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Medical Device Product Development Jobs in Arizona

Gn

Medical Device Sales

Prescott, AZ

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Beltone

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

Beltone

Medical Device Sales

Prescott, AZ · On-site

$85K/yr

Medical Device Sales - Prescott, Arizona Salary Potential: $2,500/month while training. When ... Beltone remains the most trusted brand for quality products and care among its patients and adults ...

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 ... Collaborate with cross-functional teams to support product development, manufacturing readiness ...

Erbe USA Incorporated

Sr. R&D Engineer

Tempe, AZ · On-site

$101K - $139K/yr

At least 7 years' experience in medical device R&D, product development, design controls, or other ... regulated industry. * Master's Degree preferred. * Demonstrated experience leading NPD and product ...

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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.

Staff Quality Engineer - Product Development, Tempe, AZ - (IK)

Central Business Solutions, Inc

Tempe, AZ • On-site

$110 - $115/hr

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Staff Quality Engineer - Product Development, Tempe, AZ - (IK)
  • Tempe, Arizona

Job Responsibilities:

Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance) and chemical and pharmaceutical operations (e.g., drug product manufacturing, analytical testing, process development and quality assurance)

Ability to create, support, review, and investigate analytical test methods used to support pharmaceutical combination devices.

The ability to create, support, review chemistry, manufacturing, and controls device submissions

Participates as team leader or as an active member of the team to meet company objectives and ensure department responsibilities are completed

Leads development of risk assessments and test method activities (e.g., development and validation for physical and analytical test methods)

Leads component qualifications, design validation, design verification, drug stability and process validation

Leads product investigations

Ability to make and present risked based decisions

Supports translation of design inputs into manufacturing control plans

Develop and implement procedures to comply with corporate and industry standards.

Coordinates and/or directs all aspects of product development activity related to a product line

Leads development of risk assessments and test methods

Quality engineering representation on Product Development and Design Review teams

Prepare and present project updates and technical discussions

Participate in project planning, budgeting, scheduling, and tracking

Support internal and external supplier audits

Provide support to the regulatory department in writing technical submissions

Complies with company procedures and policies, government regulations

Actively participates in training and providing input to training of employees on division procedures and policies

Ability to travel for business, project, and issues approximately up to 25% of time.

Other duties and projects, as assigned

Required Education and Experience:

BS in Engineering, Biological Science, or a related engineering field (Masters or Ph.D preferred). Fields of study include Chemical Engineering, Bioengineering, Pharmacy, or Biochemistry

Minimum of eight years of experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry

Extensive proven understanding of design controls in development stage

Pharmaceutical or combination product experience

Required Qualifications:

Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)

Ability to lead creation of risk management files

Ability to develop solutions with business impact

Advanced statistical and risk assessment techniques

Working knowledge of test method (development and validation), equipment qualifications, process and design validation, risk assessment techniques, and component qualification methodologies

Ability to make and present risk-based decisions

Strong interpersonal skills

Ability to analyze and optimize manufacturing and quality systems

Product, design & prototyping

Ability to create and provide training

Problem solving ability

Ability to create, review and coordinate test protocols and reports

Ability to generate engineering proposals

Oral and written presentation skills

Ability to lead cross functional teams

Understanding of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 210/211/820 , ICH Guidelines

Skills and Certifications

Drug Device delivery combination products

Compensation

Base Salary -USD $110,000 to $115,000

Candidate Details

Full-time

Benefits -Full

Relocation Assistance Available -Possible for ideal candidate

Ideal Candidate

8+ years experience in New Product Development of combination devices

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