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Medical Device Risk Management Jobs in Lees Summit, MO

Corbion

Procurement Category Manager II

Lenexa, KS

... risk management. Understanding and experience within basic organic and inorganic chemicals (e.g ... Job Segment: Supply Chain Manager, Supply Chain, Procurement, Medical Device, Food Science ...

Actalent

Regulatory Affairs Specialist

Olathe, KS

Support the Quality Assurance Manager in maintaining, monitoring, and improving the Quality Management System (QMS) for medical device products. * Lead or support activities to prepare the ...

Actalent

Regulatory Affairs Specialist

Olathe, KS

Support the Quality Assurance Manager in maintaining, monitoring, and improving the Quality Management System (QMS) for medical device products. * Lead or support activities to prepare the ...

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Showing results 21-40

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Lees Summit, MO

Medical Device Risk Management information

See Lees Summit, MO salary details

$50.1K

$108.5K

$165.4K

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

As of Aug 9, 2026, the average yearly pay for medical device risk management in Lees Summit, MO is $108,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,600.00 and $125,500.00 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.
Medical Device Risk Management jobs near you

Clinical Specialist - Kansas City

Jacobs Management Group

Kansas City, MO • On-site

$110K/yr

Full-time

Medical, Retirement, PTO

Posted 3 days ago

New

Job description

Clinical Specialist – Cardiac Medical Device

Position Overview
We are partnering with a growing medical device company focused on advancing innovative solutions for patients with complex cardiac conditions. The Clinical Specialist will provide clinical and technical support to physicians, hospital teams, and patients while helping ensure successful procedures and optimal outcomes.

This role is ideal for a clinically driven professional with cardiac device experience who enjoys working directly with physicians, supporting procedures, and educating healthcare teams in a hospital environment.

Responsibilities

· Provide clinical support during procedures, implants, and follow-up visits

· Work directly with physicians, nurses, and hospital staff to support patient care

· Educate clinical teams on device technology, procedures, and best practices

· Assist with clinical studies, documentation, and data collection as needed

· Provide technical expertise and troubleshooting support for healthcare providers

· Partner with sales teams to support customer relationships and account growth

· Maintain strong knowledge of cardiac device therapies and competitive technologies

· Travel throughout an assigned territory to provide case coverage and customer support

Qualifications

· Bachelor’s degree preferred or equivalent clinical experience

· Cardiac device certification or pacemaker training required

· Experience working with physicians and healthcare teams in a clinical setting

· Background in cardiac rhythm management, electrophysiology, cardiovascular devices, or related specialties preferred

· Strong communication, organizational, and problem-solving skills

· Ability to work independently in a fast-paced field environment

· Willingness to travel approximately 75%, including occasional weekends

Compensation & Benefits

· Base Salary: $90-110k

· Annual bonus/incentive opportunity

· Comprehensive medical benefits

· Paid vacation, holidays, floating holidays, and sick time

· 401(k) match up to 6%

· Career growth opportunities within a growing medical device organization

Apply