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Medical Device Risk Management Jobs in Denver, CO

Actalent

Medical Device Engineer

Aurora, CO · Hybrid

$57.69/hr

Support risk management activities in accordance with ISO 14971 methodologies. * Participate in ... Experience supporting medical device development or work within a highly regulated industry.

South metro

Risk Management Administrator

Centennial, CO · On-site

$120K - $141K/yr

RISK MANAGEMENT ADMINISTRATOR CLOSES ON AUGUST 14, 2026 AT 5:00 P.M. MST REPORTS TO: Human ... Acts as primary liaison between the employer, the injured worked, medical providers, and claims ...

South metro

Risk Management Administrator

Centennial, CO · On-site

$120K - $141K/yr

RISK MANAGEMENT ADMINISTRATOR CLOSES ON AUGUST 14, 2026 AT 5:00 P.M. MST REPORTS TO: Human ... Acts as primary liaison between the employer, the injured worked, medical providers, and claims ...

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Showing results 1-20

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Denver, CO

Medical Device Risk Management information

See Denver, CO salary details

$53K

$114.8K

$175K

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

As of Aug 10, 2026, the average yearly pay for medical device risk management in Denver, CO is $114,822.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,600.00 and $132,800.00 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.
What are popular job titles related to Medical Device Risk Management jobs in Denver, CO? For Medical Device Risk Management jobs in Denver, CO, the most frequently searched job titles are:
What job categories do people searching Medical Device Risk Management jobs in Denver, CO look for? The top searched job categories for Medical Device Risk Management jobs in Denver, CO are:
Medical Device Risk Management jobs near you
Infographic showing various Medical Device Risk Management job openings in Denver, CO as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $114,822 per year, or $55.2 per hour.

Medical Device Engineer

Actalent

Aurora, CO • Hybrid

$57.69/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago

Job description

Job Title: Electrical Engineer

Job Description

We're seeking an experienced Electrical Engineer to join a team focused on the development, testing, and regulatory compliance of innovative medical devices. In this role, you'll play a critical part in ensuring products meet global safety and performance standards while helping bring life-changing technologies to market.

This position offers a unique opportunity to work at the intersection of engineering, product development, quality, and regulatory compliance. You'll collaborate with cross-functional teams to support product development activities, electrical safety testing, risk management efforts, and regulatory initiatives, including compliance with EU MDR and IEC 60601 standards.

What You'll Do

As an Electrical Engineer, you will:

  • Design, evaluate, and support electrical systems used in medical devices.
  • Plan, execute, and document electrical safety testing in accordance with IEC 60601 standards.
  • Support compliance efforts related to EU Medical Device Regulation (EU MDR 2017/745).
  • Develop technical documentation required for product development and regulatory submissions.
  • Partner with Quality, Regulatory Affairs, Manufacturing, and R&D teams throughout the product lifecycle.
  • Support risk management activities in accordance with ISO 14971 methodologies.
  • Participate in design reviews, verification activities, and product investigations.
  • Work with third-party testing laboratories and certification organizations during compliance testing.
  • Analyze product issues and implement effective corrective actions.
  • Assist with audit readiness and regulatory inspections.
Required Qualifications
  • Bachelor's degree in Electrical Engineering or a related engineering discipline.
  • Experience supporting medical device development or work within a highly regulated industry.
  • Strong understanding of electrical design principles and product development processes.
  • Experience supporting or executing testing to IEC 60601 standards.
  • Knowledge of EU MDR requirements and medical device compliance activities.
  • Experience with electrical safety testing equipment and laboratory environments.
  • Familiarity with design controls, engineering documentation, and quality systems.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent communication and collaboration abilities.
Preferred Experience

Candidates with any of the following will stand out:

  • IEC 60601-1-2 EMC testing experience.
  • CE Marking support for medical devices.
  • Knowledge of FDA medical device regulations.
  • Experience with ISO 13485 quality systems.
  • Experience facilitating risk management activities under ISO 14971.
  • Verification and validation testing experience.
  • Embedded systems, power electronics, or medical device software integration experience.
  • Direct interaction with Notified Bodies or third-party compliance laboratories.
Technologies & Standards

You may work with:

  • EU MDR (2017/745)
  • IEC 60601-1 Electrical Safety Standards
  • IEC 60601-1-2 EMC Standards
  • ISO 13485 Quality Systems
  • ISO 14971 Risk Management
  • Design Controls & Technical Documentation
  • Electrical Safety Testing Equipment
Why Join Us?
  • Help deliver safe and compliant medical devices that impact patient outcomes worldwide.
  • Collaborate with experienced engineering, regulatory, and quality teams.
  • Gain exposure to global regulatory requirements and advanced medical technologies.
  • Work on challenging projects involving product safety, compliance, and innovation.
  • Influence products from development through commercialization and regulatory approval.
Job Type & Location

This is a Contract position based out of Centennial, CO.

Pay and Benefits

The pay range for this position is $57.69 - $57.69/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Centennial,CO.

Application Deadline

This position is anticipated to close on Aug 5, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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About Actalent

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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

Social media

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