Regulatory Affairs Supervisor - Abu Dhabi, United Arab Emirates - Kinetic
Description
A multinational pharmaceutical company is actively recruiting aRegulatory Affairs Supervisor to be based in
Abu Dhabi, UAE.
***
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
:
- Performancedriven 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 facetoface interviews in the location mentioned above.
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