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Staff Quality Assurance Engineer

Stryker

Irvine, CAJob$103–171K/yrSeen 4 days agoSeen in employer's feed 4 days ago

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At a glance

Compensation
$103–171K/yr
Location
Irvine, CA
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker is hiring a Staff Quality Engineer for its Peripheral Vascular division in Irvine, California. The role provides quality engineering support across manufacturing operations, products, and processes, partnering with cross-functional teams and suppliers to resolve quality issues and improve performance. It supports compliance with regulatory requirements, industry standards, and quality system expectations.

Skills & qualifications

RequiredNice to have

Skills

Quality System PrinciplesRisk ManagementCAPAAuditingStatistical MethodologiesCompliance Risk AssessmentsMicrosoft OfficeSupplier Quality ManagementSupplier QualificationSupplier Performance MonitoringMedical Device RegulationsISO 1348521 CFR Part 820Good Documentation PracticesGood Manufacturing PracticesRegulatory InspectionsRegulatory Agency InteractionCQECRESix Sigma Green BeltSix Sigma Black Belt

Qualifications

Bachelor's in Science, Engineering or Related4+ Years Quality Engineering Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Stryker is hiring a Staff Quality Engineer for our Peripheral Vascular division in Irvine, CA to provide Quality Engineering support for quality assurance, quality control, and continuous improvement activities across manufacturing operations, products, and processes. Partner closely with cross-functional teams and suppliers to resolve quality issues, drive corrective and preventive actions, and enhance overall quality performance. Lead and support initiatives that improve product quality, operational efficiency, and customer satisfaction while ensuring compliance with applicable regulatory requirements, industry standards, and quality system expectations.

What you will do

  • Partner with Operations, suppliers, and cross-functional teams to drive product and process quality performance, resolve quality issues, and support continuous improvement initiatives.

  • Own and support nonconformances (NCs), CAPAs, MRB activities, and product disposition, ensuring timely investigation, root cause analysis, corrective actions, and closure within quality systems.

  • Collaborate with suppliers to address quality concerns, manage supplier corrective actions, evaluate supplier changes, perform PPAP activities, and support supplier part certification programs.

  • Monitor, analyze, and report quality and process performance metrics, applying statistical methods, process controls, and risk management principles to identify trends and drive improvements.

  • Support manufacturing-related complaints, field actions, commercial holds, and containment activities to ensure product quality and regulatory compliance.

  • Develop, review, and improve quality system documentation, procedures, inspection methods, sampling plans, and Human Factors practices that enhance product and process effectiveness.

  • Support process, equipment, and supplier validations/qualifications, measurement system analysis (MSA), engineering changes, supplier-initiated changes, and manufacturing transfer activities.

  • Participate in internal and external audits and provide quality subject matter expertise to ensure compliance with applicable quality system and regulatory requirements.

What you need:

Required

  • Bachelors degree in a science, engineering or related discipline

  • Minimum of 4 years of quality engineering experience with demonstrated knowledge of quality system principles, including risk management, CAPA, auditing, and statistical methodologies.

  • Experience applying risk management principles and conducting compliance risk assessments within a regulated environment.

  • Demonstrated proficiency using Microsoft Office tools to analyze data, create reports, and support cross-functional business activities.

Preferred

  • Experience managing supplier quality activities, including supplier qualification, performance monitoring, and quality issue resolution.

  • CQE, or CRE and Six Sigma Green or Black belt preferred Or related

  • Experience in the medical device industry with knowledge of U.S. and international medical device regulations, including familiarity with ISO 13485, 21 CFR Part 820, Good Documentation Practices (GDP), and Good Manufacturing Practices (GMP).

  • Experience with regulatory inspections and audits, including direct interaction with regulatory agencies such as FDA, TUV, MoH, etc.

$102,700 - $171,100 USD Annual

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 1,055 open Quality Engineering jobs on Olive Jobs, counted November 3, 2026.

Pay
  • This posting$103–171K/yr
  • California median$126–194K/yr113 salary ranges
  • US median$116–181K/yr591 salary ranges

This range's midpoint, $137K, is 16% below the California median midpoint ($163K) — in the middle half of Quality Engineering salary ranges in California.

Openings
Olive Jobs lists 181 open Quality Engineering jobs in California and 1,055 across the US. 7% of them nationwide are listed as remote or flexible.
Hiring the most in California
Experience
This posting asks for at least 4 years of experience; Quality Engineering postings that state a minimum ask for 6 years at the median (766 postings).
Education
This posting asks for a bachelor's degree; 451 of the 1,055 open Quality Engineering jobs (43%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 3, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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