Staff Product Safety Engineer

Posted 16 Days Ago
Be an Early Applicant
Portage, MI, USA
In-Office
89K-149K Annually
Mid level
Healthtech
The Role
The Staff Product Safety Engineer leads safety initiatives for medical devices, ensuring compliance with regulatory standards and collaborating with R&D teams on safety programs.
Summary Generated by Built In
Work Flexibility: Hybrid

What You Will Do:

As Staff Product Safety Engineer, you will lead safety initiatives for new and existing products for our Ortho Tech Orthopaedic Instruments (OI) business. Collaborating with cross-functional leadership, you'll drive the strategic vision of the Product Safety organization, ensuring consistent safety practices throughout the product lifecycle. This role is responsible for product safety and compliance, providing guidance and solutions to meet safety and regulatory standards for successful medical device design.

Check out our portfolio: Orthopaedic Instruments

  • Support product safety activities for New Product Development and Product Engineering teams to ensure compliance of our products to the global safety requirements.
  • Work with R&D teams to define and implement a product safety program plans for large, complex development programs.
  • Participate in product safety activities to represent and advance the interests of the product safety community across the division, including both technical and organizational initiatives.
  • Support initiatives for product development teams with the technical understanding of 60601 and other required safety standards during the design & development of medical devices.
  • Positively influence the R&D project teams to ensure compliance to the product safety standards.
  • Collaborate with the team on design analysis to support the development of products within the boundaries of safety standards.
  • Partner with R&D on identification of problems and solutions, analysis, and implementation of design elements relevant for product safety.
  • Conduct, coordinate and evaluate results of safety testing, including EMI/EMC and Wireless.
  • Serve as an interface between development teams and NRTLs (e.g. CSA, UL, ETL, TUV) or other regulatory agencies.

What You Will Need:

Required Qualifications:

  • Bachelor's degree in Electrical Engineering, Biomedical Engineering, or related discipline
  • 4+ years of work experience
  • 2+ years of work experience in the field of product safety

Preferred Qualifications:

  • Working knowledge of regulations and standards related to Medical (60601) products
  • Medical devices safety testing experience
  • Demonstrated expertise in electrical testing equipment and processes
  • Experience driving global wireless regulatory approvals/registrations (e.g., FCC/ISED/CE RED), including test planning, documentation, and coordination with external labs/certification bodies
  • Participation in an active Certified Test Facility (CTF) program with CSA, UL, or ETL

  


  • $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, Biomedical Engineering, or related discipline
  • 4+ years of work experience
  • 2+ years in product safety
  • Working knowledge of regulations and standards related to Medical (60601) products
  • Medical devices safety testing experience
  • Expertise in electrical testing equipment and processes
  • Experience driving global wireless regulatory approvals
  • Participation in an active Certified Test Facility (CTF) program

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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