Regulatory Affairs Associate

We are looking for a detail-oriented and motivated Regulatory Affairs Associate to join our team and support the lifecycle management of pharmaceutical products across multiple markets.

• Regulatory Submissions:
• Prepare, review, and submit registration dossiers (including CTD and DMF) for new products, renewals, and post-approval updates.
• Health Authority Interaction:
• Manage correspondence with regulatory authorities (mainly the Israeli Ministry of Health), respond to deficiency letters and Q&A, and support timely approvals.
• Lifecycle Management / Variations:
• Handle regulatory variations and updates to existing registrations, ensuring compliance with current guidelines and internal timelines.
• Documentation & Compliance:
• Maintain accurate and compliant regulatory documentation, ensuring alignment with global regulatory standards and company procedures.

• Education:
• B.Sc. or M.Sc. in Life Sciences (Pharmacy, Biology, Chemistry, or related field).
• Pharmacist certification – strong advantage.
• Experience:
• Prior experience in Regulatory Affairs (pharma) – advantage.
• Skills & Competencies:
• High level of English (written and verbal)
• Strong attention to detail and organizational skills
• Ability to manage multiple tasks and deadlines
• Structured, precise, and compliance-oriented mindset

• This role offers the opportunity to work in a dynamic regulatory environment, contribute to bringing high-quality medicines to market, and be part of a team committed to excellence, compliance, and continuous growth.