Regulatory Affairs Executive

Key Responsibilities• Prepare the registration documents for initial registration/new registration, renewal, supplementation, changes, and GMP evaluation for pharmaceuticals in the treatment of various fields such as Oncology, Cardiology, Gastroenterology, Neurology, Respiratory.• Reporting to the RA manager to implement Regulatory Affairs activities. Complete relevant reports within designated timeframes.• Ensures that all product...

1. Pharmacist Degree2. Good Knowledge in pharmaceuticals & medical.3. Min 3 years of RA experience in Drug Registration4. Good English and Good communication