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Medical Device Project Manager Jobs in Arizona (NOW HIRING)

Roche

Global Project Manager

Tucson, AZ · On-site

$87K - $163K/yr

You have 6+ years project management experience in diagnostics and medical device hardware product development * You have Leading SAFE, Safe for HW or equivalent Scaled Agile certifications * You ...

Three Point Solutions

Principal R&D Engineer

Tempe, AZ · On-site

$55 - $65/hr

Medical Device Manufacturing * Cross-Functional Project Leadership * Quality Management Systems (QMS) * Technical Problem Solving * Project Management * Risk Management * Technical Documentation ...

Streimer Sheet Metal

Project Manager

Phoenix, AZ · On-site

$90 - $130/hr

Estimating to Job Cost interface, Forefront upgrades, mobile device options, 3D, and 4D / BIM, etc ... It is important that Project Managers are active participants in company and department team ...

Socket.dev

Mechanical Project Coordinator

Chandler, AZ · On-site

$60 - $90/hr

... Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical ... Support project managers with day-to-day project coordination and project-related activities ...

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All JobsMedical Device Project JobsMedical Device Project Manager JobsMedical Device Project Manager Jobs in Arizona

Medical Device Project Manager information

See Arizona salary details

$35.9K

$95.7K

$151K

How much do medical device project manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for medical device project manager in Arizona is $95,688.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,200.00 and $114,600.00 per year, depending on experience, location, and employer.

What is a medical device project manager?

A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.

What are the day-to-day responsibilities of a medical device project manager?

As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.

What are the key skills and qualifications needed to thrive in a medical device project manager position, and why are they important?

To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.

What are popular job titles related to Medical Device Project Manager jobs in Arizona?

For Medical Device Project Manager jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Medical Device Project Manager jobs in Arizona look for?

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What cities in Arizona are hiring for Medical Device Project Manager jobs?

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Medical Device Project Manager jobs near you
Infographic showing various Medical Device Project Manager job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $95,688 per year, or $46 per hour.

X-Ray Engineer (Medical Device)

Ziehm Orthoscan

Scottsdale, AZ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Key responsibilities

  • Lead all engineering and production aspects of X-Ray Generation, including electrical high voltage design, glassware, heat management, and manufacturing processes.

  • Serve as the technical bridge between engineering design and manufacturing operations by developing and validating high-voltage subsystems, insulation systems, and assemblies.

  • Troubleshoot manufacturing, assembly, test, and performance issues related to High-Voltage and X-ray systems, collaborating across departments to implement technical solutions.

