Stryker
Staff Quality Engineer
Kalamazoo, Michigan
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.5M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Lead / management
- Stated salary
- $89,300 – $148,800 per year
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 24 Sept 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
Work Flexibility: Onsite
Stryker is seeking a Staff Quality Engineer to support product and process quality across manufacturing operations for Instruments in Portage, Michigan . In this role, you will partner with operations, engineering, suppliers, and quality teams to drive compliance, resolve quality issues, support new product introductions and manufacturing scale up activities, lead continuous improvement initiatives, and ensure products meet applicable regulatory and quality requirements.
What You Will Do
Partner with manufacturing, engineering, and quality teams to monitor and improve product and process quality performance.
Support the transfer, launch, and scale-up of new products and manufacturing processes, partnering cross-functionally to establish robust quality systems and ensure successful production readiness.
- Lead investigations and timely closure of non-conformances and corrective and preventive actions, including root cause analysis and implementation of corrective actions.
- Review and disposition nonconforming materials and products through Material Review Board processes.
- Collaborate with suppliers to address quality issues, manage supplier corrective actions, and support supplier quality improvement initiatives.
- Evaluate and support manufacturing, supplier, and engineering changes to ensure compliance with quality and regulatory requirements.
- Monitor quality performance indicators, analyze trends, and implement actions to address identified risks and improvement opportunities.
Lead or support continuous improvement initiatives focused on quality enhancement, scrap reduction, efficiency gains, and cost savings.
- Support process validation, equipment qualification, inspection methods, measurement system analysis, and statistical process controls.
- Participate in internal and external audits, complaint investigations, field actions, and continuous improvement projects across manufacturing operations.
What You Will Need
Required Qualifications
- Bachelor's degree in Engineering, Science, or a related technical discipline.
- Minimum 4 years of quality engineering, manufacturing engineering, or related engineering experience.
- Experience supporting non-conformance investigations, corrective and preventive actions, or quality management systems.
Preferred Qualifications
Experience in the medical device industry.
Experience analyzing quality data and applying statistical methods to support manufacturing or process improvements.
- Six Sigma Green Belt or Six Sigma Black Belt certification.
- Experience with geometric dimensioning and tolerancing (GD&T).
- Experience using metrology equipment such as calipers, micrometers, pin gauges, or coordinate measuring machines (CMMs).
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: 20%
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.
Similar jobs
- Quality Engineer – APQP Program LeadSacoma Specialty Products, LLC · Edinburgh, INFirst seen today
- Lead Software Quality EngineerVizient · Irving, TX 75062 Vizient Corporate HQFirst seen today
- Principal/Senior Principal, Quality Engineer ValidationRoche · HillsboroFirst seen today
- Quality Engineer/Principal Quality Engineer 2/3Ngc · United States-Maryland-SykesvilleFirst seen today
- Principal Software Quality EngineerNgc · United States-Florida-MelbourneFirst seen today
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job