- Ensures timely preparation, submission and appropriate follow-up of new applications to the local authorities.
- Maintenance of assigned, authorized products through timely submission of variations, renewal applications.
- Updated on relevant local regulations and guidelines.
- Maintain a positive relationship with internal and external regulatory contacts.
Desired Skills and Experience
- Minimum 2-3 years in the regulatory of pharmaceutical or medical devices Industries
- Ability to communicate well verbally and in writing both in English and Arabic
- Proficiency in computer system with regard to word-processing, spreadsheets, database application, and internet
- Good organizational and planning skills
- Meticulous attention to detail, and be flexible enough in handling conflicting time pressures and a large volume of work
- Must be able to work both alone and as part of a team
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