Regulatory Affairs Specialist

Novo Nordisk A/S • Kefar Sava, Center District • Posted April 12, 2026

Position Overview

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 ensur...