Senior Supplier Quality Controls Engineer with French Global Capability Centre
Senior Supplier Quality Controls Engineer with French Global Capability Centre
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Job Description
What you will do:
The Supplier Quality Senior 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 Senior Engineer focuses on developing processes that build quality into the products we sell and driving a culture of continuous improvement to support Strykers 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 inclass Supplier Quality Controls organization.
Work with site and divisional counterparts to own Corporate Purchasing Controls NCs and CAPAs
What you need:
Bachelors degree in a Science Engineering or related discipline preferred.
3 years of experience in Supply Management Quality or Engineering within a regulated industry (medical device industry preferred).
Fluent spoken and written English and French
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 thirdparty inspection (FDA Notified Body) within the medical device industry.
Required Experience:
Exec
Employment Type
Full-Time
