Sr.Executive-Regulatory Affairs(ROW)

Roles and Responsibilities :

• Prepare and compile dossiers for registration and renewal submissions to regulatory authorities in the European region (ROW).
• Ensure compliance with relevant regulations, guidelines, and timelines for drug product registrations.
• Collaborate with cross-functional teams to gather required information and documentation for dossier preparation.
• Review and finalize dossiers before submission to ensure accuracy, completeness, and quality.

Job Requirements :

• 2-6 years of experience in Regulatory Affairs or related field in the pharmaceutical industry.
• Strong understanding of drug regulatory affairs in the ROW market.
• Proficiency in dossier compilation, dossier preparation, RA (Regulatory Affairs), registration processes.