Nyprax Pharma is a growing Regulatory Affairs Consultancy with 20+ years of experience. We provide expert guidance to ensure smooth regulatory submissions for medical devices to be imported, distributed, and marketed in Singapore.

You will coordinate and submit regulatory documentation to the Health Sciences Authority, compile and format medical device dossiers, verify report accuracy, and respond to Ministry queries while managing multiple tasks under deadlines.

• Coordinate and submit formatted regulatory documents online to the Health Sciences Authority (Ministry of Health)
• Compile client dossiers for medical devices and applications according to Ministry requirements
• Format medical dossier documents to meet regulatory standards
• Verify accuracy of reports through detailed validation and checking
• Respond promptly and accurately to queries from the Minis...