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Medical Device Manufacturing Engineer Jobs in Arizona

Intellectt INC

Collaborate with manufacturing, quality, and engineering teams * Maintain accurate validation documentation Requirements: * 5+ years of automation validation experience (medical device preferred)

Intel Corporation

Device Engineer

Phoenix, AZ · On-site

$72K - $93K/yr

Manufacturing Development and Customer Engineering (MDCE) organization serves as the bridge between ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Intel

Device Engineer

Phoenix, AZ

$72K - $93K/yr

Manufacturing Development and Customer Engineering (MDCE) organization serves as the bridge between ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Ralliant

Manufacturing Engineer

Chandler, AZ · On-site

$71K - $92K/yr

... Medical Device, Automotive, or other highly regulated manufacturing experience preferred. • Lean ... With engineering and manufacturing capability in Arizona and California, our associates work ...

Amphenol Borisch Technologies

Manufacturing Engineer

Mesa, AZ · On-site

$72K - $93K/yr

The Manufacturing Engineer III is a Senior Engineer, responsible to develop and drive quality ... Full Medical, Dental and Prescription Drug Insurance * Flexible Spending Accounts * Generous 401(k) ...

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All JobsMedical Device Manufacturing Engineer JobsMedical Device Manufacturing Engineer Jobs in Arizona

Medical Device Manufacturing Engineer information

See Arizona salary details

$44.3K

$79.8K

$111.8K

How much do medical device manufacturing engineer jobs pay per year?

As of Aug 1, 2026, the average yearly pay for medical device manufacturing engineer in Arizona is $79,782.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $87,600.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Manufacturing Engineer vs Quality Assurance Engineer?

AspectMedical Device Manufacturing EngineerQuality Assurance Engineer
CredentialsBachelor's in engineering or related field; certifications like ASQ CQE beneficialBachelor's in engineering, quality assurance, or related; certifications like ASQ CQE or CQA common
Work EnvironmentManufacturing plants, production lines, R&D labsQuality labs, manufacturing sites, regulatory agencies
Industry UsageDesign, develop, and optimize manufacturing processesEnsure product quality, compliance, and process improvements

While both roles work within the medical device industry and require similar credentials, the Medical Device Manufacturing Engineer focuses on manufacturing processes and product development, whereas the Quality Assurance Engineer emphasizes maintaining quality standards and regulatory compliance.

What are the key skills and qualifications needed to thrive as a Medical Device Manufacturing Engineer, and why are they important?

To excel as a Medical Device Manufacturing Engineer, you need a solid background in engineering principles, manufacturing processes, and regulatory compliance, typically supported by a degree in biomedical, mechanical, or industrial engineering. Familiarity with CAD software, Six Sigma/Lean methodologies, and knowledge of FDA or ISO 13485 standards is essential. Strong problem-solving, teamwork, and communication skills help manage cross-functional projects and ensure product quality. These competencies are crucial for developing safe, effective devices in a highly regulated industry where precision and compliance are paramount.

What are some common challenges faced by Medical Device Manufacturing Engineers during product development?

Medical Device Manufacturing Engineers often encounter challenges in balancing strict regulatory compliance with efficient production processes. Adapting to frequent design changes, ensuring high product quality, and validating manufacturing processes are crucial tasks. Additionally, they collaborate closely with cross-functional teams—including quality assurance, R&D, and supply chain—to troubleshoot production issues and implement improvements. Addressing these challenges requires strong problem-solving skills and a keen attention to detail.

What does a Medical Device Manufacturing Engineer do?

A Medical Device Manufacturing Engineer is responsible for designing, developing, and optimizing manufacturing processes for medical devices. They ensure that products are produced efficiently, safely, and in compliance with regulatory standards such as FDA or ISO guidelines. Their work involves collaborating with design teams, troubleshooting production issues, implementing quality control procedures, and continuously improving manufacturing methods to enhance product quality. Ultimately, they play a key role in bringing safe and effective medical devices to market.
What are popular job titles related to Medical Device Manufacturing Engineer jobs in Arizona? For Medical Device Manufacturing Engineer jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Medical Device Manufacturing Engineer jobs in Arizona look for? The top searched job categories for Medical Device Manufacturing Engineer jobs in Arizona are:
Medical Device Manufacturing Engineer jobs near you
Infographic showing various Medical Device Manufacturing Engineer job openings in Arizona as of July 2026, with employment types broken down into 81% Full Time, 12% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $79,782 per year, or $38.4 per hour.

Principal R&D Engineer

Three Point Solutions

Tempe, AZ • On-site

$55 - $65/hr

Contractor

Posted 17 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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