Stryker is hiring a Staff Design Quality Engineer (Software/Electrical) in Portage, Michigan to support our Medical business. In this role, you will provide on-site quality support for new product development and partner with cross-functional teams, including R&D, Operations, Product Security, Testing, and Regulatory, throughout the development process. You will develop electrical and software development plans, support execution of those plans, and provide post-market quality support through the change control process. You may also support quality improvement projects.
What you will do:
- Partner closely with R&D to ensure product designs meet quality requirements for safety and effectiveness. Support the collection of market feedback to inform design requirements and validate the design with customers as it matures through the production launch.
- Work closely with Product Security and R&D teams to accomplish product security activities and ensure the design is in line with the cybersecurity required practices.
- Lead risk management activities for new product development teams by developing risk management plans and reports, conducting risk reviews, and verifying the implementation and effectiveness of risk controls.
- Partner with Operations and suppliers to ensure supplier processes and Stryker manufacturing processes implement robust process controls.
- Participate in design reviews and track how the design, documentation, and manufacturing process mitigate risks throughout the development process.
- Lead design validation activities including human factors usability engineering.
- Support product design and quality transfers to internal and/or external manufacturing facilities.
- Analyze and define critical quality attributes for products and processes through risk analysis techniques.
- Contribute to the completion of final design verification and validation reports.
- Support PPAP planning, communicate PPAP requirements to component suppliers, and support PPAP approval.
What you will need
- Bachelor’s Degree in Software Engineering, Electrical Engineering, or Computer Science Engineering (or other engineering degree with relevant electrical or software experience).
- 4+ years’ experience in quality, manufacturing, new product development, software or engineering.
Preferred
- Experience within medical device/manufacturing industry.
- Familiarity with ISO 13485 (medical device standard) and ISO 14971 (risk management standard), IEC-62304 (software development life cycle)
- Data analysis (statistical analysis, sampling plans, statistical process control, Minitab) experience.
- Demonstrated applied knowledge of Advanced Quality tools such as Failure Modes Effect Analysis (FMEA), GD&T, Root Cause Analysis, and Mistake Proofing/Poke Yoke.
Demonstrated ability to read and interpret CAD drawings. - Six Sigma Certification.
- ASQ CSQE certification.
United States of America Pay Ranges:
- USN: $89,300 - $148,800 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
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 Software Engineering, Electrical Engineering, Computer Science Engineering, or another engineering discipline with relevant electrical or software experience
- At least 4 years of experience in quality, manufacturing, new product development, software, or engineering
- Experience in the medical device or manufacturing industry
- Familiarity with ISO 13485 and ISO 14971
- Familiarity with IEC 62304 software development lifecycle requirements
- Experience with data analysis, statistical analysis, sampling plans, statistical process control, or Minitab
- Applied knowledge of FMEA, GD&T, root cause analysis, and mistake proofing or Poka Yoke
- Ability to read and interpret CAD drawings
- Six Sigma certification
- ASQ CSQE certification
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.
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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.
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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.
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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
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.







