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Medical Device Development Jobs in Arizona (NOW HIRING)

Banner Health

Biomedical IoMT Specialist

Chandler, AZ · On-site

Opportunities for employee development include project and time management, temperament training ... This role is integral to Banner Health's medical device security program, ensuring compliance and ...

Banner Health

Biomedical IoMT Specialist

Chandler, AZ · On-site

Opportunities for employee development include project and time management, temperament training ... This role is integral to Banner Health's medical device security program, ensuring compliance and ...

IQVIA

Medical Biller/Claims Processing

Flagstaff, AZ · Remote

$23/hr

Our teams help biopharma, medical device and diagnostic companies get their therapies to the people ... We create intelligent connections to accelerate the development and commercialization of innovative ...

AbbVie

Senior Engineer

Tempe, AZ · On-site

$109K/yr

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... Provide technical leadership for injection device development, verification, validation, and ...

AbbVie

Senior Engineer

Tempe, AZ · On-site

$100K - $137K/yr

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... Provide technical leadership for injection device development, verification, validation, and ...

AbbVie

Senior Engineer

Tempe, AZ

$100K - $137K/yr

... medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across ... Provide technical leadership for injection device development, verification, validation, and ...

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Medical Device Development information

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$27K

$49.8K

$75.5K

How much do medical device development jobs pay per year?

As of Jun 13, 2026, the average yearly pay for medical device development in Arizona is $49,779.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,600.00 and $55,900.00 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.
What are popular job titles related to Medical Device Development jobs in Arizona? For Medical Device Development jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Medical Device Development jobs in Arizona look for? The top searched job categories for Medical Device Development jobs in Arizona are:
What cities in Arizona are hiring for Medical Device Development jobs? Cities in Arizona with the most Medical Device Development job openings:
Medical Device Development jobs near you
Tech 2, Product Development Engineering

Tech 2, Product Development Engineering

Becton, Dickinson and Company

Tempe, AZ • On-site

Full-time

Posted 6 days ago

BD rating

7.3

Company rating: 7.3 out of 10

Based on 135 frontline employees who took The Breakroom Quiz

249th of 417 rated machine equipment manufacturers

Job description

We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Responsibilities:
  • Collaborate with Product Development Engineers to plan, execute, analyze, and report on research and development studies involving material, process, and device evaluations using specialized laboratory equipment including microscopes, Scanning Electron Microscopes (SEM), ovens, conditioning chambers, vacuum pumps, pouch sealers, and tensile/mechanical testers.
  • Accurately document all experimental methods, results, and observations in laboratory notebooks, protocols, and reports while remaining vigilant for unexpected results or process deviations, ensuring proper documentation and escalation of findings in accordance with cGMP, safety, and quality system requirements.
  • Support the manufacturing of medical devices in a cleanroom environment by following written and verbal work instructions to consistently produce safe and effective products, working collaboratively with technicians, operators, and engineers to meet project timelines and quality objectives while handling active pharmaceutical ingredients (APIs) and solvents safely.
  • Maintain clean, organized, and compliant cleanroom and laboratory spaces, ensure adequate stocking of supplies, place purchase orders, track deliveries, work with suppliers to receive and verify materials, and support audits, inspections, and continuous improvement activities related to cleanliness, organization, and compliance.
  • Complete all assigned training in a timely manner including safety, quality, and procedural training, while actively identifying opportunities for product, process, and workflow improvements and communicating recommendations to engineering and management teams.

Minimum Requirements:
  • Ability to recognize abnormal or unexpected results and escalate issues appropriately.
  • Effective communication and collaboration skills.
  • Comfort working with laboratory equipment and handling chemicals in a controlled environment.
  • High School Diploma or GED with 5+ years of experience in medical device manufacturing or a similar regulated industry.

Preferred Requirements:
  • Associate's Degree with 3+ years of experience in medical device manufacturing or a similar field
  • Equivalent combinations of education and experience may be considered.
  • Ability to follow detailed written and verbal instructions in a regulated manufacturing environment.
  • Strong attention to detail with a commitment to safety, quality, and documentation accuracy.

Work Environment & Physical Requirements:
  • Work is performed in cleanroom, laboratory, and office environments.
  • Required to wear appropriate personal protective equipment (PPE), including masks, hair nets, beard covers, safety glasses, gloves, and coveralls.
  • Ability to stand for significant portions of the shift and perform hands-on technical tasks.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit https://bd.com/careers.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
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Primary Work Location
USA AZ - Tempe Headquarters
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About BD

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BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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