SUPPLIER QUALITY MANAGER

Johnson & Johnson is currently seeking a Supplier Quality  Manager   to join our team located in Israel.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.
nj.
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This role leads/manages the Supplier Quality Management /Purchasing Control process and ensures that HTC Suppliers provide purchased finished goods, direct and indirect materials, or services in compliance with CSS and J&J policies/procedures, Global Regulations and industry standards.
Responsible for supplier oversight from qualifying new suppliers, monitoring and improving supplier’s performance Duties and Responsibilities.
Serves/provides management oversight focusing on Purchasing Controls/Supplier Quality Management for assigned supplier categories globally.
Leads/participates in the external supply selection process to provide quality system expertise.
Develops and deploys strategies to effectively manage direct and indirect Suppliers with appropriate risk-based controls.
Compiles and recommends data driven conclusions for Management Review Analyzes quality data and identifies trends impacting risks/benefits requirements of process, Product, and quality systems with primary responsibility for the development and maintenance of HTC external suppliers.
Utilizes key knowledge of business processes, analytical tools, and the regulatory environment to support the supplier quality management lifecycle.
Leads/assists in the maintenance of the supplier quality relationship (proactive quality reviews, risk-sensing modeling, follow-up on corrective actions, metrics development/improvements, etc.) Ensures compliance to applicable Global Regulations and standards (e.
.
QSR, ISO, EN, Medical Device Directive (MDD), and EU MDR requirements) Team development, Mentor and trains team members.
Qualifications BSc in Engineering or Practical Engineering with Qualification in Quality Assurance (CQE, CQM or CQA).
At least 5 years of experience as a quality leader in a WW manufacturing organization (preferably, Medical Devices Industry) Practical knowledge of ISO, Experience in the Medical Device industry or medical field  Demonstrated knowledge of manufacturing principles and practices, and procedures Demonstrated knowledge of Statistical Analysis Tools  Must be a self-starter/able to think outside the box, challenge the norm and drive change.   Ability to collaborate and build strong partnerships internally/externally with customer focus.
Must have excellent communication, interpersonal and presentation skills (Also in English) Significant teamwork and leadership skills Demonstrate project management skills with strong results orientation.  Self-confidence and integrity Builds relationships based on respect, listens to and incorporates diverse points of view.
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