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Medical Product Development Jobs in Arizona (NOW HIRING)

... 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 ...

... 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 ...

... 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 ...

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Showing results 1-20

Medical Product Development information

See Arizona salary details

$39.6K

$118.3K

$134.7K

How much do medical product development jobs pay per year?

As of Aug 10, 2026, the average yearly pay for medical 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 are the key skills and qualifications needed to thrive in medical product development?

To excel in Medical Product Development, you need a background in biomedical engineering, life sciences, or a related field, along with experience in product design and regulatory compliance. Familiarity with CAD software, quality management systems (QMS), and ISO or FDA regulatory standards is typically required. Strong project management, problem-solving abilities, and effective cross-functional communication are crucial soft skills for this role. These competencies ensure the creation of safe, innovative medical products that meet regulatory requirements and address patient needs.

What is medical product development?

Medical product development is the process of designing, creating, testing, and bringing medical devices, diagnostics, or pharmaceutical products to market. This multidisciplinary process involves stages such as research, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that products are safe, effective, and meet regulatory standards before being used by patients or healthcare professionals.

What are some common challenges faced in medical product development, and how can professionals effectively navigate them?

Professionals in Medical Product Development often encounter challenges such as navigating complex regulatory requirements, coordinating cross-functional teams, and managing tight project timelines. Success in this role requires strong project management skills, adaptability, and effective communication with stakeholders including engineers, clinicians, and regulatory experts. Building a thorough understanding of FDA or international guidelines, maintaining meticulous documentation, and fostering collaborative team environments can help overcome these obstacles and drive successful product launches.
What cities in Arizona are hiring for Medical Product Development jobs? Cities in Arizona with the most Medical Product Development job openings:
Infographic showing various Medical Product Development 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 $118,338 per year, or $56.9 per hour.

Product Development Engineer

SPECTRUM PLASTICS MASTER

Tucson, AZ โ€ข On-site

Full-time

Re-posted 28 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.