Job Description

- Create and manage effective communication and close collaboration with MOH, Keeping up-to-date with the latest news in MOH , syndicates and pharmaceutical industry.
- Preparing and completing Regulatory documentation, provide reports on a regular basis to QA manager.
- Familiar with TTAC website, registration of supplements and APIs, medicines & getting IRC in MOH.
- Support the commanded strategies to increase time and accuracy of regulatory compliance.
- Establish and maintain system for tracking changes in documents submitted to regulatory authorities or partners.
- Support in collecting and coordinate information and prepare regulatory documentation for submission to regulatory affairs.
- Support maintenance of regulatory files in compliance with regulation and standards applicable to company products.
- Capable of travelling and site visits

Requirements

- Junior professional (Master’s degree in health professions or chemistry) - At least 2 years of experience in the regulatory field and pharmaceutical company - Familiar with regulatory affairs and MOH procedures - Strong communication skills - High team work value - English proficiency - Gender Preference: Female

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