Quality Assurance Manager

As a Quality Manager, you will validate and control quality processes in the company's factories worldwide. Your role includes planning work processes, maintaining and improving processes, and managing quality in the company's factories in Israel and internationally.

Your Responsibilities:

• Lead quality improvement implementation as appropriate to legacy products, continuous improvement, and customer satisfaction.
• Responsible for the development, maintenance, and continuous improvement of Quality KPIs.
• Receive assignments in the form of strategic objectives and determine how to use resources to meet schedules and goals. Tracks assignments status, quality, and report-out to management
• Manage and Monitor Quality Transition plans and activities.
• Handling external audits by notified bodies, auditing organizations, and regulatory authorities
• Plan and manage implementation of internal quality audits and related findings
• Overview of training planning and effectiveness
• Formulate and recommend (changes to) policies and established procedures that affect immediate organization(s) activity, either directly or through Q&R functions.

You're the right fit if:

• BSc in Engineering or Practical Engineering with Qualification in Quality Assurance (CQE, CQM or CQA).
• At least 3 years of experience in QA/QMS management at a Medical Device Company
• Proven experience in the establishment and / or management of quality systems in compliance with ISO 13485, preferably for a multi-disciplinary product.
• Proven experience in leading MDSAP / ISO 13485 audits/ FDA-QSR Inspections
• Great communication and influential skills, Supportive and service-oriented, Team Player
• Fluent in verbal and written English.