Senior Supplier Quality Engineer, Global Capability Centre

Posted 6 Days Ago
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Warsaw, Warszawa, Mazowieckie
Mid level
Healthtech • Other • Robotics • Biotech • Manufacturing
Together with our customers, we're on a mission to make healthcare better.
The Role
The Senior Supplier Quality Engineer ensures quality improvement within the supply base by assessing supplier processes, driving continuous improvement initiatives, and providing technical support for supplier quality. They coordinate with various groups to monitor supplier performance, educate suppliers, and execute cost reduction through quality enhancements.
Summary Generated by Built In

Work Flexibility: Hybrid

What you will do:

The Supplier Quality Engineer serves as a liaison between suppliers and Stryker to drive effective continuous improvement to the supply base. Works with internal customers and suppliers to support supplier quality issues and provide technical support for activities related to supplier quality system assessment, performance evaluation and quality improvement projects.
The Supplier Quality Engineer collaborates with the strategic sourcing, auditing and development groups to understand capabilities and competencies of suppliers to fulfill quality and regulatory requirements.
Responsibilities:
• Assess and critique supplier processes and control documentation and drive improvement in the supplier QMS.
• Articulate detailed supplier performance results and trends to appropriate levels of management.
• Support tracking and reporting of KPI and other metrics associated with supplier performance.
• Provide education and training to suppliers, as necessary.
• Maintain and track completion of supplier action plans.
• Identify and execute cost reduction opportunities through quality improvements at suppliers.
• Transfer “lessons learned” from the supply base back to R&D, AO, RA, and other functions for incorporation into next generation designs
• Participate in cross-functional projects as needed.
What you need:
Bachelor’s degree in a Science, Engineering or related discipline preferred.
• 3+ years experience in manufacturing environment or equivalent.
Preferred Qualifications:
• Experience in a highly regulatory environment
• Basic knowledge of FMEA, validation programs and SPC processes
• Basic understanding of manufacturing processes, prints, tolerancing, project management and statistics
• Strong interpersonal skills, written, oral communication and negotiations skills
• Knowledge and understanding of US and International Medical Device Regulations
• Travel required.

Travel Percentage: 40%

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The Company
HQ: Kalamazoo, MI
51,000 Employees
On-site Workplace
Year Founded: 1941

What We Do

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 130 million patients annually. More information is available at www.stryker.com.

Together with our customers, we are driven to make healthcare better.

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