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Senior Quality Assurance Engineer
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-03-01
Listing for:
Stryker Group
Full Time
position Listed on 2026-03-01
Job specializations:
-
Engineering
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Join Stryker’s
Peripheral Vascular business as a Senior Quality Assurance Engineer and make a direct impact on the performance and safety of commercially released medical devices. Based in Irvine, CA, you’ll play a key role in sustaining engineering efforts that drive product quality, strengthen risk management, and ultimately improve outcomes for patients around the world.
- Partner with cross‑functional teams to support quality engineering activities for sustaining projects, ensuring commercial products continue to meet safety, performance, and regulatory expectations.
- Execute product safety risk management activities, including health risk assessments for distributed products.
- Develop, review, and approve validation strategies, plans, protocols, and reports in accordance with internal procedures and regulatory requirements.
- Evaluate and enhance test plans, methods, and sampling strategies to maintain compliance and improve product reliability.
- Monitor and analyze post‑market and field performance data; identify trends and recommend corrective or preventive actions to drive continuous improvement.
- Investigate quality issues and contribute to activities related to corrective and preventive actions, nonconformance management, and risk mitigation.
- Participate in internal and external audits, providing technical input related to risk management, CAPA, and sustaining quality activities.
- Contribute to initiatives that improve quality systems, processes, and tools across the organization.
- Serve as a technical resource and share knowledge within the Quality organization.
Required:
- Bachelor’s degree in Engineering, Science, or a related technical discipline.
- Minimum 2+ years of experience in a highly regulated environment (e.g., medical device, pharmaceutical, biotechnology, or similarly regulated industry).
Preferred:
- Advanced degree in Engineering, Science, or a related technical discipline.
- Experience supporting post‑market surveillance or field performance monitoring.
- Certification such as CQE, CQA, or equivalent
$89,400.00 - $148,900 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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