Senior Quality Assurance Engineer

Reposted 4 Days Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
89K-149K Annually
Senior level
Healthtech
The Role
Support sustaining engineering for peripheral vascular medical devices by executing risk management, validation, testing, post-market surveillance, CAPA, audits, and continuous quality improvements.
Summary Generated by Built In
Work Flexibility: Onsite

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.

What You Will Do:

  • 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.

What You Need:

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.

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.
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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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