עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
Drive regulatory excellence in a region that matters, obtaining regulatory approvals and compliance for life-saving medicines and medical devices. Apply today!
Your new role
As a Regulatory Affairs Specialist, you'll be the regulatory backbone for Novo Nordisk's operations in Israel and the Palestinian Authority. You'll manage the full lifecycle of pharmaceutical product and medical device registrations—from initial submissions through renewals and new indications—ensuring seamless compliance with local regulations and internal standards.
Day-to-day Your Tasks Will Include
- Regulatory activities for obtaining and maintaining licenses for pharmaceutical products and medical devices, including NDA submissions, variations, renewals, and new indications
- Preparing, reviewing and approving packaging materials in accordance with Ministry of Health requirements and Novo Nordisk SOPs
- Supporting National Health Basket (NHB) submissions and ensuring timely, accurate documentation
- Maintaining and updating Novo Nordisk internal regulatory affairs systems a
- Reviewing and approving promotional materials according to Ministry of Health and Novo Nordisk guidelines
- Participating in 29C procedures for importing non-registered products and leading relabelling projects
- Collaborating cross-functionally with other departments to ensure regulatory continuity and consistency
- Providing backup regulatory support to colleagues during periods of absence.
As part of International Operations, you will join our largest operational unit. Covering 194 countries and 95% of the world's population, more than 18,000 of us work passionately to serve 35 million patients each day. With a promise to outperform the competition, we continue to be the growth driver for Novo Nordisk, and to improve health at scale across the globe.
Within International Operations, our team in Israel is dedicated to ensuring our innovative medicines and medical devices reach patients who need them. You'll be instrumental in navigating the local regulatory landscape, building relationships with the Ministry of Health, and maintaining Novo Nordisk's reputation as a trusted, compliant partner in the region.
Your Skills & Qualifications
We're looking for a Regulatory Affairs Specialist with deep expertise in the Israeli regulatory environment and a strong pharmaceutical background. You'll bring with you:
- A bachelor’s or master’s degree in pharmacy A minimum of 2 years' experience in pharmaceutical product registration and regulatory affairs in Israel
- Comprehensive knowledge of Israeli Ministry of Health regulations, procedures, and requirements
- Strong experience with NDA submissions, product renewals, labelling updates, and packaging material compliance
- Excellent attention to detail and ability to manage complex regulatory documentation
- Fluent in Hebrew and English (written and verbal)
- Excellent interpersonal skills, ability to work collaboratively in a team, and a supportive approach toward others
- Strong organizational and project management skills with the ability to manage multiple registrations simultaneously
- Collaborative mindset with proven ability to work effectively across departments and with external stakeholders.
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.
What We Offer
Being part of a global healthcare company means opportunities to learn and develop are all around us. You'll work in a region where your expertise directly impacts patient access to innovative treatments, while our benefits are designed with your career and life stage in mind.
Deadline
March 15
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
שאלות ותשובות עבור משרת Regulatory Affairs Specialist
כמומחה/ית לענייני רגולציה ב-Novo Nordisk, תהיו עמוד השדרה הרגולטורי של החברה בישראל וברשות הפלסטינית. תנהלו את מחזור החיים המלא של רישום מוצרים פרמצבטיים ומכשירים רפואיים, כולל הגשות ראשוניות, חידושים ואינדיקציות חדשות, תוך הבטחת עמידה מלאה בתקנות המקומיות ובתקנים הפנימיים של החברה. תכללו גם הכנה ואישור חומרי אריזה, תמיכה בהגשות סל שירותי הבריאות הלאומי, ואישור חומרי קידום מכירות.
משרות נוספות מומלצות עבורך
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Regulatory Affairs Specialist
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כפר סבא
Novo Nordisk
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Regulatory Affairs Specialist
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כרמיאל
LV Recruiting
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משרת רגולציה בחברה יצרנית כחוללבן
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הרצליה
זיו השמות
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Regulatory Affairs Specialist
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תל אביב - יפו
ICON plc
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Regulatory Affairs Specialist
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תל אביב - יפו
ICON Plc
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למחלקת הרישום אנו מחפשים את האחד /אחת למשרת רשמ /ת ברגולציה קלינית ופרה-קל
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אור עקיבא
דקסל פארמה
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14,000-18,000 ₪