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CQ Staff Specialist EP Israel

Johnson & Johnson MedTechשפיים, מחוז המרכז, ישראללא צויןFull-timeדרגה: בכיר/ה

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תובנת Willbi

התפקיד במילים פשוטות

תפקיד זה אחראי על ניהול והובלת מערך ואמצעי איכות הסביבה והמוצר עבור תחום האלקטרופיזיולוגיה בישראל. העבודה כוללת ניהול חריגות ותלונות איכות, תמיכה בתהליכי מבדקים (אורדיטים), מעקב אחר מדדי איכות ועבודה מול צוותים מקומיים וגלובליים.

חובה
  • Bachelor’s degree in Engineering, Science, Business, or a related field
  • Minimum 5 years of experience in a regulated industry
  • Experience with Quality Management Systems (QMS) and compliance activities
  • Strong organizational, communication, and stakeholder management skills
  • Fluent Hebrew and English with excellent spoken English
יתרון

    חולץ מתיאור המשרה · מתעדכן אוטומטית

    למי זה מתאים

    התפקיד מתאים למקצועני איכות בעלי תואר ראשון רלוונטי ולפחות 5 שנות ניסיון בתעשייה מבוקרת (עדיפות למכשור רפואי או פארמה). התפקיד פחות מתאים למי שאינו שולט באנגלית ברמה גבוהה או למי שחסר ניסיון עם מערכות ניהול איכות (QMS).

    תיאור המשרה המלא

    המשרה המקורית · נשמר לעיון

    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 jnj.com.

    As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

    Job Function

    Quality

    Job Sub Function

    Customer/Commercial Quality

    Job Category

    Professional

    All Job Posting Locations:

    Kibbutz Shefayim, Center District, Israel

    Job Description

    About Johnson & Johnson MedTech

    Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

    Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

    We are searching for the best talent for a CQ Staff Specialist EP role, to join our team located in Shefayim, Israel.

    Purpose: Under the general direction of the Lead Commercial Quality Electrophysiology Mid-size markets cluster, this position is responsible for establishing and leading Johnson & Johnson overall quality management framework and quality system for Electrophysiology business in Israel, establishing preventive and corrective actions to mitigate potential or actual non-compliance risks and ensuring compliance to attain world-class operational/customer focused capabilities.

    The overall management responsibilities also require exerting leadership in regional projects and initiatives providing strategic direction to achieve established goals. Role complexity includes but is not limited to ability to interact cross functional and representation of the country in global projects and initiatives.

    The lead is responsible to lead activities towards the integration of the quality management systems for Electrophysiology in Israel. This position is responsible for ensuring the QMS requirements are effectively executed in the country in accordance with local regulations, corporate and segment policies and procedures.

    The role will interface with related organizations to ensure a consistent and systematic process is followed and that metrics are reported timely.

    You Will Be Responsible For

    • Support Quality Management System (QMS) activities and compliance processes.

    • Participate in audits, inspections, and supplier assessments.

    • Manage product quality complaints and support field actions.

    • Drive complaint vigilance execution, ensuring the timely closure of product related complaints.

    • Monitor quality metrics.

    • Collaborate with local, regional, and global stakeholders.

    • Support compliance with regulatory requirements and ISO standards.

    • Define, document, and control operational processes and procedures to ensure compliance, consistency, and continuous improvement.

    Qualifications And Requirements

    • Bachelor’s degree in Engineering, Science, Business, or a related field.

    • Minimum 5 years of experience in a regulated industry, preferably Medical Devices, Pharma, or Healthcare.

    • Experience with Quality Management Systems (QMS) and compliance activities.

    • Strong organizational, communication, and stakeholder management skills.

    • Ability to work in a fast-paced, international environment.

    • Fluent Hebrew and English, with excellent spoken English for daily interaction with global teams.

    Required Skills

    Preferred Skills:

    Audit Management, Business Savvy, Coaching, Communication, Compliance Management, Continuous Improvement, Fact-Based Decision Making, ISO 9001, Issue Escalation, Problem Solving, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment, Standard Operating Procedure (SOP)

    אודות Johnson & Johnson MedTech
    פרופיל החברה · בקרוב

    ביקורות עובדים · בקרובעוד משרות ב-Johnson & Johnson MedTech

    שאלות על המשרה

    • המשרה לא ציינה שכר. אנחנו מציגים שכר רק כשהמעסיק מפרסם אותו.
    Johnson & Johnson MedTech
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