Regulatory Affairs Post-Approval Associate-Europe - DEMO Global Services Center

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