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מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.

Regulatory Affairs Associate

SK Pharma

תל אביב - יפו

Regulatory Affairs Associate

SK Pharma

תל אביב - יפו
היברידית
9,000-13,000 ₪ (הערכה מבוססת AI)
זוהי הערכת טווח שכר מבוססת AI ולא פרסום של המעסיק

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.

Key Responsibilities

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.

Requirements

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

Why Join Us

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.