- 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