Job description

Ziehm Imaging - Orthoscan Inc. is currently seeking a motivated, career-oriented professional with a positive can-do attitude to join our team as a full-time X-Ray Engineer located in Scottsdale, AZ.
Why Work for Ziehm Imaging - Orthoscan Inc.?
There's something special about Ziehm-Orthoscan. There's a sense of pride that comes from building a product that helps improve people’s lives and making the most of ourselves as a company and as individuals. We know the success of Ziehm-Orthoscan depends on every employee in our organization; it is our people who make the difference.
What do we offer?
  • The challenge of meaningful work - we offer constant opportunities to grow and develop world-class skills and a truly rewarding career.
  • A unique culture where people convert their passion into action.
  • The kind of competitive compensation you would expect from a world leader.
  • Nine paid holidays plus a generous PTO and vacation time plan.
  • Great benefit plans, major medical, dental and vision.
  • Company 401(k) plan with an employer match.
  • Competitive salary commensurate with experience
​JOB SUMMARY:
Lead all engineering and production aspects of X-Ray Generation, including electrical high voltage design, glassware, heat management, and lean and quality production processes. Working closely with R amp;D, QARA, and Production, the X-Ray Engineer serves as the critical technical bridge between engineering design and manufacturing operations, architecting, designing, and developing next-generation X-ray generator assemblies, high-voltage subsystems, high-voltage insulation systems, and oil-filled assemblies from initial engineering concepts through final mass production. Leveraging a strong background in high-voltage testing methodologies and robust manufacturing processes, this role translates research and development concepts into scalable, manufacturable, high-power hardware by applying advanced root-cause analysis and problem-solving techniques. The position also utilizes excellent written and verbal communication skills to develop automated test procedures, manufacturing process documentation, work instructions, validation protocols, and factory acceptance criteria that ensure product quality, clinical reliability, manufacturing efficiency, and strict regulatory compliance
ESSENTIAL FUNCTIONS:
  • Own the electrical engineering design, conceptualization, and manufacturing transfer of X-ray generator assemblies, High-Voltage subsystems, High-Voltage insulation systems, and oil-filled assemblies, ensuring sound manufacturing methodologies are engineered directly into the initial layout. Develop technical solutions to achieve marketing/sales requirements to ISO13485 standards
  • Develop, maintain, and improve manufacturing processes, fixtures, work instructions, and acceptance criteria while designing and refining the underlying product architectures
  • Drive reliability improvements for X-ray generator assemblies, High-Voltage subsystems, insulation systems, and oil-filled assemblies by developing, implementing, and executing advanced, physical High-Voltage testing methodologies and validation protocols, ensuring all products are built, tested, and validated to IEC60601-1 4th edition standards
  • Lead data-driven failure analysis, root-cause investigations, corrective actions, and field-return evaluations to implement Engineering Change Orders (ECOs) that directly improve product performance and production yield.
  • Troubleshoot manufacturing, assembly, test, and performance issues related to High-Voltage and X-ray systems, verbally collaborating across R amp;D, QARA, and Production to deploy rapid, permanent technical solutions.
  • Identify and implement continuous improvement opportunities across processes, work instructions, product quality, and manufacturing efficiency to maintain statistical control of the production line.
  • Own the entire generator technical lifecycle—from incoming parts and assembly processes through burn-in, clinical reliability, and field-return investigations.
Basic Qualifications:
Education:
  • Bachelor's degree in Electrical Engineering (BSEE) or a closely related engineering discipline with a strong academic focus in Power Electronics, Electromagnetic Field Theory, or High-Voltage Physics. An advanced Master’s degree in Manufacturing Engineering or related disciplines is a plus.
  • 3+ years of progressive electrical or hardware engineering experience designing, developing, validating, and implementing complex high-power or high-voltage (kV-level) electrical systems, with demonstrated expertise in product development and production readiness.
  • 2+ years of progressive electrical engineering experience with demonstrated manufacturing engineering expertise, including manufacturing process development and new product introduction (NPI), is required, preferably in a medical device industry environment.
Experience
  • High-Voltage testing amp; process transition experience in engineering or production test engineering (preferably in the medical/industrial X-ray industry), with a proven track record of implementing sound manufacturing processes and safely configuring high-power test benches operating between 40kV and 150kV
  • Structured failure investigation experience leading structured root-cause analysis and problem-solving techniques to dissect generator breakdowns, electrical arcs, and contamination events from factory burn-in failures through clinical field returns.
  • Cross-Functional technical communication: Demonstrated history of utilizing excellent written and verbal communication skills to bridge the gap between R amp;D, QARA, and Production—specifically transforming complex engineering requirements into audit-ready documentation and manufacturing work instructions.
Competencies:
  • Mastery of specialized high-voltage test equipment, including digital oscilloscopes, high-voltage probes, insulation resistance testers, power analyzers, and partial discharge measurement systems
  • Comprehensive knowledge of high-voltage insulation systems, creepage and clearance design, dielectric breakdown, oil insulation systems, electric field management, and vacuum/altitude effects
  • Deep understanding of tube current regulation, filament and anode operation, dark current, tube aging, and tube vacuum behavior.
  • Strong understanding of switching power supplies, resonant converters, inverters, PWM systems, feedback loops, and high-voltage multipliers.
  • Advanced proficiency in evaluating manufacturing processes to maintain strict control, determine process capabilities, design assembly fixtures, and establish compliant process validation (IQ/OQ/PQ) and acceptance criteria
  • Solid understanding of cleanliness and contamination control during assembly, with specific expertise regarding fluid contamination in oil-filled assemblies
  • Application of structured reliability principles and problem-solving techniques to identify root-cause failures, evaluate field returns, and directly improve production yields.
  • Experience in verifying products that meet regulatory/safety standards, using outside test agencies.
  • Keep abreast of new products, trends, and practices within the field/scope of practice as needed
Working Conditions:
  • Majority of the work is performed in a manufacturing and office environment.
  • Typical working hours and days are Monday – Friday 7am – 4pm, however this is subject to change depending on work demands
  • Periodic travel may be required (visit vendors, customers, training activities, etc.).
  • May require PPE and periodic exposure to low dose radiation.
We support a drug free work environment
EOE/M/F/Disability/Vet All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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