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Medical Device Risk Management Jobs (NOW HIRING)

Intellectt INC

Senior medical device risk management experience -- 7-10+ yrs preferred * Deep expertise in ISO 14971 and FDA QMSR risk management requirements * Experience building or remediating complete risk ...

Intellectt INC

Design Transfer Risk SME

Yuma, AZ · On-site

Medical device risk management experience with focus on design transfer * Familiarity with ISO 14971 and QMSR risk expectations * Experience reviewing design transfer documentation with risk ...

INCOG

QA Risk Management Sr Engineer

Fishers, IN

Provide QA risk management oversight for medical device and combination product (autoinjector, prefilled syringe, and similar device) assembly operations, ensuring compliance with ISO 13485 and ISO ...

Deegit Inc

QARA

Plymouth, MN · On-site

Experience with ISO 14971 risk management activities * Experience with the post market medical device support (complaint or risk analysis) Skill and Experience Details: Minimum Experience Required:

Collabera

Medical Reviewer/Safety Reviewer

Richmond, VA · On-site

$40K - $65K/mo

... device risk management and associated risk management documents such as Clinical Hazards List ... Provides medical support which may include: Adverse Event Reporting - the investigation and ...

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Medical Device Risk Management information

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$51.5K

$111.6K

$170K

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

As of Jun 6, 2026, the average yearly pay for medical device risk management in the United States is $111,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,000.00 and $129,000.00 per year, depending on experience, location, and employer.

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 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.
More about Medical Device Risk Management jobs
What cities are hiring for Medical Device Risk Management jobs? Cities with the most Medical Device Risk Management job openings:
What states have the most Medical Device Risk Management jobs? States with the most job openings for Medical Device Risk Management jobs include:
What job categories do people searching Medical Device Risk Management jobs look for? The top searched job categories for Medical Device Risk Management jobs are:
Medical Device Risk Management jobs near you
Infographic showing various Medical Device Risk Management job openings in the United States as of May 2026, with employment types broken down into 3% Locum Tenens, 3% As Needed, 43% Full Time, and 51% Part Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $111,556 per year, or $53.6 per hour.
Medical Device Risk Management Advisor (Part-Time, Remote)

Medical Device Risk Management Advisor (Part-Time, Remote)

FocusKPI Inc.

Boston, MA • Remote

Contractor

Posted 18 days ago

Job description

We are building an AI-powered platform to support medical device risk management and regulatory documentation (including ISO 14971 and design controls), and are looking for a few professionals to serve as ongoing product feedback advisors.

This is a flexible, part-time opportunity for experienced professionals who can periodically test new features, review workflows, and provide practical feedback based on real-world medical device and regulatory experience. Your input will directly shape how the product supports day-to-day work in regulated environments.

What You’ll Do
  • Test new features and prototypes periodically
  • Provide feedback on usability and regulatory alignment
  • Review risk management and documentation workflows
  • Suggest improvements based on real industry practice
  • Join occasional 30–45 minute feedback sessions
Time Commitment
  • Flexible, ongoing engagement
  • Approximately 1–2 hours per week or biweekly
  • Fully remote
Preferred Background
  • Medical device regulatory affairs or quality assurance
  • Experience with ISO 14971 risk management
  • Design controls / DHF documentation
  • 510(k), De Novo, or PMA experience is a plus
  • Risk management file, FMEA, or hazard analysis experience

Consultants and industry professionals are welcome.

How to Apply

If you’re interested, please complete this short screening form so we can better understand your background:
https://forms.gle/jgj1ZN2jtAGGAbYQA

We’ll follow up with selected candidates to schedule an initial session and discuss next steps.

NOTICE: Please be aware of fraudulent emails regarding job postings, job offers and fake checks. FocusKPI's recruiting team will strictly reach out via @focuskpi.com email domain. If you have received fraudulent emails now or in the past, please report it to https://reportfraud.ftc.gov/ .
The domain @focuskpijobs.com is fraudulent and not related to FocusKPI. Please do not not reply or communicate to anyone with @focuskpijobs.com.

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About FocusKPI

Sourced by ZipRecruiter

Industry

Computing infrastructure providers, data processing, web hosting

Company size

51 - 200 Employees

Headquarters location

Santa Clara, CA, US

Year founded

2010

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