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Medical Device Product Development Engineer Jobs in Phoenix, AZ

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Principal R&D Engineer Client: Medical Device Manufacturing Company Duration: 8.5 Months ... Collaborate with cross-functional teams to support product development, manufacturing readiness ...

CPR is seeking a Product Development Engineer (PDE) to join our team. The PDE section is ... Hired applicants may be eligible for benefits, including but not limited to, medical, dental ...

Designs, validates and brings new products to market. Specifies precise new product functional ... Vascular device engineering preferred Technical ability to develop and optimize designs for medical ...

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... products and services in our Allergan Aesthetics portfolio. For more information about AbbVie ...

Sr. R&D Engineer

Scottsdale, AZ · On-site

$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 ...

Develop a strong understanding of the complete medical device system, including electrical ... New Product Development * Contribute to next‑generation product development efforts.

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Showing results 1-20

Medical Device Product Development Engineer information

See Phoenix, AZ salary details

$39.2K

$87.3K

$131.6K

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

As of Aug 31, 2026, the average yearly pay for medical device product development engineer in Phoenix, AZ is $87,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,500.00 and $99,300.00 per year, depending on experience, location, and employer.

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 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 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 Phoenix, AZ?

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

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

The top searched job categories for Medical Device Product Development Engineer jobs in Phoenix, AZ are:

Infographic showing various Medical Device Product Development Engineer job openings in Phoenix, AZ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $82,351 per year, or $39.6 per hour.

Principal R&D Engineer

Tempe, AZ • On-site

Three Point Solutions
Recruiting and Staffing Services • 11 - 50 employees

$55 - $65/hr

Contractor

Re-posted 18 days ago


Job description

Job Title:         Principal R&D Engineer

Client:             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 medical device manufacturing processes.
  • Design and execute process characterization, validation (IQ/OQ/PQ), DOE, and TMV activities.
  • Analyze manufacturing data using statistical methods to drive process improvements and solve complex engineering problems.
  • Collaborate with cross-functional teams to support product development, manufacturing readiness, and commercialization.
  • Conduct root cause investigations and implement corrective actions using DMAIC, 5 Whys, and Lean Six Sigma methodologies.
  • Ensure compliance with quality management systems, regulatory requirements, and validation standards.
  • Lead technical projects, mentor team members, and communicate project progress, risks, and solutions.
  • Support research, product development, and continuous improvement initiatives for medical devices.

Required Skills:

  • Process Development & Validation (DOE, IQ/OQ/PQ, TMV)
  • Statistical Analysis
  • Root Cause Analysis
  • Medical Device Manufacturing
  • Cross-Functional Project Leadership
  • Quality Management Systems (QMS)
  • Technical Problem Solving
  • Project Management
  • Risk Management
  • Technical Documentation

Preferred Skills:

  • HPLC, LCMS, FTIR, Mass Spectrometry
  • Lean Six Sigma / DFSS / DRM
  • Green Belt Certification
  • Technical Writing
  • Investigation & CAPA
  • Medical Device Regulatory Compliance

Education:

  • Advanced degree in Mechanical Engineering, Biomedical Engineering, Materials Science, Physics, Chemistry, Chemical Engineering, or a related engineering/science discipline.

Experience:

  • 7+ years of relevant R&D or manufacturing engineering experience, or
  • 5+ years of relevant experience with an advanced degree.
  • Experience in medical device process development, validation, and cross-functional project leadership is required.

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