Job Details
The Supplier Quality Engineer serves as a key role for leading Supplier Quality Controls activities and process improvement initiatives at Stryker sites. In this role, you will interface with many functions of the business and own the development and continuous improvement of Global Supplier Quality Controls systems, tools, policies, and procedures at assigned Stryker sites across the globe.
The Supplier Quality Engineer focuses on developing processes that build quality into the products we sell and driving a culture of continuous improvement to support Stryker’s mission & strategic goals.
- Lead Supplier Quality Controls activities and drive continuous improvement initiatives across assigned Stryker sites.
- Develop, maintain, and improve supplier quality processes, tools, policies, and procedures aligned with global standards.
- Partner closely with Procurement, Quality, Regulatory, and Supplier Quality teams to support supplier performance and compliance.
- Monitor, analyze, and report supplier performance metrics and trends to management.
- Support internal and external audits, including FDA, Notified Body, and corporate quality inspections.
- Execute and manage Supplier Quality Agreements and Supplier Change Control Agreements.
- Lead corrective and preventive actions related to purchasing controls, including root cause analysis and remediation.
- Provide best-in-class support to business partners to ensure compliant, efficient, and sustainable supplier quality programs.
Bachelor’s degree
2 years of experience in Quality, Supply Management, or Engineering within a regulated industry
Strong communication skills and ability to work cross-functionally
Experience with Quality Management Systems
Knowledge of ISO 13485, FDA, EU MDR, or other medical device regulations
Experience supporting third-party audits (FDA, Notified Body)
Medical device, supply chain, or quality-related certifications (e.g., ISO 13485 Lead Auditor)
Salary information will be provided during the recruitment process.
