Regulatory

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 CDAKB certificate that has never been used in other company.
• 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