---
title: Senior Quality Systems Specialist at Stryker
description: Stryker is hiring for the Senior Quality Systems Specialist role in Redmond, WA.
  Pays $83.4K–$139K per year. See the full description and apply.
type: job
url: https://www.foundrole.com/jobs/senior-quality-systems-specialist-at-stryker-01a16495-0582-73c6-98f4-a2b07f15fa9d
date: 2026-11-15T01:26:44Z
og_description: Join Stryker as Senior Quality Systems Specialist in Redmond, WA. Pays $83.4K–$139K
  per year. Full-time, hybrid role.
og_image: https://www.foundrole.com/og/q3177l.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** | Redmond, WA (Hybrid) |
| **Salary** | $83.4K/yr - $139K/yr |
| **Type** | Full Time |
| **Posted** | Oct 21, 2026 |

## Is this job real?

**Ghost job check:** A- · 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 $76,000 – $117,000 a year (median $97,000).

## Description

Work Flexibility: Hybrid

As a **Senior Quality Systems Specialist**, you will play a critical role in ensuring the effectiveness of Stryker's quality management system by driving compliance, leading problem-solving efforts, and partnering with cross-functional teams to resolve quality issues. This position offers the opportunity to influence quality excellence, continuous improvement, and regulatory compliance across the organization. This role is **Hybrid** in **Redmond, Washington.**

**What You Will Do**

- Own and oversee the Nonconformance (NC) and Corrective and Preventive Action (CAPA) processes to ensure compliance, effectiveness, and efficiency in addressing quality issues.
- Review and approve NCs and CAPAs for completeness, accuracy, effectiveness, and timeliness.
- Partner with cross-functional teams to facilitate investigations, root cause analysis, and corrective action implementation.
- Serve as the site subject matter expert and super user for the eCAPA system, ensuring records are maintained with appropriate supporting evidence..
- Coach and mentor teams on problem-solving methodologies, including 5 Whys, Fishbone Diagrams, Process Mapping, Human Error Reduction, and 4-D methodologies.
- Lead accountability meetings, CAPA review boards, and root cause analysis workshops to drive quality improvements.
- Monitor and report NC/CAPA key performance indicators (KPIs), providing updates for quality and business review forums.
- Develop, maintain, and deliver training programs related to CAPA processes and quality systems.
- Identify and implement continuous improvement initiatives to optimize quality systems and business processes.
- Participate in cross-site and corporate quality system improvement projects.
- Support internal, corporate, customer, and third-party audits, including preparation, participation, and follow-up activities.

**What You Need**

- Bachelor’s degree in Science, Engineering, or a related discipline.
- Minimum 3+ years of experience in a manufacturing environment or equivalent.
- Strong communication, project management, and influencing skills.
- Demonstrated ability to manage multiple priorities in a fast-paced, matrixed environment.
- Strong analytical, critical thinking, and problem-solving capabilities.
- Ability to work independently and drive issues to resolution.
- Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.

**Preferred**

- 2+ years of experience in CAPA, Quality Systems, Quality Engineering, or a related field.
- Experience interacting with regulatory agencies such as FDA, TUV, and other international regulatory bodies.
- Knowledge of U.S., European, and international medical device regulations and standards.
- Strong understanding of quality system processes, including audits, management review, and quality planning.
- Experience working in compliance-risk environments.
- Demonstrated success leading projects and driving results across cross-functional teams.
- Excellent written, verbal, and negotiation skills.
- Ability to facilitate teams through complex investigations and root cause analyses.
- Experience supporting multi-site or global quality initiatives.
- Willingness to travel as needed.

**United States of America Pay Ranges:**

- **US15**: $83,400 - $139,000 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.

Travel Percentage: None

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

- Project Management
- Influencing
- Quality Management System (Qms)
- Influencing Skills
- Training And Development
- Investigation
- Microsoft Excel
- Problem Solving
- Planning
- Third-Party Auditing
- Key Performance Indicators (KPIs)
- Critical Thinking
- Negotiation
- Quality Engineering
- Root Cause Analysis
- International Regulatory Affairs
- Microsoft Word
- Continuous Improvement Process
- Process Mapping
- Microsoft Office
- Corrective And Preventive Action (Capa)
- Medical Device Regulations
- Microsoft PowerPoint
- Ability to Work Independently
- FDA Regulations
- Communication

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