The Role
As a Regulatory specialist , you will be in charge of the following tasks:
- Main Responsibilities: (Assist regulatory manager in all regulatory activities such as)
- Preparation of registration documents (CTD review, checking received forms and files)
- Communicating with Commercial department for customs release
- Preparation of import documents
- Preparation of new systemic release documents
- Documentation preparation in Regulatory Department
- Following the open cases from MOH
- Having discipline in working and archiving documents
- Participate in training programs
Requirements
– University Qualifications: Pharmacist or relevant Master degree
– Good command of written, read and spoken English
– Effective time management skills, ability to handle multiple projects and tasks simultaneously
– Ability to work in a team
– Preferable age between 25-30 years
– Good command of computer knowledge (MS. Office)
– (1-2) years working experience in Pharmaceutical Company
– having Flexibility and perseverance attitudes