https://bayt.page.link/RqoQ8sTv5YXk17sJ9
أنشئ تنبيهًا وظيفيًا للوظائف المشابهة

الوصف الوظيفي

Work Flexibility: Hybrid

What you will do


Primary responsibilities include:


  • Liaison between suppliers and Stryker to drive effective continuous improvement to the supply base.
  • Works with internal customers and suppliers to support supplier quality issues and provide technical support for activities related to supplier quality system assessment, performance evaluation and quality improvement projects.
  • collaborates with the strategic sourcing, auditing and development groups to understand capabilities and competencies of suppliers to fulfill quality and regulatory requirements
  • Assess and critique supplier processes and control documentation and drive improvement in the supplier QMS
  • Articulate detailed supplier performance results and trends to appropriate levels of management
  • Support tracking and reporting of KPI and other metrics associated with supplier performance
  • Provide education and training to suppliers, as necessary
  • Maintain and track completion of supplier action plans
  • Identify and execute cost reduction opportunities through quality improvements at suppliers.
  • Transfer “lessons learned” from the supply base back to R&D, AO, RA, and other functions for incorporation into next generation designs
  • Participate in cross-functional projects as needed.

What you need


Basic Qualifications:


  • B. Eng. in a science, engineering or related discipline preferred, or equivalent years of experience
  • 2+ years’ experience in manufacturing environment or equivalent
  • Overall, 3-5 years career experience in Supplier Quality roles.

Preferred Qualifications:


  • Experience in a highly regulatory environment
  • Basic knowledge of FMEA, validation programs and SPC processes
  • Basic understanding of manufacturing processes, prints, tolerancing, project management and statistics
  • Strong interpersonal skills, written, oral communication and negotiations skills
  • Knowledge and understanding of US and International Medical Device Regulations
  • Travel required.
Travel Percentage: 20%

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