Job Role International Regulatory Affairs Responsible for compilation submission of Dossier of a generic drug Hand on experience in Filing dossiers to regulated emerging and ROW markets Experienced in CTD ACTD and Regional Module Experience in Filing in EU ASEAN MIDDLE EAST AND LATAM regions To obtain approvals for relevant product marketing Registration Certificates and export permission Key Responsibilities 1 The Responsible for task involving evaluating dossiers queries and compilation of critical dossiers and queries as and when required This includes search retrieval editing of data logically for preparation of dossier query 2 Will be responsible for maintaining high moral discipline and secrecy of the Regulatory Affairs Department with effective correspondence liaison with manufacturing plants for timely procuring the required data for dossier preparation 3 Experience with Injectable is a must A combination of medical devices and pharma will be a plus Desired candidate profile 1 Minimum 4-8 years of experience in Pharmaceutical Regulatory Affairs 2 Worked with Pharmaceutical Formulation Regulatory department 3 Hands on experience to manage formulation regulatory Job Type Full time Pay 30 000 00 - 70 000 00 per month Work Location In person

📌 Manager - Regulatory Affairs (row) (New Delhi)
🏢 Curiza LIfeciences
📍 New Delhi