Regulatory Affairs Pharmacist - Temporary Position

Do you want to make a real impact on patients’ lives in Israel?

Are you looking to work in a dynamic, professional environment where you can express your expertise and be part of a multidisciplinary team?

If so – we invite you to join our winning team!

Kamada, a global biopharmaceutical company, is looking for a Regulatory Affairs Pharmacist for a temporary position (maternity leave cover) to join our vibrant Regulatory team and lead registration and regulatory activities for a diverse portfolio of medicinal products in Israel.

About the Role

As a Regulatory Affairs Pharmacist, you will play a key role in our mission to bring new products to market and ensure that registered products remain compliant, up-to-date, and aligned with Israeli Ministry of Health (MOH) regulatory requirements.

You will be involved in the full lifecycle of regulatory activities, from submission to maintenance, with a direct and meaningful impact on both the organization and patients.

Key Responsibilities

• Preparation and submission of registration dossiers and regulatory documents to the Israeli Ministry of Health.
• Maintenance and lifecycle management of registration files, including variations and renewals of imported medicinal products.
• Preparation, review, and updates of patient leaflets, physician leaflets, and packaging materials.
• Ongoing communication with overseas manufacturers and the Israeli Ministry of Health regarding product registration.
• Providing regulatory guidance and support to internal stakeholders across the company.
• Review of regulatory and scientific documentation.
• Ensuring full compliance with Israeli regulatory requirements and MOH guidelines.

Requirements

• B.Sc. in Pharmacy – mandatory (M.Sc. – an advantage).
• Experience in the pharmaceutical industry.
• Regulatory affairs experience – a significant advantage.
• Experience working with the Israeli Ministry of Health – an advantage.
• High proficiency in Hebrew and English (written and spoken).
• Experience in scientific writing.
• High attention to detail and accuracy.
• Fast learner with strong self-motivation, ability to work independently, and excellent interpersonal skills.

Why Join Us?

If you are looking for a role that combines regulatory excellence, precision, and a true impact on life-saving medicines – this is the place for you.

Position scope: Full-time, temporary (~9 months)

Location: Rehovot site, Israel