Job descriptions:

Create an account for companies to register products in MOH and other relevant authorities
Setting up registration document and applying for product registration to the relevant department.
Follow up and monitor every product that had been registered
Communicate and consult with the relevant department for any shortfall of document
Documenting each registration documents
Make payment for registration and verify the documents' completeness
Identify the validity of the registration number
Responsible for inspections conducted by the MOH and other relevant authorities
Able to handle trading (purchase and import process)
Checking and monitoring the condition of medical equipment
Coordinate / monitor the recording, management and reporting of medical equipment
Manage and monitor the import process including compliance with applicable import regulations, starting from document processing to receiving goods at the warehouse.
Developed and monitored goods delivery schedules to ensure timeliness, including import.
Coordinate with other departments such as marketing, sales, and production to ensure the smooth flow of goods and information needed.
ISO Document control

Requirements:

Major in pharmacy from reputable university or any related major with minimum IPK 3.0
Have CDAKB certificate is additional value.
Must Have Pharmacist Certificate and pharmacist practice license that has never been used in other pharmacies.
Have experience about MOH regulatory at least 2-3 years (Having experience in this field is preferred) and understand about AKL/AKD, CDAKB, SNI etc.
Have experience in managing documents, permits on related government institutions
Updates related to new regulations in terms of certification of import products
Good communication In English