Sr Product Safety Engineer
Portage, MI · On-site
Support a third-generation medical device/product currently undergoing UL certification and ... and risk management per the Quality Management System. · Partner within design teams to drive ...
Portage, MI · On-site
Support a third-generation medical device/product currently undergoing UL certification and ... and risk management per the Quality Management System. · Partner within design teams to drive ...
Portage, MI · On-site
Support a third-generation medical device/product currently undergoing UL certification and ... and risk management per the Quality Management System. · Partner within design teams to drive ...
... of medical device products, including toxicological risk assessments based on data from ... Support biocompatibility and toxicology processes initiated by department management and help ...
... of medical device products, including toxicological risk assessments based on data from ... Support biocompatibility and toxicology processes initiated by department management and help ...
Arlington, VA · On-site
$70 - $85/hr
Airbus US is looking for a Cyber Security Product Risk Manager to who works with specialists from the Cyber, Space Engineering, and Contracts departments to ensure our products meet the applicable ...
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Arlington, VA · On-site
$70 - $85/hr
Airbus US is looking for a Cyber Security Product Risk Manager to who works with specialists from the Cyber, Space Engineering, and Contracts departments to ensure our products meet the applicable ...
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 ...
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 ...
Plano, TX · On-site
$134K - $145K/yr
... device product lifecycle, including premarket and postmarket initiatives. This high-impact role ... Drive risk management, data quality, and continuous process improvement Requirements: * Bachelor ...
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Plano, TX · On-site
$134K - $145K/yr
... device product lifecycle, including premarket and postmarket initiatives. This high-impact role ... Drive risk management, data quality, and continuous process improvement Requirements: * Bachelor ...
Embedded Systems Testing, Mobile Testing, Defect Management, Risk Management, Continuous ... Coordinate daily with Client project teams, product owners, QA teams, and offshore resources to ...
Embedded Systems Testing, Mobile Testing, Defect Management, Risk Management, Continuous ... Coordinate daily with Client project teams, product owners, QA teams, and offshore resources to ...
... products, and Pre-Submissions, as applicable. The candidate will apply expertise in mechanical ... Risk Management * ANSI/AAMI/ISO 14971 - Medical Devices - Application of Risk Management to Medical ...
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... products, and Pre-Submissions, as applicable. The candidate will apply expertise in mechanical ... Risk Management * ANSI/AAMI/ISO 14971 - Medical Devices - Application of Risk Management to Medical ...
Beverly, MA · On-site
$120K - $140K/yr
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 ...
Beverly, MA · On-site
$120K - $140K/yr
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 ...
Dallas, TX · On-site
$88K - $119K/yr
Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... product knowledge by completing required training courses, working with your managers, and ...
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Dallas, TX · On-site
$88K - $119K/yr
Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... product knowledge by completing required training courses, working with your managers, and ...
... product risk management, usability engineering and medical device software. Detailed understanding and working knowledge of US and International regulations including 21 CFR part 820, is required, as ...
... product risk management, usability engineering and medical device software. Detailed understanding and working knowledge of US and International regulations including 21 CFR part 820, is required, as ...
Alameda, CA · On-site
$130K - $261K/yr
... medical device development activities, including design controls, system requirements, risk ... Product Management DIVISION: ADC Diabetes Care LOCATION: United States > Alameda : 2601 Harbor Bay ...
Alameda, CA · On-site
$130K - $261K/yr
... medical device development activities, including design controls, system requirements, risk ... Product Management DIVISION: ADC Diabetes Care LOCATION: United States > Alameda : 2601 Harbor Bay ...
Beverly, MA · On-site
$120K - $140K/yr
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 ...
Beverly, MA · On-site
$120K - $140K/yr
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 ...
$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 ...
$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 ...
San Francisco, CA · On-site
$150 - $200/hr
Support risk management, usability engineering, and validation activities. * Participate in design ... Familiarity with FDA, ISO 13485, MDR, and medical device product development processes.
San Francisco, CA · On-site
$150 - $200/hr
Support risk management, usability engineering, and validation activities. * Participate in design ... Familiarity with FDA, ISO 13485, MDR, and medical device product development processes.
Indianapolis, IN · On-site
... medical device product development. • Experience with Design History File (DHF) development, review, and remediation. • Hands-on experience with Risk Management activities including: o dFMEA o ...
Indianapolis, IN · On-site
... medical device product development. • Experience with Design History File (DHF) development, review, and remediation. • Hands-on experience with Risk Management activities including: o dFMEA o ...
Newark, DE · On-site
$70K - $90K/yr
... scale production documentation and remediation initiative at our client's Newark, Delaware ... These professionals will play a critical role in strengthening risk management practices ...
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Newark, DE · On-site
$70K - $90K/yr
... scale production documentation and remediation initiative at our client's Newark, Delaware ... These professionals will play a critical role in strengthening risk management practices ...
Arlington, VA · On-site
$127K - $172K/yr
Position Overview SET Development is seeking a Cyber Security Product Risk Manager to support the security and resilience of space-based systems, including spacecraft and associated hardware. This ...
Arlington, VA · On-site
$127K - $172K/yr
Position Overview SET Development is seeking a Cyber Security Product Risk Manager to support the security and resilience of space-based systems, including spacecraft and associated hardware. This ...
Irvine, CA · On-site
$130K - $172K/yr
This role bridges software engineering, cybersecurity, and medical device product integration for a ... MDCG ). • Manage integration of third-party libraries and drivers while maintaining software ...
Irvine, CA · On-site
$130K - $172K/yr
This role bridges software engineering, cybersecurity, and medical device product integration for a ... MDCG ). • Manage integration of third-party libraries and drivers while maintaining software ...
Mentor, OH · On-site
$137K/yr
... Product Management /Marketing Preferred * MBA preferred * Experience with chemistry products and/ or consumables is helpful * Medical device product marketing experience preferred * Experience ...
Mentor, OH · On-site
$137K/yr
... Product Management /Marketing Preferred * MBA preferred * Experience with chemistry products and/ or consumables is helpful * Medical device product marketing experience preferred * Experience ...
San Jose, CA · On-site
$151K - $195K/yr
... production monitoring. You do not need to be an ML engineer. * Working knowledge of regulated medical-device development practices, including design controls, risk management, verification and ...
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San Jose, CA · On-site
$151K - $195K/yr
... production monitoring. You do not need to be an ML engineer. * Working knowledge of regulated medical-device development practices, including design controls, risk management, verification and ...
$51.5K - $64.7K
0% of jobs
$64.7K - $78K
1% of jobs
$78K - $91.2K
3% of jobs
$91.2K - $104.4K
4% of jobs
$104.4K - $117.6K
5% of jobs
$117.6K - $130.9K
5% of jobs
$136.5K is the 25th percentile. Wages below this are outliers.
$130.9K - $144.1K
14% of jobs
$144.1K - $157.3K
5% of jobs
The median wage is $165.9K / yr.
$157.3K - $170.5K
18% of jobs
$180.6K is the 75th percentile. Wages above this are outliers.
$170.5K - $183.8K
24% of jobs
$183.8K - $197K
19% of jobs
$51.5K
$159.4K
$197K
For Medical Device Product Risk Manager jobs, the most frequently searched job titles are:

Portage, MI • On-site
Other
Posted 6 days ago
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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Recruiting and staffing services
501 - 1,000 Employees
Beverly, MA, US
1984