Company: Sun Pharmaceutical Industries Ltd
Responsibilities:
- Compilation and review of dossier for US, EU, AU, Canada & IL markets.
- Review of query responses prepared and compiled by regulatory associates.
- Manage all activities pertaining to dossier submissions for the aforementioned markets.
- Meet dossier submission and query response timelines as per given targets.
- Review all documents received from stakeholders for dossier compilation, query response, and lifecycle management.
- Allocate projects to regulatory associates and manage the team for all regulatory submission activities.
- Lifecycle management for US, Canada & IL markets.
- Act as the single point of contact for all regulatory submission activities for IL and Palestine markets.
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