---
title: Staff Quality Engineer New Product Introduction
description: Stryker is hiring for the Staff Quality Engineer New Product Introduction role
  in Irvine, CA. See the full description and apply.
type: job
url: https://www.foundrole.com/jobs/staff-quality-engineer-new-product-introduction-at-stryker-01a14425-b5d7-7fdb-9b4d-34f09538ac5b
date: 2026-11-15T01:26:44Z
og_description: Join Stryker as Staff Quality Engineer New Product Introduction in Irvine, CA.
  Pays $102.7K–$171.1K per year. Full-time, on-site role.
og_image: https://www.foundrole.com/og/p0awcm.png
breadcrumbs:
  - label: Home
    url: https://www.foundrole.com/
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    url: https://www.foundrole.com/jobs
---

| | |
|---|---|
| **Company** | [Stryker](https://www.foundrole.com/companies/stryker?utm_source=ai_markdown) |
| **Location** | Irvine, CA |
| **Salary** | $102.7K/yr - $171.1K/yr |
| **Type** | Full Time |
| **Posted** | Oct 14, 2026 |

## Is this job real?

**Ghost job check:** B · Low risk. Probably a real opening.

## Visa sponsorship

- **H-1B:** Stryker sponsors H-1B visas. It filed 77 H-1B petitions (FY2026 Q1 – FY2026 Q4).
- **E-Verify:** No E-Verify enrollment on record for Stryker.

## Pay for similar jobs

Most similar jobs pay $132,000 – $190,000 a year (median $162,000).

## Description

Work Flexibility: Onsite

**Staff Quality Engineer, New Product Introduction**

*Irvine, CA*

Join Stryker’s Quality Engineering team supporting the development, transfer, and introduction of new medical devices, manufacturing processes, and technologies. In this role, you will provide technical quality leadership across design transfer, process validation, risk management, inspection strategy, supplier quality, and manufacturing readiness within a regulated environment.

**What you will do**

- Lead quality engineering activities for new product and process introductions, ensuring design transfer deliverables are completed, documented, and aligned with quality and regulatory requirements.
- Evaluate manufacturing and process risks using Process Failure Mode and Effects Analysis (PFMEA), identify mitigation and control strategies, and support risk management activities in accordance with ISO 14971.
- Develop inspection strategies, sampling plans, First Article Inspection approaches, and Measurement System Analysis (MSA) strategies that support repeatable, scalable, and efficient manufacturing.
- Develop and approve process validation strategies, protocols, reports, and data analyses to support capable, scalable manufacturing processes and high production yield.
- Apply statistical methods and structured problem-solving tools to process characterization, capability analysis, nonconformances, corrective and preventive actions, root-cause investigations, and process improvements.
- Support Design for Manufacturing and Assembly by influencing process design, production specifications, inspection optimization, tooling, fixtures, and human-error risk controls.
- Lead quality activities for supplier qualification, supplier validation, Production Part Approval Process (PPAP), supplier certification, and quality agreements.
- Represent Quality during design reviews and design transfer, tracking launch-quality measures including right-first-time performance, manufacturing loss, inspection cost, and product escapes.

**What you will need**

**Required**

- Bachelor of Science degree in Engineering or a related technical discipline.
- Minimum 4 years of experience in quality, engineering or technical discipline
- Experience in a regulated manufacturing environment.
- Experience with risk-based and statistical quality techniques, including FMEA, statistical sampling, process capability, and MSA.

**Preferred**

- Experience in new product or process introduction.
- Certified Quality Engineer (CQE) certification or equivalent quality engineering coursework or experience.
- Experience with medical device manufacturing and applicable quality requirements, including ISO 13485, Good Manufacturing Practices, and Good Documentation Practices.
- Lean Six Sigma training and experience applying structured problem-solving methods such as DMAIC.

- Experience with supplier qualification and supplier quality activities supporting new product introduction and manufacturing.  

$102,700 - $171,100 USD Annual

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.
## Skills

- Measurement System Analysis
- Influencing
- Medical Device Manufacturing
- Inspection
- Lean Project Management
- Investigation
- Sampling (Statistics)
- First Article Inspection
- Certified Quality Engineer
- Process Design
- Process Failure Mode and Effects Analysis (Pfmea)
- Problem Solving
- Sampling Plans
- Good Manufacturing Practices
- Design for Manufacturing (Dfm)
- Risk Management
- Quality Engineering
- Root Cause Analysis
- Supplier Quality Management
- Supplier Qualification
- Define Measure Analyze Improve And Control (Dmaic)
- ISO 13485
- BCSI Good Documentation Practices
- Lean Six Sigma
- Corrective And Preventive Action (Capa)
- Design Review
- New Product Introduction (Npi)
- Production Part Approval Process (Ppap)
- Data Analysis
- Process Characterization
- ISO 14971
- Quality Agreements
- Process Capability
- Regulatory Compliance

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