Regulatory Affairs Project Manager

We are a leading consulting and services group providing comprehensive, end-to-end regulatory solutions to major local and global pharmaceutical and medical device companies. We are currently expanding and looking for an experienced Regulatory Affairs Project Manager to join our professional team.

The role includes managing submissions for new products and maintaining existing licenses in a dynamic, global environment.

What we offer:

• 🏡 Hybrid Model (Full-Time): Work from home with 1-2 days per week at our offices (located in both the Central and Sharon regions).
• 🌍 High-level exposure to international markets and global stakeholders.

Requirements:

• ✔️ At least 5 years of experience in Regulatory Affairs for medicinal products – Must.
• ✔️ Proven experience in generic product submissions – Must.
• ✔️ High-level English and the ability to communicate independently with global counterparts – Must.
• ✔️ Strong project management skills, including the ability to multitask and meet strict deadlines.
• ➕ Experience in the registration of food supplements – A significant advantage.
• https://app.civi.co.il/promo/id=960330&src=8691