Job Opportunities API

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented  Regulatory Affairs Associate  to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe and other global markets for sterile, non-sterile and oral solid/liquid products. This position is based at  Hyderabad, India. Responsibilities: Understanding of Regulatory strategy and documentation requirements for EU variations including renewals, extensions for Sterile (SVP, LVP, lyophilized, ophthalmic etc.), non-sterile and oral solid/liquid products. Collect, prepare, compile regulatory documentation, for the product’s lifecycle maintenance (administrative, quality, safety variations and renewal procedures). Prepare and coordinate responses to Deficiency Letters (DLs) and other CMC-related regulatory queries in collaboration with cross-functional teams Preparation of module 1 documentation for as per assigned timelines for out-licensing and in-licensing products in EU countries Liaise with various departments to collect all necessary information and documentation, in accordance with defined guidelines for Pharmaceutical Dossier submission and product registration Liaise with external Regulatory authorities as required Act as responsible Regulatory Team member for assigned regulatory projects Support internal activities of Regulatory department in order to ensure regulatory compliance of registered products