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Medical Device Risk Management Jobs in Kansas (NOW HIRING)

Engenious Design

Systems Engineer

Prairie Village, KS · On-site

... manage risk, and tackle complex integration challenges to deliver life-changing medical and high ... Experience interpreting and applying medical device standards such as ISO 60601-1, ISO 13485 etc ...

Steadily

Catastrophe Risk Manager

Overland Park, KS · On-site

Required * 5+ years of catastrophe modeling experience or risk management * Expertise with third ... Medical, dental, vision, life, disability, HSA, FSA * Retirement : 401(k) * Perks : Free snacks ...

Steadily

Catastrophe Risk Manager

Overland Park, KS · On-site

Required * 5+ years of catastrophe modeling experience or risk management * Expertise with third ... Medical, dental, vision, life, disability, HSA, FSA * Retirement : 401(k) * Perks : Free snacks ...

ProPharma Group

... risk and accelerate our partners' most high-profile drug and device programs. The Medical ... Other activities as assigned as delegated by the Manager. Qualified candidates must have: Pharmacy ...

ProPharma Group

... risk and accelerate our partners' most high-profile drug and device programs. The Medical ... Other activities as assigned as delegated by the Manager. Qualified candidates must have: Nursing ...

Pfizer

PMO Sr. Project Manager

Mcpherson, KS · On-site

$99K - $165K/yr

Master's degree with specific experience in managing pharmaceutical, technical, or medical device ... Ability to analyze data from detailed schedule and risk management tools. * Interface effectively ...

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Medical Device Risk Management information

See Kansas salary details

$45.9K

$99.5K

$151.6K

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

As of Sep 11, 2026, the average yearly pay for medical device risk management in Kansas is $99,491.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,300.00 and $115,000.00 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 Kansas look for?

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

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

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

Medical Device Risk Management jobs near you
Infographic showing various Medical Device Risk Management job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $99,491 per year, or $47.8 per hour.

Systems Engineer

Prairie Village, KS • On-site

Engenious Design
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Engenious Designexternal

Full-time

Re-posted 28 days ago

Job description

We're seeking an experienced product development Systems Engineer who can think big-picture while staying hands-on across diverse technologies. You'll define user needs, drive system-level requirements, and unite electrical, mechanical, and software disciplines into cohesive products. Acting as the connective tissue across designers, engineers, and clients, you'll navigate tradeoffs, manage risk, and tackle complex integration challenges to deliver life-changing medical and high-tech products.
What You'll Do:
  • Maintain the System View: Act as the holistic thinker for the product-maintaining a clear mental model of the system, identifying roadblocks early, and guide the team toward effective solutions.
  • Lead Cross-Functional Integration: Coordinate electrical, mechanical, software, industrial design, and test workstreams to ensure the product functions as a cohesive system.
  • Drive Requirements & Traceability: Lead the definition of user needs and product requirements, maintaining clear traceability from requirements to design decisions, risk management, and verification.
  • Own Risk Management: Proactively identify, prioritize, document, and manage technical and program risks, working closely with the design team to develop and execute mitigation strategies.
  • Act as a Technical Investigator: Use prototypes, proof-of-concept builds, and engineering testing to validate concepts and inform design direction.
  • Enable Informed Decisions: Communicate system architecture, progress, risks, and tradeoffs clearly to teams and clients, empowering confident design decisions.
  • Guide Compliance & Documentation: Ensure development follows the governing QMS and regulatory standards while maintaining a right-sized Design Development File.

Position Details:
This is a full-time, permanent position. This leadership position is based in our Kansas City design center, and not available as a remote job.
Qualifications:
  • 5+ years of applicable experience in electromechanical/embedded system product development
  • Degree in a relevant engineering background (e.g Biomedical, Mechanical, Electrical, Software), or equivalant experience.
  • Experience interpreting and applying medical device standards such as ISO 60601-1, ISO 13485 etc., or similar experience in a regulated industry
Nice to haves:
  • Experience leading cross-functional teams of engineers and designers

While we recognize that top talent comes from all over the world, we are a small team and are not able to offer visa sponsorship at this time. Candidates must be authorized to work in the United States without requiring visa sponsorship

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