Ra specialist

Company Description

Rekah Pharmaceutical Industries Ltd. is a publicly traded Israeli company focused on developing and delivering high-quality generic pharmaceutical products. With a portfolio of approximately 250 prescription (Rx) and over-the-counter (OTC) products, Rekah specializes in various therapeutic areas. The company manufactures and distributes an array of dosage forms, including sterile solutions, tablets, liquids, creams, and powders. In addition to pharmaceuticals, Rekah is also a provider of dermo-cosmetics and vitamins, catering to a wide range of healthcare needs.

Role Description

Rekah Pharmaceutical Industries Ltd. is seeking a full-time Regulatory Affairs (RA) Specialist for a hybrid role based in Binyamina - Givat Ada, with flexibility for partial remote work. The RA Specialist will be responsible for preparing regulatory submissions to support product registration and compliance. This includes compiling dossiers, coordinating with R&D and manufacturing teams, ensuring adherence to regulatory guidelines, and maintaining up-to-date knowledge of global regulatory requirements. The role requires attention to detail, strong organizational skills, and the ability to manage multiple projects simultaneously.

Qualifications

• Experience in regulatory submissions, documentation preparation, and compliance with regulatory guidelines
• Strong understanding of pharmaceuticals across dosage forms such as sterile solutions, tablets, liquids, creams, and powders
• Excellent communication, organizational, and multitasking skills
• Proficiency in technical writing and document management
• Ability to collaborate effectively with cross-functional teams including R&D and manufacturing
• Knowledge of global regulatory requirements and processes
• Proficiency in English, both written and spoken
• Bachelor's degree in Life Sciences, Pharmacy, or a related field is required
• Experience in the pharmaceutical industry and familiarity with regulatory authority interactions are advantageous