Senior Manufacturing Engineer

Stryker; Salt Lake City (UT); On-site; USD 82,000 - 136,000; Full time

Job summary

Stryker’s Neurovascular division advances stroke therapies with Complete Stroke Care solutions, delivering innovative products and clinical education to improve patient outcomes.

This role focuses on designing and validating manufacturing processes, conducting data-driven analysis, and driving improvements in a regulated medical-device environment to ensure quality, cost efficiency, and throughput.

Qualifications

• Bachelor’s degree in Engineering or related discipline required or preferred.
• Minimum 2 years of engineering experience in manufacturing, production, or industrial environments.
• Experience creating, interpreting, and modifying engineering drawings using design software.
• Experience conducting statistical or data-driven analysis to support engineering decisions.
• Proficiency with Microsoft Office applications.

Responsibilities

• Design, document, validate, and improve manufacturing processes for safe, effective medical device production.
• Conduct process qualifications, verifications, and validations per quality system and regulatory requirements.
• Analyze manufacturing data to identify trends, investigate issues, and implement corrective actions.
• Troubleshoot manufacturing challenges affecting quality, cost, delivery, yield, or throughput.
• Design, develop, procure, and implement manufacturing equipment, tooling, and fixtures with safety compliance.
• Plan, execute, and document engineering tests; analyze results and provide data-based recommendations.
• Lead or contribute to cross-functional projects on process optimization, new product introduction, technology development, and manufacturing readiness.
• Train and provide technical guidance to operators and technicians to support production goals and continuous improvement.

Job description

Stryker’s Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions. The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes.

What You Will Do

• Design, document, validate, and continuously improve manufacturing processes that support the safe and effective production of medical devices.
• Conduct process qualifications, verifications, and validations in accordance with quality system and regulatory requirements.
• Analyze manufacturing data using statistical methods to identify trends, investigate issues, and implement corrective actions.
• Troubleshoot and resolve manufacturing challenges that impact product quality, cost, delivery, yield, or throughput.
• Design, develop, procure, and implement manufacturing equipment, tooling, and fixtures while ensuring compliance with applicable safety requirements.
• Plan, execute, and document engineering tests and experiments; analyze results and provide recommendations, and present results based on data.
• Lead or contribute to cross-functional projects focused on process optimization, new product introduction, technology development, and manufacturing readiness.
• Train and provide technical guidance to operators and technicians while supporting production goals, process performance, and continuous improvement initiatives.

What You Will Need

Required Qualifications

• Bachelor’s degree; Engineering or related discipline preferred.
• Minimum 2 years of engineering experience in a manufacturing, production, or industrial environment.
• Experience creating, interpreting, and modifying engineering drawings using engineering design software.
• Experience conducting statistical, mathematical, or data-driven analysis to support engineering decisions.
• Proficiency with Microsoft Office applications.

Preferred Qualifications

• Experience in a regulated industry such as medical device, pharmaceutical, or life sciences manufacturing.
• Experience with process validation, qualification, verification, or quality system requirements.
• Proficiency with Minitab or similar statistical analysis software.
• Experience with Continuous Improvement projects and/or LEAN Six Sigma Certification.

$81,600 - $136,000 USD Annual