Quality Assurance Intern Jobs in Irvine, CA
Quality Assurance Intern jobs in Irvine are concentrated across medtech, software, and consumer electronics firms in the Irvine Spectrum, Irvine Business Complex, and Great Park neighborhoods, with employers like Stryker, Glidewell Laboratories, and NURA posting openings regularly. Demand is steady given Irvine's dense cluster of life sciences and tech companies. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 316+ Quality Assurance Intern jobs
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.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
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.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
See All 316+ Quality Assurance Intern Jobs in Irvine
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Find Quality Assurance Intern JobsQuality Assurance Intern Job Market in Irvine
Who's Hiring
- Stryker57
- Glidewell Laboratories57
- NURA29
- Circuit Assembly29
- MV Transportation29
Quality Assurance Intern Jobs in Irvine: Frequently Asked Questions
How do I get a quality assurance intern job in Irvine?
Focus your search on Irvine's medtech, semiconductor, and SaaS companies, which hire the most quality assurance interns locally. The Irvine Spectrum and Irvine Business Complex are where most postings originate. Candidates who can demonstrate hands-on lab work, familiarity with ISO or FDA quality standards, or coursework in engineering or life sciences stand out with Irvine employers. Applying directly through company career portals tends to move faster than broad job-board submissions in this market.
Which companies hire quality assurance interns in Irvine?
Irvine quality assurance intern roles are posted by Stryker, Glidewell Laboratories, and NURA and others right now, based on current listings on Migrate Mate as of November 2026. Irvine's employer mix skews toward medical device manufacturers, enterprise software firms, and consumer electronics companies, so most openings come from mid-size to large technology or regulated-industry employers rather than early-stage startups.
Are there remote quality assurance intern jobs in Irvine?
Yes, though availability depends heavily on the role. Analytical and documentation-focused quality assurance intern work can transfer well to remote settings, while lab-based or hardware testing positions almost always require on-site presence. About 50% of quality assurance intern openings tied to Irvine are remote or hybrid as of November 2026, with the remote share concentrated in software QA and compliance documentation roles rather than in Irvine's medical device or semiconductor segments.
How can I get a quality assurance intern job in Irvine with little or no experience?
The most realistic entry path in Irvine is applying to internship programs at the city's medtech and software companies, many of which are structured specifically for students with limited professional experience. UC Irvine and Irvine Valley College both have employer partnerships that funnel students into local QA intern roles. Highlighting coursework in quality systems, statistics, or engineering lab work helps, and applying for test associate or quality coordinator aide roles at smaller Irvine manufacturers can open the door to formal QA intern positions.
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See All 316+ Quality Assurance Intern Jobs in Irvine
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