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Senior Engineer, Quality Process

Stryker

Phoenix, AZJob$78–130K/yrSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$78–130K/yr
Location
Phoenix, AZ
Work Authorization
Not specified

Olive focuses on jobs in the United States, including remote roles you can work from there.

Requirements

Credentials this posting asks for.

Bachelor's degree, required

Job overview

Stryker is hiring a Senior Quality Engineer in Phoenix to support Sustainability Solutions. The role focuses on resolving production and quality issues, monitoring process performance, and improving manufacturing, inspection, and quality-system processes. It also supports audits, product complaints and field actions, validation, risk management, and supplier quality, while promoting continuous improvement and quality practices.

Skills & qualifications

RequiredNice to have

Skills

Medical Device Manufacturing, nice to haveISO 13485, nice to haveGMP, nice to haveLean Six Sigma, nice to haveCommunication, nice to haveAttention to Detail, nice to haveRisk Management, nice to haveCAPA, nice to haveAudits, nice to haveStatistics, nice to haveStatistical Sampling, nice to haveProcess Capability, nice to haveGauge R&R, nice to haveMicrosoft Word, nice to haveMicrosoft Excel, nice to haveMicrosoft PowerPoint, nice to haveRegulatory Agency Interaction, nice to haveQuality Concepts, nice to haveCross-Functional Collaboration, nice to haveTask Management, nice to haveTeamwork, nice to have

Qualifications

Bachelor's in Engineering or Related, required2+ Years Quality Engineer Experience, requiredManufacturing Environment Experience, required

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Stryker is hiring a Senior Quality Engineer in Phoenix, Arizona , to support Sustainability Solutions ! In this role, you will be responsible for analyzing and resolving production issues through collaboration with engineering and material procurement teams. Furthermore, you will perform monitoring of process data and analysis of trends, financial results, and customer feedback. You will exhibit a commitment to quality first culture, compliance, and continuous improvement through the implementation of projects which optimize production, inspection, and quality system processes.

What you will do

  • Work closely with operations and the business functions to ensure quality performance of product and processes

  • Collaborate cross-functionally with internal and external teams to resolve quality issues

  • Manages internal and supplier-driven Non-Conformances (NCs), ensuring timely investigation and closure

  • Owns Corrective and Preventive Actions (CAPAs) through root cause analysis to closure

  • Disposition of non-conforming product through MRB, issuing NCs as appropriate

  • Initiates and leads in the development and improvement of the manufacturing processes for existing and new products.

  • Review and approval of change management activities, challenges change effectiveness and drives strong review.

  • Interpret KPI trends, act as necessary, driving a continuous improvement process.

  • Support the execution and analysis of manufacturing complaints and product field actions

  • Provide QA support during internal and external audits

  • Advocate of Human Factor practices, proficient in the science of Human Factor identification and mitigation.

  • Proficient in risk management practices and concepts and applies knowledge to manufacturing operations and identify opportunities and weaknesses

  • Lead and participate in the Lean philosophy – standardization and elimination of waste

  • Understanding of Human Error Prevention and the application of those principles to the manufacturing environment.

  • Support process/equipment validation, qualification, and Measurement System Analysis (MSA)

  • Support with product holds and executing containment plans

  • Manage supplier relationships, including but not limited to, coordinating communications, monitoring performance, managing in house and external nonconformities and ensuring timely delivery of quality materials and services.

What you need

  • B.S. in engineering, or related discipline

  • 2+ years as a Quality Engineer in a manufacturing environment.

Preferred

  • Proficient in understanding of Med Device manufacturing processes, ISO 13485, GMP.

  • Lean Six Sigma training is a distinct advantage.

  • Excellent communication skills and attention to detail.

  • Proficient understanding of engineering and quality principles, including Risk Management, CAPA, Audits, and Statistics

  • High level knowledge/experience of Risk Based and statistical techniques, in particular process risk, statistical sampling plans, Process Capability, Gauge R&Rs.

  • High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.

  • Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.) desired.

  • Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics).

  • Confident representing Quality in cross-functional settings

  • Self-starter able to manage multiple tasks in a fast-paced environment

  • Willing to work as part of a multi-site team; some travel required

United States of America Pay Ranges:

  • Puerto Rico : $69,500 - $110,900 USD Annual

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

  • US5 : $81,600 - $136,000 USD Annual

  • US10 : $85,500 - $142,500 USD Annual

  • US15 : $89,400 - $148,900 USD Annual

  • US20 : $93,200 - $155,400 USD Annual

  • US30 : $101,000 - $168,400 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.

How this job compares

Set against the 1,078 open Quality Engineering jobs on Olive Jobs, counted November 15, 2026.

Pay
  • This posting$78–130K/yr
  • US median$116–184K/yr675 salary ranges

This range's midpoint, $104K, is 31% below the US median midpoint ($150K) — in the lowest quarter of Quality Engineering salary ranges across the US.

Openings
Olive Jobs lists 15 open Quality Engineering jobs in Arizona and 1,078 across the US. 8% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 2 years of experience — less than three in four Quality Engineering postings that state a minimum ask for (median 7 years, across 819 postings).
Education
This posting asks for a bachelor's degree; 408 of the 1,078 open Quality Engineering jobs (38%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 15, 2026. Figures based on too few postings are left out.

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