Job Description
-Team working in analyzing the tablets and capsules based on quality-related parameters.
-Team working in preparing the required documentation for submitting the pharmaceutical dossier into the ministry of health includes CTDs, SOPs, reports.
-Create and manage effective communication and close collaboration with MOH, Keeping up-to-date with the latest news in MOH and pharmaceutical industry.
-Follow up all affairs of technical department, provide reporting on a regular basis to executive management to ensure timely execution of regulatory strategies to support launch activities and compliance status for maintenance projects and activities.
-Routine maintenance of regulatory files international regulation, guidance and standards applicable to company products.
