Supplier Quality Controls Engineer

Work Flexibility: Hybrid

What you will do:
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.
Responsibilities:
• Responsible for the development, revision, maintenance, and inactivation of the local Stryker site procedures ensuring the alignment with the corporate guidelines for purchasing controls.
• Collaborate with Procurement, Site Quality, Regulatory, and Regional Supplier Quality teams on strategic initiatives and sustaining activities to support successful supplier quality controls programs.
• Support tracking and reporting of KPI and other metrics associated with supplier performance. Articulate detailed supplier performance results and trends to appropriate levels of management.
• Support Third Party inspection (FDA, Notified Body etc.) and Stryker Corporate audits of the quality system.
• Execute supplier quality agreements (SQA) and Supplier Change Control Agreements (CCA).
• Provide best in class support to our business partners across Stryker for successful implementation of compliant and efficient Supplier Quality Controls programs.
• Support local initiatives and projects for improvement, and implementation of processes to build a best in-class Supplier Quality Controls organization.
• Work with site and divisional counterparts to own Corporate Purchasing Controls NC’s and CAPA’s.
What you need:

• Bachelor’s degree in a Science, Engineering or related discipline preferred.
• 1+ years of experience in Supply Management, Quality, or Engineering within a regulated industry (medical device industry preferred).

• Fluency in English.

Preferred Qualifications:
• Experience in quality management systems is desired.
• Supply Chain and/or Medical Device quality certifications or related training.
• ISO 13485 Lead Auditor certification or equivalent.
• Knowledge of ISO 13485, FDA, EUMDR and regional medical device regulatory requirements.
• Strong communication skills with the ability to relay technical information to both internal teams and external stakeholders.
• Experience in supporting third-party inspection (FDA, Notified Body) within the medical device industry.

Travel Percentage: 10%