11 Sep
|
Lyka Labs
|
Mumbai
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.
- Robust understanding of drug regulatory affairs in the ROW market.
- Proficiency in dossier compilation, dossier preparation, RA (Regulatory Affairs), registration processes.
📌 Sr.Executive-Regulatory Affairs(ROW) (Mumbai)
🏢 Lyka Labs
📍 Mumbai