×
Register Here to Apply for Jobs or Post Jobs. X

Senior Staff Engineer, Design Quality

Job in Irvine, Orange County, California, 92713, USA
Listing for: Stryker Group
Full Time position
Listed on 2025-12-22
Job specializations:
  • Engineering
    Quality Engineering, Product Engineer, Biomedical Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 115600 - 190400 USD Yearly USD 115600.00 190400.00 YEAR
Job Description & How to Apply Below

Stryker - Inari Medical is hiring a Sr. Staff Engineer, Design Quality in Irvine
, California
! In this role, you will partner with Engineering and Advanced Operations to define design requirements and develop manufacturing processes that support new product development projects. You will also lead risk management activities to ensure the highest level of product and process quality!

What You Will Do:
  • Develop quality documentation to support new product development and regulatory submissions.
  • Maintain and improve quality systems by identifying and correcting procedural deficiencies.
  • Lead risk management activities and present final risk/benefit justifications to leadership.
  • Help create, maintain, and manage risk files throughout the product lifecycle.
  • Drive product and process design activities in cross‑functional teams.
  • Define and validate design verification and validation (V&V) test requirements and methods.
  • Present product risks during design reviews and ensure mitigation through development.
  • Support manufacturing process development and product design transfer to internal/external sites.
  • Apply statistical analysis and problem‑solving techniques to define acceptance criteria and resolve quality issues.
  • Review and approve inspection plans, routers, and product drawings.
  • Evaluate predicate devices and define critical quality attributes through risk analysis.
  • Contribute to final V&V reports with statistically valid conclusions and graphical summaries.
  • Support early market feedback collection and resolution of initial product concerns.
What You Need:

Required:
  • Bachelor’s degree in science, engineering or related discipline.
  • 6+ years’ related experience required.
  • Medical device industry experience required.
  • Familiarity with New Product Development (NPD) processes and/or involvement in cross‑functional activities supporting product development and commercialization.
Preferred:
  • MS, CQE, or CRE preferred.
  • Six Sigma Green or Black belts are preferred.
  • Experience with the medical device development lifecycle, including risk management and design/process verification and validation.
  • Proficient in quality tools such as FMEA, GD&T, root cause analysis, and Poka‑Yoke, as well as core quality concepts.
  • Proficient in data analysis tools (e.g., Minitab) and interpreting CAD drawings to support design and process evaluations.
  • Proven project management and cross‑functional collaboration skills.
  • Excellent communication, problem‑solving, and analytical abilities.

115, salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary