עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לחפש לבד בין מאות מודעות – תנו ל-Jobify לנתח את קורות החיים שלכם ולהציג לכם רק הזדמנויות שבאמת שוות את הזמן שלכם מתוך מאגר המשרות הגדול בישראל.
השימוש חינם, ללא עלות וללא הגבלה.
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
If you have experience in regulatory compliance and enjoy working with cutting-edge medical technologies, we’d love to hear from you. Join us as a Regulatory Affairs Specialist.
Our products include different technologies (active and non-active, hardware, software and AI) and are sold in more than 30 countries.
The Regulatory Affairs Specialist will be part of the Regulatory team at the Yokneam site, reporting to Senior Regulatory Affairs Manager, supporting a wide range of activities with frequent interactions with corporate teams in the U.S. and globally.
Responsibilities may include the following and other duties may be assigned:
Coordinate and prepare document packages for regulatory submissions, internal audits, and inspections
Lead or compile materials required for submissions, license renewal, and annual registrations
Write, update and maintain technical files for class IIa products
Perform Regulatory operations activities, including updating databases and coordination with Medtronic cross functions to release products
Collaborate closely with internal stakeholders including global post market teams to ensure consistent and compliant execution of post-market activities including design changes
Stay updated on regulatory procedures and changes
Required Knowledge and Experience:
Bachelor’s degree in scientific discipline
Minimum of 2 years’ experience in regulatory affairs
Experience in the medical device industry
Working knowledge of global regulatory frameworks including MDR (Medical Device Regulation)
Excellent attention to details, proactive approach and ability to work independently
High learning agility and ability to work under pressure
Detail-oriented and organized, capable of managing multiple priorities while meeting strict regulatory deadlines
Fluency in Hebrew and English, both written and verbal, is essential
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
About Medtronic
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
במקום לחפש לבד בין מאות מודעות – תנו ל-Jobify לנתח את קורות החיים שלכם ולהציג לכם רק הזדמנויות שבאמת שוות את הזמן שלכם מתוך מאגר המשרות הגדול בישראל.
השימוש חינם, ללא עלות וללא הגבלה.
שאלות ותשובות עבור משרת Regulatory Affairs Specialist
המוצרים של מדטרוניק, בהם יעסוק מומחה הרגולציה, כוללים מגוון טכנולוגיות מתקדמות כמו מכשור רפואי אקטיבי ולא אקטיבי, חומרה, תוכנה ובינה מלאכותית. מוצרים אלו נמכרים בלמעלה מ-30 מדינות ברחבי העולם.
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