in Arizona as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 90% In-person, 4% Hybrid, and 6% Remote job distribution, with an average salary of $118,338 per year, or $56.9 per hour.

Senior Software Engineer

Orthoscan, Inc.

Scottsdale, AZ • On-site

$123K - $163K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 26 days ago

Job description

Ziehm Imaging - Orthoscan Inc. is currently seeking a motivated, career-oriented professional with a positive can-do attitude to join our team as a full-time Senior Software Engineer located in Scottsdale, AZ.
Why Work for Ziehm Imaging - Orthoscan Inc.?
There's something special about Ziehm-Orthoscan. There's a sense of pride that comes from building a product that helps improve people's lives and making the most of ourselves as a company and as individuals. We know the success of Ziehm-Orthoscan depends on every employee in our organization, it is our people who make the difference.
What do we offer?
  • The challenge of meaningful work - we offer constant opportunities to grow and develop world-class skills and a truly rewarding career.
  • A unique culture where people convert their passion into action.
  • The kind of competitive compensation you would expect from a world leader.
  • Nine paid holidays plus a generous PTO and vacation time plan.
  • Great benefit plans, major medical, dental and vision.
  • Company 401(k) plan with an employer match.
  • Competitive Salary

JOB SUMMARY:
As a Senior Software Engineer, you will be developing primarily C++ applications for medical devices. This position has hands-on access to the final product at every stage of development. In this capacity, you will be working primarily on a Linux-based platform, creating and maintaining a modern QT multi-touch/keyboard optimized GUI application with a strong emphasis on safety-critical software development and regulatory compliance (IEC 62304 / ISO 13485 environments).
Essential Functions:
  • Develop, verify, and validate software solutions for our C-Arm (Linux based computer) in compliance with medical device software lifecycle standards (IEC 62304).
  • Develop and maintain touchscreen-friendly GUI software using QT and QML with a focus on performance, usability, and embedded system constraints.
  • Adapt existing architectural design patterns to realize a modern software architecture with a focus on platform technology and long-term maintainability/scalability.
  • Perform code reviews, support verification by unit tests, automated and manual system integration tests, and enforce coding standards and software quality best practices across the team.
  • Support designing and specifying requirements and work packages in collaboration with systems engineering and regulatory teams to ensure traceability.
  • Maintaining source control branches and performing integrations with merge requests following Git-based branching strategies and release management practices.

Basic Qualifications:
Education:
  • Bachelor's degree in software engineering, computer science, or a related field is required or equivalent combination of education and relevant industry experience.

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 developing C++ applications (preferably modern C++17/20 practices, including memory management, concurrency, and performance optimization).
  • Knowledge in C++17, QT, QML, bash, python, gtest, boost libs and postgres (strong preference for experience with Qt application frameworks in embedded or medical device environments).
  • Profound knowledge of design patterns and software architecture principles (SOLID, modular design, clean architecture).
  • Experience working in Agile (Scrum) project management.
  • Knowledge of GIT, Docker, Jenkins, and CI/CD pipelines in a regulated development environment.
  • Experience with Linux systems, specifically Ubuntu and Debian, including system-level debugging and deployment considerations.
  • Experience working in collaboration with Electrical Engineering, Mechanical Engineering, Quality, Regulatory, Production, and Sales in a cross-functional product development environment.
  • Proven ability to collaborate across cross-functional and international engineering, manufacturing, and quality teams, with clear and effective communication in globally distributed product development environments.
  • Knowledge of DICOM and IEC62304 Medical Device Software, Software Life Cycle Processes (strongly preferred and highly valued for this role).

Competencies:
  • Excellent critical thinking and problem-solving abilities with a structured engineering mindset.
  • This is a hands-on position that requires a high level of trust with unrestricted access to products, code, and documentation, and a strong sense of accountability for software quality and product safety.
  • Excellent verbal and written communication skills. Must feel comfortable asking questions when clarity is needed and documenting technical decisions clearly for audit and regulatory traceability.
  • Ability to adapt and work efficiently in a rapidly changing, dynamic environment with a willingness to manage multiple simultaneous projects and prioritize effectively in a fast-paced product development lifecycle.
  • Having knowledge of and demonstrating a willingness to work through different cultures' beliefs, values, and traditions is a must in a global engineering environment with distributed teams.

Working Conditions:
  • Majority of the work is performed in an office and manufacturing environment.
  • Typical work schedule is Monday through Friday, 7:00 a.m. to 4:00 p.m. Work hours may vary based on business and operational needs. Regular, reliable, and punctual attendance is an essential function of this position.
  • Occasional travel to Germany may be required.
  • May require PPE and periodic exposure to low-dose radiation.

We support a drug free work environment
Ziehm Orthoscan is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status and disability, or other legally protected status, and we will ensure that all employment decisions are based only on valid job requirements.

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