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Medical Device Risk Management Jobs in Orem, UT (NOW HIRING)

... medical, dental, vision, life insurance, defined contribution retirement program, and potential for incentive compensation). The Risk Analyst reports to the VP-Risk Manager and is primarily ...

Risk Analyst

South Jordan, UT · On-site

$57K - $85K/yr

... medical, dental, vision, life insurance, defined contribution retirement program, and potential for incentive compensation). The Risk Analyst reports to the VP-Risk Manager and is primarily ...

... medical, dental, vision, life insurance, defined contribution retirement program, and potential for incentive compensation). The Risk Analyst reports to the VP-Risk Manager and is primarily ...

Experience in Risk Management is preferred. * Strong critical thinking and analytical abilities ... of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time ...

... Device Industry required • Minimum of 2-3 years writing experience within the Medical Device ... Working knowledge of Excel. • Proficiency with a PC • Excellent time management skills, and ...

... Device Industry required • Minimum of 2-3 years writing experience within the Medical Device ... Working knowledge of Excel. • Proficiency with a PC • Excellent time management skills, and ...

... medical, claims, litigation, and employee information appropriately. Education & Experience * Bachelor's degree in Occupational Safety, Human Resources, Business, Risk Management, or a related field ...

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Showing results 1-20

Medical Device Risk Management information

See Orem, UT salary details

$44.8K

$97K

$147.8K

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

As of Aug 28, 2026, the average yearly pay for medical device risk management in Orem, UT is $96,983.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,200.00 and $112,100.00 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 are popular job titles related to Medical Device Risk Management jobs in Orem, UT?

For Medical Device Risk Management jobs in Orem, UT, the most frequently searched job titles are:

What job categories do people searching Medical Device Risk Management jobs in Orem, UT look for?

The top searched job categories for Medical Device Risk Management jobs in Orem, UT are:

Medical Device Assembler - Day Shift

Spherion of Utah

Draper, UT

$19 - $22/hr

Full-time

Posted 2 days ago

New


Job description

Elevate your manufacturing career with a dynamic, growing industry leader launching cutting-edge wireless technologies for interventional medicine. In this high-impact cleanroom role, you will perform precision guide wire assembly, hydrophilic coating, and Tyvek packaging using advanced tools and microscopes. This temp-to-hire opportunity offers a consistent first-shift schedule, structured on-the-job training, and a collaborative team environment dedicated to making a difference in patient lives.
Responsibilities:

  • Precision Assembly: Perform precision guide wire assembly, hydrophilic coating, and Tyvek bag sealing/pouching.
  • Quality Inspection: Use microscopes and advanced custom fixtures to inspect components and ensure strict adherence to quality metrics.
  • Documentation & Compliance: Read, follow, and execute technical drawings and written manufacturing procedures in English.
  • Cleanroom Maintenance: Work comfortably within an Environmentally Controlled Area (ECA) cleanroom, adhering to strict gowning and PPE protocols. Perform routine sanitization and cleaning of workbenches, walls, and floors.
  • Team Collaboration: Maintain a strong work ethic and collaborate with team members to meet daily production targets.
  • Working hours: 7:00 AM - 3:30 PM


Skills:

  • Advanced Equipment Handling: Prior experience operating microscope inspection tools and precision hand tools.
  • Specialized Processes: Specific familiarity with guidewire assembly, hydrophilic coating application, and Tyvek pouch sealing.
  • Soft Skills: High precision, keen attention to detail, strong active listening, and proactive troubleshooting abilities.


Education:

  • No Degree Required


Experience:

  • 1-4 years


Qualifications:

  • Experience: Proven background in medical device or high-precision manufacturing assembly.
  • Technical Literacy: Ability to interpret and accurately follow technical drawings and written instructions in English.
  • Cleanroom Proficiency: Strict adherence to ECA cleanroom protocols, including wearing required PPE (cleanroom gown, hairnet, face mask, and protective gloves).
  • Physical Capabilities: Ability to lift up to 20 lbs and comfortably manage a physical workload that is approximately 70% sitting and 30% standing/walking.
  • Availability: Ability to work the standard Day Shift (Monday-Friday, 7:00 AM - 3:30 PM) and work overtime as needed.
  • Screening: Must be able to pass a pre-employment background check and a drug screen.


Ready to launch your career in medical technology? If you have the precision, drive, and cleanroom experience we are looking for, we want to hear from you! Click Apply Now to submit your resume and to schedule your interview. Secure your spot on this premier day shift today!


Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Company Description

We believe that a job should offer more than a paycheck—it should provide clarity, confidence, and hope. Spherion is a national recruiting powerhouse powered by independent, local owners who are personally invested in your success. Whether you’re looking for your next big break or a flexible way to work, we have the local expertise and global reach to get you there.