Regulatory Affairs Associate for managing new drug registrations and preparing documentation in the India Market. Collaborating with stakeholders and supporting compliance in bulk drug registration.
Responsibilities
Actively participate in the file preparation and management of new drug registrations
Support in preparation of documents for tenders
Update and manage internal databases and tools for artworks and dossiers
Participate in the planning, strategy for bulk drug registration
Support the team for new product registrations, labelling, variations
Requirements
1-3 years of experience
Looking for India Market experience
Hands on Experience in SUGAM Portal
Benefits
We are passionate about developing our people, through career development and progression
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