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Senior Quality Engineer

Stryker

Kalamazoo, MIJob$78–130K/yrSeen 2w agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$78–130K/yr
Location
Kalamazoo, MI
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Senior Quality Engineer at Stryker develops and implements quality methods for process control, inspection, testing and defect prevention, investigates nonconformances, leads root cause analysis, and supports supplier quality improvement within regulated medical device manufacturing.

Skills & qualifications

RequiredNice to have

Skills

Statistical MethodsRisk ManagementProcess ControlInspectionTestingDefect PreventionRoot Cause AnalysisCorrective Action ManagementSupplier Quality ImprovementMaterial Review ProcessAudit Support

Qualifications

Bachelor’s Degree in Engineering, Science, or a Related Technical FieldMinimum 2 Years of Quality Engineering or Related Quality Experience Within a Regulated IndustryExperience Working With U.S. And International Medical Device Regulatory RequirementsExperience Managing Nonconformance Investigations and Corrective Action Activities in a Regulated Quality SystemExperience Supporting Supplier Quality Activities or Manufacturing Process ImprovementsExperience Applying Risk Management and Statistical Process Control Methods in Manufacturing Environments

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

At Stryker, our quality engineers play a critical role in ensuring products consistently meet defined quality and regulatory requirements.

We are hiring a Senior Quality Engineer in Kalamazoo, MI supporting Instruments! In this role, you will develop and implement methods and procedures for process control, process improvement, testing, and inspection to ensure products function as designed and meet established quality standards. You will work closely with operations, engineering, and suppliers, with direct impact across product quality, supplier performance, and manufacturing process control throughout the product lifecycle.

What You Will Do

  • Develop, implement, and maintain quality methods for process control, inspection, testing, and defect prevention within manufacturing operations

  • Investigate internal and supplier-related nonconformances, lead root cause analysis, and manage timely corrective and preventive actions in alignment with quality system requirements

  • Review, disposition, and document nonconforming product through formal material review processes, including containment and escalation when required

  • Analyze quality data and key performance indicators, identify trends, and initiate actions to address emerging product or process risks

  • Evaluate manufacturing and supplier changes, including process updates and component changes, to assess quality and risk impacts prior to implementation

  • Support supplier quality improvement activities, including corrective action management, part certification initiatives, and ongoing performance monitoring

  • Apply statistical methods and risk management practices to support process capability, inspection strategies, and sampling plans

  • Support internal and external audits, manufacturing transfers, engineering changes, and field-related quality investigations as a subject matter resource

  • Collaborate closely with manufacturing and engineering teams to identify, investigate, and resolve quality issues impacting production

What You Will Need

Required Qualifications

  • Bachelor’s degree in Engineering, Science, or a related technical field

  • Minimum 2 years of quality engineering or related quality experience within a regulated industry

Preferred Qualifications

  • Experience working with U.S. and international medical device regulatory requirements

  • Experience managing nonconformance investigations and corrective action activities in a regulated quality system

  • Experience supporting supplier quality activities or manufacturing process improvements

  • Experience applying risk management and statistical process control methods in manufacturing environments

United States of America Pay Ranges:

USN : $77,700 - $129,500 USD Annual

View the U.S. work location and transparency guide (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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.

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