Senior Product Safety Engineer, Electrical

Posted 4 Days Ago
Be an Early Applicant
Enterprise, FL, USA
In-Office
89K-149K Annually
Senior level
Healthtech
The Role
Develops and evaluates electrical and system-level product safety for robotic-assisted surgical devices. Responsibilities include hazard analysis, FMEAs, risk mitigation, IEC 60601 and ISO 14971 compliance, electrical safety and EMC testing, laboratory coordination, troubleshooting, root cause analysis, corrective actions, documentation, and regulatory support. Collaborates with electrical, systems, mechanical, and software engineering teams throughout product development.
Summary Generated by Built In
Work Flexibility: Onsite

It's Time to Join Stryker!

Join Stryker's Mako Robotics team as a Senior Product Safety Engineer, helping ensure the safety, reliability, and regulatory compliance of advanced robotic-assisted surgical technologies.


In this hands-on engineering role, you will partner closely with electrical, systems, and cross-functional engineering teams to identify and mitigate product safety risks throughout development. You will support electrical safety and electromagnetic compatibility (EMC) testing, troubleshoot technical challenges, and help ensure products meet applicable industry standards.


This opportunity is ideal for an engineer with a strong electrical foundation who enjoys practical problem-solving, laboratory testing, and collaborating with design teams to develop safe, high-quality medical devices.


What You Will Do
  • Product Safety & Risk Management: Identify, evaluate, and document electrical and system-level safety hazards. Develop and maintain risk management documentation, including hazard analyses, FMEAs, and safety assessments, while recommending practical risk mitigation strategies.
  • Electrical Safety & EMC: Apply electrical safety and electromagnetic compatibility principles to evaluate product designs, identify potential compliance concerns, and support troubleshooting and design improvements.
  • Standards & Compliance: Interpret and apply relevant medical device safety standards, with particular emphasis on IEC 60601 and its relationship to ISO 14971 and applicable regulatory requirements.
  • Testing & Laboratory Coordination: Plan, coordinate, and support electrical safety and EMC testing with internal teams and external laboratories, including UL, CSA, TÜV, and other recognized testing organizations. Prepare test documentation, coordinate samples, evaluate results, and help resolve identified issues.
  • Design Collaboration: Work closely with electrical, systems, mechanical, and software engineers to integrate safety requirements into product development, identify potential issues early, and support iterative design testing.
  • Technical Troubleshooting: Investigate safety-related test failures and nonconformances, perform root cause analysis, and collaborate with engineering teams to develop and verify effective corrective actions.
  • Documentation & Regulatory Support: Maintain accurate safety documentation, test evidence, and requirements traceability. Provide technical input supporting design reviews, verification activities, and regulatory submissions.
  • Continuous Improvement: Contribute to improvements in product safety processes, testing practices, and engineering documentation while sharing technical knowledge and best practices across project teams.

What You Need
  • Bachelor's degree in Electrical Engineering or a related engineering discipline is required.
  • Minimum of 2 years of relevant engineering experience in electrical engineering, product development, hardware testing, product safety, or a closely related technical field is required.

Preferred Qualifications (You do not need all of these)
  • Demonstrated understanding of electrical engineering fundamentals, including electrical circuits, system behavior, and troubleshooting methodologies.
  • Working knowledge of electromagnetic compatibility (EMC/EMI) principles and their application to electrical systems, testing, or design troubleshooting.
  • Ability to interpret technical standards, analyze test results, investigate technical issues, and recommend practical engineering solutions.
  • Strong analytical, problem-solving, documentation, and communication skills, with the ability to collaborate effectively across engineering disciplines.
  • Experience supporting medical device development or engineering in another regulated industry.
  • Familiarity with IEC 60601, ISO 14971, FDA requirements, and medical device risk management practices, including hazard analysis, FMEA, or fault tree analysis.
  • Hands-on experience with EMC or electrical safety testing, including test setup, troubleshooting, data interpretation, or coordination with external testing laboratories.
  • Understanding of EMC design considerations, including conducted and radiated interference, shielding, grounding, coupling mechanisms, PCB and cable parasitics, and current return paths.
  • Familiarity with medical electrical safety concepts such as essential performance, insulation diagrams, means of operator protection (MOOP), means of patient protection (MOPP), and programmable electrical medical systems.
  • Experience collaborating with electrical, mechanical, software, and systems engineering teams to resolve product safety or compliance challenges.
  • Familiarity with engineering tools such as Altium, Jama, Jira, or equivalent design and documentation systems.

Additional Information

This position is based in Weston, Florida, and may require occasional travel to other Stryker locations and external testing laboratories to support product safety and compliance activities.

  


  • $89,300 - $148,800 USD Annual

  


Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills Required

  • Bachelor's degree in Electrical Engineering or a related engineering discipline
  • At least 2 years of relevant engineering experience in electrical engineering, product development, hardware testing, product safety, or a closely related technical field
  • Understanding of electrical engineering fundamentals, including circuits, system behavior, and troubleshooting
  • Working knowledge of electromagnetic compatibility and interference principles
  • Ability to interpret technical standards, analyze test results, investigate technical issues, and recommend engineering solutions
  • Strong analytical, problem-solving, documentation, and communication skills
  • Experience supporting medical device development or engineering in another regulated industry
  • Familiarity with IEC 60601, ISO 14971, FDA requirements, and medical device risk management practices
  • Hands-on experience with EMC or electrical safety testing
  • Understanding of EMC design considerations, including shielding, grounding, coupling, PCB and cable parasitics, and current return paths
  • Familiarity with medical electrical safety concepts, including essential performance, MOOP, MOPP, and programmable electrical medical systems
  • Experience collaborating with electrical, mechanical, software, and systems engineering teams
  • Familiarity with Altium, Jama, Jira, or equivalent engineering tools

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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