Specialist, Regulatory Affairs FDF

Centrient Pharmaceuticals Netherlands
Job description
📍 India
💼 Full time
💰 Competitive
📅 Posted 19/02/2026

Job description

Supporting the RA-FDF Team and contributing in the regulatory activities in order to achieve the objectives of the department which are: obtaining global approval for CENTRIENT products, including the lifecycle management of the registration dossiers according to business planning. Key Individual Accountabilities Collection of information and preparation of dossiers and variation packages as and when required. Compilation and update of the product dossiers in portfolio for global and for custom…

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