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Medical Device Product Risk Manager Jobs (NOW HIRING)

Medical Device Assembler

Irvine, CA · On-site

$17 - $19/hr

May be required based on production needs Role Overview Build medical technology that makes a ... Support Quality Management System (QMS), Environmental Management System (EMS), and applicable ...

Drive all phases of the product development cycle, including feasibility, concept, validation ... Managing efforts for compliance ensure design control, DMR/DHF compliance, risk analysis, and ...

... medical device development activities, including design controls, system requirements, risk ... Product Management DIVISION: ADC Diabetes Care LOCATION: United States > Alameda : 2601 Harbor Bay ...

Senior Director, Program Management

$118K - $119K/yr

Strong knowledge of medical device product development processes, Design Controls, risk management, and FDA and international regulatory requirements. * Demonstrated ability to proactively identify ...

Showing results 41-60

Medical Device Product Risk Manager information

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$51.5K

$159.4K

$197K

How much do medical device product risk manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for medical device product risk manager in the United States is $159,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,000.00 and $197,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Device Product Risk Manager jobs?

For Medical Device Product Risk Manager jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Product Risk Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $159,405 per year, or $76.6 per hour.

Sr Product Safety Engineer

Portage, MI • On-site

Oxford Global Resources
Recruiting and Staffing Services • 501 - 1,000 employees

Other

Posted 6 days ago


Job description

Job Title: Sr Product Safety Engineer

Location: Portage, MI (3-4 days ONSITE)
Duration: 6 months

Ideal Start Date: Aug 10th

Background or Drug Screen required: Yes

Project Details: Support a third-generation medical device/product currently undergoing UL certification and verification testing, with a focus on electrical product safety, V&V, EMC, and regulatory compliance activities. The immediate priority is assisting with final testing execution, documentation, and certification reporting under IEC/ISO 60601 (3rd Edition). The consultant will also provide compliance and regulatory input for an early-stage second-generation product program. Most testing is performed internally, with some testing conducted at UL's Northbrook, IL facility.

·      Define and implement product safety program plans for complex device development programs.

·      Create product safety test plans and ensure they meet third-party certifier requirements.

·      Support lab personnel on compliance testing, design conformance, and product safety issues.

·      Interface with Nationally Recognized Test Labs (NRTLs) and external bodies to achieve product certification.

·      Apply design controls, change controls, and risk management per the Quality Management System.

·      Partner within design teams to drive product safety, compliance, and industry best practices.

·      Mentor and support early-career engineers in the product safety discipline (as needed).

Musts:

Hands-on IEC/ISO 60601 3rd Edition testing experience

Strong electrical product safety testing background

Verification & Validation (V&V) experience

EMC testing and compliance experience

Experience supporting UL and/or CSA certification activities

Ability to execute testing, analyze results, and prepare technical reports

5–10 years of relevant experience (targeting approximately 7–8 years)

Pluses:

Former UL or CSA test engineer experience

Product Safety Engineer background

Regulatory Affairs and compliance experience

Experience supporting medical device development programs

Experience with both testing execution and regulatory strategy

Familiarity with next-generation product development and design planning activities

Prior work in accredited test lab environments (UL, CSA, or similar)


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About Oxford Global Resources

Sourced by ZipRecruiter

Oxford Global Resources delivers tailored solutions for any technical challenges you face using our partnership-first approach. We specialize in workforce mobilization, digital transformation, and modern enterprise. We are committed to providing you with The Right Talent. Right Now. In 1984, we started Oxford with a handful of employees in a converted schoolhouse in Reading, Massachusetts. The people that shape our organization are some of the best in the industry. They are dedicated to making an impact and are with you every step of the way. We strive to meet the most pressing needs, solve the most complex problems, and go beyond expectations for our clients and our consultants. Together, we drive great outcomes. Whether you’d like to join the thousands of professionals who trust Oxford to advance their careers or partner with us to solve a challenge your business is facing, contact us at any of our 35 global offices.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Beverly, MA, US

Year founded

1984

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