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Medical Device Development Jobs in Phoenix, AZ (NOW HIRING)

Orthoscan, Inc.

X-Ray Engineer (Medical Device)

Scottsdale, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Working closely with R&D, QARA, and Production, the X-Ray Engineer serves as the critical technical ... medical device industry environment. Experience * High-Voltage testing & process transition ...

Ziehm-OrthoScan

X-Ray Engineer (Medical Device)

Scottsdale, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Working closely with R&D, QARA, and Production, the X-Ray Engineer serves as the critical technical ... medical device industry environment. Experience * High-Voltage testing & process transition ...

Ziehm Orthoscan

X-Ray Engineer (Medical Device)

Scottsdale, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... development concepts into scalable, manufacturable, high-power hardware by applying advanced root ... medical device industry environment. Experience * High-Voltage testing amp; process transition ...

Ziehm Orthoscan

X-Ray Engineer (Medical Device)

Scottsdale, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Working closely with R&D, QARA, and Production, the X-Ray Engineer serves as the critical technical ... medical device industry environment. Experience: * High-Voltage testing & process transition ...

Hanger, Inc.

QA/QC Engineer II

Phoenix, AZ · On-site

$71K - $92K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Hanger, Inc.

QA/QC Engineer II

Phoenix, AZ · On-site

$71K - $92K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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 ...

Intel Corporation

Device Engineer

Phoenix, AZ · On-site

$72K - $93K/yr

  • Medical

  • Retirement

  • PTO

Manufacturing Development and Customer Engineering (MDCE) organization serves as the bridge between ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Intel

Device Engineer

Phoenix, AZ

$72K - $93K/yr

  • Medical

  • Retirement

  • PTO

Manufacturing Development and Customer Engineering (MDCE) organization serves as the bridge between ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Three Point Solutions

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Medical Device Manufacturing Company Duration: 8.5 Months (Possibility of Extension) Location: Tempe, AZ 85281 Shift: 1st Shift Description: * Lead the development, validation, and optimization of ...

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All JobsMedical Device Development JobsMedical Device Development Jobs in Phoenix, AZ

Medical Device Development information

See Phoenix, AZ salary details

$28.8K

$53K

$80.4K

How much do medical device development jobs pay per year?

As of Aug 14, 2026, the average yearly pay for medical device development in Phoenix, AZ is $53,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,200.00 and $59,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

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

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Phoenix, AZ as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $53,039 per year, or $25.5 per hour.

R&D Advanced Therapeutics Manager

Innovative Health LLC

Scottsdale, AZ • On-site

Full-time

Re-posted 4 days ago

Job description

The R&D Advanced Therapeutics Manager role is responsible for leading the development of advanced medical device reprocessing platforms, including Class III devices and complex electromechanical systems. This role provides both strategic and hands-on leadership across advanced therapeutic device reverse engineering and process development, with a focus on system-level architecture, disassembly/reassembly processes, component replacement strategies, and validation of functional equivalence.Essential Duties and Responsibilities:Strategic & Technical LeadershipDefine system-level architecture across different therapeutics platforms.Establish engineering requirements framework in compliance with FDA, ISO, and internal design controls.Define electrical performance criteria, functional equivalence requirements, and acceptance criteria for reprocessed devices.Lead cross-platform engineering strategy to ensure reuse of validation frameworks.Advanced Reprocessing DevelopmentDevelop and implement disassembly, component replacement, and reassembly strategies for complex devices.Lead reverse engineering and second-life device design approaches.Define critical-to-function components and replacement thresholds.Validation & Test ArchitectureBuild validation architecture covering: Electrical performanceMechanical performanceSystem-level functional equivalenceOversee development of test methods, protocols, and design verification and validation strategies.Program ExecutionLead R&D programs from concept through production.Manage timelines, technical risk, and resource allocation.Partner with RA/QA to define regulatory pathways and validation expectations.Team DevelopmentLead, mentor, and develop engineering team (Sr Engineers, Engineers, Technicians).Support hiring strategy aligned with technical roadmap.Foster a collaborative, high-performance culture. Supervisory Responsibilities:· Direct supervision of R&D engineering team members· Responsible for hiring, coaching, and performance managementEducation, Qualifications and Skills:· Bachelor's degree in engineering (Electrical, Mechanical, Biomedical or related); advanced degree preferred· 8 – 10+ years of experience in medical device R&D· Strong experience in Class III medical device development· Experience with system-level architecture and electromechanical systems· Deep understanding of design controls, risk management, and validation for FDA-regulated products· Strong leadership, problem-solving, and communication skills· Ability to work in a fast-paced, collaborative environment