Boston Scientific
- 24/10/2023
- יקנעם עילית
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.
Lead suppliers to comply with Quality level requirements and directives, supplier qualification, evaluation, and supplier communication. Suppliers' Material Monitoring activities and constant improvement.
Main Duties
- New supplier qualification and reevaluation.
- Establish an annual Supplier quality audit plan and lead to full implementation according to the yearly goal. Supplier’s audits execution and lead to full completion, including corrective actions follow-up, and effectiveness where applicable.
- Maintaine approved supplier list within SAP system and signed hardcopy, monitor supplier classification, and change according to supply chain needs.
- Define Vendor rating KPI’s and establish a rating system that will be presented to Quality, purchasing, and operational management in defined time intervals. Define action plans for improvement for low-rating suppliers.
- Define KPI and crucial activities supporting quality engineers for Production line transfer processes and qualification.
- Establish and maintain Quality agreements with critical suppliers in compliance with Boston's Scientific requirements based on former quality issues and in adequacy to notified body and directive requirements.
- Ensure the quality of deliverable parts/materials and services by the suppliers.
- Manage the monitoring of rejected material and Supplier corrective action requests follow-up.
- Improvement of Boston Scientific supplier quality processes in Boston Scientific systems
- Supplier QA SOP’s related, establish, and maintenance.
- Bachelor’s Degree in relevant academic area.
- Minimum of 2 years of experience in Quality.
- Experience with Multidiscipline products & medical devices.
- The ability to approve test protocols and V&V (production-related only)
- Knowledge in Process Validation, PFMEA
- Knowledge of product Life Cycle methods and control, medical standards /regulations, and general standards knowledge (for example, ISO13485 , FDA – QSR, MDD, IEC 60601, etc.’)
- Familiar with Failure analysis and statistic techniques methods and Expertise
- Multi-tasking and objective dedication
- Good interpersonal relationship
- Auditors' certification and experience
- Working knowledge of Supplier Corrective Actions (SCAR), non-conformance management, and complaint investigations
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
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