Opportunity Description
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:
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