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Senior Supplier Quality Controls Engineer, Global Capability Centre (2 year FTC)

Senior Supplier Quality Controls Engineer, Global Capability Centre (2 year FTC)

Stryker Poland Services sp. z o.o.Warsaw, Poland
17 days ago
Job description

Work Flexibility : Hybrid

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 Company-wide 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 in-class Supplier Quality Controls organization.
  • Work with site and divisional counterparts to own Corporate Purchasing Controls NC’s and CAPA’s (containment actions, root cause, corrective / preventive action, etc.).

What you need :

  • Bachelor’s degree in a Science, Engineering or related discipline preferred.
  • 5+ years of experience in Supply Management, Quality, or Engineering within a regulated industry
  • 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 : 20%

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    Supplier Quality Engineer • Warsaw, Poland

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