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Regulatory Affairs Supervisor
3 weeks ago
A multinational pharmaceutical company is actively recruiting a **Regulatory Affairs Supervisor** to be based in **Abu Dhabi, UAE.**
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**Key aspects of the role include**:
- Prepare and complete the registration process for assigned products.
- Reviewing new product submission and variation dossiers for submission.
- Collate and distribute all technical and regulatory documentation internally and externally.
- Prepare and maintain relevant SOPs.
- Defining and execute regulatory plans and manage timelines to achieve the stated goals.
- Updated on relevant local regulations and guidelines.
- Collects relevant regulatory information.
- Maintain a positive relationship with internal and external regulatory contacts.
**To be successful you will need to meet the following**:
- **Bachelor’s or master’s degree in pharmacy or similar.**:
- **Must have a minimum 10 years’ Regulatory Affairs experience in a biotech/pharmaceutical industry**. Previous experience working with international regulatory organizations.
- **Proven Experience** **and knowledge in regulatory submissions.** Preferably Marketing Authorization Application
- **Strong Knowledge and understanding of GCC, FDA and EMA regulations.**:
- Performance-driven individual, with a strong sense of urgency, exceptional organizational credibility, and deep understanding of the business.
- Excellent verbal and written in English.
- Applicants should be available for face-to-face interviews in the location mentioned above.
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