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Inari Medical

Senior Manufacturing Engineer

Posted Yesterday
Be an Early Applicant
In-Office
Irvine, CA, USA
89K-149K Annually
Senior level
In-Office
Irvine, CA, USA
89K-149K Annually
Senior level
Support and improve medical device manufacturing through process and equipment design, validation, data analysis, troubleshooting, and continuous improvement. Lead tests and investigations, document results, mentor junior engineers, and collaborate with production, suppliers, and cross-functional teams to ensure quality, safety, and regulatory compliance.
The summary above was generated by AI
Work Flexibility: Onsite

*This role will be Monday-Friday on second shift (3 pm - 12 am PST) with some flexibility on the hours. *

Join a team focused on delivering high-quality medical devices through robust manufacturing processes and continuous improvement. In this role, you will support manufacturing operations by applying engineering principles to materials, products, equipment, and processes while maintaining a strong commitment to patient safety, product quality, and regulatory compliance. This position offers the opportunity to work across product development, process improvement, validation, and production support activities in a collaborative manufacturing environment.

What You Will Do

  • Design and improve manufacturing processes, equipment, tooling, and fixtures to support safe, efficient, and compliant production operations.

  • Execute qualification, verification, and validation activities for manufacturing processes and equipment, ensuring compliance with quality and regulatory requirements.

  • Analyze manufacturing data, conduct statistical studies, and troubleshoot issues impacting product quality, yield, cost, delivery, or process performance.

  • Lead and document engineering tests, experiments, and process improvement projects, including data analysis, reporting, and implementation of corrective actions.

  • Collaborate with production teams, technicians, suppliers, and cross-functional project teams to support production goals, project timelines, and continuous improvement initiatives.

What You Will Need

Required:

  • Minimum 2 years of manufacturing engineering experience.

  • Bachelor’s degree in Engineering or a related technical discipline.

  • Experience conducting statistical, geometric, and mathematical analysis in a manufacturing environment.

  • Experience creating, reading, and interpreting engineering drawings using Computer Aided Design (CAD) software.

  • Proficiency with Microsoft Office applications.

  • Experience supporting process validation, qualification, or verification activities.

  • Support and drive Quarantine Ticket (QT) and Non-conformance (NC) report dispositions and investigations.

  • Mentor entry to junior engineers and provide technical guidance

Preferred:

  • Experience using Minitab or similar statistical analysis software.

  • Experience sourcing, evaluating, or managing external suppliers and service providers.

  


United States of America Pay Ranges:

$89,400 - $148,900 USD Annual

  


Travel Percentage: 10%

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.
HQ

Inari Medical Irvine, California, USA Office

6001 Oak Canyon, Suite 100, Irvine, CA, United States, 92618

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