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Medical Device Risk Management Jobs in Arizona (NOW HIRING)

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 ...

ASRC

Senior Risk Management Analyst

Tempe, AZ · On-site

Maintain all related files and filing, including confidential medical records, police reports, payroll records, etc. * Develop and update risk management and insurance reports, policies and ...

Talented Medical Solutions

RN - Risk Manager

Peridot, AZ · On-site

$2.2K - $2.4K/wk

At Talented Medical Solutions we breed winners. Responsibilities * Plans, directs and coordinates the Risk Management and Compliance Program to minimize the risk of personal injury to patients ...

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Medical Device Risk Management information

See Arizona salary details

$48K

$104K

$158.4K

How much do medical device risk management jobs pay per year?

As of Sep 9, 2026, the average yearly pay for medical device risk management in Arizona is $103,958.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,900.00 and $120,200.00 per year, depending on experience, location, and employer.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a medical device risk management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.

What are the key skills and qualifications needed to thrive in medical device risk management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What job categories do people searching Medical Device Risk Management jobs in Arizona look for?

The top searched job categories for Medical Device Risk Management jobs in Arizona are:

What cities in Arizona are hiring for Medical Device Risk Management jobs?

Cities in Arizona with the most Medical Device Risk Management job openings:

Medical Device Risk Management jobs near you

Principal R&D Engineer

Tempe, AZ • On-site

Three Point Solutions
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Three Point Solutionsexternal

$55 - $65/hr

Contractor

Re-posted 26 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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