Execution and follow-up of the request for legal documents from Regulatory Affairs.
Keep internal regulatory databases and records up to date.
Track and monitor the status of submissions and ensure timely follow-up of requests and feedback from the Health Authority.
Assist in the review and formatting of regulatory documentation to ensure accuracy, consistency, and compliance.
Support and follow-up throughout the entire process for Good Manufacturing Practices certification.
Collaborate closely with local and global cross-functional teams (Quality, Manufacturing, Medical Affairs, etc.) to support regulatory deliverables.
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Job Profile
Bachelor's degree in Pharmacy, Biological Pharmaceutical Chemistry, Biotechnology, Industrial Chemistry or a related field.
Interest in developing a career in Regulatory Affairs.
Strong organizational and project management skills.
* Excellent attention to detail and ability to manage multiple tasks.
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