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Biomedical Product Development Engineer Jobs in Arizona

Becton, Dickinson and Company

Sr. R&D Engineer

Tempe, AZ

$100K - $137K/yr

The position designs, develops and implements new products, focusing on project planning ... B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other ...

Becton, Dickinson and Company

Sr. R&D Engineer

Tempe, AZ · On-site

$100K - $137K/yr

The position designs, develops and implements new products, focusing on project planning ... B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other ...

Lectric eBikes

Director, Product Development

Phoenix, AZ · On-site

$135K - $145K/yr

Director, Product Development Department: Product Reports to: CINO Location(s): In-Person, Phoenix ... Foster strong collaboration between Product Managers, Engineering, Operations, Marketing, and other ...

AbbVie

Development Engineer

Tempe, AZ · On-site

AbbVie is seeking a Development Engineer to join the PDS&T Injection Devices group. In this role ... Experience in medical devices, combination products, or related product development environments ...

AbbVie

Development Engineer

Tempe, AZ

AbbVie is seeking a Development Engineer to join the PDS&T Injection Devices group. In this role ... Experience in medical devices, combination products, or related product development environments ...

AbbVie

Development Engineer

Tempe, AZ

AbbVie is seeking a Development Engineer to join the PDS&T Injection Devices group. In this role ... Experience in medical devices, combination products, or related product development environments ...

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All JobsBiomedical Product Development Engineer JobsBiomedical Product Development Engineer Jobs in Arizona

Biomedical Product Development Engineer information

See Arizona salary details

$36.8K

$81.9K

$123.5K

How much do biomedical product development engineer jobs pay per year?

As of Jun 16, 2026, the average yearly pay for biomedical 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 in the Biomedical Product Development Engineer position, and why are they important?

To thrive as a Biomedical Product Development Engineer, you need a solid background in biomedical engineering, product design, and regulatory compliance, usually supported by a relevant engineering degree. Familiarity with CAD software, simulation tools, FDA regulations, and ISO standards is highly valuable, and some roles may require certification such as a Professional Engineer (PE) license. Excellent problem-solving skills, creativity, project management abilities, and effective communication are key soft skills that distinguish top performers in this field. These competencies ensure the successful development, testing, and delivery of safe and innovative biomedical devices that meet industry standards.

What does a Biomedical Product Development Engineer do?

A Biomedical Product Development Engineer is responsible for designing, developing, and testing medical devices and healthcare-related products. They collaborate with cross-functional teams, including scientists, regulatory specialists, and manufacturing engineers, to ensure products meet safety and regulatory standards. Their work involves prototyping, conducting validation studies, and optimizing designs for production. Additionally, they stay updated on industry advancements and compliance requirements to bring innovative solutions to market.

What are the typical challenges a Biomedical Product Development Engineer faces when bringing a new medical device to market?

Biomedical Product Development Engineers often encounter challenges such as navigating complex regulatory requirements, integrating multidisciplinary feedback, and ensuring device safety and efficacy through rigorous testing. Balancing innovative design with manufacturability and cost constraints is common, especially when working under tight deadlines. Collaboration with clinicians, quality assurance teams, and regulatory affairs professionals is an essential part of the process. Adapting quickly to feedback and addressing unforeseen technical issues are key to successfully advancing a product from concept to commercialization.

What are the most commonly searched types of Biomedical Product Development Engineer jobs in Arizona? The most popular types of Biomedical Product Development Engineer jobs in Arizona are:
What are popular job titles related to Biomedical Product Development Engineer jobs in Arizona? For Biomedical Product Development Engineer jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Biomedical Product Development Engineer jobs in Arizona look for? The top searched job categories for Biomedical Product Development Engineer jobs in Arizona are:
Biomedical Product Development Engineer jobs near you
Infographic showing various Biomedical Product Development Engineer job openings in Arizona as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $81,898 per year, or $39.4 per hour.

Product Development Engineer

SPECTRUM PLASTICS MASTER

Tucson, AZ • On-site

Full-time

Posted 2 days ago

Job description

JOB PURPOSE:
To design new devices/components and make design changes or improvements to existing devices/components. Leads or is a team member on projects to bring new designs or design changes through the applicable phases of the Product Development Process.
ESSENTIAL DUTIES:
  • Functions as leader or team member for projects involving all phases of product design and development, leading Core Team through the execution of project activities
  • Drives execution of project activities through the applicable project phases to the final phase of Commercial Release for ongoing production
  • Applies the Risk Management Policy to the development process for identifying hazards, estimating and evaluating associated risks, controlling these risks and monitoring the effectiveness of risk controls
  • Optimizes design and technology to drive innovation and significantly improve patient outcome
  • Ensures all applicable aspects of product design including design for manufacturability, scalability, testing, variability, and usability
  • Diligently develops product requirements and design inputs based on the applicable standards as well as other relevant sources, such as Post-Market Surveillance
  • Oversees and participates in creation of sub-assembly and final assembly drawings to serve as design specifications for a medical device
  • Develops verification and validation plans for the protocols, test methods, and reports for execution of design verification and validation testing
  • Verifies connection between product requirements, design inputs, design outputs, and verification/validation is clear in traceability matrix
  • Leads and ensures thoroughness of risk management activities as documented in Risk Management File, dFMEA, and pFMEA (design/process Failure Mode Effects Analysis)
  • Evaluates and designs products, parts, or processes for cost efficiency to minimize the cost for patient care
  • Coordinates project activities for Commercial Release of product and corresponding manufacturing processes while meeting expectations for sustainable, efficient, repeatable, and reproducible manufacturing operations
  • Defines activities for project execution to meet the requirements of the Product Development Process
  • Supports requests for quotes by outlining necessary project activities and timing for new product introduction
  • Upholds SPG and Dupont vision and core values
  • Performs all other duties as assigned

QUALIFICATIONS (Education/Experience/Knowledge, Skills & Abilities)
Required:
  • Bachelor's degree in engineering or equivalent experience in a related field.
  • 3-7 years industry experience
  • Demonstrated history to problem solve, identify errors and deficiencies and perform research
  • High degree of understanding of ISO 13485 requirements for Design Controls
  • Ability to provide guidelines and instructions applicable to the job function
  • Accuracy, attention to detail, and thoroughness
  • Proficient computer skills
  • Proficient communications skills
  • Ability to comprehend and comply with company safety and quality standards
  • Ability to provide oral and written instructions to others
  • Responsible for understanding and complying with all SPG and DuPont safety policies and procedures

Preferred:
  • Master's degree in Engineering discipline
  • Experience as project manager on a project which involved all phases of product design and development, leading Core Team through the execution of project activities
  • Knowledge on developing full-scale project plans
  • Effectively communicated project expectations to team members and stakeholders in a timely and clear fashion
  • Experience planning and driving execution of project activities through the applicable project phases to the final phase of Commercial Release for ongoing production
  • Has knowledge of commonly used concepts, practices, and procedures within medical device design and development
  • Can handle financial responsibilities for project such as budget accountability and revenue recognition
  • Experience developing Gantt Charts in Microsoft Project
  • Demonstrated ability to complete product design transfers

WORKING CONDITIONS:
Works with supervision from manager as necessary. Requires light physical activity performing non-strenuous daily activities.

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