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 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 eye and ear drop solutions, tablets, caplets, liquids, creams, suspensions, suppositories 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 role located in Binyamina site. 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 QA teams, ensuring adherence to regulatory guidelines, and maintaining up-to-date knowledge of local and 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 QA
• Knowledge of local and 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 Mandatory