Job Duties 

• Review and Compile Regulatory Dossiers for submission to NMRA/CDDA, Sri Lanka
• Streamlining product registration and approval process.
• Assessing regulatory acceptance of new initiative or new products.
• Providing strategic recommend to balance organization on product registration/regulatory issue
• Handling health related consumer complaint and product regulatory related issue
• Anticipating and leverage changes in the product and environment related to regulatory issue Liaison with NMRA/CDDA personnel and follow up the application status
• Liaison with CHA and custom personnel to get on time shipment clearance

Requirements:

• Male/ Female
• Age below 45
• Bachelor of Pharmacy /Diploma in pharmacy/B.Sc. Pharmacology/B.Sc. Chemistry
• Good knowledge of NMRA Act no. 5 of 2015 /CDD Act No.27 of 1980 and SLS Act 1984.
• Minimum 4 year experience of Products registration with NMRA/CDDA, Sri Lanka