Staff Engineer, Supplier Quality Controls (1 year FTC)
Staff Engineer, Supplier Quality Controls (1 year FTC)
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Job Description
What you will do:
The Supplier Quality Staff 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.
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.
- Implement strategy for supplier controls procurement and strategic sourcing processes and procedures in coordination with Site Supplier Quality teams and Companywide Supplier Quality Controls team.
- Own 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.
- Lead local and support global 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 (containment actions root cause corrective/preventive action etc.).
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
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:
Staff IC
Employment Type
Full-Time
