| Job Location | Dubai, United Arab Emirates |
| Education | Not Mentioned |
| Salary | Not Mentioned |
| Industry | Pharmacies; Pharmaceutical Manufacturing |
| Functional Area | Not Mentioned |
Specialist with expertise in eCTD submissions for the United Arab Emirates (UAE). The Regulatory Affairs Specialist will be responsible for ensuring compliance with applicable regulatory requirements for submissions of Documents & registration of products with UAE MOH. He or She will be responsible for developing and implementing eCTD submission strategies for our products in the UAE market.˙Responsibilities:? Develop and implement eCTD submission strategies for our products registration & compliance in the UAE market? Ensure compliance with applicable regulatory requirements.? Prepare and submit eCTD submissions to regulatory agencies in the UAE.? Review and interpret regulatory requirements.? Communicate with regulatory team of principles to coordinate the documentations for registration process.? Monitor regulatory changes in UAE & update our compliance accordingly.? Maintain eCTD submission records and documentations.
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