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Job Description
- Preparing and submitting dossiers including CTD & eCTD
- Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals or registrations.
- May compile and prepare materials for submission to regulatory agencies.
- Ensure submission and approval of Medical Devices registration files to the MOH for new launches, and registration renewal applications to keep licenses valid.
Job Requirements
- 3-5 Years of experience
- Bachelor of pharmaceutical
