Eagle Eye Limited BD offers an exciting opportunity for a Regulatory Affairs Specialist to join their pharmaceutical export operations team in Bangladesh. This full-time position involves managing contract manufacturing and export processes, requiring expertise in Bangladesh’s pharmaceutical regulatory framework and experience with DGDA registration procedures. The role provides a chance to work with international pharmaceutical supply chains and contribute to the company’s mission of delivering high-quality generic drugs to global markets.
The successful candidate will enjoy a competitive salary package with performance bonuses, comprehensive benefits including social and medical insurance, and professional development opportunities. Working in a modern office environment with flexible arrangements, you’ll collaborate with both local manufacturing partners and the Hong Kong headquarters team. This position is ideal for professionals passionate about pharmaceutical regulatory affairs who want to make an impact in the growing generic drug export industry while building expertise in international pharmaceutical supply chain management.